Skip to main content
NCBI home page
Springer logoLink to Springer
. 2011 Oct 18;19(5):1618–1627. doi: 10.1245/s10434-011-2114-4

Outcome of Microscopic Incomplete Resection (R1) of Colorectal Liver Metastases in the Era of Neoadjuvant Chemotherapy

Ninos Ayez 1, Zarina S Lalmahomed 2, Alexander M M Eggermont 3, Jan N M Ijzermans 2, Jeroen de Jonge 1,2, Kees van Montfort 4, Cornelis Verhoef 1,✉
PMCID: PMC3332355  PMID: 22006375

Abstract

Background

Data from patients with colorectal liver metastases (CRLM) who received neoadjuvant chemotherapy before resection were reviewed and evaluated to see whether neoadjuvant chemotherapy influences the predictive outcome of R1 resections (margin is 0 mm) in patients with CRLM.

Methods

Between January 2000 and December 2008, all consecutive patients undergoing liver resection for CRLM were analyzed. Patients were divided into those who did and did not receive neoadjuvant chemotherapy. The outcome after R0 (tumor-free margin >0 mm) and R1 (tumor-free margin 0 mm) resection was compared.

Results

A total of 264 were eligible for analysis. Median follow-up was 34 months. Patients without chemotherapy showed a significant difference in median disease-free survival (DFS) after R0 or R1 resection: 17 [95% confidence interval (CI) 10–24] months versus 8 (95% CI 4–12) months (P < 0.001), whereas in patients with neoadjuvant chemotherapy the difference in DFS between R0 and R1 resection was not significant: 18 (95% CI 10–26) months versus 9 (95% CI 0–20) months (P = 0.303). Patients without chemotherapy showed a significant difference in median overall survival (OS) after R0 or R1 resection: 53 (95% CI 40–66) months versus 30 (95% CI 13–47) months (P < 0.001). In patients with neoadjuvant chemotherapy, the median OS showed no significant difference: 65 (95% CI 39–92) months for the R0 group versus the R1 group, in whom the median OS was not reached (P = 0.645).

Conclusions

In patients treated with neoadjuvant chemotherapy, R1 resection was of no predictive value for DFS and OS.

Without treatment, patients with colorectal liver metastases (CRLM) have a median survival of 5–8 months.1–3 Unfortunately, only approximately 20–30% of patients with CRLM have resectable disease at the time of diagnosis.4,5 After resection, 5-year survival rates of 21–48% have been reported.6–8 Nowadays, chemotherapy regimens are highly effective and can result in response rates of 50–80% and seem to convert 10–30% of formerly irresectable CRLM to a resectable size or situation.6,7,9,10

Several studies have described risk factors for the outcome of patients with CRLM.8,11–17 Surgical margin status has been described as the major determinant of survival after resection, with R1 resections doing worse compared to R0 resections. However, the impact of the several proposed cutoff points regarding R0 resections remains controversial.

Some older studies proposed a surgical margin of ≤1 cm as a contraindication for resection.16,18–20 Others demonstrated that a resection margin ≤1 cm is not a contraindication, providing a radical resection (minimal margin of 1 mm) is performed.21–25

However, these studies did not evaluate the specific group of patients who received neoadjuvant chemotherapy before resection of CRLM. Therefore, the present study analyzes whether a resection margin of 0 mm is sufficient in the era of effective neoadjuvant chemotherapy.

Methods

Between January 2000 and December 2008, all consecutive patients who underwent liver resection for CRLM were analyzed. Patients were eligible for this study if they fulfilled the following criteria: macroscopic complete resection; clear description of surgical margin status by the pathologist for each metastasis; no evidence of concomitant extrahepatic disease; no simultaneous use of local treatment modalities (radiofrequency ablation and/or cryotherapy).26

All patients underwent preoperative screening to assess the extent of the metastases by clinical examination and chest and abdominal imaging (ultrasound, computed tomography [CT], magnetic resonance imaging). In our institute, positron emission tomography is not routinely used. Also, serum tumor marker levels (carcinoembryonic antigen, CEA) and colonoscopy were performed preoperatively.

Chemotherapy

We are a tertiary referral hospital, and we do not administer perioperative chemotherapy as a standard treatment protocol for patients with CRLM. Most patients had already received neoadjuvant chemotherapy in the referring hospital. In our clinic, patients received neoadjuvant chemotherapy in cases of initially difficult/unresectable liver metastases (poor location) or multiple synchronous metastases ≥4. Patients received a combination of 5-fluorouracil/capecitabine and oxaliplatin or irinotecan, with or without bevacizumab. The response to neoadjuvant chemotherapy was assessed after two or three cycles by CT scan and CEA levels. Further treatment was discussed according to the tumor response and extent of the disease. When the liver metastases were resectable, a laparotomy was planned more than 3 weeks after the last course of systemic neoadjuvant chemotherapy. Bevacizumab had to be excluded from the last course of chemotherapy to ensure an interval of at least 6 weeks. None of the patients received adjuvant chemotherapy as standard therapy after liver resection. The time period from 2000 was chosen because of the introduction of more effective chemotherapy and also because after 2000 the definition of resectability was not changed in our clinic.

Liver Resection

Hepatic parenchymal resection was performed with an ultrasonic surgical aspirator (Cavitron; Valleylab, Boulder, CO) and a monopolar coagulator. R0 was defined by the absence of microscopic tumor invasion of the resection margin (tumor-free margin >0 mm), and R1 was defined by the presence or microscopic tumor invasion of the resection margin (tumor-free margin 0 mm).

Follow-up

Postoperative follow-up consisted of clinical examination and measurement of CEA every 3 months. Abdominal imaging (ultrasound, CT of thorax and abdomen) was performed at 3, 6, 9, and 12 months in the first year; every 6 months the second year; and once a year thereafter. If disease recurred, a decision on whether to initiate chemotherapy treatment again was made by the multidisciplinary team.

Outcome

Overall survival (OS) was defined as the interval in months between resection of CRLM and death, or the date of last follow-up. Disease-free survival (DFS) was defined as the interval in months between resection of CRLM and recurrence, death without recurrence, or date of last follow-up without recurrence.

Statistical Analysis

Descriptive values are expressed as median (range). Comparison between categorical variables was determined by the chi-square test or Fisher’s exact test as appropriate. Survival analysis was performed by the Kaplan–Meier method. Comparison between survival curves was made by log rank tests. Univariate analysis was performed by Cox regression analysis. For the multivariate analysis, only parameters with a P value of <0.25 in the univariate model were entered in the Cox regression model. Backward elimination was applied. Variables were included if P values were ≤0.05 and were removed if P values were >0.10. SPSS statistical software, version 17.0 (SPSS, Chicago, IL), was used for statistical analysis; a P value of ≤0.05 was considered statistically significant.

Results

Between January 2000 and December 2008, a total of 352 patients underwent liver resection for CRLM (Fig. 1). Of these, 81 patients (23%) were excluded because of extrahepatic disease, concomitant local treatment, and/or macroscopic incomplete liver resection. Seven patients (2%) had unknown margin status. Finally, 264 patients (75%) were eligible for analysis. One patient was lost to follow-up at 21 months. Neoadjuvant chemotherapy was provided to 92 (35%) of 264 patients. Thirty-eight patients (41%) received concomitant bevacizumab.

Fig. 1.

Fig. 1

Open in a new tab

Flowchart of the study

Patient characteristics are listed in Tables 1 and 2. An R1 resection was found in 33 patients (13%). R1 resections in patients without chemotherapy and with chemotherapy were comparable: 13 vs. 12% (P = 0.845).

Table 1.

Characteristics of patients by chemotherapy treatment

Characteristic No chemotherapy (n = 172) Chemotherapy (n = 92) P value All patients (n = 264)
Value Value Value
Male sex 107 (62%) 62 (67%) 0.403 169 (64%)
Age 65 (30–86) 62 (36–84) 0.714 64 (30–86)
Primary tumor
 Rectal cancer 84 (49%) 45 (49%) 0.991 129 (49%)
 T stage
  T3 124 (72%) 66 (72%) 190 (72%)
  T4 12 (7%) 8 (9%) 20 (8%)
  Missing data – 2 (2%) 2 (1%)
 Positive lymph node 97 (56%) 56 (61%) 0.364 153 (58%)
 Missing data – 2 (2%) 2 (1%)
Liver metastases
 Synchronous 52 (30%) 67 (73%) <0.001 119 (45%)
 Diameter (cm)
  Median (range) 3.3 (0.9–15) 3.5 (0.5–18) 0.068 3.4 (0.5–18)
  Missing data 2 (1%) 2 (2%) 4 (2%)
 No. of metastases <0.001
  Median (range) 1 (1–8) 2.0 (1–8) 2 (1–8)
  Missing data 1 (1%) – 1 (0.5%)
 Bilobar 43 (25%) 36 (39%) 0.017 79 (30%)
 Resection type 0.544
  Anatomical 78 (45%) 41 (45%) 119 (45%)
  Nonanatomical 69 (40%) 33 (36%) 102 (39%)
  Combined 25 (15%) 18 (20%) 43 (16%)
 R1 resection 22 (13%) 11 (12%) 0.845 33 (13%)
Open in a new tab

Data are presented as n (%) unless otherwise indicated

Table 2.

Characteristics of patients by resection margin

Characteristic R0 (n = 231) R1 (n = 33) P value All patients (n = 264)
Male 152 (66%) 17 (52%) 0.123 169 (64%)
Age, median (range) 64 (31–86) 62 (30–77) 0.499 64 (30–86)
Primary tumor
 Rectal cancer 117 (51%) 12 (36%) 0.139 129 (49%)
 T stage 0.682
  T3 163 (71%) 27 (82%) 190 (72%)
  T4 18 (8%) 2 (6%) 20 (8%)
  Missing data 2 (1%) – 2 (1%)
 Positive lymph node 127 (55%) 26 (79%) 0.011 153 (58%)
 Missing data 2 (1%) 2 (1%)
Liver metastases
 Synchronous 106 (46%) 13 (39%) 0.483 119 (45%)
 Diameter (cm) 0.048
  Median (range) 3.2 (0.5–18) 3.9 (1.6–7.0) 3.4 (0.5–18)
  Missing data 4 (2%) – 4 (2%)
 No. metastases 0.173
  Median 1 (1–8) 3.0 (1–8) 2 (1–8)
  Missing data 1 (1%) – 1 (0.5%)
 Bilobar 61 (26%) 18 (55%) 0.001 79 (30%)
 Resection type 0.513
  Anatomical 107 (46%) 12 (37%) 119 (45%)
  Nonanatomical 88 (38%) 14 (42%) 102 (39%)
  Combined 36 (16%) 7 (21%) 43 (16%)
Chemotherapy
 Neoadjuvant chemotherapy 81 (35%) 11 (33%) 0.845 92 (35%)
Open in a new tab

Data are presented as n (%) unless otherwise indicated

The median follow-up was 34 (range 0–121) months. Five patients (1.9%) died postoperatively, 3 due to liver and kidney failure and 2 due to aspiration followed by sepsis.

The median DFS was 14 [95% confidence interval (CI) 10–18] months for patients without chemotherapy, and for patients with neoadjuvant chemotherapy it was 16 (95% CI 8–24) months (P = 0.962). In patients without chemotherapy, the median DFS showed a significant difference between the R0 and R1 resection: 17 (95% CI 10–24) months versus 8 (95% CI 4–12) months (P < 0.001). In patients with neoadjuvant chemotherapy, the median DFS showed no significant difference between the R0 and R1 resection: 18 (95% CI 10–26) months versus 9 (95% CI 0–20) months (P = 0.303) (Fig. 2).

Fig. 2.

Fig. 2

Open in a new tab

R0 versus R1 resection in patients without and with chemotherapy for DFS and OS

During follow-up, 171 patients (65%) developed recurrence. Local treatment was performed in 74 patients (43%) (surgery, radiofrequency ablation, stereotactic radiotherapy), 80 patients (47%) received palliative chemotherapy, and 17 patients (10%) did not receive chemotherapy or local treatment. There was no difference in treatment of the recurrence between patients who were treated with or without neoadjuvant chemotherapy (P = 0.253).

In total, 54 patients (20%) had intrahepatic recurrence only, 87 patients (33%) had extrahepatic recurrence only, and 30 patients (11%) had intrahepatic and extrahepatic recurrence. There was no difference in recurrences located at the surgical liver margins between R0 and R1 resection in patients with and without chemotherapy (P = 0.853 and P = 0.839, respectively).

The median OS was 48 (95% CI 39–57) months for patients without chemotherapy and 65 months (95% CI not reached) for patients with neoadjuvant chemotherapy (P = 0.103). In patients without chemotherapy, the median OS showed a significant difference between R0 and R1 resection: 53 (95% CI 40–66) months versus 30 (95% CI 13–47) months (P < 0.001). In patients with neoadjuvant chemotherapy, the median OS showed no significant difference between the R0 resection, 65 (95% CI 39–92) months, and the R1 resection, where the median OS was not reached (P = 0.645) (Fig. 2).

A similar trend was found if a tumor-free margins of 0–2 mm versus >2 mm and 0–5 mm versus >5 mm was chosen. The 5-year OS was 35% for patients without neoadjuvant chemotherapy who had R0 resection with ≤2 mm from the resection margin (n = 42), whereas for patients who had a R0 resection with >2 mm from the resection margin (n = 100), the 5-year OS was 51% (P = 0.04). In patients with neoadjuvant chemotherapy, this phenomenon could not be demonstrated: 65% (n = 28) versus 45% (n = 48) (P = 0.564). When comparing 0–5 mm versus >5 mm, the 5-year OS was 55 vs. 36% in patients without chemotherapy (P = 0.062) and 44 vs. 63% in patients with chemotherapy (P = 0.361).

Predictive factors in univariate and multivariate analysis are listed in Table 3. In the total study population of 264 patients, multivariate analysis showed four factors predictive for survival: T stage primary tumor [hazard ratio (HR) = 2.0 [95% CI 1.1–3.5]; P = 0.016]. Positive lymph nodes in primary tumor (HR = 1.5 [95% CI 1.0–2.2]; P = 0.039), number of metastases (≥4) (HR = 1.8 [95% CI 1.1–2.9]; P = 0.028) and neoadjuvant chemotherapy (HR = 0.62 [95% CI 0.4–0.9]; P = 0.027).

Table 3.

Data on univariate and multivariate analysis

Characteristic Without chemotherapy With chemotherapy
Median survival (95% CI) Univariate HR (95% CI), P value Multivariate HR (95% CI) Median survival (95% CI) Univariate HR (95% CI), P value Multivariate HR (95% CI)
Disease-free survival
 Sex
  Male 14 (10–18) 0.95 (0.65–1.39), 0.789 NS 17 (6–28) 1.03 (0.60–1.77), 0.914 NS
  Female 13 (7–19) 14 (3–25)
 Age
  <60 years 14 (4–24) 1.09 (0.72–1.64), 0.692 NS 11 (6–16) 0.87 (0.52–1.48), 0.617 NS
  ≥60 years 14 (10–18) 21 (13–29)
 Primary tumor
  Rectum 13 (10–16) 0.86 (0.60–1.25), 0.440 NS 17 (3–31) 1.23 (0.73–2.08), 0.440 NS
  Colon 15 (9–21) 15 (4–26)
 T stage primary tumor
  T1–3 15 (11–19) 2.00 (1.07–3.73), 0.029 2.52 (1.33–4.76) 18 (11–25) 2.56 (1.16–5.67), 0.021 2.4 (1.08–5.34)
  T4 6 (0–14) 0.004 4 (1–7) 0.032
 Lymph node
  Negative 26 (0–57) 1.70 (1.4–2.5), 0.009 1.53 (1.02–2.29) 16 (0–36) 1.29 (0.74–2.24), 0.371 2.35 (1.28–4.31)
  Positive 10 (6–14) 0.042 17 (8–26) 0.006
Hepatic metastases
 Time diagnosis
  Metachronous 15 (8–22) 1.30 (0.9–1.9), 0.174 NS 19 (8–30) 1.10 (0.61–1.98), 0.751 NS
  Synchronous 13 (8–18) 14 (7–21)
 No. of metastases
  ≤3 26 (0–57) 2.00 (1.1–3.5), 0.024 NS 21 (9–33) 2.47 (1.37–4.44), 0.003 NS
  ≥4 10 (6–14) 6 (5–7)
 Largest metastasis size
  <4 16 (10–22) 1.10 (0.75–1.62), 0.637 NS 12 (6–18) 0.74 (0.40–1.37), 0.338 NS
  ≥4 11 (8–140 23 (0–64)
 Tumor distribution
  Unilobar 16 (8–24) 1.41 (0.94–2.10), 0.093 NS 21 (0–44) 1.80 (1.07–3.03), 0.027 NS
  Bilobar 10 (8–12) 11 (7–15)
 CEA level
  <50 16 (11–21) 1.39 (0.91–2.11), 0.129 NS 15 (7–23) 1.06 (0.48–2.35), 0.880 NS
  ≥50 8 (4–12) 21 (0–50)
 Resection margin
  R0 17 (10–24) 3.08 (1.90–5.01), <0.001 2.86 (1.70–4.78) 18 (10–26) 1.44 (0.71–2.94), 0.315 NS
  R1 8 (4–12) <0.001 9 (0–20)
Overall survival
 Sex
  Male 46 (38–54) 0.84 (0.55–1.30), 0.434 NS 65 (NR) 0.98 (0.47–2.03), 0.951 NS
  Female 54 (27–81) NR
 Age
  <60 years 53 (41–65) 1.13 (0.72–1.77), 0.600 NS NR 0.81 (0.40–1.62), 0.544 NS
  ≥60 years 43 (33–53) 65 (NR)
 Primary tumor
  Rectum 42 (28–56) 0.92 (0.61–1.39), 0.691 NS 65 (NR) 0.74 (0.37–1.49), 0.397 NS
  Colon 51 (36–66) NR
 T stage primary tumor
  T1–3 51 (40–62) 1.72 (0.86–3.43), 0.122 NS NR 2.84 (1.08–7.49), 0.035 2.84 (1.08–7.59)
  T4 34 (3–65) 32 (16–48) 0.035
 Lymph node
  Negative 64 (44–84) 1.45 (0.95–2.22), 0.084 NS 65 (31–99) 1.53 (0.70–3.34), 0.287 NS
  Positive 42 (28–56) NR
Hepatic metastases
 Time diagnosis
  Metachronous 54 (41–67) 1.18 (0.77–1.82), 0.443 NS 46 (NR) 0.93 (0.43–2.01), 0.851 NS
  Synchronous 42 (38–46) NR
 No. of metastases
  ≤3 48 (37–59) 1.68 (0.87–3.26), 0.123 NS NR 2.24 (1.06–4.75), 0.036 NS
  ≥4 32 (14–50) 43 (27–59)
 Largest metastasis size
  <4 46 (37–55) 1.05 (0.69–1.62), 0.811 NS 65 (35–95) 0.55 (0.21–1.43), 0.220 NS
  ≥4 48 (27–69) NR
 Tumor distribution
  Unilobar 51 (39–63) 1.11 (0.71–1.74), 0.639 NS NR 2.13 (1.06–4.29), 0.035 NS
  Bilobar 42 (29–55) 45 (NR)
 CEA level
  <50 51 (41–61) 1.37 (0.85–2.10), 0.208 NS 65 (NR) 0.49 (0.12–2.07), 0.335 NS
  ≥50 36 (16–56) NR
 Resection margin
  R0 53 (40–66) 2.42 (1.45–4.03), 0.001 2.58 (1.54–4.33) 65 (NR) 0.78 (0.27–2.24), 0.647 NS
  R1 30 (13–47) <0.001 NR
Open in a new tab

NS not significant, NR not reached

Discussion

This study reviews patients with CRLM who received neoadjuvant chemotherapy before resection and evaluates whether neoadjuvant chemotherapy affects the predictive value of resection margins. In patients with neoadjuvant chemotherapy, those with a R1 resection did not fare worse than those with a R0 resection (P = 0.303 and P = 0.645, respectively). In our series, we found 13% R1 resections, which is comparable to data in found at other centers (5–46%).11,18,21,26–29

Earlier studies found that a clear resection margin of 1 cm was found to be a good predictor of survival.30,31 Others have confirmed these results.16,18–20 With new insights in CRLM surgery in the last decade, some report that the 1-cm rule is outdated and should not preclude resection, provided a complete resection is possible.21–25,32 De Haas et al. even reported that they did not find any difference in DFS and OS between R0 and R1 resections (P = 0.12 and P = 0.27, respectively).26 In their study, 74% of the patients received neoadjuvant chemotherapy and 26% did not receive neoadjuvant chemotherapy; however, they did not describe these two groups separately. In 83% of their patients, surgery was followed by adjuvant chemotherapy.

The present study demonstrates comparable results when we divide the cohort into patients who did and did not receive neoadjuvant chemotherapy. However, one major difference is that none of our patients received adjuvant chemotherapy after CRLM surgery. As yet, to our knowledge, there are no randomized data to support adjuvant chemotherapy alone after liver resection. The liver represents the predominant site of cancer relapse after curative resection of CRLM, with up to 50% in the first 2 years.33,34 Thus, there is a rationale for perioperative chemotherapy, although controversy remains. The role of perioperative chemotherapy in the case of resectable metastases was investigated in one randomized controlled trial, which compared perioperative chemotherapy with surgery alone.35 It remains unknown whether the positive effects reported in the treatment arm were related to neoadjuvant chemotherapy and/or to adjuvant chemotherapy. A study by Adam et al. answered the pending question whether perioperative chemotherapy is really beneficial in patients developing solitary metastases.36 Although preoperative chemotherapy does not seem to benefit the outcome of patients with solitary metachronous CRLM, postoperative chemotherapy is associated with better OS and DFS, mainly when the tumor diameter exceeds 5 cm.36 In four randomized trials, liver resection was followed by adjuvant systemic chemotherapy or observation.37–40 None of the studies displayed an OS or DFS benefit. Mitry et al. performed a meta-analysis from two trials above.41 In multivariate analysis, adjuvant chemotherapy was independently associated with progression-free survival. Although there are strong theoretical arguments in favor of adjuvant systemic chemotherapy after resection of liver metastases, the evidence to suggest an improvement in survival after this regime is still lacking.42

Hou et al. found no difference in OS between R0 and R1 resections in patients with colorectal metastases (P = 0.0776). In their study, patients did not receive neoadjuvant chemotherapy but were administered adjuvant hepatic arterial chemotherapy after resection. Furthermore, they used additional cryotherapy after resection of CRLM.43 Yan et al. also suggested that cryotherapy is useful after resection of CRLM; they found no difference between close or involved surgical margins (P = 0.084).44 It is possible that in case of additional cryotherapy, the micrometastases that were not resected were eliminated by the edge cryotherapy because edge cryotherapy can provide an area of tumor eradication of up to another 1 cm.

To explain these results, it is necessary to consider several characteristics of CRLM. One feature is micrometastases.45–47 Some found that approximately 95% of intrahepatic micrometastases are found in the close zone of < 1 cm from the gross hepatic tumor, and therefore suggested that a resection margin of 1 cm should remain the goal for resection of CRLM.47 Others collected positive samples only within 4 mm of the tumor border.46,48 Nanko et al. state that the bigger the macrometastases, the more micrometastases, and the further away they are located.45 Yamamoto et al. could not demonstrate a relationship between distance and tumor size.49 Because there are several methods for detection of micrometastases, not all investigators report similar results on incidence. For example, when genetic analysis is used, only 2% of micrometastases were detected, whereas with basic histopathology, a detection rate of 56% was achieved, and with immunohistochemical staining, the detection rate is 58%.45–47 These differences in detection method might explain why micrometastases distribution is very different in these studies.

It is widely accepted that neoadjuvant chemotherapy can decrease the size of metastases. But how neoadjuvant chemotherapy decreases the size of CRLM remains unclear. Ng et al. showed that cell death is randomly distributed, probably as a result of variations in chemosensitivity of tumor cells, and that tumor shrinkage occurs in a concentric manner.48 They also found that viable tumor cells were more frequent in the periphery of metastases, whether or not they were treated with chemotherapy. Mentha et al. reported similar results with the finding of a dangerous “halo” (regrowth occurring at the periphery rather than in the center of the metastasis when chemotherapy is interrupted).50 They state that the surgeon should aim for a wider resection margin than 1 mm. Nevertheless, Klinger et al. rarely observed a dangerous halo.51 In their study, the tumor glands were located mostly in the periphery of the metastases but were still covered by a layer of fibrotic tissue, and therefore parenchymal transection could be performed within the new borders (after response to chemotherapy) without increasing the incidence of local recurrence.51 This phenomenon supports our results.

Neoadjuvant chemotherapy is able to shrink the tumor, as described before. We believe that this is a concentric rather than a scattering response, as sometimes seen in primary tumors; perhaps micrometastases in the periphery of the tumor were destroyed.52 This could explain why recurrence was similar in R0 and R1 resection in patients who received neoadjuvant chemotherapy. This also explains the successful downsizing of formerly unresectable metastases into resectable metastases with almost the same outcome in primary resectable cases. A concern of neoadjuvant chemotherapy might be the disappearance of smaller lesions after several lines of chemotherapy and the difficulty identifying these lesions during surgery. The need to resect all tumors observed on the prechemotherapy imaging was demonstrated previously.53,54 Another concern of chemotherapy is additional complications after liver resection. However, it is known from the literature that if limited cycles of chemotherapy are provided in the neoadjuvant setting, the morbidity or mortality of liver surgery is not increased.55,56 Therefore, we administer to our patients <6 cycles of chemotherapy and evaluate after 2–3 cycles.

Several authors state that the width of the negative margins (R0) does not show a correlation with survival.21,22,25,57 In all these studies, a considerable proportion of the patients received neoadjuvant chemotherapy and/or adjuvant chemotherapy. In our study, we demonstrated in both univariate and multivariate analyses that the 5-year OS for patients without neoadjuvant chemotherapy showed a marked difference between R0 and R1 resection. Others proposed that margin widths of 2 and 5 mm, respectively, were acceptable and led to similar outcomes compared with 1-cm margin resection.28,29,46 We also analyzed whether margin width ≤2 mm or >2 mm influenced survival. This proved to be the case (P = 0.04) in patients who had a R0 resection without neoadjuvant chemotherapy. In patients with neoadjuvant chemotherapy, this phenomenon could not be demonstrated (P = 0.564). A similar trend was found if a tumor-free margins of 0–5 mm versus >5 mm was chosen. It seems that the width of the resection margin still correlates with survival, but this only applies to patients who did not receive chemotherapy. This supports our hypothesis that neoadjuvant chemotherapy is able to destroy micrometastases in the periphery, and that in patients, the same survival rate, regardless of the width of the negative margins, is achieved. Therefore, data should be revised, and patients who did and did not receive chemotherapy should be investigated separately.

Yamamoto et al. described another feature of some CRLM.49 They found that one third of their patients have a thick fibrous pseudocapsule and suggested that a generous surgical margin is not required for resection. Later, the same group reported on a larger cohort and demonstrated that a thicker pseudocapsule leads to fewer R1/R2 resections.58 Although not significant, there was some relation between the presence of a pseudocapsule and the ability to achieve complete resection. Pseudocapsule formation was not available in our data set, so we could not compare this in the different chemotherapy groups.

In conclusion, in the present series, the DFS and OS in patients with neoadjuvant chemotherapy is similar for patients with either R0 or R1 resection.

Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

References

  • 1.Bengmark S, Hafstrom L. The natural history of primary and secondary malignant tumors of the liver. I. The prognosis for patients with hepatic metastases from colonic and rectal carcinoma by laparotomy. Cancer. 1969;23:198–202. doi: 10.1002/1097-0142(196901)23:1<198::AID-CNCR2820230126>3.0.CO;2-J. [DOI] [PubMed] [Google Scholar]
  • 2.Simmonds PC. Palliative chemotherapy for advanced colorectal cancer: systematic review and meta-analysis. Colorectal Cancer Collaborative Group. BMJ. 2000;321(7260):531–535. doi: 10.1136/bmj.321.7260.531. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Seymour MT, Stenning SP, Cassidy J. Attitudes and practice in the management of metastatic colorectal cancer in Britain. Colorectal Cancer Working Party of the UK Medical Research Council. Clin Oncol (R Coll Radiol) 1997;9:248–251. doi: 10.1016/S0936-6555(97)80010-6. [DOI] [PubMed] [Google Scholar]
  • 4.Adam R. Chemotherapy and surgery: new perspectives on the treatment of unresectable liver metastases. Ann Oncol. 2003;14(Suppl. 2):ii13–ii16. doi: 10.1093/annonc/mdg731. [DOI] [PubMed] [Google Scholar]
  • 5.Scheele J, Stangl R, Altendorf-Hofmann A. Hepatic metastases from colorectal carcinoma: impact of surgical resection on the natural history. Br J Surg. 1990;77:1241–1246. doi: 10.1002/bjs.1800771115. [DOI] [PubMed] [Google Scholar]
  • 6.Scheele J, Altendorf-Hofmann A. Resection of colorectal liver metastases. Langenbecks Arch Surg. 1999;384:313–327. doi: 10.1007/s004230050209. [DOI] [PubMed] [Google Scholar]
  • 7.Adam R, Avisar E, Ariche A, et al. Five-year survival following hepatic resection after neoadjuvant therapy for nonresectable colorectal. Ann Surg Oncol. 2001;8:347–353. doi: 10.1007/s10434-001-0347-3. [DOI] [PubMed] [Google Scholar]
  • 8.Nordlinger B, Guiguet M, Vaillant JC, et al. Surgical resection of colorectal carcinoma metastases to the liver. A prognostic scoring system to improve case selection, based on 1568 patients. Association Francaise de Chirurgie. Cancer. 1996;77:1254–1262. doi: 10.1002/(SICI)1097-0142(19960401)77:7<1254::AID-CNCR5>3.0.CO;2-I. [DOI] [PubMed] [Google Scholar]
  • 9.Giacchetti S, Itzhaki M, Gruia G, et al. Long-term survival of patients with unresectable colorectal cancer liver metastases following infusional chemotherapy with 5-fluorouracil, leucovorin, oxaliplatin and surgery. Ann Oncol. 1999;10:663–669. doi: 10.1023/A:1008347829017. [DOI] [PubMed] [Google Scholar]
  • 10.Nikfarjam M, Shereef S, Kimchi ET, et al. Survival outcomes of patients with colorectal liver metastases following hepatic resection or ablation in the era of effective chemotherapy. Ann Surg Oncol. 2009;16:1860–1867. doi: 10.1245/s10434-008-0225-3. [DOI] [PubMed] [Google Scholar]
  • 11.Fong Y, Fortner J, Sun RL, et al. Clinical score for predicting recurrence after hepatic resection for metastatic colorectal cancer: analysis of 1001 consecutive cases. Ann Surg. 1999;230:309–318. doi: 10.1097/00000658-199909000-00004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Iwatsuki S, Dvorchik I, Madariaga JR, et al. Hepatic resection for metastatic colorectal adenocarcinoma: a proposal of a prognostic scoring system. J Am Coll Surg. 1999;189:291–299. doi: 10.1016/S1072-7515(99)00089-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Nagashima I, Takada T, Nagawa H, et al. Proposal of a new and simple staging system of colorectal liver metastasis. World J Gastroenterol. 2006;12:6961–6965. doi: 10.3748/wjg.v12.i43.6961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Konopke R, Kersting S, Distler M, et al. Prognostic factors and evaluation of a clinical score for predicting survival after resection of colorectal liver metastases. Liver Int. 2009;29:89–102. doi: 10.1111/j.1478-3231.2008.01845.x. [DOI] [PubMed] [Google Scholar]
  • 15.Rees M, Tekkis PP, Welsh FK, et al. Evaluation of long-term survival after hepatic resection for metastatic colorectal cancer: a multifactorial model of 929 patients. Ann Surg. 2008;247:125–135. doi: 10.1097/SLA.0b013e31815aa2c2. [DOI] [PubMed] [Google Scholar]
  • 16.Lise M, Bacchetti S, Da Pian P, et al. Patterns of recurrence after resection of colorectal liver metastases: prediction by models of outcome analysis. World J Surg. 2001;25:638–644. doi: 10.1007/s002680020138. [DOI] [PubMed] [Google Scholar]
  • 17.Schindl M, Wigmore SJ, Currie EJ, et al. Prognostic scoring in colorectal cancer liver metastases: development and validation. Arch Surg. 2005;140:183–189. doi: 10.1001/archsurg.140.2.183. [DOI] [PubMed] [Google Scholar]
  • 18.Cady B, Jenkins RL, Steele GD, Jr, et al. Surgical margin in hepatic resection for colorectal metastasis: a critical and improvable determinant of outcome. Ann Surg. 1998;227:566–571. doi: 10.1097/00000658-199804000-00019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Scheele J, Stang R, Altendorf-Hofmann A, et al. Resection of colorectal liver metastases. World J Surg. 1995;19:59–71. doi: 10.1007/BF00316981. [DOI] [PubMed] [Google Scholar]
  • 20.Shirabe K, Takenaka K, Gion T, et al. Analysis of prognostic risk factors in hepatic resection for metastatic colorectal carcinoma with special reference to the surgical margin. Br J Surg. 1997;84:1077–1080. doi: 10.1002/bjs.1800840810. [DOI] [PubMed] [Google Scholar]
  • 21.Pawlik TM, Scoggins CR, Zorzi D, et al. Effect of surgical margin status on survival and site of recurrence after hepatic resection for colorectal metastases. Ann Surg. 2005;241:715–722. doi: 10.1097/01.sla.0000160703.75808.7d. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Figueras J, Burdio F, Ramos E, et al. Effect of subcentimeter nonpositive resection margin on hepatic recurrence in patients undergoing hepatectomy for colorectal liver metastases. Evidences from 663 liver resections. Ann Oncol. 2007;18:1190–1195. doi: 10.1093/annonc/mdm106. [DOI] [PubMed] [Google Scholar]
  • 23.Elias D, Cavalcanti A, Sabourin JC, et al. Resection of liver metastases from colorectal cancer: the real impact of the surgical margin. Eur J Surg Oncol. 1998;24:174–179. doi: 10.1016/S0748-7983(98)92878-5. [DOI] [PubMed] [Google Scholar]
  • 24.Elias D, Cavalcanti A, Sabourin JC, et al. Results of 136 curative hepatectomies with a safety margin of less than 10 mm for colorectal metastases. J Surg Oncol. 1998;69:88–93. doi: 10.1002/(SICI)1096-9098(199810)69:2<88::AID-JSO8>3.0.CO;2-X. [DOI] [PubMed] [Google Scholar]
  • 25.Bodingbauer M, Tamandl D, Schmid K, et al. Size of surgical margin does not influence recurrence rates after curative liver resection for colorectal cancer liver metastases. Br J Surg. 2007;94:1133–1138. doi: 10.1002/bjs.5762. [DOI] [PubMed] [Google Scholar]
  • 26.de Haas RJ, Wicherts DA, Flores E, et al. R1 resection by necessity for colorectal liver metastases: is it still a contraindication to surgery? Ann Surg. 2008;248:626–637. doi: 10.1097/SLA.0b013e31818a07f1. [DOI] [PubMed] [Google Scholar]
  • 27.Choti MA, Sitzmann JV, Tiburi MF, et al. Trends in long-term survival following liver resection for hepatic colorectal metastases. Ann Surg. 2002;235:759–766. doi: 10.1097/00000658-200206000-00002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Nuzzo G, Giuliante F, Ardito F, et al. Influence of surgical margin on type of recurrence after liver resection for colorectal metastases: a single-center experience. Surgery. 2008;143:384–393. doi: 10.1016/j.surg.2007.09.038. [DOI] [PubMed] [Google Scholar]
  • 29.Poultsides GA, Schulick RD, Pawlik TM. Hepatic resection for colorectal metastases: the impact of surgical margin status on outcome. HPB (Oxford) 2010;12:43–49. doi: 10.1111/j.1477-2574.2009.00121.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Cady B, McDermott WV. Major hepatic resection for metachronous metastases from colon cancer. Ann Surg. 1985;201:204–209. doi: 10.1097/00000658-198502000-00012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Ekberg H, Tranberg KG, Andersson R, et al. Determinants of survival in liver resection for colorectal secondaries. Br J Surg. 1986;73:727–731. doi: 10.1002/bjs.1800730917. [DOI] [PubMed] [Google Scholar]
  • 32.Pawlik TM, Vauthey JN. Surgical margins during hepatic surgery for colorectal liver metastases: complete resection not millimeters defines outcome. Ann Surg Oncol. 2008;15:677–679. doi: 10.1245/s10434-007-9703-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Fong Y, Cohen AM, Fortner JG, et al. Liver resection for colorectal metastases. J Clin Oncol. 1997;15:938–946. doi: 10.1200/JCO.1997.15.3.938. [DOI] [PubMed] [Google Scholar]
  • 34.Petrelli NJ. Perioperative or adjuvant therapy for resectable colorectal hepatic metastases. J Clin Oncol. 2008;26:4862–4863. doi: 10.1200/JCO.2008.18.5868. [DOI] [PubMed] [Google Scholar]
  • 35.Nordlinger B, Sorbye H, Glimelius B, et al. Perioperative chemotherapy with FOLFOX4 and surgery versus surgery alone for resectable liver metastases from colorectal cancer (EORTC Intergroup trial 40983): a randomised controlled trial. Lancet. 2008;371(9617):1007–1016. doi: 10.1016/S0140-6736(08)60455-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Adam R, Bhangui P, Poston G, et al. Is perioperative chemotherapy useful for solitary, metachronous, colorectal liver metastases? Ann Surg. 2010;252:774–787. doi: 10.1097/SLA.0b013e3181fcf3e3. [DOI] [PubMed] [Google Scholar]
  • 37.Langer B, Bleiberg H, Labianca R, Shepherd L, Nitti D, Marsoni S, Tu D, Sargeant A-M, Fields A. Fluorouracil (FU) plus l-leucovorin (l-LV) versus observation after potentially curative resection of liver or lung metastases from colorectal cancer (CRC): results of the ENG (EORTC/NCIC CTG/GIVIO) randomized trial. Proc Am Soc Clin Oncol. 2002;21:592.
  • 38.O’Connell MJ, Adson MA, Schutt AJ, et al. Clinical trial of adjuvant chemotherapy after surgical resection of colorectal cancer metastatic to the liver. Mayo Clin Proc. 1985;60:517–520. doi: 10.1016/s0025-6196(12)60567-9. [DOI] [PubMed] [Google Scholar]
  • 39.Lopez-Ladron A, Salvador AJ, Bernabe R, Bernardos A, Arriola E, Serrano J, Reina JJ, Gomez MA, Barneto I, Moreno-Nogueira JA Observation versus postoperative chemotherapy after resection of liver metastases in patients with advanced colorectal cancer. Proc Am Soc Clin Oncol. 2003;22:1497.
  • 40.Portier G, Elias D, Bouche O, et al. Multicenter randomized trial of adjuvant fluorouracil and folinic acid compared with surgery alone after resection of colorectal liver metastases: FFCD ACHBTH AURC 9002 trial. J Clin Oncol. 2006;24:4976–4982. doi: 10.1200/JCO.2006.06.8353. [DOI] [PubMed] [Google Scholar]
  • 41.Mitry E, Fields AL, Bleiberg H, et al. Adjuvant chemotherapy after potentially curative resection of metastases from colorectal cancer: a pooled analysis of two randomized trials. J Clin Oncol. 2008;26:4906–4911. doi: 10.1200/JCO.2008.17.3781. [DOI] [PubMed] [Google Scholar]
  • 42.Taylor I. Adjuvant chemotherapy after resection of liver metastases from colorectal cancer. Eur J Cancer. 2008;44:1198–1201. doi: 10.1016/j.ejca.2008.04.007. [DOI] [PubMed] [Google Scholar]
  • 43.Hou RM, Chu F, Zhao J, et al. The effects of surgical margin and edge cryotherapy after liver resection for colorectal cancer metastases. HPB (Oxford) 2007;9:201–207. doi: 10.1080/13651820701275113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Yan TD, Padang R, Xia H, et al. Management of involved or close resection margins in 120 patients with colorectal liver metastases: edge cryotherapy can achieve long-term survival. Am J Surg. 2006;191:735–742. doi: 10.1016/j.amjsurg.2005.05.055. [DOI] [PubMed] [Google Scholar]
  • 45.Nanko M, Shimada H, Yamaoka H, et al. Micrometastatic colorectal cancer lesions in the liver. Surg Today. 1998;28:707–713. doi: 10.1007/BF02484616. [DOI] [PubMed] [Google Scholar]
  • 46.Kokudo N, Miki Y, Sugai S, et al. Genetic and histological assessment of surgical margins in resected liver metastases from colorectal carcinoma: minimum surgical margins for successful resection. Arch Surg. 2002;137:833–840. doi: 10.1001/archsurg.137.7.833. [DOI] [PubMed] [Google Scholar]
  • 47.Wakai T, Shirai Y, Sakata J, et al. Appraisal of 1 cm hepatectomy margins for intrahepatic micrometastases in patients with colorectal carcinoma liver metastasis. Ann Surg Oncol. 2008;15:2472–2481. doi: 10.1245/s10434-008-0023-y. [DOI] [PubMed] [Google Scholar]
  • 48.Ng JK, Urbanski SJ, Mangat N, et al. Colorectal liver metastases contract centripetally with a response to chemotherapy: a histomorphologic study. Cancer. 2008;112:362–371. doi: 10.1002/cncr.23184. [DOI] [PubMed] [Google Scholar]
  • 49.Yamamoto J, Sugihara K, Kosuge T, et al. Pathologic support for limited hepatectomy in the treatment of liver metastases from colorectal cancer. Ann Surg. 1995;221:74–78. doi: 10.1097/00000658-199501000-00009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Mentha G, Majno PE, Andres A, et al. Neoadjuvant chemotherapy and resection of advanced synchronous liver metastases before treatment of the colorectal primary. Br J Surg. 2006;93:872–878. doi: 10.1002/bjs.5346. [DOI] [PubMed] [Google Scholar]
  • 51.Klinger M, Tamandl D, Eipeldauer S, et al. Bevacizumab improves pathological response of colorectal cancer liver metastases treated with XELOX/FOLFOX. Ann Surg Oncol. 2010;17:2059–2065. doi: 10.1245/s10434-010-0972-9. [DOI] [PubMed] [Google Scholar]
  • 52.Burger JW, de Graaf EJ, Doornebosch PG, et al. Local excision of rectal cancer after chemoradiation: feasibility depends on the primary stage. Int J Colorectal Dis. 2010;25:1141–1142. doi: 10.1007/s00384-010-0920-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Brouquet A, Abdalla EK, Kopetz S, et al. High survival rate after two-stage resection of advanced colorectal liver metastases: response-based selection and complete resection define outcome. J Clin Oncol. 2011;29:1083–1090. doi: 10.1200/JCO.2010.32.6132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Benoist S, Brouquet A, Penna C, et al. Complete response of colorectal liver metastases after chemotherapy: does it mean cure? J Clin Oncol. 2006;24:3939–3945. doi: 10.1200/JCO.2006.05.8727. [DOI] [PubMed] [Google Scholar]
  • 55.Karoui M, Penna C, Amin-Hashem M, et al. Influence of preoperative chemotherapy on the risk of major hepatectomy for colorectal liver metastases. Ann Surg. 2006;243:1–7. doi: 10.1097/01.sla.0000193603.26265.c3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Allen PJ, Kemeny N, Jarnagin W, et al. Importance of response to neoadjuvant chemotherapy in patients undergoing resection of synchronous colorectal liver metastases. J Gastrointest Surg. 2003;7:109–115. doi: 10.1016/S1091-255X(02)00121-X. [DOI] [PubMed] [Google Scholar]
  • 57.Hamady ZZ, Cameron IC, Wyatt J, et al. Resection margin in patients undergoing hepatectomy for colorectal liver metastasis: a critical appraisal of the 1 cm rule. Eur J Surg Oncol. 2006;32:557–563. doi: 10.1016/j.ejso.2006.02.001. [DOI] [PubMed] [Google Scholar]
  • 58.Okano K, Yamamoto J, Kosuge T, et al. Fibrous pseudocapsule of metastatic liver tumors from colorectal carcinoma. Clinicopathologic study of 152 first resection cases. Cancer. 2000;89:267–275. doi: 10.1002/1097-0142(20000715)89:2<267::AID-CNCR10>3.0.CO;2-1. [DOI] [PubMed] [Google Scholar]

Articles from Annals of Surgical Oncology are provided here courtesy of Springer

RESOURCES