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. 2019 Jul 3;19:75. doi: 10.1186/s12893-019-0534-4

A score model based on pancreatic steatosis and fibrosis and pancreatic duct diameter to predict postoperative pancreatic fistula after Pancreatoduodenectomy

Guo Xingjun 1,#, Zhu Feng 1,#, Yang Meiwen 2,#, Jiang Jianxin 3, He Zheng 4, Gao Jun 5, Huang Tao 6, Zhao Rui 7, Zhang Leida 2,, Wang Min 1,, Qin Renyi 1,; FACS
PMCID: PMC6610813  PMID: 31269932

Abstract

Purposes

To establish a scoring model for the risk of postoperative pancreatic fistula (POPF) following pancreatoduodenectomy (PD).

Methods

PD Patients from 7 institutions in 2 independent sets: developmental (n = 457) and validation cohort (n = 152) were retrospectively enrolled and analyzed. Pancreatic Fibrosis (PF) and Pancreatic Steatosis (PS) were assessed by pathological examination of the pancreatic stump.

Results

Stepwise univariate and multivariate analysis indicated that pancreatic duct diameter ≤ 3 mm, increased PS and decreased PF were independent risk factors for POPF and Clinically Relevant Postoperative Pancreatic Fistula (CR-POPF). Based on the relative weight and odds ratio of each factor in the POPF, a simplified scoring model was developed. And patients were stratified into high-risk group (22~28 points), medium-risk group (15~21 points) and low-risk group (8~14 points). The receiver operating characteristic curve demonstrated that the Area under the curve for the predictive model was 0.868 and 0.887 in the model design group and the external validation group.

Conclusions

This study establishes a simplified scoring model based on accurately and quantitatively measuring the PS, PF and pancreatic duct diameter. The scoring model accurately predicted the risk of POPF.

Electronic supplementary material

The online version of this article (10.1186/s12893-019-0534-4) contains supplementary material, which is available to authorized users.

Keywords: Pancreatic fibrosis, Pancreatic steatosis, Postoperative pancreatic fistula, Scoring model

Introduction

Pancreatoduodenectomy (PD) is the optimal treatment for most malignant and benign neoplasms of the pancreatic head and periampullary region. Serious postoperative complications raise concerns for surgeons [1], along with surgical technical difficulty. Postoperative pancreatic fistula (POPF) is one of the most common complications [2]. POPF not only may result in massive intra-abdominal hemorrhaging and severe intraperitoneal infection [3, 4], but is also the most important determinant of death after PD [5]. Surgeons and researchers have attempted to develop various strategies to decrease the incidence of pancreatic leakage after PD such as anastomosis of the pancreas and intestine or placing a tube to support the pancreatic duct [68]. Despite many such attempts, the incidence of POPF following PD is still in the 10–28% range [9]. It has been well known that some chronic morbidities, such as alcohol and smoking, contribute to diverse conditions in each patient, especially in regards to the texture of the pancreas [10, 11]. Questions have been raised as to whether pancreatic texture is a potential factor causing high incidence of POPF and if individualized management based on pancreatic texture might change the status quo.

It is believed that the softness or hardness of the pancreas is related to POPF. A soft pancreas makes performing anastomosis of the pancreas and intestine more difficult and makes it easier for the suture line to tear pancreatic tissue. Pancreatic texture can also affect pancreatic exocrine function [12]. The robustness of pancreaticojejunostomy and pancreatic exocrine function both contribute to the occurrence of pancreatic fistula after surgery [13]. However, current research is controversial as to whether a hard pancreas can decrease, or a soft pancreas increase, the incidence of POPF [1416]. The controversy is not surprising because there are no consensus criteria for quantitatively evaluating pancreatic texture, and when assessed subjectively by each operator, results may differ in perceptions of softness and hardness. Moreover, the cut-off for defining a soft or hard pancreas is also unclear. Using preoperative imaging modalities (CT or MRI) to assess the texture of the pancreas has been attempted. However, imaging modalities only indirectly reflected the texture of the pancreas and can be impacted by many factors. For example, artifacts in MRI can significantly interfere with the evaluation of the fat content of the pancreas.

The softness or hardness of pancreatic texture is determined by the composition of the pancreatic parenchyma which is influenced by the balance of fibrous and fatty tissue [17, 18]. Therefore, pathological analysis of the pancreatic microstructure is the most accurate method to assess pancreatic texture. The aim of this study was to investigate the correlation between the microscopic pathological structure of the pancreas, including level of pancreatic fibrosis (PF) and pancreatic steatosis (PS), and the incidence of POPF after PD in a multicenter retrospective study.

Methods

Ethics statement

This study was approved by the Human Research Ethics Committees at the Huazhong University of Science and Technology and was carried out in accordance with the principles embodied in the Declaration of Helsinki. Informed consent for the use of the specimen was obtained from all participants.

Retrospective study population and patient selection

Seven pancreatic surgery centers contributed to the study (see the institutional affiliations of the authors). The patients’ data from January 2014 to December 2017 were collected and analyzed retrospectively. The eligibility criteria included age greater than 18 years old; died within 1 week. A total of 609 consecutive patients were included in the study for risk factor analysis and the development of a risk score. The risk score was calculated retrospectively after the review of patient records. The patients were represented in the study by code numbers and their personal data were concealed.

Surgical technique and perioperative management

Each patient was placed in the supine position. The Open Pancreaticoduodenectomy.

(OPD) usually required a long midline incision or straight incision through right rectus abdominis. The Laparoscopic Pancreaticoduodenectomy (LPD) required drilling five small holes in the patient’s abdomen. The supporting stent of the pancreatic duct was placed in some of the patients. Closed rubber drainage tubes were placed near the pancreatic anastomosis and choledochojejunostomy sites. Pancreatic texture and pancreatic duct diameter were assessed by the surgeons.

Broad-spectrum antibiotics (Paclitaxel sulbactam sodium) were intravenously administered to all patients for 3 days after surgery. If there was a clear sign of infection, the period of antibiotic treatment was prolonged. All patients received an H2 blocker every 12 h intravenously during the period after surgery when there was no oral intake. After 5d of postoperative octreotide treatment by a 24 h intravenous pump, octreotide dosing was switched to subcutaneous administration (100 mg every 6 h for 7d). The amount of fluid drainage from the peripancreatic site was measured daily and the amylase levels of serum and fluid drainage were measured on postoperative day 1, 3, 5, 7 and 10. On postoperative day 7 an abdominal CT scan was performed and the peripancreatic drainage tube was removed, provided there was no evidence of leakage or fluid collection.

Hematoxylin and eosin analysis of paraffin embedded sections

The paraffin embedded sections from the pancreatic stump specimens were stained with hematoxylin and eosin (HE) and reviewed by two experienced pathologists who were blinded to the surgical outcome. Based on the criteria of Klopper and Maillet [19], pancreatic fibrosis and pancreatic steatosis was evaluated. The degree of intralobular and interlobular fibrosis was separately scored from 0 to 6 and the total score (0–12) was calculated. According to the total score, fibrosis was classified into normal (Grade 0, score 0–3), mild fibrosis (Grade 1, score 4–6), moderate fibrosis (Grade 2, score 7–9) and severe fibrosis (Grade 3, score 10–12). The degree of pancreatic fat infiltration was assessed based on the percentage of the interlobular fat to total interlobular space and the percentage of the intralobular fat to total intralobular space. The sum of the intralobular and interlobular fat percentages was calculated. Pancreatic steatosis was graded into 4 categories: normal (Grade 0: 0–10%), mild lipomatosis (Grade 1: 11–40%), moderate lipomatosis (Grade 2: 41–70%), and severe lipomatosis (Grade 3: 71–100%).

Definition of pancreatic fistula

The International Study Group of Pancreatic Fistula (ISGPF) definition on POPF was used in our study [20].

Statistical analysis

Statistical analyses were performed using SAS version 9.4 (SAS Inc., Chicago, IL, USA). Univariable analysis was performed on the various parameters of the POPF and non-POPF, CR-POPF and non-CR-POPF groups. The variables were then selected into multivariable logistic regression models, with forward stepwise selection procedures. Statistically significant differences were defined as p < 0.05.

Results

Demographic and Clinicopathologic characteristics of cohort

Patient demographics and perioperative characteristics are listed in Additional file 1: Table S1. During the study period, a total of 609 patient underwent PD at the 7 participating centers. The patients were comprised of 383 men (62.9%) and 226 women (37.1%), with a median age of 54.6 years (range: 18–82 years). The median BMI was 22.0 kg/m2 (range: 15.1–34.0 kg/m2). Most patients had ASA scores of II (74.1%) or III (17.2%). The mean preoperative TBIL was 138.2 μmol/L (range: 3.7–570.2 μmol/L) and the mean preoperative DBIL was 72.3 μmol/L (range: 0.5–278.4 μmol/L). The mean preoperative ALT was 147.0 U/L (range: 1.2–1099.0 U/L); the mean preoperative AST was 113.2 U/L (range: 9.0–1628.0 U/L). The mean preoperative CT Hu value was 39.6 (range: 16.3~65.7). Prior abdominal surgery had been performed in 23.6% of the patients. Preoperative jaundice and abdominal pain were the most common clinical symptoms. The preoperative diagnoses of mass location were pancreatic head (66.3%), duodenum (7.2%), biliary duct (17.6%), and ampulla (9.0%).

Intraoperative details are shown in Additional file 1: Table S1. Laparoscopic pancreaticoduodenectomy was performed in 79 patients (13.0%) and OPD in 530 patients (87.0%). The median operative time was 398.8 min (SD = 120.1 min). The methods of pancreatic remnant anastomosis included PJ (85.6%) and PG (14.4%). Stenting of the pancreatic duct was required in 554 cases (92.0%). The median estimated intraoperative blood loss was 489.6 mL (SD = 345.7 mL). Intraoperative blood transfusions were needed in 129 patients (21.2%); the median estimated volume of intraoperative blood transfusion was 173.0 mL (SD = 231.5 mL).

Postoperative details are shown in Additional file 1: Table S1. According to the ISGPF, 73 patients (12.0%) had a grade A POPF; these patients were treated conservatively and fed orally without additional intervention. Grade B POPF occurred in 41 patients (6.7%) and grade C POPF in 27 patients (4.4%).

Pathological outcomes are shown in Additional file 1: Table S1. Lesions were caused by chronic inflammation in 82 cases (13.5%), cystic neoplasia of the pancreas in 82 cases (13.5%), ampullary carcinoma in 55 cases (9.0%), duodenal lesions in 43 cases (7.1%), cholangiocarcinoma in 107 cases (17.6%), and pancreatic carcinoma in 245 cases (40.2%). The grade of pancreatic fibrosis of the pancreatic stump was normal in 168 cases (27.6%), mild in 181 cases (29.7%), moderate in 204 cases (33.5%), and severe in 56 cases (9.2%). The grade of pancreatic steatosis of the pancreatic stump was normal in 292 cases (47.9%), mild in 205 cases (33.7%), moderate in 95 cases (15.6%), and severe in 17 cases (2.8%).

Univariate analysis and correlation of variables with POPF

A total of 640 patient was identified, with 31 being excluded from analysis because of missing data. Postoperative pancreatic fistula occurred in 141 of the 609 patients (23.2%). Univariate analyses of the variables and their association with POPF are shown in Table 1. In total, the 10 variables (BMI, AST, CT Hu value, pancreatic texture, pancreatic duct diameter, surgery approach, operating time, histopathology, PF and PS) were significantly different between the no-POPF group and POPF group. Univariate analyses of the variables and their association with CR-POPF are shown in Table 3. In total, the 4 variables (pancreatic texture, pancreatic duct diameter, PF and PS) were significantly different between the no-CR-POPF group and CR-POPF group.

Table 1.

Univariate Analysis and Relationship of Variables With POPF

Variables No POPF P CR-POPF P
no yes no yes
Sex: Male / Female 383/226 285/183 98/43 0.064 340/201 43/25 0.173
Age: ≤55/> 55 300/309 227/241 73/68 0.281 265/276 35/33 0.699
BMI: ≤23/> 23 327/282 268/200 59/82 0.001 290/251 37/31 0.900
Diabetes: No/Yes 551/58 423/45 128/13 0.889 489/52 62/6 0.546
Abdominal surgery history: No/Yes 465/144 352/166 133/28 0.227 403/128 52/16 0.917
RBC: normal / abnormal 392/217 305/163 87/54 0.451 348/193 44/24 0.951
PCT: ≤0.5/> 0.5 ng/mL 374/235 288/180 86/55 0.907 231/210 43/25 0.095
ALT: ≤40/> 40 U/L 204/405 166/302 38/103 0.060 181/360 23/45 0.952
AST: ≤40 / > 40 U/L 229/380 189/279 40/101 0.009 203/338 26/42 0.909
Platelet: normal / abnormal 466/143 362/106 104/37 0.378 408/127 52/16 0.969
Total Bilirubin: ≤171 / > 171 μmol/L 424/185 334/134 90/51 0.088 377/164 47/21 0.923
Direct Bilirubin: ≤110 / > 110 μmol/L 350/259 272/196 78/63 0.555 311/230 39/29 0.913
CT Hu value: ≤40Hu / >40Hu 423/186 336/132 87/54 0.023 371/110 52/16 0.903
Surgery approach: OPD / LPD 530/79 397/71 133/8 0.003 467/74 63/5 0.143
Pancreatic texture (evaluation by surgeon)
 soft 318 211 107 < 0.001 276 42 < 0.001
 middle 205 174 31 179 26
 hard 86 83 3 86 0
Operating time: ≤240 min / > 240 min 273/336 222/246 51/90 0.018 241/300 32/36 0.695
Pancreatic duct diameter: ≤3 / > 3 mm 312/297 206/262 106/35 < 0.001 298/243 14/54 < 0.001
Intraoperative bleeding: ≤400 / > 400 mL 387/222 298/170 73/50 0.905 244/197 43/25 0.221
Intraoperative blood transfusion: ≤400 / > 400 mL 563/46 432/36 131/10 0.813 500/41 63/5 0.859
Histopathology
 Chronic inflammation 77 63 14 < 0.001 68 9 0.074
 Cystic neoplasia of the pancreas 82 63 19 73 9
 Ampullary carcinoma 55 42 13 49 6
 Duodenal lesions 43 22 21 38 5
 Cholangiocarcinoma 107 68 39 95 12
 Pancreatic cancinoma 245 210 35 218 27
Pancreatic Fibrosis
 0 168 79 89 < 0.001 126 42 < 0.001
 1 181 152 29 158 23
 2 204 182 22 201 3
 3 56 55 1 56 0
Pancreatic Steatosis
 0 292 258 34 < 0.001 288 4 < 0.001
 1 205 156 49 181 24
 2 95 48 47 64 31
 3 17 6 11 8 9

Data are expressed as whole numbers, with P values from Fisher exact test

Table 3.

Risk scoring model for POPF

Risk Factor Risk Factor Weight OR Points contributed
Pancreatic duct diameter
  > 3 mm 2.81 1.00 2
  ≤ 3 mm 2.81 2.93 8
Pancreatic Steatosis
 0 3.79 1 4
 1 3.79 1.62 6
 2 3.79 2.62 10
 3 3.79 4.25 16
Pancreatic Fibrosis
 3 1.60 1 2
 2 1.60 1.41 2
 1 1.60 1.99 3
 0 1.60 2.81 4

Score max = 28, score min = 8

Low-risk: 8~14

Medium-risk: 15~21

High-risk: 22~28

Multivariate analysis and correlation of variables with POPF

Next, the 609 patients were divided into two groups. Data from 3/4 of the patients (n = 457) was used for a multivariate analysis and design model and the remaining 1/4 patient’s (n = 152) data was used for external validation for the logistic regression model. In the multivariate logistic regression analysis between the no-POPF group and POPF group, pancreatic duct diameter, PS and PF were independent factors with significance (Table 2). Patients with a pancreatic duct diameter > 3 mm were 0.341-fold risk of POPF compared with a diameter ≤ 3 mm. Both PS and PF are ordinal variables with numerical values from 0 to 3. The risk of POPF for each additional grade of PS is 1.621 times the lower grade. The risk of POPF for each additional grade of PF is 0.709 times the lower grade. In the multivariate logistic regression analysis between the no-CR-POPF group and CR-POPF group, pancreatic duct diameter, PS and PF were independent factors with significance (Table 2).

Table 2.

Multivariate logistic regression models of independent risk factors for POPF

Odds ratio 95% CI P value
No POPF VS. POPF
 Pancreatic duct diameter 0.34 0.19–0.59 < 0.001
 Pancreatic Steatosis 1.62 1.76–3.31 < 0.001
 Pancreatic Fibrosis 0.71 0.52–0.96 0.03
No CR-POPF VS. CR-POPF
 Pancreatic duct diameter 3.33 1.96–5.64 < 0.001
 Pancreatic Steatosis 0.78 0.67–0.91 0.01
 Pancreatic Fibrosis 2.42 1.47–3.97 < 0.001

POPF risk score model

The weighting of each risk factor can be calculated based on the coefficient of each variable in the multivariate linear regression analysis. An odds ratio was also revealed in the multivariate linear regression analysis (Table 2). The authors assumed each risk factor contributes to POPF, with respect to weighting and odds ratios, and each variable was given a certain value by calculating the product of weighting times odds ratio (Table 3). Therefore, a simplified scoring model was generated, and 3 variables, pancreatic duct diameter, PS and PF, were included. The scores ranged from 8 to 28 and were stratified into into high-risk group (22~28 points), medium-risk group (15~21 points) and low-risk group (8~14 points) (Table 3). The receiver operating characteristic (ROC) curve (Fig. 1a) in the model design group shows that the Area under the curve (AUC) of the score was 0.868. The ROC curve in the external validation database (Fig. 1b) shows that the AUC of the score was 0.887.

Fig. 1.

Fig. 1

Receiver operating characteristic curve. a: Receiver operating characteristic (ROC) curve for the predictive scoring model of the study group. Area under the receiver operator characteristics curve was 0.868. b: ROC curve for the predictive scoring model of the validate group. Area under the receiver operator characteristics curve was 0.88

Discussion

Postoperative pancreatic fistula continues to be a challenge in postoperative management. It increases patient distress, prolongs hospitalization and escalates the medical cost. In high volume institutions, POPF rates are high and are a primary detrimental factor causing modality and mortality. In this study, the overall incidence of POPF after PD was 23.2%, which was similar to the POPF rate in several large multicenter cohort studies [2123].

Incorporating various risk factors into a scores model that predicts POPF risk has been reported by various groups [21, 2431]. However, most of these models are built with single-center data, either not having been externally validated or having poor to fair performance at external validation, which restricts the applicability for clinical practice. The Fistula Risk Score (FRS) created by Callery and colleagues [27], which is based on gland texture, pancreatic duct diameter, intraoperative blood loss and definitive pathology, is the most cited and widely accepted POPF prediction model. It has been reported that the internal validation of AUC for Models I, II, and III are 0.936, 0.938 and 0.942, respectively. However, Olga and colleagues’ [32] recent research, based on NSQIP data, showed a Modified FRS (without blood loss) prediction model with poor external validation performance, where the AUC was only 0.62. In addition, included the most recently published Alternative FRS (without blood loss) study [33], these models rely heavily on pancreas texture to stratify risk groups. Despite pancreas texture being widely recognized as a strong prediction factor for POPF and applied universally in clinical practice, the subjective assessment is affected by many factors including but not limited to perceptions and experience, ultimately limiting its predictive value. To address these limitations, a new predictive model that can objectively reflect pancreas consistency and incorporate other risk factors, as well as predict and stratify POPF risk, needs to be developed. In this study, pancreatic texture was accurately evaluated based on the microstructure of the pancreas. In addition, the scoring model contain 3 main factors. We give each factor the appropriate score based on the relative weight of the three factors, which is more reasonable than the average score given in previous studies.

Pancreatic fibrosis and PS are well known for affecting the consistency of the pancreas. In this study’s systematic reviews, research indicated that low PF and high PS were risk factors for pancreatic leakage after pancreatic resection. One of the hypotheses is that the fiber and adipose tissue replace the normal pancreatic parenchyma destroying the normal microstructure of the pancreas, ultimately leading to changes in pancreatic texture [3436]. Fatty infiltration in the pancreas makes the tissue more fragile, making anastomosis of the pancreas and intestine more easily disrupted, while deposition of fibrous tissue in the pancreas makes the tissue firm and reduces the complications in surgical operation [37]. Another hypothesis is that a fibrotic pancreas can decrease the incidence of POPF because of decreased pancreatic exocrine function. This study revealed that patients with severe PF had lower incidences of pancreatic fistula following PD and those with severe pancreatic fat infiltration had higher incidences. These results are consistent with several reported studies [16, 38, 39]. Many studies also concluded pancreatic duct diameter to be a major determinant of POPF [26, 4042]. In this study, the data revealed that a pancreatic duct diameter less than 3 mm was a risk factor, with an odds ratio of 2.93 in POPF after PD. It is proposed that smaller pancreatic ducts are more prone to occlude or dehisce after a challenging duct-to-mucosa anastomosis procedure and obstructed or leaking pancreatic juice might corrode the pancreatic intestinal anastomosis, leading to pancreatic leakage. Wada et al. [43] suggested that using surgical microscope magnification for better visualization would decrease POPF rates.

The authors of this study were able to successfully develop and validate a POPF prediction model. This simplified scoring model consists of only three variables: PS, PF and pancreatic duct diameter. Using only three variables was shown to not sacrifice predictive capacity, where the AUC of the ROC curve for the model design group and external validation group were 0.868 and 0.887, respectively. This predictive model stratifies patients into three risk groups.

The limit of this study is that the three key variables used in the predictive model are intraoperative variables, limiting the model’s applicability for preoperative patient counseling. Next we should carry on a multicenter, prospective study to analyze whether this scoring system can guide clinicians in choosing the right pancreatic anastomosis. There are many ways to reconstruction the pancreas, but there is no uniform opinion on the choice of anastomosis. And we should also evaluate whether or not we can get accurate data of pancreatic fibrosis, pancreatic steatosis and pancreatic duct diameter during the surgery. After establishing the scoring system, we need to evaluate whether the surgeon can choose a more reasonable match according to the score.

Conclusion

Changes in pancreatic microstructure, such as severe fatty tissue infiltration in the pancreas, decreased pancreatic fibrosis and a smaller pancreatic duct diameter are the major risk factors for POPF following PD. A new predictive model can stratify patients into different POPF risk groups.

Additional files

Additional file 1: (70KB, doc)

Table S1. Demographic and Clinicopathologic Characteristics of Cohort (DOC 70 kb)

Acknowledgements

We thank Xuehan Liu, PhD, from the Department of Epidemiology and Biost atistics, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, for her statistical support. We thank Dong Chen, PhD and Ke Zuo, PhD, from the School of Pathology, Tongji Medical College, Huazhong University of Science and Technology, for their pathological analysis. We thank Chencheng Xie, PhD, from the Department of Internal Medicine, Sanford School of Medicine, University of South Dakota for his lingual support.

Abbreviations

ALT

Alanine aminotransferase

AST

Aspartate aminotransferase

BMI

Body Mass Index

CP

Chronic Pancreatitis

CR-POPF

Clinically Relevant Postoperative Pancreatic Fistula

DP

Distal Pancreatectomy

HE

hematoxylin and eosin

LPD

Laparoscopic Pancreaticoduodenectomy

OPD

Open Pancreaticoduodenectomy

PC

Pancreatic Carcinoma

PCT

Procalcitonin

PD

Pancreatoduodenectomy

PF

Pancreatic Fibrosis

PG

Pancreaticogastrostomy

PJ

Pancreaticojejunostomy

POPF

Postoperative Pancreatic Fistula

PS

Pancreatic Steatosis

RBC

Red blood cell

Authors’ contributions

Study concept and design: GX, WM, QR. Acquisition of data: ZF, YM, JJ, HZ, GJ, HT, ZR, ZL, QR. Analysis and interpretation of data: GX, YM, ZL, WM. Drafting of the manuscript: GX, WM. Critical revision of the manuscript for important intellectual content: QR. Statistical analysis: GX, WM, ZL. Obtained funding: QR, WM. Study supervision: QR, WM, ZL. All authors have read and approved the manuscript.

Funding

Not applicable.

Availability of data and materials

The datasets used and analysed during the current study are available from the corresponding author on reasonable request.

Ethics approval and consent to participate

This study was approved by the Human Research Ethics Committees at the Huazhong University of Science and Technology and was carried out in accordance with the principles embodied in the Declaration of Helsinki.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no conflicts of interest.

Footnotes

Publisher’s Note

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

Guo Xingjun, Zhu Feng and Yang Meiwen contributed equally to this work.

Contributor Information

Zhang Leida, Phone: +023-65318301, Email: 2518569931@qq.com.

Wang Min, Phone: +27-8366-5295, Email: wangmin0013128@aliyun.com.

Qin Renyi, Phone: +27-8366-5295, Email: ryqin@tjh.tjmu.edu.cn.

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Associated Data

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

Supplementary Materials

Additional file 1: (70KB, doc)

Table S1. Demographic and Clinicopathologic Characteristics of Cohort (DOC 70 kb)

Data Availability Statement

The datasets used and analysed during the current study are available from the corresponding author on reasonable request.


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