Skip to main content
Springer logoLink to Springer
. 2026 Jul 23;40(10):8670–8686. doi: 10.1007/s00464-026-13143-3

Robotic versus open pancreatoduodenectomy after completion of the learning curve: a propensity score–matched and CUSUM analyses of perioperative outcomes

Matteo Aulicino 1, Giuseppe Quero 1,2,4,✉, Claudio Fiorillo 1,2, Roberta Menghi 1,2, Giuseppe Daloiso 1, Flavia Taglioni 1, Claudia Ferrantone 1, Davide De Sio 1, Antonio Pio Tortorelli 1,2, Vincenzo Tondolo 2,3, Sergio Alfieri 1,2
PMCID: PMC13633149  PMID: 42489883

Abstract

Background

Robotic pancreatoduodenectomy (R-PD) has emerged as a minimally invasive alternative to open pancreatoduodenectomy (O-PD), although its role remains debated due to technical complexity and heterogeneous outcomes. This study compared perioperative outcomes between R-PD and O-PD in a high-volume center while minimizing the impact of the learning curve, and additionally evaluated the progressive improvement in surgical outcomes between the early and late phases of the robotic experience through comparative analyses and CUSUM assessment.

Methods

A single-center propensity score–matched retrospective cohort study was conducted using a prospectively maintained database of patients undergoing PD between January 2020 and December 2025. The most recent 50 consecutive R-PDs (late group, LR-PD) were compared with O-PD after 2:1 matching (matched open group, MO-PD) to balance baseline characteristics. Perioperative, postoperative, and pathological outcomes were compared, and multivariable analyses were performed to identify independent predictors of key outcomes. A subgroup analysis comparing the first 50 R-PDs (early group, ER-PD) with the subsequent 50 cases (LR-PD) was also performed, along with CUSUM analyses of outcomes showing differences between the two phases of the robotic experience.

Results

After matching, 100 MO-PD patients were compared with 50 LR-PD patients. LR-PD was associated with significantly lower estimated blood loss (EBL) (200 vs 300 mL; p = 0.0012) and shorter length of hospital stay (LOS) (12 vs 14 days; p = 0.038), but longer operative time (OT) (582 vs 362 minutes; p < 0.001). Rates of major complications (Clavien–Dindo ≥ III) and pancreas-specific complications were comparable between groups. A significantly lower incidence of postoperative lymphatic fistula was observed in the LR-PD (4 vs 15%; p = 0.045). At multivariable analysis, the LR-PD was independently associated with lower EBL (β − 116.80; p = 0.023), shorter LOS (β − 1.48; p = 0.041), and a reduced risk of postoperative lymphatic fistula (OR 0.30; p = 0.047), while remaining an independent predictor of longer OT (β 99.75; p < 0.001). Within the R-PD, OT was significantly shorter in the LR-PD compared with the ER-PD (582 vs 705 minutes; p < 0.001). CUSUM analyses identified inflection points at cases 51, 55, and 53 for OT, major complications, and clinically relevant PPH, respectively.

Conclusions

In a high-volume setting after the learning curve, R-PD is a potentially safe and feasible alternative to O-PD, offering reduced EBL, shorter LOS, and lower incidence of lymphatic fistula, despite longer OT. Further prospective studies are warranted to confirm these findings.

Graphical abstract

graphic file with name 464_2026_13143_Figa_HTML.webp

Supplementary Information

The online version contains supplementary material available at https://doi.org/10.1007/s00464-026-13143-3.

Keywords: Robot-assisted pancreaticoduodenectomy, Pancreaticoduodenectomy, CUSUM analysis, Perioperative outcomes, Learning curve


Pancreatoduodenectomy (PD) is one of the most complex procedures in abdominal surgery and represents the standard surgical treatment for malignant and selected benign diseases of the pancreatic head and periampullary region [1–4]. Despite substantial improvements in surgical technique, perioperative management, and the centralization of pancreatic surgery, PD remains associated with considerable morbidity, even in high-volume centers [5, 6].

In recent years, minimally invasive approaches have been increasingly adopted in pancreatic surgery with the aim of reducing surgical trauma while preserving oncological adequacy [7–9]. In this context, robotic pancreatoduodenectomy (R-PD) has gained growing attention as a potential alternative to conventional open pancreatoduodenectomy (O-PD) [10, 11]. The robotic platform offers several technical advantages, including three-dimensional high-definition visualization, tremor filtration, and articulated instruments, which may facilitate more precise dissection and the execution of complex reconstructive steps [12, 13].

Despite these potential benefits, the effectiveness of R-PD remains debated. Its adoption is still limited by the technical complexity of the procedure, longer operative times, and the substantial learning curve required to achieve stable perioperative outcomes [14–17]. Moreover, the currently available literature reports heterogeneous results compared with other approaches, likely reflecting differences in patient selection, institutional experience, and the inclusion of cases performed during the early phases of robotic program implementation [14, 15].

In this setting, comparative studies controlling for baseline differences between surgical approaches are essential to better define the role of R-PD in clinical practice. Propensity score–matched (PSM) analyses may help reduce selection bias and provide a more balanced comparison between robotic and open techniques.

Therefore, the aim of the present study was to compare perioperative outcomes between R-PD and O-PD in a high-volume tertiary referral center using a propensity score–matched cohort. To minimize the impact of the learning curve, the analysis was limited to cases performed by a single surgeon after completion of the initial robotic experience. In addition, a comparison of perioperative outcomes between the early and late phases of the robotic surgical experience was performed, together with a CUSUM analysis of the outcomes that differed between the early and late phases of the learning curve.

Methods

This single-center propensity score–matched retrospective cohort study analyzed data from a prospectively maintained institutional database of patients undergoing R-PD or O-PD between January 2020 and December 2025 at the Pancreatic Surgery Unit of the Fondazione Policlinico Universitario A. Gemelli IRCCS of Rome.

Inclusion criteria were adult patients (≥ 18 years) diagnosed with pancreatic or periampullary diseases, including pancreatic ductal adenocarcinoma (PDAC), periampullary neoplasms (tumors of the ampulla of Vater or distal bile duct), cystic pancreatic neoplasms requiring surgical resection, pancreatic neuroendocrine tumors, and other benign or malignant conditions requiring pancreatic head resection.

All cases were evaluated by a multidisciplinary team (MDT) to determine surgical indication and resectability. All patients were thoroughly informed about the potential risks and benefits of the procedure, and written informed consent for surgery was obtained.

The following baseline characteristics were collected: age, sex, body mass index (BMI), American Society of Anesthesiologists (ASA) score [18], Charlson Comorbidity Index (CCI) [19], insulin-dependent diabetes, histological diagnosis, tumor size, tumor resectability according to National Comprehensive Cancer Network (NCCN) criteria [20] (resectable or borderline resectable), neoadjuvant treatment (NAT), vascular resection, pancreatic texture (soft or hard), main pancreatic duct diameter, and Fistula Risk Score (FRS) [21].

Perioperative variables included operative time (OT), estimated blood loss (EBL), perioperative blood transfusion, length of hospital stay (LOS), reintervention, and readmission rates. Postoperative complications were graded according to the Clavien–Dindo (CD) classification [22]. Pancreas-specific complications, including postoperative pancreatic fistula (POPF) [23], delayed gastric emptying (DGE) [24], bile leak [25], and postpancreatectomy hemorrhage (PPH) [26], were defined according to the International Study Group of Pancreatic Surgery (ISGPS) criteria. The occurrence of postoperative lymphatic (chylous) fistula was also recorded.

Histopathological outcomes included the number of harvested lymph nodes and resection margin status (R status), defined according to the Royal College of Pathologists criteria [27]. Postoperative mortality was defined as death occurring within 30 days after surgery.

Study outcomes

The primary endpoint of the study was the comparison between O-PD and R-PD in terms of postoperative outcomes, including major postoperative complications (CD grade ≥ III), pancreas-specific complications, reintervention rate, readmission rate, and length of hospital stay.

Secondary endpoints included intraoperative and pathological outcomes, specifically OT, EBL, perioperative blood transfusion, number of harvested lymph nodes, and resection margin status.

For this analysis, only the most recent 50 consecutive R-PD procedures (late group: LR-PD) were included, based on evidence suggesting that approximately 40–60 cases are required to overcome the learning curve and achieve stable perioperative outcomes [16, 28, 29]. This approach was adopted to reduce the potential impact of the learning curve and to ensure a more homogeneous level of surgical proficiency.

To minimize selection bias, outcomes were compared after PSM. Propensity scores were estimated using a logistic regression model, with surgical approach (O-PD vs LR-PD) as the dependent variable and baseline characteristics as covariates. Matching was performed using a 2:1 nearest-neighbor method without replacement. The matched groups (matched open group: MO-PD and LR-PD) were subsequently compared in terms of baseline characteristics as well as intraoperative, postoperative, and pathological outcomes.

Outcomes showing statistically significant differences between groups were subsequently included in multivariable regression analyses to assess the independent effect of surgical approach and to identify additional factors associated with each outcome.

Furthermore, an additional supplementary comparison was also performed between the overall O-PD population and the overall R-PD population. Finally, in order to further evaluate the impact of the learning curve, a subgroup analysis was performed comparing the entire cohort of patients undergoing O-PD with the first 50 R-PD procedures (early robotic group: ER-PD) and the subsequent 50 cases (late robotic group: LR-PD), assessing differences in baseline characteristics as well as perioperative and pathological outcomes among the groups. Subsequently, a CUSUM analysis was performed for the outcomes that showed differences between the ER-PD and LR-PD groups in order to identify the turning point of the robotic learning curve and to evaluate the progressive improvement in surgical performance and perioperative outcomes with increasing operative experience.

Robotic pancreatic surgery program and surgical training

The robotic pancreatic surgery program at our institution was initiated in 2023 within an established high-volume pancreatic surgery unit performing more than 80 PD annually.

Implementation of R-PD followed a structured and progressive institutional pathway supported by prior experience in advanced minimally invasive pancreatic procedures and extensive training in hepatopancreatobiliary surgery. The surgeon performing all R-PDs included in the present study had previously completed dedicated robotic surgical training and had gained progressive experience in complex robotic abdominal surgery before initiating the R-PD program.

During the initial phase of the program, patient selection was deliberately restricted to technically favorable cases, including absence of major vascular involvement, lower BMI, and tumors without locally advanced features. With increasing experience, indications were progressively expanded to include more complex resections requiring vascular reconstruction, reflecting maturation of the robotic program and completion of the learning curve.

Open pancreatoduodenectomies included during the study period were performed by experienced pancreatic surgeons within the same high-volume institutional setting according to standardized perioperative management protocols shared across the unit.

Statistical analysis

Continuous variables were reported as median (minimum–maximum) and compared using the Student’s t-test or the Mann–Whitney U test, as appropriate based on data distribution. Categorical variables were expressed as frequencies and percentages and compared using the χ2 test.

Propensity score matching was performed using a logistic regression model, with surgical technique (O-PD vs LR-PD) as the dependent variable. Covariates included baseline characteristics showing a potential imbalance between groups (p ≤ 0.100). Propensity scores were matched using a 2:1 nearest-neighbor matching method without replacement.

Multivariable analyses were performed including variables with a univariate p-value ≤ 0.100. Logistic regression models were used for binary outcomes, whereas linear regression models were applied for continuous outcomes.

Cumulative sum (CUSUM) analyses were performed for the outcomes that showed differences or trends toward significance between the ER-PD and LR-PD groups (p ≤ 0.100).CUSUM curves were constructed by sequentially calculating the cumulative sum of the difference between each individual outcome and the overall cohort mean (for continuous variables) or expected event rate (for binary outcomes). The inflection point of each curve was considered indicative of the transition from the initial learning phase to a more stable phase of surgical performance.

Statistical significance was defined as a two-sided p-value < 0.05, and confidence intervals (CI) were calculated at the 95% level. All statistical analyses were performed using IBM SPSS Statistics version 25.

Results

Comparison of outcomes between unmatched O-PD and R-PD cohorts

During the study period, 398 consecutive PDs were performed at the Pancreatic Surgery Unit of the Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy. Of these, 298 patients (74.9%) underwent O-PD and 100 (25.1%) R-PD.

Baseline characteristics of O-PD and R-PD cohorts are summarized in Supplementary Material 1. No statistically significant differences were observed between groups regarding age, sex, BMI, ASA score, CCI, pancreatic texture, Wirsung duct diameter, or FRS. However, patients undergoing R-PD presented significantly smaller tumors (25 (6–32) vs 28 (17–41); p = 0.041), lower rates of borderline-resectable disease (9 (9%) vs 57 (19.1%); p = 0.018), lower rates of NAT (13 (13%) vs 77 (25.8%); p = 0.007), and significantly fewer vascular resections (6 (6%) vs 62 (20.8%); p < 0.001) compared with the O-PD cohort.

Intraoperative and postoperative outcomes of O-PD and R-PD cohorts are reported in Supplementary Material 2.

OT was significantly longer in the R-PD group compared with O-PD (640 (479–980) vs 389 (210–760) minutes; p < 0.001), whereas EBL was significantly lower following R-PD (200 (0–1500) vs 350 (0–2400) mL; p < 0.001). In addition, R-PD was associated with a significantly shorter LOS (13 (5–94) vs 15 (6–91) days; p = 0.022). No statistically significant differences were observed between groups regarding harvested lymph nodes, R1 resection rate, perioperative blood transfusion, major postoperative complications, CR-PPH, CR-POPF, bile leak, DGE, reinterventions, or readmission rates.

Comparison of outcomes between unmatched O-PD cohort and early and late phases of R-PD

Baseline characteristics of patients undergoing O-PD, ER-PD and LR-PD are reported in Table 1.

Table 1.

Baseline characteristics comparison between unmatched O-PD, ER-PD, and LR-PD cohorts

Variable O-PD
298
ER-PD
50
LR-PD
50
P (O vs ER) P (O vs LR) P (ER vs LR)
Age, median (min–max) 68 (31–85) 67 (18–79) 66.5 (40–80) 0.458 0.114 0.909
Gender, n (%) 0.404 0.449 0.224
 Male 172 (57.71) 32 (64) 26 (52)
 Female 126 (42.28) 18 (36) 24 (48)
BMI, median (min–max) 24.87 (17–38) 24.12 (18–34) 23.72 (19–37) 0.586 0.387 0.547
ASA, n (%) 0.432 0.837 0.656
 < 3 204 (68.45) 37 (74) 35 (70)
 ≥ 3 94 (31.54) 13 (26) 15 (30)
CCI, median (min–max) 5 (2–10) 4 (3–7) 4 (2–7) 0.295 0.214 0.709
Insulin-dependent diabetes, n (%) 0.748 0.362 0.662
 Yes 77 (25.83) 14 (28) 16 (32)
 No 221 (74.16) 36 (72) 34 (68)
Hystological type, n (%)
 PDAC of the pancreatic head 229 (76.84) 33 (66) 35 (70) 0.092 0.245 0.668
 Ampully tumor 10 (3.35) 2 (4.25) 3 (6.38) 0.611 0.288 0.645
 IPMN 19 (6.37) 5 (10.64) 4 (8.51) 0.215 0.585 0.725
 Distal cholangiocarcinoma 10 (3.35) 2 (4) 2 (4) 0.808 0.534 1
 Other 30 (10.06) 8 (17.02) 6 (12.76) 0.119 0.573 0.562
Tumor size, n (%) 28 (17–41) 23.5 (6–31) 26 (16–32) 0.038 0.095 0.117
Bordeline-resectable, n (%) 0.023 0.225 0.294
 Yes 57 (19.12) 3 (6) 6 (12)
 No 241 (80.87) 47 (94) 44 (88)
Neoadjuvant treatment, n (%) 0.034 0.097 0.766
 Yes 77 (25.83) 6 (12) 7 (14)
 No 221 (74.16) 44 (88) 43 (86)
Vascular resection, n (%) 0.002 0.072 0.092
 Yes 62 (20.8) 1 (2) 5 (10)
 No 236 (79.19) 48 (98) 45 (90)
Pancreatic texture, n (%) 0.953 0.829 0.826
 Soft 106 (35.57) 18 (36) 17 (34)
 Hard 192 (64.42) 32 (64) 33 (66)
Wirsung diameter, median (min–max) 4 (1–12) 4 (1–10) 3.5 (1–10) 0.864 0.923 0.833
Fistula risk score, median (min–max) 9 (4–14) 7 (3–13) 8 (3–14) 0.128 0.256 0.799

Statistical significance was set at p < 0.05): statistically significant values are given in bold

BMI body mass index, ASA American Society of Anesthesiologists Score, CCI Charlson Comorbidity Index, PDAC pancreatic ductal adenocarcinoma, IPMN Intraductal papillary mucinous neoplasm

Compared with the O-PD cohort, patients undergoing ER-PD showed significantly smaller tumor size (23.5 (6–31) vs 28 (17–41); p = 0.038), lower rates of borderline-resectable disease (3 (6%) vs 57 (19.2%); p = 0.023), lower rates of neoadjuvant treatment (6 (12%) vs 77 (25.83%); p = 0.034), and significantly fewer vascular resections (1 (2%) vs 62 (20.8%); p = 0.002). However, when comparing O-PD with LR-PD, these differences did not reach statistical significance. No significant differences were found among groups regarding age, sex, BMI, ASA score, CCI, Wirsung duct diameter, or FRS.

When comparing the two robotic subgroups, no statistically significant differences were observed in demographic, clinical, or tumor related characteristics. However, a non-significant trend toward larger tumor size (23.5 (6–31) vs 26 (16–32); p = 0.117), and an hight rate of vascular resections (1 (2%) vs 5 (10%); p = 0.092) was observed in the LR-PD group.

Conversion to open surgery occurred in 3 of 50 ER-PDs (6%) and 3 of 50 LR-PDs (6%) because of intraoperative technical difficulties and/or oncological concerns.

Intraoperative and postoperative outcomes of patients undergoing O-PD, ER-PD and LR-PD are summarized in Table 2.

Table 2.

Intraoperative and postoperative outcomes of unmatched O-PD, ER-PD and R-PD cohorts

Variable O-PD
298
ER-PD
50
LR-PD
50
P (O vs ER) P (O vs LR) P (ER vs LR)
OT, median (min–max) 389 (210–760) 705 (497–980) 582 (479–810)  < 0.001  < 0.001  < 0.001
EBL, median (min–max) 350 (0–2400) 200 (0–1100) 200 (0–1500) 0.011 0.006 0.397
Harvested nodes, median (min–max) 19 (6–72) 17 (9–38) 18 (11–43) 0.283 0.365 0.412
R1, n (%) 89 (29.86) 12 (24) 14 (28) 0.397 0.789 0.674
Peri-operative blood transfusion, n (%) 0.516 0.219 0.663
 Yes 91 (30.53) 13 (26) 11 (22)
 No 207 (70.14) 37 (74) 39 (78)
Major complications (CD grade ≥ III), n (%) 116 (38.92) 23 (46) 15 (30) 0.227 0.359 0.099
 Grade IIIa 61 (20.46) 11 (22) 8 (16) 0.307 0.463 0.444
 Grade IIIb 27 (9.06) 3 (6) 3 (6) 0.475 0.475 1.000
 Grade IV 16 (5.36) 7 (14) 2 (4) 0.023 0.685 0.088
 Grade V/30-day mortality 12 (4.03) 2 (4) 2 (4) 0.992 0.992 1.000
PPH grade B/C, n (%) 45 (15.10) 14 (28) 7 (14) 0.024 0.839 0.076
 Grade B 28 (9.39) 9 (18) 4 (8) 0.067 0.751 0.137
 Grade C 17 (5.70) 5 (10) 3 (6) 0.248 0.933 0.460
POPF grade B/C, n (%) 87 (29.19) 15 (30) 14 (28) 0.907 0.863 0.826
 Grade B 75 (25.17) 13 (26) 11 (22) 0.900 0.630 0.640
 Grade C 12 (4.03) 2 (4) 3 (6) 0.992 0.524 0.646
Post operative bile leak grade B/C, n (%) 24 (8.05) 6 (12) 4 (8) 0.357 0.989 0.504
 Grade B 14 (4.70) 4 (8) 3 (6) 0.329 0.692 0.695
 Grade C 10 (3.36) 2 (4) 1 (2) 0.817 0.612 0.557
DGE grade B/C, n (%) 62 (20.80) 14 (28) 9 (18) 0.254 0.648 0.234
 Grade B 47 (15.77) 10 (20) 6 (12) 0.454 0.492 0.275
 Grade C 15 (5.03) 4 (8) 3 (6) 0.392 0.775 0.695
Post operative lymphatic fistula, n (%) 0.492 0.026 0.140
 Yes 47 (15.77) 6 (12) 2 (4)
 No 253 (84.23) 44 (88) 48 (96)
Re-interventions, n (%) 116 (38.92) 23 (46) 17 (34) 0.344 0.507 0.220
 Radiological 51 (19.46) 10 (20) 9 (18) 0.619 0.878 0.799
 Endoscopic 21 (7.38) 3 (6) 2 (4) 0.511 0.422 0.646
 Surgical reoperation 34 (11.41) 10 (20) 6 (12) 0.091 0.903 0.275
LOS, median (min–max) 15 (6–91) 14 (5–94) 12 (6–40) 0.492 0.019 0.154
Re-admission, n (%) 65 (21.81) 10 (20.0) 11 (22) 0.773 0.976 0.806

Statistical significance was set at p < 0.05): statistically significant values are given in bold

OT operative time, EBL estimate blood loss, CD Clavien Dindo, PPH postpancreatectomy haemorrhage, POPF postoperative pancreatic fistula, DGE delayed gastric emptying, LOS lenght of stay

OT was significantly longer in both ER-PD and LR-PD than in O-PD (705 (497–980) vs 389 (210–760) minutes; p < 0.001 and 582 (479–810) vs 389 (210–760) minutes; p < 0.001, respectively). Nevertheless, a significant reduction in OT was observed between the ER-PD and LR-PD groups (705 (497–980) vs 582 (479–810) minutes; p < 0.001).

EBL was significantly lower in both robotic groups than in O-PD (200 (0–1100) vs 350 (0–2400) mL; p = 0.011 for ER-PD and 200 (0–1500) vs 350 (0–2400) mL; p = 0.006 for LR-PD), whereas no statistically significant difference emerged between ER-PD and LR-PD (p = 0.397).

The ER-PD group showed significantly higher rates of CD grade IV complications (7 (14%) vs 16 (5.36%); p = 0.023) and clinically relevant PPH (14 (28%) vs 45 (15.1%); p = 0.024) than O-PD, while these differences were no longer evident in the LR-PD cohort.

Conversely, LR-PD was associated with a significantly lower rate of postoperative lymphatic fistula (1 (4%) vs 47 (15.77%); p = 0.026) and a shorter LOS (12 (6–40) vs 15 (6–91) days; p = 0.019) relative to O-PD.

Within the robotic cohort, a non-significant trend toward higher rates of major postoperative complications (CD ≥ III) was observed in the ER-PD compared with the LR-PD (23 (46% vs 15 (30%); p = 0.099), with more evident differences for CD grade IV complications (7 (14%) vs 2 (4%); p = 0.088) and CR-PPH (14 (28%) vs 7 (14%); p = 0.076).

No significant differences were observed among groups regarding harvested lymph nodes, R1 resection rate, perioperative blood transfusion, CR-POPF, bile leak, DGE, reinterventions, or readmission rates.

CUSUM analysis of outcomes showing differences between early and late phases of the R-PD learning curve

Operative time

CUSUM analysis of OT demonstrated a clear learning curve effect throughout the study period (Fig. 1). During the initial phase of the robotic experience, the curve showed a progressive upward trend, reflecting OT above the cohort mean and greater variability between consecutive procedures. This phase was followed by a plateau and subsequent downward slope, indicating progressive improvement in operative efficiency and increasing procedural standardization. The main inflection point of the CUSUM curve was identified at case 51, suggesting transition from the initial learning phase to a more reproducible phase of operative performance.

Fig. 1.

Fig. 1

Flow chart of patient’s selection

Major complications

CUSUM analysis for major postoperative complications (CD ≥ III) also demonstrated a learning curve effect during the study period (Fig. 2). The curve showed a progressive increase during the initial and intermediate phases of the robotic experience, indicating accumulation of major postoperative events above the expected cohort rate. After reaching the main inflection point at case 55, the curve progressively stabilized and subsequently declined, suggesting improvement in postoperative outcomes with increasing surgical experience.

Fig. 2.

Fig. 2

CUSUM analysis of operative time during the robotic pancreatoduodenectomy learning curve

Clinically relevant PPH

CUSUM analysis for CR-PPH demonstrated a similar trend throughout the robotic experience (Fig. 3). During the initial phase, the curve showed a progressive upward slope, reflecting a higher incidence of clinically relevant hemorrhagic events. Following the main inflection point identified at case 53, the curve progressively stabilized and subsequently declined, suggesting improved bleeding control and increasing technical proficiency during the later phase of the robotic learning curve.

Fig. 3.

Fig. 3

CUSUM analysis of major postoperative complications (Clavien–Dindo ≥ III) during the robotic pancreatoduodenectomy learning curve

Post-PSM comparison of perioperative outcomes between MO-PD and LR-PD

To minimize the impact of baseline imbalances between the O-PD and LR-PD cohorts, a PSM analysis was performed. As reported in Table 1, vascular resection (62 (20.8%) vs 5 (10%); p = 0.072), tumor size (28 (17–41) vs 26 (16–32); p = 0.095) and NAT (77 (25.83%) vs 7 (14%); p = 0.097) showed a trend toward imbalance. These variables were therefore included as covariates in the propensity score model (Fig. 4).

Fig. 4.

Fig. 4

CUSUM analysis of clinically relevant postpancreatectomy hemorrhage (CR-PPH) during the robotic pancreatoduodenectomy learning curve

After PSM, 100 patients in the MO-PD group were compared with 50 patients in the LR-PD group. Post-matching analysis confirmed adequate balance between groups, with no statistically significant differences in baseline characteristics (Supplementary Material 3).

Intraoperative and postoperative outcomes are reported in Table 3. MO-PD was associated with a significantly shorter OT compared with LR-PD (362 (210–680) vs 582 (479–810) minutes; p < 0.001), whereas EBL was significantly lower in the LR-PD group (200 (0–1500) vs 300 (0–2100) mL; p = 0.007). No significant differences were observed in the number of harvested lymph nodes and R status. Rates of perioperative blood transfusion and CD ≥ III complications were comparable between groups. Similarly, no significant differences were found in terms of CR-POPF, PPH, bile leak, or DGE. A significantly lower incidence of postoperative lymphatic fistula was observed in the LR-PD group compared with the MO-PD group (2 (4%) and 15 (15%), respectively; p = 0.045).

Table 3.

Intraoperative and postoperative outcomes of MO-PD vs LR-PD

Variable MO-PD
100
LR-PD
50
P-value
OT, median (min–max) 362 (210–680) 582 (479–810)  < 0.001
EBL, median (min–max) 300 (0–2100) 200 (0–1500) 0.012
Harvested nodes, median (min–max) 20 (6–69) 18 (11–43) 0.348
R1, n (%) 28 (28) 15 (30) 0.798
Peri-operative blood transfusion, n (%) 0.685
 Yes 25 (25) 11 (22)
 No 75 (75) 39 (78)
Major complications (CD grade ≥ III), n (%) 36 (36) 16 (32) 0.809
 Grade IIIa 19 (19) 9 (18) 0.882
 Grade IIIb 8 (8) 3 (6) 0.657
 Grade IV 4 (4) 2 (4) 1
 Grade V/30-day mortality 5 (5) 2 (4) 0.784
PPH grade B/C, n (%) 13 (13) 7 (14) 0.865
 Grade B 8 (8) 4 (8) 1
 Grade C 5 (5) 3 (6) 0.797
POPF grade B/C, n (%) 28 (28) 14 (28) 1
 Grade B 25 (25) 11 (22) 0.685
 Grade C 4 (4) 3 (6) 0.584
Post Operative Bile leak grade B/C, n (%) 7 (7) 4 (8) 0.824
 Grade B 4 (4) 3 (6) 0.584
 Grade C 3 (3) 1 (2) 0.720
DGE grade B/C, n (%) 19 (19) 9 (18) 0.882
 Grade B 15 (15) 6 (12) 0.617
 Grade C 5 (5) 3 (6) 0.797
Post operative lymphatic fistula, n (%)
 Yes 15 (15) 2 (4) 0.045
 No 85 (85) 48 (96)
Re-interventions, n (%) 36 (36) 17 (34) 0.809
 Radiological 18 (18) 9 (18) 1.000
 Endoscopic 7 (7) 2 (4) 0.466
 Surgical reoperation 11 (11) 6 (12) 0.855
LOS, median (min–max) 14 (6–91) 12 (6–40) 0.038
Re-admission, n (%) 20 (20) 11 (22) 0.676

Statistical significance was set at p < 0.05): statistically significant values are given in bold

OT operative time, EBL estimate blood loss, CD Clavien Dindo, PPH postpancreatectomy haemorrhage, POPF postoperative pancreatic fistula, DGE delayed gastric emptying, LOS lenght of stay

Reintervention rates (radiological, endoscopic, or surgical) and hospital readmission were similar between groups. LOS was significantly shorter in the LR-PD group compared with the MO-PD group (12 (6–36) vs 14 (6–91) days; p = 0.038).

Multivariable analysis of predictors of perioperative outcomes in the matched population

The results of the univariate and multivariable analyses for OT and EBL are reported in Table 4.

Table 4.

Univariate and multivariable analyses of factors associated with OT and EBL in the matched population

All patients
N 150
Prognostic factors analysis for OT (multivariable linear regression) Prognostic factors analysis for EBL (multivariable linear regression)
Univariate Analysis Multivariate Analysis Univariate Analysis Multivariate Analysis
Variable N (%)/median (min–max) B [95% CI] P value B [95% CI] P value B [95% CI] P value B [95% CI] P value
Age 67 (31–83) 1.14 [0.96–3.24] 0.286 0.96 [− 1.23–3.89] 0.386
Gender
 Male 82 (54.66) 17.20 [1.45–33.95] 0.044 8.95 [− 7.78–25.65] 0.270 72.18 [9.24–132.58] 0.027 20.46 [− 36.20–89.67] 0.477
 Female 68 (45.33)
BMI 23.93 (17–37) 1.86 [− 1.92–5.64] 0.333 2.18 [− 3.88–8.24] 0.481
ASA score
 I-II 104 (69.33)
 III 46 (30.66) 16.80 [1.35–32.25] 0.034 14.70 [2.36–27.64] 0.026 37.66 [− 18.32–93.50] 0.187
Charlson Comorbidity Index 4.5 (2–9) 1.62 [− 1.74–7.94] 0.336 8.40 [− 7.20–24.00] 0.290
Insulin-dependent diabetes
 Yes 42 (28) 7.26 [− 5.19–15.54] 0.288 53.20 [− 17.60–124.00] 0.140
 No 108 (72)
Hystological Type
 PDAC of the pancreatic head* 109 (72.66) * * * *
 Ampully tumor 7 (4.66)  − 13.80 [− 41.62–6.26] 0.214  − 16.54 [− 59.83–13.23] 0.305
 IPMN 13 (8.66)  − 7.18 [− 22.44–13.90] 0.392  − 29.17 [− 70.86–16.91] 0.207
 Distal cholangiocarcinoma 6 (4) 2.25 [− 29.82–27.97] 0.561  − 10.12 [− 47.62–16.29] 0.482
 Other 15 (10) 5.40 [− 26.83–34.86] 0.681  − 6.807 [− 30.40–12.12] 0.601
Surgical approach
 Robotic 50 (30) 105.65 [93.39–118.27]  < 0.001 99.75 [84.90–112.50]  < 0.001 −164.47 [−231.2–95.6]  < 0.001  − 116.80 [− 326.1– − 76.2] 0.026
 Open 100 (70)
Tumor size 26 (15–35) 1.18 [− 1.13–3.46] 0.307 3.15 [0.62–5.68] 0.015 1.02 [− 1.29–3.34] 0.386
Neoadjuvant treatment
 Yes 24 (16) 32.14 [9.73–58.59] 0.012 37.26 [5.33–69.17] 0.022 117.434 [22.82–209.02] 0.016 89.70 [62.23–189.63] 0.041
 No 126 (84)
Vascular resection
 Yes 16 (10.66) 35.10 [21.94–63.83] 0.003 61.86 [41.27–82.44]  < 0.001 352.63 [267.82–437.44]  < 0.001 315.05 [216.48–414.67]  < 0.001
 No 134 (89.33)
Harvested nodes 19.5 (6–69) 0.86 [− 0.88–2.61] 0.330 0.78 [− 1.90–3.46] 0.567
Pancreatic texture
 Soft 53 (35.33) 10.46 [− 2.72–22.97] 0.121 134.92 [37.89–226.63] 0.006 144.23 [86.62–287.82] 0.009
 Hard 97 (64.66)
Wirsung diameter 4 (1–12) 1.05 [− 1.30–6.43] 0.380  − 0.58 [− 13.40–4.84] 0.349
Fistula Risk Score 9 (3–14) 2.61 [− 0.76–11.93] 0.181 6.50 [− 5.83–18.84] 0.298

Statistical significance was set at p < 0.05): statistically significant values are given in bold

OT operative time, EBL estimated blood loss, BMI body mass index, ASA American Society of Anesthesiologists score, PDAC pancreatic ductal adenocarcinoma, IPMN intraductal papillary mucinous neoplasm

*Reference category

Operative time

On univariate analysis, male sex (B = 17.20 [1.45–33.95]; p = 0.044), ASA score III–IV (B = 16.80 [1.35–32.25]; p = 0.034), LR-PD (B = 105.65 [93.39–118.27]; p = < 0.001), NAT (B = 32.14 [9.73–58.59]; p = 0.012), and vascular resection (B = 35.10 [21.94–63.83]; p = 0.003) were associated with longer OT.

After adjustment in the multivariable model, ASA score III–IV (B = 14.70 [2.36–27.64]; p = 0.026), LR-PD (B = 99.75 [84.90–112.50]; p < 0.001), NAT (B = 37.26 [5.33–69.17]; p = 0.022), and vascular resection (B = 61.86 [41.27–82.44]; p < 0.001) remained independently associated with longer OT.

Estimated blood loss

At univariate analysis, male sex (B = 72.18 [9.24–132.58]; p = 0.027), tumor size (B = 3.15 [0.62–5.68]; p = 0.015), NAT (B = 117.434 [22.82–209.02]; p = 0.016, vascular resection (B = 352.63 [267.82–437.44]; p < 0.001, and soft pancreatic texture (B = 134.92 [37.89–226.63]; p = 0.006) were associated with higher EBL, whereas LR-PD (B = −164.47 [−231.2–95.6]; p < 0.001) was associated with lower EBL.

In the multivariable model, the robotic approach remained independently associated with lower EBL compared with the open approach (B = − 116.80 [− 326.1 to − 76.2]; p = 0.026), whereas NAT (B = 89.70 [62.23–189.63]; p = 0.041), vascular resection (B = 315.05 [216.48–414.67]; p < 0.001), and soft pancreatic texture (B = 144.23 [86.62–287.82]; p = 0.009) were independently associated with increased EBL.

Multivariable analysis of predictors of length of hospital stay

Factors associated with prolonged LOS are reported in Table 5.

Table 5.

Univariate and multivariable analyses of factors associated with LOS in the matched population

All patients
N 150
Prognostic factors analysis for length of hospitalization (multivariable linear regression)
Univariate analysis Multivariate analysis
Variable N (%)/median (min–max) B [95% CI] P value B [95% CI] P value
Age 67 (31–83) 0.09 [−0.03–0.13] 0.401
Gender 0.79 [−0.31–2.47] 0.191
 Male 82 (54.66)
 Female 68 (45.33)
BMI 23.93 (17–37) 0.16 [−0.09–0.31] 0.387
ASA score
 I-II 104 (69.33)
 III 46 (30.66) 1.59 [0.21–2.98] 0.031 1.31 [0.19–2.27] 0.013
Charlson Comorbidity Index 4.5 (2–9) 0.19 [−0.21–0.59] 0.247
Insulin-dependent diabetes
 Yes 42 (28) 1.46 [−0.81–2.92] 0.156
 No 108 (72)
Hystological type
 PDAC of the pancreatic head * 109 (72.66) * *
 Ampully tumor 7 (4.66) − 0.61 [–1.93–1.68] 0.289
 IPMN 13 (8.66) − 0.76 [–1.25–1.12] 0.192
 Distal cholangiocarcinoma 6 (4) 0.37 [−0.19–1.24] 0.521
 Other 15 (10) 0.29 [−0.29–1.64] 0.512
Surgical approach
 Robotic 50 (30) − 1.82 [–2.85–−0.63]  < 0.001 − 1.48 [−2.38 – −0.39] 0.041
 Open 100 (70)
Tumor size 26 (15–35) 0.03 [−0.01–0.12] 0.268
Neoadjuvant treatment
 Yes 24 (16) 1.19 [−0.13–2.47] 0.081 0.91 [−0.67–1.77] 0.318
 No 126 (84)
Vascular resection
 Yes 16 (10.66) 2.29 [0.69–3.93] 0.021 1.58 [−0.54–2.35] 0.231
 No 134 (89.33)
Harvested nodes 19.5 (6–69) 0.05 [−0.04–0.17] 0.587
Pancreatic texture
 Soft 53 (35.33) 0.73 [−0.39–2.36] 0.219
 Hard 97 (64.66)
Wirsung diameter 4 (1–12) 0.04 [−0.19–0.41] 0.607
Fistula risk score 9 (3–14) 0.25 [−0.25–0.78] 0.391
OT 428 (210–810) 0.008 [0.004–0.009]  < 0.001 0.005 [0.002–0.008] 0.017
EBL 250 (0–2100) 0.002 [0.001–0.005] 0.001 0.0014 [0.0003–0.0024] 0.010
Peri-operative blood transfusion
 Yes 36 (24) 2.04 [1.12–3.01] 0.024 1.29 [−0.98–2.31] 0.142
 No 114 (76)
Major complication (CD ≥ 3)
 Yes 52 (34.66) 5.22 [2.11–6.96]  < 0.001 4.03 [1.08–6.92]  < 0.001
 No 98 (65.33)

Statistical significance was set at p < 0.05): statistically significant values are given in bold

LOS lenght of stay, BMI body mass index, ASA American Society of Anesthesiologists score, PDAC pancreatic ductal adenocarcinoma, IPMN intraductal papillary mucinous neoplasm, OT operative time, EBL estimate blood loss, CD Clavien Dindo

*Reference category

On univariate analysis, ASA score III–IV (B = 1.59 [0.21–2.98]; p = 0.031), vascular resection (B = 2.29 [0.69–3.93]; p = 0.021), OT (B = 0.008 [0.004–0.009]; p < 0.001), EBL (B = 0.002 [0.001–0.005]; p = 0.001), perioperative blood transfusion (B = 2.04 [1.12–3.01]; p = 0.024), and CD ≥ III complications (B = 5.22 [2.11–6.96]; p < 0.001) were associated with prolonged LOS. Conversely, the robotic surgical approach was associated with a shorter LOS (B = −1.82 [–2.85 to −0.63]; p < 0.001).

Following adjustment in the multivariable model, ASA score III–IV (B = 1.31 [0.19–2.27]; p = 0.013), OT (B = 0.005 [0.002–0.008]; p = 0.017), EBL (B = 0.0014 [0.0003–0.0024]; p = 0.010, and CD ≥ III complications (B = 4.03 [1.08–6.92], p < 0.001) were confirmed as independent predictors of prolonged LOS. In contrast, LR-PD remained independently associated with reduced LOS (B = −1.48 [−2.38 to −0.39]; p = 0.041).

Multivariable analysis of predictors of chylous fistula

The variables associated with the development of postoperative chylous fistula are reported in Table 6.

Table 6.

Univariate and multivariable analyses of factors associated with lymphatic fistula in the matched population

Variable Chyle Leak (+)
N 17 pts
Chyle Leak (−)
N 133 pts
Prognostic factors analysis for postoperative chile leak (multivariable logistic regression)
Univariate Analysis Multivariate Analysis
N (%)/Median (min–max) N (%)/median (min–max) OR [95% CI] P value OR [95% CI] P value
Age 69 (45–81) 66 (31–83) 1.04 [0.72–1.11] 0.164
Gender
 Male 11 (64.70) 71 (53.38) 1.89 [0.68–4.94] 0.221
 Femal 6 (35.29) 59 (46.61)
BMI 24.92 (19–32) 24.22 (17–37) 1.05 [0.79–1.21] 0.481
ASA score
 I-II 9 (53) 95 (71.42)
 III 8 (47) 38 (28.57) 2.21 [0.82–5.98] 0.091 1.57 [0.48–4.38] 0.368
Charlson Comorbidity Index 5 (2–9) 4 (2–8) 1.13 [0.86–1.33] 0.216
Insulin-dependent diabetes
 Yes 6 (35) 36 (27.06) 1.55 [0.53–4.53] 0.409
 No 11 (65) 97 (72.93)
Hystological type
 PDAC of the Pancreatic head 12 (70.6) 97 (72.93) * *
Ampully tumor 1 (5.9) 6 (4.51) 1.47 [0.16–13.2] 0.716
 IPMN 1 (5.9) 12 (9.02) 0.67 [0.08–5.2] 0.793
 Distal cholangiocarcinoma 1 (5.9) 5 (3.75) 1.92 [0.17–17.9] 0.526
 Other 2 (11.8) 13 (9.7) 1.29 [0.23–7.1] 0.772
Surgical approach
 Robotic 2 (11.8) 48 (36.09) 0.22 [0.08–0.97] 0.034 0.30 [0.09–0.99] 0.047
 Open 15 (88.2) 85 (63.90)
Tumor size 27 (18–35) 26 (15–34) 1.02 [0.92–1.07] 0.152
Neoadjuvant Treatment
 Yes 6 (35.3) 18 (13.53) 3.32 [1.12–10.87] 0.029 3.02 [1.04–9.05] 0.049
 No 11 (64.7) 115 (86.46)
Vascular resection
 Yes 5 (29.4) 11 (8.27) 5.24 [1.38–18.80] 0.013 2.19 [0.74–9.13] 0.264
 No 12 (70.6) 122 (91.73)
Harvested nodes 22 (12–69) 18 (6–52) 1.07 [1.02–1.18] 0.029 1.03 [0.64–1.11] 0.307
Pancreatic texture
 Soft 5 (29.4) 48 (36.09) 1.52 [0.65–3.94] 0.534
 Hard 12 (70.6) 85 (63.90)
Wirsung diameter 4 (2–11) 4 (1–12) 0.86 [0.63–1.21] 0.837
Fistula risk score 9 (3–9) 8.5 (3–14) 1.08 [0.87–1.21] 0.446

Statistical significance was set at p < 0.05): statistically significant values are given in bold

BMI body mass index, ASA American Society of Anesthesiologists score, PDAC pancreatic ductal adenocarcinoma, IPMN intraductal papillary mucinous neoplasm, CD Clavien Dindo

*Reference category

Univariate analysis identified NAT (OR = 3.32 [1.12–10.87]; p = 0.029), vascular resection (OR = 5.24 [1.38–18.80]; p = 0.013), and increasing number of harvested lymph nodes (OR = 1.07 [1.02–1.18]; p = 0.029) as related to a higher rate of chylous fistula, whereas the robotic surgical approach was associated with a significantly lower risk of this complication (OR = 0.22 [0.08–0.97]; p = 0.034).

When these variables were entered into the multivariable model, only robotic surgical approach (OR = 0.30 [0.09–0.99]; p = 0.047) and NAT (OR = 3.02 [1.04–9.05]; p = 0.049) remained independently associated with the occurrence of chylous fistula, with the robotic approach acting as a protective factor.

Discussion

The present study provides a comparative analysis of R-PD versus MO-PD performed in a high-volume tertiary referral center, with the additional strength of controlling for selection bias through propensity score matching and minimizing the influence of the learning curve. According to our findings, LR-PD was associated with significantly lower EBL and shorter LOS, at the expense of longer OT, while no significant differences were observed in terms of major postoperative complications, pancreas-specific complications, or oncological outcomes.

These results are in line with the current body of evidence comparing minimally invasive and open approaches for PD [30, 31]. One of the most consistent findings in the literature is the trade-off between OT and perioperative benefits. In the present study, LR-PD was associated with a significantly longer OT compared with the open approach, which remained an independent predictor at multivariable analysis. This evidence has been consistently reported across both retrospective series and meta-analyses, with robotic procedures requiring on average 60–90 additional minutes [30, 31]. However, despite longer OT, robotic surgery appears to reduced LOS and EBL, likely due to improved visualization, enhanced dexterity, more precise dissection, and reduced surgical trauma.

In this context, the analysis of the learning curve within the robotic cohort provides additional insight into the evolution of operative performance over time. When comparing the early and late phases of the robotic experience, OT was significantly reduced in the LR-PD, while other intraoperative and postoperative outcomes remained comparable between groups. This finding was further supported by the CUSUM analysis for OT, which identified a clear inflection point at case 51, followed by a progressive downward trend of the curve, suggesting increasing operative efficiency and procedural standardization with growing surgical experience. A non-significant trend toward lower rates of major postoperative complications, including CD grade IV complications and clinically relevant PPH, was also observed in the late phase. Although these differences did not reach statistical significance, the corresponding CUSUM analyses demonstrated a progressive stabilization and subsequent decline of both major complications and clinically relevant PPH after cases 55 and 53, respectively. These results support the hypothesis that increasing robotic experience may contribute to improved perioperative management, bleeding control, and reduction of severe postoperative morbidity over time. Notably, these findings emerged despite a trend toward increased case complexity, characterized by larger tumor size and a higher rate of vascular resections, suggesting progressive expansion of surgical indications with increasing experience. These results are consistent with previous reports demonstrating improvement and stabilization of perioperative outcomes after completion of the learning curve for R-PD [16, 28, 29].

Nevertheless, the persistence of longer OT in the robotic group compared with the open approach, even after completion of the learning curve, deserves specific consideration. R-PD inherently includes additional procedural steps, such as docking and instrument exchange, which are not required in open surgery, while the fully intracorporeal reconstructive phase remains technically demanding and time-consuming even in experienced hands. Moreover, the later phase of the robotic experience was characterized by a progressive expansion of surgical indications toward more complex cases, which may have contributed to maintaining longer OT despite increasing surgical proficiency. Similar results have been reported in other high-volume series [30, 31], suggesting that OT may remain longer than in open surgery even after stabilization of perioperative outcomes and completion of the learning curve, without negatively affecting postoperative morbidity or oncological adequacy.

Two other important results of the present study are the significantly lower EBL and shorter LOS observed in the LR-PD group, both of which remained independently associated with the robotic approach after adjustment for potential confounding factors. This finding are strongly supported by the literature [30, 31]. In particular, a large meta-analysis including more than 50,000 patients reported significantly lower EBL and shorter LOS in the robotic group, while rates of major complications and oncological outcomes remained comparable between approaches [31]. From a clinical perspective, reduced EBL may translate into lower transfusion requirements and potentially improved postoperative recovery, although no significant differences in transfusion rates were observed in our cohort. Similarly, the shorter LOS associated with R-PD may reflect the minimally invasive nature of the procedure, resulting in reduced surgical trauma, faster recovery of gastrointestinal function, and earlier postoperative mobilization.

In contrast, no significant differences were observed between the two approaches in terms of major postoperative complications, including CR-POPF, DGE, PPH, and bile leak. These findings are consistent with both randomized and non-randomized studies [32, 33], which have demonstrated comparable perioperative safety between robotic and open pancreatoduodenectomy. Importantly, the absence of increased complication rates in the robotic group supports the safety of this approach when performed in experienced centers.

From an oncological standpoint, the two approaches yielded similar results in terms of lymph node harvest and R status. These findings are in line with previous studies demonstrating equivalent oncological adequacy between R-PD and O-PD [30, 34, 35]. The preservation of oncological outcomes is a critical prerequisite for the adoption of minimally invasive techniques in pancreatic surgery, and the present study further supports the oncological safety of R-PD in a high-volume setting.

An interesting finding of the present study concerns postoperative lymphatic/chylous fistula. In our analysis, the LR-PD was associated with a significantly lower incidence of lymphatic fistula compared with the open technique, and this protective effect was confirmed at multivariable analysis. Although data on this specific complication are relatively limited in the literature, this finding may be explained by the technical advantages of the robotic platform. Enhanced three-dimensional visualization and improved instrument articulation may allow for more precise identification and sealing of lymphatic vessels during lymphadenectomy and dissection along major vascular structures. In addition, the stability of the robotic platform may contribute to more meticulous tissue handling, potentially reducing lymphatic leakage.

These findings are in line with emerging evidence suggesting that minimally invasive approaches, particularly robotic surgery, may reduce certain procedure-specific complications through improved surgical precision. However, given the relatively low incidence of chylous fistula and the heterogeneity in its definition and reporting across studies, further investigations are warranted to confirm this potential benefit and to better elucidate the underlying mechanisms.

A key strength of the present study is the deliberate exclusion of the initial learning curve for R-PD from the comparative PSM comparison with the open approach. It is well established that outcomes of minimally invasive pancreatic surgery are highly dependent on surgeon experience and institutional volume [29, 32, 33, 36]. By including only cases performed after completion of the learning curve, the present analysis provides a more accurate representation of the “steady-state” performance of the robotic approach. This methodological choice likely reduces heterogeneity and enhances the validity of the comparison with open surgery.

In addition, the use of PSM represents another important strength, as it allows for adjustment of baseline differences between groups and reduces selection bias inherent to retrospective studies. Although randomized controlled trials remain the gold standard, they are still limited in this field, and high-quality observational studies with robust statistical adjustment continue to play a crucial role in informing clinical practice.

Despite these strengths, several limitations of the present study should be acknowledged. First, the retrospective design inherently exposes the analysis to residual confounding, even after PSM. Second, this is a single-center study conducted in a high-volume tertiary referral center, which may limit the generalizability of the results to lower-volume institutions. In addition, all R.PD were performed by a single experienced surgeon, whereas open procedures were carried out by multiple surgeons, potentially introducing a surgeon-related bias. Third, long-term oncological outcomes, including disease-free and overall survival, were not evaluated and therefore no conclusions can be drawn regarding the long-term effectiveness of the robotic approach. Finally, although the learning curve effect was minimized, the relatively small sample size of the robotic cohort may limit the statistical power for detecting differences in less frequent outcomes.

Therefore, despite the relevant findings of the present study, further prospective and multicenter investigations are required to confirm these results and to better define the role of robotic pancreatoduodenectomy in contemporary pancreatic surgical practice.

Conclusion

In a high-volume tertiary referral center and after completion of the learning curve, R-PD represents a valid alternative to O-PD, being associated with reduced EBL, shorter LOS, and a lower incidence of postoperative lymphatic fistula, albeit at the cost of longer OT. Importantly, no differences were observed in major postoperative complications or oncological outcomes, supporting the safety and feasibility of the robotic approach in experienced centers.

Supplementary Information

Below is the link to the electronic supplementary material.

Funding

Open access funding provided by Università Cattolica del Sacro Cuore within the CRUI-CARE Agreement. This research received no external funding.

Declarations

Disclosures

Dr. Matteo Aulicino, Dr. Giuseppe Quero, Dr. Claudio Fiorillo, Dr. Roberta Menghi, Dr. Giuseppe Dalioso, Dr. Flavia Tagliani, Dr. Claudia Ferrantone, Dr. Davide De Sio, Dr. Antonio Pio Tortorelli, Dr. Vincenzo Tondolo, and Prof. Sergio Alfieri declare that they have no conflicts of interest or financial ties to disclose.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.D’Cruz JR, Misra S, Menon G, Shamsudeen S (2026). Pancreaticoduodenectomy (Whipple procedure). In: StatPearls. Treasure Island, FL: StatPearls Publishing [PubMed]
  • 2.Hidalgo M (2010) Pancreatic cancer. N Engl J Med 362:1605–1617. 10.1056/NEJMra0901557 [DOI] [PubMed] [Google Scholar]
  • 3.Winter JM, Cameron JL, Campbell KA, Arnold MA, Chang DC, Coleman J et al (2006) 1423 pancreaticoduodenectomies for pancreatic cancer: a single-institution experience. J Gastrointest Surg 10:1199–1210. 10.1016/j.gassur.2006.08.018. (discussion 1210-1) [DOI] [PubMed] [Google Scholar]
  • 4.Cameron JL, He J (2015) Two thousand consecutive pancreaticoduodenectomies. J Am Coll Surg 220:530–536. 10.1016/j.jamcollsurg.2014.12.031 [DOI] [PubMed] [Google Scholar]
  • 5.Gooiker GA, Lemmens VEPP, Besselink MG, Busch OR, Bonsing BA, Molenaar IQ et al (2014) Impact of centralization of pancreatic cancer surgery on resection rates and survival. Br J Surg 101:1000–1005. 10.1002/bjs.9468 [DOI] [PubMed] [Google Scholar]
  • 6.van der Geest LGM, van Rijssen LB, Molenaar IQ, de Hingh IH, Groot Koerkamp B, Busch ORC et al (2016) Volume-outcome relationships in pancreatoduodenectomy for cancer. HPB (Oxford) 18:317–324. 10.1016/j.hpb.2016.01.515 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Ricci C, D’Ambra V, Alberici L, Ingaldi C, Minghetti M, Bonini G et al (2025) Minimal invasive pancreatoduodenectomy: a comprehensive systematic review and metanalysis of randomized controlled clinical trials. Ann Surg Oncol 32:3614–3622. 10.1245/s10434-025-16990-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.de Rooij T, Lu MZ, Steen MW, Gerhards MF, Dijkgraaf MG, Busch OR et al (2016) Minimally invasive versus open pancreatoduodenectomy: systematic review and meta-analysis of comparative cohort and registry studies. Ann Surg 264:257–267. 10.1097/SLA.0000000000001660 [DOI] [PubMed] [Google Scholar]
  • 9.Zhang X-P, Xu S, Zhao Z-M, Yu G-S, Han B, Chen X et al (2023) Outcomes of robotic versus laparoscopic pancreatoduodenectomy following learning curves of surgeons: a multicenter study on 2255 patients. Ann Surg. 10.1097/SLA.0000000000006167 [DOI] [PubMed] [Google Scholar]
  • 10.Zureikat AH, Moser AJ, Boone BA, Bartlett DL, Zenati M, Zeh HJ (2013) 250 robotic pancreatic resections: safety and feasibility. Ann Surg 258:554–559. 10.1097/SLA.0b013e3182a4e87c. (discussion 559-62) [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Nickel F, Wise PA, Müller PC, Kuemmerli C, Cizmic A, Salg GA et al (2024) Short-term outcomes of robotic versus open pancreatoduodenectomy: propensity score-matched analysis. Ann Surg 279:665–670. 10.1097/SLA.0000000000005981 [DOI] [PubMed] [Google Scholar]
  • 12.Khachfe HH, Nassour I, Hammad AY, Hodges JC, AlMasri S, Liu H et al (2023) Robotic pancreaticoduodenectomy: increased adoption and improved outcomes: is laparoscopy still justified? Ann Surg 278:e563–e569. 10.1097/SLA.0000000000005687 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Giulianotti PC, Sbrana F, Bianco FM, Elli EF, Shah G, Addeo P et al (2010) Robot-assisted laparoscopic pancreatic surgery: single-surgeon experience. Surg Endosc 24:1646–1657. 10.1007/s00464-009-0825-4 [DOI] [PubMed] [Google Scholar]
  • 14.Zureikat AH, Postlewait LM, Liu Y, Gillespie TW, Weber SM, Abbott DE et al (2016) A multi-institutional comparison of perioperative outcomes of robotic and open pancreaticoduodenectomy. Ann Surg 264:640–649. 10.1097/SLA.0000000000001869 [DOI] [PubMed] [Google Scholar]
  • 15.Liu Q, Li M, Gao Y, Jiang T, Han B, Zhao G et al (2024) Effect of robotic versus open pancreaticoduodenectomy on postoperative length of hospital stay and complications for pancreatic head or periampullary tumours: a multicentre, open-label randomised controlled trial. Lancet Gastroenterol Hepatol 9:428–437. 10.1016/S2468-1253(24)00005-0 [DOI] [PubMed] [Google Scholar]
  • 16.Napoli N, Kauffmann EF, Palmeri M, Miccoli M, Costa F, Vistoli F et al (2016) The learning curve in robotic pancreaticoduodenectomy. Dig Surg 33:299–307. 10.1159/000445015 [DOI] [PubMed] [Google Scholar]
  • 17.Speicher PJ, Nussbaum DP, White RR, Zani S, Mosca PJ, Blazer DG et al (2014) Defining the learning curve for team-based laparoscopic pancreaticoduodenectomy. Ann Surg Oncol 21:4014–4019. 10.1245/s10434-014-3839-7 [DOI] [PubMed] [Google Scholar]
  • 18.Hendrix JM, Garmon EH (2025) American Society of Anesthesiologists physical status classification system. In: StatPearls. Treasure Island, FL: StatPearls Publishing [PubMed]
  • 19.Charlson M, Wells MT, Ullman R, King F, Shmukler C (2014) The Charlson comorbidity index can be used prospectively to identify patients who will incur high future costs. PLoS ONE 9:1–16. 10.1371/journal.pone.0112479 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Tempero MA, Malafa MP, Al-Hawary M, Asbun H, Bain A, Behrman SW et al (2017) Pancreatic adenocarcinoma, version 2.2017, NCCN clinical practice guidelines in oncology. J Natl Compr Canc Netw 15:1028–1061. 10.6004/jnccn.2017.0131 [DOI] [PubMed] [Google Scholar]
  • 21.Callery MP, Pratt WB, Kent TS, Chaikof EL, Vollmer CM (2013) A prospectively validated clinical risk score accurately predicts pancreatic fistula after pancreatoduodenectomy. J Am Coll Surg 216:1–14. 10.1016/j.jamcollsurg.2012.09.002 [DOI] [PubMed] [Google Scholar]
  • 22.Clavien PA, Barkun J, de Oliveira ML, Vauthey JN, Dindo D, Schulick RD et al (2009) The Clavien-Dindo classification of surgical complications: five-year experience. Ann Surg 250:187–196. 10.1097/SLA.0b013e3181b13ca2 [DOI] [PubMed] [Google Scholar]
  • 23.Bassi C, Marchegiani G, Dervenis C, Sarr M, Abu Hilal M, Adham M et al (2016) The 2016 update of the International Study Group (ISGPS) definition and grading of postoperative pancreatic fistula: 11 years after. Surgery 161:584–591. 10.1016/j.surg.2016.11.014 [DOI] [PubMed] [Google Scholar]
  • 24.Wente MN, Bassi C, Dervenis C, Fingerhut A, Gouma DJ, Izbicki JR et al (2007) Delayed gastric emptying (DGE) after pancreatic surgery: a suggested definition by the International Study Group of Pancreatic Surgery (ISGPS). Surgery 142:761–768. 10.1016/j.surg.2007.05.005 [DOI] [PubMed] [Google Scholar]
  • 25.Koch M, Garden OJ, Padbury R, Rahbari NN, Adam R, Capussotti L et al (2011) Bile leakage after hepatobiliary and pancreatic surgery: a definition and grading of severity by the International Study Group of Liver Surgery. Surgery 149:680–688. 10.1016/j.surg.2010.12.002 [DOI] [PubMed] [Google Scholar]
  • 26.Wente MN, Veit JA, Bassi C, Dervenis C, Fingerhut A, Gouma DJ et al (2007) Postpancreatectomy hemorrhage (PPH): an International Study Group of Pancreatic Surgery (ISGPS) definition. Surgery 142:20–25. 10.1016/j.surg.2007.02.001 [DOI] [PubMed] [Google Scholar]
  • 27.Verbeke C, Webster F, Brosens L, Campbell F, Del Chiaro M, Esposito I et al (2021) Dataset for the reporting of carcinoma of the exocrine pancreas: recommendations from the International Collaboration on Cancer Reporting (ICCR). Histopathology 79:902–912. 10.1111/his.14540 [DOI] [PubMed] [Google Scholar]
  • 28.Müller PC, Kuemmerli C, Cizmic A, Sinz S, Probst P, de Santibanes M et al (2022) Learning curves in open, laparoscopic, and robotic pancreatic surgery: a systematic review and proposal of a standardization. Ann Surg Open 3:e111. 10.1097/AS9.0000000000000111 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Abu Hilal M, van Ramshorst TME, Boggi U, Dokmak S, Edwin B, Keck T et al (2024) The Brescia internationally validated European guidelines on minimally invasive pancreatic surgery (EGUMIPS). Ann Surg 279:45–57. 10.1097/SLA.0000000000006006 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Neshan M, Padmanaban V, Chick RC, Pawlik TM (2024) Open vs robotic-assisted pancreaticoduodenectomy, cost-effectiveness and long-term oncologic outcomes: a systematic review and meta-analysis. J Gastrointest Surg 28:1933–1942. 10.1016/j.gassur.2024.08.013 [DOI] [PubMed] [Google Scholar]
  • 31.Waseem MH, Abideen ZU, Durrani R, Dilawar E, Kamran MS, Butt HT et al (2025) Comparing operative outcomes and resection quality in robotic vs open pancreaticoduodenectomy: a meta-analysis of 54,000 patients. J Gastrointest Cancer 56:57. 10.1007/s12029-025-01177-0 [DOI] [PubMed] [Google Scholar]
  • 32.Yan Q, Xu L-B, Ren Z-F, Liu C (2020) Robotic versus open pancreaticoduodenectomy: a meta-analysis of short-term outcomes. Surg Endosc 34:501–509. 10.1007/s00464-019-07084-3 [DOI] [PubMed] [Google Scholar]
  • 33.Polychronidis G, Joos MC, Merz DC, Holze M, Kalkum E, Probst P et al (2026) Non-inferiority of robotic versus open pancreatoduodenectomy - a systematic review and meta-analysis of prospective non-randomized and randomized trials. EClinicalMedicine 92:103761. 10.1016/j.eclinm.2026.103761 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Klotz R, Mihaljevic AL, Kulu Y, Sander A, Klose C, Behnisch R et al (2024) Robotic versus open partial pancreatoduodenectomy (EUROPA): a randomised controlled stage 2b trial. Lancet Reg Health Eur 39:100864. 10.1016/j.lanepe.2024.100864 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Da Dong X, Felsenreich DM, Gogna S, Rojas A, Zhang E, Dong M et al (2021) Robotic pancreaticoduodenectomy provides better histopathological outcomes as compared to its open counterpart: a meta-analysis. Sci Rep 11:3774. 10.1038/s41598-021-83391-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Fu Y, Qiu J, Yu Y, Wu D, Zhang T (2022) Meta-analysis of robotic versus open pancreaticoduodenectomy in all patients and pancreatic cancer patients. Front Surg 9:989065. 10.3389/fsurg.2022.989065 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials


Articles from Surgical Endoscopy are provided here courtesy of Springer

RESOURCES