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Publications > Journals > Journal of Clinical and Translational Hepatology > Article Full Text

  • Review Article
  • OPEN ACCESS

Prognostic Impact of Surgical Margin Width in Hepatectomy for Colorectal Liver Metastasis

  • Katsunori Sakamoto1,* ,
  • Toru Beppu2,
  • Kohei Ogawa1,
  • Kei Tamura1,
  • Masahiko Honjo1,
  • Naotake Funamizu1  and
  • Yasutsugu Takada1
 Author information
Journal of Clinical and Translational Hepatology   2023;11(3):705-717

doi: 10.14218/JCTH.2022.00383

Abstract

As for resection for colorectal liver metastasis (CRLM), securing an adequate surgical margin is important for achieving a better prognosis. However, it is often difficult to achieve adequate margins for the resection of CRLM. So the current survival impact of sub-centi/millimeter surgical margins in hepatectomy for CRLM should be evaluated. In the current era of multidisciplinary treatment options, this review focused on the prognostic impact of a sub-centi/millimeter surgical margin width in hepatectomy for CRLM. We systematically reviewed retrospective studies that clearly described the surgical margin width for hepatectomy for CRLM. We selected studies conducted since 2000 that involved patients diagnosed as having CRLM. We focused on studies that investigated not only surgical margins, but also microscopic surgical curability such as R0 (microscopically complete resection) or R1 (microscopically incomplete resection), which clearly describe their definitions. Based on our literature review, 1, 2, or 5 mm was considered the minimum surgical margin width for hepatectomy for CRLM. Although a surgical margin width of 1 mm is acceptable for hepatectomy for CRLM, submillimeter margins, which are defined as R1 in many reports, are only acceptable for limited patients such as those who have undergone preoperative chemotherapy. Zero-mm margins are also acceptable in limited patients such as those who show a good response to preoperative chemotherapy. New chemotherapy agents have been reported to reduce the prognostic impact of a narrow surgical margin width. The incidence of margin recurrence, which is a major concern regarding R1 resection of CRLM, is about 20–30% according to the majority of earlier reports. As evaluations of the actual prognostic impact of the surgical margin remain difficult, further study is warranted.

Keywords

Surgical margin, Colorectal liver metastasis, Chemotherapy

Introduction

The liver is the most frequent metastatic site in colorectal cancer.1 Colorectal liver metastasis (CRLM) occurs in about 50% of patients with colorectal cancer.1 Five-year overall survival rates among all patients with CRLM and those who undergo hepatectomy are 36.3% and 57.1%, respectively, according to nationwide reports in Japan.2 As for resection for CRLM, securing a proper surgical margin is important for achieving a better prognosis.3–6 For better survival outcomes in hepatectomy for CRLM, margins >10 mm have been recommended.3–6 However, it is often difficult to achieve margins >10 mm in patients with multiple bilobar CRLM or whose tumor is adjacent to major vessels.3 Recent advances in surgical procedures and perioperative chemotherapies have led to an increase in the number of patients indicated for potentially curative resection, even for multiple bilobar CRLM.7,8 Regarding surgical procedures, two-stage hepatectomy including associating liver partition and portal vein ligation for staged hepatectomy, major vascular resection and reconstruction, combined local ablation therapy, and parenchymal-sparing hepatectomy (PSH) are reportedly useful options to treat multiple bilobar CRLM.1,7–13 Furthermore, more precise evaluation of hepatic function reserve, portal vein embolization, and conversion chemotherapy, including molecular targeted agents, are considered useful perioperative management strategies for multiple bilobar CRLM. However, for these multidisciplinary treatments, the surgical margin for multiple bilobar CRLM is too narrow to preserve remnant liver volume. In addition, to preserve hepatic function reserve and enable re-hepatectomy for intrahepatic recurrences, PSH is reportedly a useful surgical option with comparable prognostic outcomes and fewer postoperative complications compared with major hepatectomy (MH).10–13 However, unlike MH, PSH can reduce the surgical margin width to preserve liver parenchyma or major vessels. Therefore, reports of the usefulness of sub-centi/millimeter surgical margins have been increasing.3 A sub-centi/millimeter surgical margin can provide a better prognosis than if the patient does not undergo resection, and is considered an acceptable treatment strategy, especially for patients undergoing perioperative chemotherapy for multiple CRLM.3 In addition, R1 resection may be possible for patients who undergo hepatectomy after showing a good response to preoperative chemotherapy.14 Therefore, the current survival impact of sub-centi/millimeter margin surgical margins in hepatectomy for CRLM should be evaluated. In the current era of multidisciplinary treatment options, this review focused on the prognostic impact of a sub-centi/millimeter surgical margin width in hepatectomy for CRLM.

Literature search

As it is difficult to determine the surgical margins for hepatectomy for tumor resection preoperatively, to our knowledge, no randomized controlled trials regarding the surgical margin width for CRLM have been conducted. So we systematically reviewed retrospective studies that clearly described the surgical margin width for hepatectomy for CRLM. We selected studies conducted since 2000 that involved patients diagnosed as having CRLM. We focused on studies that investigated not only surgical margins, but also microscopic surgical curability such as R0 (microscopically complete resected) or R1 (microscopically incomplete resected), which clearly describe their definitions. The definition of R0/1 was varied among studies, and surgical margin widths of <1 mm14–29 and 0 mm1,30–34 were both defined as R1. We conducted a meta-analysis using RevMan software (version 5.4.1; Cochrane Collaboration, Oxford, UK). Dichotomous outcomes were shown by risk difference and 95% confidence intervals. Heterogeneity among the included trials was evaluated by a forest plot. The I-squared and chi-squared statistics were used to evaluate statistical heterogeneity. When I2<50% or p>0.1 in the chi-squared test, indicating significant heterogeneity, a fixed-effects model was adopted. Otherwise, a random-effects model was used.

Subcentimeter surgical margins

We reviewed previous studies that evaluated subcentimeter surgical margins (Table 1).11,15,18,21,22,25,31,32,35-39 The majority of earlier reports that evaluated the feasibility of subcentimeter surgical margins were published before 2014. Angelsen et al.15 and Nuzzo et al.31 reported that compared with >5 mm, a surgical margin of <5 mm increased the margin/local recurrence rate and reduced the time to recurrence. Kokudo et al.35 investigated micrometastases classified into groups based on the distance from the tumor (<2 mm, 2–4 mm, 5–9 mm, and ≥10 mm), and found that 2 mm was the minimum acceptable surgical margin width because micrometastases were rare beyond 2 mm. Konopke et al.36 reported that surgical margin widths of 0 mm or 1–2 mm were associated with poor recurrence-free survival (RFS) compared with those of 3–5 mm and 6–9 mm, but no significant difference in overall survival (OS) was seen. According to Pawlik et al.,18 no significant differences in OS were found among 1–4, 5–9, and ≥10 mm, all of which had better prognosis than <1 mm. In addition, several reports suggested that 1 mm was the minimum acceptable surgical margin width to achieve better survival, and that other factors such as tumor biology or features had a stronger impact on survival.21,22,37,38 Hamady et al.38 reported no significant difference in recurrence rates between subcentimeter and ≥10-mm margins based on propensity-matched analyses. Several papers concluded that hepatectomy for CRLM with subcentimeter margins provided a survival benefit.14,32,37,39,40 Based on our literature review (Table 1), 1, 2, or 5 mm was considered the minimum surgical margin width for hepatectomy for CRLM.

Table 1

Studies evaluating subcentimeter surgical margins

AuthorYear of publicationPeriodFollow-up period, MMarginSummaryMinimum acceptable margin width
Kokudo et al.3520021980–2000Median 29.1<2 mm (n=45)Surgical margin width did not have a negative impact on survival. Cut-end recurrence was rare in margins <2 mm. Micrometastasis was rarely seen within <2 mm around the main tumor.≥2 mm
2–4 mm (n=36)
5–9 mm (n=53)
≥10 mm (n=49)
Pawlik et al.1820051990–2004Median 29<1 mm (n=45)Positive surgical (<1 mm) margin had a negative impact on survival. However, surgical margin width, if negative, did not affect survival or recurrence.≥1 mm
1–4 mm (n=129)
5–9 mm (n=85)
≥10 mm (n=298)
Bodingbauer et al.2520072000–2003Median 33<1 mm (n=43)Margin status did not correlate with either OS or DFS.Positive margin (<1 mm) accepted
1–9 mm (n=110)
>9 mm (n=23)
Are et al.3220071991–2003Median 42Involved (n=112)Margin width of >10 mm is optimal, but subcentimeter resection was also associated with favorable outcomes.>10 mm
<1 mm (n=138)
1–5 mm (n=261)
5–10 mm (n=164)
>10 mm (n=344)
Konopke et al.36200810 yearsMedian 280 mm (n=29)Surgical margins of 0 mm and 1–2 mm had a negative impact on RFS and hepatic-RFS, but not OS.>2 mm
1–2 mm (n=51)
3–5 mm (n=58)
6–9 mm (n=48)
≥10 (n=147)
Nuzzo et al.3120081992–2005Mean 390 mm (n=9)Surgical margin width was a strong prognostic factor and surgical margins ≤5 mm worsened surgical margin recurrence, OS, and DFS.>5 mm
≤2 mm (n=16)
3–5 mm (n=29)
6–9 mm (n=20)
≥10 mm (n=111)
Vandeweyer et al.3720091992–2007Median 48.7≤1 mm (n=67)No significant differences in OS were found among subcentimeter margins other than those ≤1 mm. Beneficial effect of margins >1 mm could not be demonstrated.>1 mm
>1 <4 mm (n=44)
≥4 <10 mm (n=63)
≥10 mm (n=87)
Muratore et al.2120101999–2007Median 56.5<1 mm (n=175)No significant differences in RFS among subcentimeter margins other than those <1 mm. Tumor biology, but not the width of the negative resection margin, affected RFS.≥1 mm
1–2 mm (n=42)
3–5 mm (n=81)
6–10 mm (n=52)
Lordan et al.2220101996–2006NR<1 mm (n=14)No significant differences in OS among subcentimeter margins other than those <1 mm. Clear margin did not affect survival.≥1 mm
1–3 mm (n=48)
>3 mm, 5 mm < (n=17)
>5 mm, 10 mm < (n=55)
≥10 mm (n=104)
Postriganova et al.3920141998–2012Median 310 mm (n=17)Surgical margins <1 mm had comparable survival compared with those ≥10 mm.0 mm
0 mm <1 mm (n=16)
1 mm <3 mm (n=31)
3 mm <10 mm (n=55)
≥10 mm (n=36)
Angelsen et al.1520141998–2010NR<1 mm (n=48)R1 resection was a poor prognostic factor. Resection margins <5 mm increased local recurrence and shortened RFS.≥5 mm
1–4 mm (n=77)
5–9 mm (n=46)
≥10 mm (n=71)
Hamady et al.3820141987–2010Median 33<1 mm (n=663)No significant difference in DFS in the ≥1 mm groups. The <1 mm group showed worse DFS than did the others.≥1 mm
1–4.9 mm (n=852)
5–9.9 mm (n=439)
≥10 mm (n=761)
Memeo et al.1120172006–2013NR0 mm (patient number NR)R1 had a negative impact on OS, even after propensity score matching.≥1 mm
1–5 mm (patient number NR)
>5 mm (patient number NR)

DFS, disease-free survival; NR, not reported; OS, overall survival; RFS, recurrence-free survival.

Submillimeter surgical margins

To evaluate the survival impact of submillimeter margins, we reviewed studies that assessed differences in survival at a surgical margin width cutoff point of 1 mm (Table 2).11,14-20,23-29,32,34,37-39,41–43 In contrast to studies that evaluated subcentimeter margin widths, the majority of the studies evaluating the clinical impact of submillimeter margins were published after 2014, which may imply that subcentimeter margins have recently become an acceptable treatment option.3

Table 2

Studies evaluating submillimeter surgical margins

AuthorYear of publicationStudy periodFollow-up periodSurgical margin widthPatient numberSynchronous, %Tumor numberLargest tumor size, mmPre-CTx, %Post-CTx, %5-yearOS, %p-value5-year DFS, %p-value
Pawlik et al.1820051990–2004Median 29<1 mm4542≥2, 55%Median, 35NR6017.10.005RR, 510.003
≥1 mm512≥62.3RR, 39.5
Are et al.3220071991–2003Median 42Involved11264.9≥2, 49.7%>50, 33.3%33NR26RefNRNR
<1 mm138290.59
≥1 mm76935–450.07–<0.01
Bodingbauer et al.2520072000–2003Median 33<1 mm4358≥2, 70%>50, 19%55–5990.1MST 38.90.373MST, 11.20.343
≥1 mm13352–56.4≥2, 53.4%>50, 21.8%Not reachedMST, 12.4–15.9
Welsh et al.2420081987–2005Median 26.4<1 mm8042.5>3, 35%≥50, 36.3%46.2NRCSS, 17.8<0.001IHRFS, 26.60.001
≥1 mm84944.3>3, 14.3%≥50, 35.0%338839.760.2
de Haas et al.1420081990–2006NR0 mm20258≥2, 68%Mean, 568188570.27290.12
≥1 mm23446≥2, 50%Mean, 3967786120
Vandeweyer et al.3720091992–2007Median 56.4≤1 mm6727NRNRNRNR250.0418.60.14
>1 mm19442.723.6
Andreou et al.1620131997–2010Median 32<1 mm5265≥2, 62%≥30, 49%10069260.017NRNR
≥1 mm32655
Angelsen et al.1520141998–2010NR<1 mm4845.5Median, 2Median, 3032.825.016.10.01100.127
≥1 mm19415.142.524.5
Postriganova et al.3920141998–2012Median 31<1 mm3354.5≥2, 42%Median, 29NRNR540.988360.978
≥1 mm12259.8≥2, 26.2%45–5337–49
Hamady et al.3820141993–2001NR<1 mm, R266349.9≥5, 14%≥50, 36.549NRNRNR20<0.001
≥1 mm2,05233
Pandanaboyana et al.1920151993–2011Median 31.4<1 mm39061.3NR≥50, 40.340.0NRMST, 2.28Y<0.001MST, 1.04Y<0.001
≥1 mm86552.6≥50, 32.642.1MST, 2.7YMST, 1.52Y
Truant et al.2620152000–2010Mean 43<1 mm5967.8Mean, 3.3Mean, 4772.952.539.10.0115.20.021
≥1 mm21453.8Mean, 2.6Mean, 3562.159.354.231.1
Vigano et al.4120162004–2013Median 33.2<1 mm parenchyma10747.7>3, 55.1%>50, 24.3%53.339.332.50.068LR, 19.60.002
<1 mm vascular4650.0>3, 63.0%>50, 19.6%63.039.159.4LR, 4.3NS
≥1 mm9548.4>3, 30.5%>50, 21.1%46.345.354.3LR, 5.3Reference
Laurent et al.2320161999–2010Median 32<1 mm1953>3, 32%Median, 508655440.04780.082
≥1 mm17267>3, 20%Median, 356122
Brudvik et al.1720162005–2013Mean 26<1 mm4822.9≥2, 54.2%Mean, 3585.4NRHazard ratio, 2.4230.001NRNR
≥1 mm58530.1≥2, 52.3%Mean, 2786.2Reference
Sadot et al.4220161992–2012NR0 mm24552>3, 43%≥50, 39%Perioperative, 93%24ReferenceNRNR
0.1–0.9 mm16026<0.05
≥1 mm1,95650>3, 21%≥50, 29%46–48<0.05
Takamoto et al.2720162007–2015Median 30≤1 mm16364≥8, 37%>50, 32%49NR36.60.0043.5<0.001
>1 mm7275.529.7
Margonis et al.3420162003–2015Median 28.9≤1 mm10557.1Median, 2Median, 2579.069.242.40.001NRNR
>1 mm38057.1
Sasaki et al.2020172000–2015Median 30.3Largest tumor <1 mm45NRMedian, 3Median, 2777.881.0MST 36.50.002NRNR
Non-largest tumor <1 mm50Median, 3Median, 2566.075.5MST 53.30.66
≥1 mm156Median, 2Median, 2365.476.0MST 66.6Ref
Hosokawa et al.4320162000–2009At least >600 mm14162.1≥2, 7555.993.2NR360.37NRNR
≥1 mm130NRNRNRNR34
Memeo et al.1120172006–2013NR0 mmNR48.4≥2, 75.1≥50, 25.164.7NR580.0002NRNR
≥1 mmNR39.3≥2, 54.9≥50, 16.770.9NR76–80
Xu et al.2820192006–2016Median 30<1 mm67NRMedian, 3Median, 3010077.638.20.00110.50.002
≥1 mm147Median, 2Median, 2572.853.226.5
Procopio et al.2920202008–2016Median 26<1 mm Parenchyma14153%>3, 62%>50, 28%7450300.00215<0.0001
<1 mm Vascular91>3, 63%>50, 18%7852290.062250.010
≥1 mm142>3, 40%>50, 15%725937Reference39Reference

CSS, cancer-specific survival; CTx, chemotherapy; DFS, disease-free survival; IHRFS, intrahepatic recurrence-free survival; MST, median survival time; NR, not reported; NS, not significant; OS, overall survival; RFS, recurrence-free survival; RR, recurrence rate.

The number of hepatic lesions was greater and the greatest tumor diameter was larger in the <1 mm than in the ≥1 mm group (Fig. 1A, B), and more aggressive disease was considered to have been included in the <1 mm group. Although the rate of preoperative chemotherapy varied, >70% of the patients in the studies published after 2016 underwent preoperative chemotherapy (Fig. 1C, D). Moreover, de Haas et al.14 reported a significantly higher rate of preoperative chemotherapy in the 0 mm than in the ≥1 mm group.

Meta-analysis of studies evaluating the prognostic impact of a surgical margin width ≥1 mm in hepatectomy for colorectal liver metastasis.
Fig. 1  Meta-analysis of studies evaluating the prognostic impact of a surgical margin width ≥1 mm in hepatectomy for colorectal liver metastasis.

(A) Proportion of multiple tumors; (B) Proportion of tumors sized ≥50 mm; (C) Proportion of patients undergoing preoperative chemotherapy; (D) Proportion of patients undergoing postoperative chemotherapy; (E) 5-year overall survival; (F) 5-year recurrence-free survival.

Both 5-year OS and 5-year RFS were poor in the <1 mm group compared with the ≥1 mm group usually (Fig. 1E, F).14–17,19–21,23–26,41–42,44 However, neither Bodingbauer et al.25 nor Postriganova et al.39 found any significant differences in OS or disease-free survival (DFS) between the <1 and ≥1 mm groups.25,39 Furthermore, several reports concluded that even if a surgical margin width <1 mm had a worse prognosis in univariate analyses, it was not an independent prognosticator in multivariate analysis.15,18,21,25,26 In other words, a narrow surgical margin could result from more aggressive disease, which might have led to worse survival.

As for subgroups with a surgical margin <1 mm, Vigano et al.29 and Procopio et al.41 reported that surgical margins of <1 mm adjacent to major vessels had a better prognosis than those not adjacent to major vessels (<1 mm at parenchyma) and was comparable with that of ≥1 mm surgical margins. Takamoto et al.27 reported that ≤1 mm margins had worse OS than did those >1 mm, but narrow ≤1 mm margins (≤4 cm2) showed better survival than did broad ≤ mm margins. In addition, Sasaki et al.20 reported that except for the largest tumor, surgical margins <1 mm had a prognosis comparable to that of those with margins ≥1 mm and better than with <1 mm margins in the largest tumor. Other reports found no differences in long-term prognosis among ≥1 and <1 mm margin groups when patients were limited to those who had undergone preoperative chemotherapy with a good response or had KRAS wild-type tumors.16,23,28–30 Based on our literature review, a surgical margin width of 1 mm is acceptable for hepatectomy for CRLM. However, submillimeter margins, which are defined as R1 in many reports, are acceptable only for a limited number of patients such as those who have undergone preoperative chemotherapy.

Zero-mm margins

Zero-mm margins (exposed tumor, involved margin) are associated with poor survival in many cases.22,31,33,42,45,46 Memeo et al.11 reported that R1 (0 mm) had poor OS compared with R0 (≥1 mm) even after propensity-matched analysis. In the most recent report, Ausania et al.1 reported that 0 mm margins had significantly worse survival, compared with <1 mm margins. However, de Haas et al.14 reported that 0 mm margin resection (R1) had comparable OS/DFS compared with R0 (≥1 mm). Ayez et al.30 also reported that patients who underwent preoperative chemotherapy had comparable survival (OS and DFS) between R0 (>0 mm) and R1 (0 mm). In addition, 0 mm margins, which are defined as R1, in patients with highly advanced bilobar tumor or who had a good response to chemotherapy had a better prognosis compared with R2.34,43,47,48 Therefore, 0 mm margins are acceptable only in a limited number of patients such as those who had a good response to preoperative chemotherapy.

Margin (local, cut-end) recurrence

One major concern regarding R1 resection of CRLM is margin (local, cut-end) recurrence. However, even for patients with R1 resection, the incidence of margin recurrence is about 20–30% according to the majority of previous reports (Table 3).1,15,18,21,26,29,31,35,39,41,46 Vigano et al.41 found no significant difference in the incidence of margin recurrence between R0 and R1-vascular groups, but the R1-parenchyma group was associated with a significantly higher incidence of margin recurrence compared with the others. Furthermore, they found no differences in the isolated margin recurrence rate among the three groups, or in the margin recurrence rate when limited to patients with a good response to preoperative chemotherapy or with large/multiple CRLM.41 Truant et al.26 reported a similar margin recurrence rate between R0 and R1 among patients who underwent preoperative chemotherapy. Postriganova et al.39 reported comparative OS among R1 and R0 after salvage re-hepatectomy in patients with liver recurrence, including margin recurrences. Salvage resection for margin recurrence was reportedly performed in 32.1–78.6% of the patients with margin recurrence,1,15,26,35,41,46 and may improve OS.

Table 3

Studies evaluating margin (local, cut-end) recurrence

AuthorYear of publicationStudy periodFollow-up periodSurgical margin widthPatient numberPre-CTx, %Response* to pre-CTx, %Margin recurrence, %p- value5-year OS, %p-value
Kokudo et al.3520021980–2000Median 29.1<2 mm45NRNR20NR34.70.90
≥2 mm1387.243.8–50.2
Pawlik et al.1820051990–2004Median 29<1 mm45NRNR11NR17.10.005
≥1 mm5123.1≥62.3
Wakai et al.4620081989–2004Median 1270 mm100-300.015MST, 18<0.0001
<10 mm513.9MST, 33
≥10 mm290MST, 89
Nuzzo et al.3120081992–2005Mean 390 mm9NRNR71.4NR00.01
>0 mm1744.039.1
Angelsen et al.1520141998–2010NR<1 mm4832.895.533.30.000116.10.011
≥1 mm19412.442.5
Muratore et al.2120101999–2007Median 56.5<1 mm5545.5NR23.6<0.001NR
≤1 cm17536.26.944.50.9
>1 cm8434.53.645.9
Postriganova et al.3920141998–2012Median 31<1 mm,33NRNR6.10.232540.988
≥1 mm1220.845–53
Truant et al.2620152000–2010Mean 43<1 mm5972.995.316.9 (31.3% of recurrences)0.02539.10.01
≥1 mm21462.193.25.6 (13.4% of recurrences)54.2
Vigano et al.4120162004–2013Median 33.2<1 mm parenchyma10753.368.419.60.00232.50.068
<1 mm vascular4663.072.44.3NS59.4
≥1 mm9546.393.25.3Reference54.3
Procopio et al.2920202008–2016Median 26<1 mm parenchyma141749221.3<0.001300.002
<1 mm vascular91787.7NS290.062
≥1 mm142726.3Reference37Reference
Ausania et al.120222009–2018Median 46.3R1 contact5360.49030.20.036MST, 460.038
R1<1 mm2450908.3MST, 69

*Including complete/partial/stable. CTx, chemotherapy; MST, median survival time; NR, not reported; NS, not significant; OS, overall survival.

Conditions for improved prognosis after R1 hepatectomy

To evaluate the survival impact of new chemotherapy agents such as oxaliplatin or irinotecan for patients with a narrow surgical margin, we evaluated papers published since 2000, mainly from Europe and the USA, where more than 80% of patients in the study cohort had undergone preoperative chemotherapy with new chemotherapy agents. Pandanaboyana et al.19 reported that preoperative chemotherapy did not have a positive impact on OS in patients with R1 (<1 mm) compared with R0 (≥1 mm), but Ayez et al.30 found no significant difference in OS or DFS between R1 (0 mm) and R0 (>0 mm) among patients had undergone preoperative chemotherapy. Andreau et al.16 found no significant difference in OS between R1 (<1 mm) and R0 (≥1 mm) among patients with a good pathological response (0–49% residual possible tumor cells pathologically) to preoperative chemotherapy. In addition, de Haas et al.14 conducted a study that included a high rate of good responders to preoperative chemotherapy (90.0% with response + stabilization and 73.6% of whom had undergone preoperative chemotherapy), and found no significant difference in OS or DFS between R1 (0 mm) and R0 (≥1 mm). Tanaka et al.47 reported significantly poorer OS in an R1 (0 mm) group compared with an R0 (>0 mm) group among all patients, but no significant difference when limited to patients with unresectable/marginally resectable cases who underwent preoperative chemotherapy. Hosokawa et al.43 found no significant difference in OS between R1 (0 mm) and R0 (≥1 mm), and the patients who responded to preoperative chemotherapy achieved cure in 18% of R1 resections. New chemotherapy agents have been reported to reduce the prognostic impact of micrometastases around the resected tumor, and may provide comparable 5-year OS between R1 (<1 mm) and R0 (≥1 mm) groups.14,15,23

R1-vascular, small-R1 (≤4 cm2), and R1 in smaller lesions in multiple metastases might be considered acceptable for improved prognoses in patients undergoing R1 hepatectomy.20,27,29,41 Margonis et al.48 reported that intraoperative re-resection in patients with R1 did not show a survival benefit and that tumor factors showed a stronger survival impact. Margonis et al.34 also showed that R0 resection (>1 mm) only provided a survival benefit in patients with KRAS wild-type, and R1 (≤1 mm) had no survival impact on patients with KRAS mutant type. In contrast, Xu et al.28 reported that R1 (<1 mm) was not an independent predictor of OS in patients with RAS wild-type with a good response to chemotherapy. Therefore, genetic mutation status might affect survival after hepatectomy for CRLM, but to the best of our knowledge, this has yet to be confirmed.

Prognostic factors other than surgical margins

Among the reports that did not find the surgical margin to be a prognostic factor, high preoperative carcinoembryonic antigen (CEA) value, node-positive primary lesion, larger tumor size, and higher number of tumors were identified as independent prognosticators in multivariate analysis.14,15,18,20,21,26,35,40 CEA values of 10, 50, or 200 ng/mL, a tumor size >50 mm, and more than two, four, or five tumors were reported cutoff values.14,18,20,21,35,40 Tumor or biologic factors are often considered prognostic factors stronger than surgical margin width.

Discussion

Earlier reports on hepatectomy for CRLM, considered that tumor surgical margins ≥10 mm were sufficient or desirable,3,44 and subcentimeter surgical margins were also acceptable in many studies (Tables 1 and 2). Therefore, if it was difficult to secure a surgical margin ≥10 mm, large of a margin of subcentimeter length should be secured. This review found that a surgical margin of 5, 2, or 1 mm may be appropriate as a reference value.15,31,35,36 Recent studies have reported that even a surgical margin ≥1 mm provides a sufficient prognostic advantage and might be a minimally acceptable surgical margin (Table 2 and Fig. 1). A possible explanation of why acceptable minimal surgical margin widths have become smaller over time may be advances in chemotherapy.14 However, the 1 mm margin has become acceptable even for patients who have not undergone chemotherapy.25 Therefore, another explanation could be the substantial advances in surgical techniques.14 Regarding surgical procedures, various subgroup analyses of surgical margin status have been reported. Takamoto et al.27 reported that narrow R1 (≤4 cm2) was associated with better survival than broad R1. Vigano et al.41 reported that R1-vascular had better survival than did R1-parenchyma. Recently, Procopio et al.29 also reported that R1-parenchyma showed a worse prognosis than both R1-vascular and R0, but no significant difference was seen between R1-vascular and R0. These studies stress the importance of a precise surgical procedure for dissection at a point close to the tumor because dissection between the tumor and adjacent major vessels requires more accurate techniques to prevent both tumor exposure and injury to vessels. However, evaluating real surgical margins is difficult because they are affected by procedures such as parenchymal ablation/suction, that are considered a major limitation of studies assessing surgical margins.2

In contrast to a 1 mm surgical margin width, a 0 mm margin had worse survival in many studies.1,11,22,31,33,42,45,46 It is possible, however, that preoperative chemotherapy with a good response may counteract the observed negative impact of a 0 mm margin width. The margin recurrence also rate was not high (20–30%), even in patients with R1 resection (Table 3). Furthermore, even if margin recurrence has occurred, recent improvements in surgical procedures may provide a higher rate of salvage hepatectomy for margin recurrence and improve patient prognoses.1,15,26,35,41,46 Because several previous reports that did not find a narrow surgical margin to be an independent predictor of survival found that aggressive tumor status was an independent predictor,14,15,18,21,25,26 a narrow surgical margin might result from a more aggressive disease status. Indicators of aggressive status such as large tumor size, multiple tumors, bilobar distribution, or RAS mutant status are reportedly independent predictors of R1 resection.14,17,24,31,32,36 In the case of multiple bilobar CRLM, the surgical margin must be narrow to preserve a sufficient remnant liver.27,49 Continued advances in chemotherapy, including molecular targeted agents and genomic evaluation, may help solve the problem regarding surgical margin widths, but surgical procedures to achieve an adequate surgical margin width still are an important part of achieving a good long-term prognosis.3 In contrast to the impact of preoperative chemotherapy for the prognosis of patients with a narrow surgical margin width, evidence supporting post-hepatectomy chemotherapy is weak. Although several studies have reported that the absence of post-hepatectomy chemotherapy was a poor prognostic factor,20,21,26,28,41 to our knowledge, no reports have compared the prognosis of patients with a narrow surgical margin with or without post-hepatectomy chemotherapy.

A minimum surgical margin width (≥1 mm) might not be necessary and sufficient for all patients with CRLM. The appropriate surgical margin may differ for individual patients with CRLM. For example, a margin of >10 mm is recommended for patients such those with a solitary, small CRLM at the surface of the liver and distant from the major vessels. In contrast, a 1 mm surgical margin may be suitable for preserving the remnant liver in patients with multiple bilobar CRLM who undergo preoperative chemotherapy. Similarly, a narrow surgical margin width may be suitable for solitary lesions adjacent to major vessels. In Figure 2, we provide a flowchart of the treatment strategy for CRLM considering surgical margin width and various other factors. A prospective study that randomizes tumor resection with a narrow or wide margin for solitary, small, and superficial lesions distant from major vessels is needed to investigate the actual survival impact of narrow margins. However, as hepatectomy with a narrow margin requires a highly technically and precise parenchymal transection procedure, such a study should be undertaken by expert hepatic surgeons. In conclusion, evaluations of the actual prognostic impact of the surgical margin remain difficult and further study is needed.

Flowchart of the treatment strategy for colorectal liver metastasis considering surgical the margin width and other factors.
Fig. 2  Flowchart of the treatment strategy for colorectal liver metastasis considering surgical the margin width and other factors.

*Extrahepatic lesion-positive or node-positive primary. †Detach from major vessels (SM 0 mm) and consider salvage HTx if local recurrence occurs. CEA, carcinoembryonic antigen; CLRM, colorectal liver metastasis; HTx, hepatectomy; SM, surgical margin width.

Abbreviations

CEA: 

carcinoembryonic antigen

CRLM: 

colorectal liver metastasis

DFS: 

disease-free survival

MH: 

major hepatectomy

OS: 

overall survival

PSH: 

parenchymal-sparing hepatectomy

RFS: 

recurrence-free survival

Declarations

Funding

None to declare.

Conflict of interest

The authors have no conflict of interests related to this publication.

Authors’ contributions

Study concept and design (KS, TB), acquisition of data (KS), analysis and interpretation of data (KS, TB), drafting of the manuscript (KS), critical revision of the manuscript for important intellectual content (TB, KO, KT, MH, NF, YT), administrative, technical, or material support (KS, TB), and study supervision (TB). All authors have made a significant contribution to this study and have approved the final manuscript.

References

  1. Ausania F, Landi F, Martínez-Pérez A, Sandomenico R, Cuatrecasas M, Pages M, et al. Impact of microscopic incomplete resection for colorectal liver metastases on surgical margin recurrence: R1-Contact vs R1 < 1 mm margin width. J Hepatobiliary Pancreat Sci 2022;29(4):449-459 View Article PubMed/NCBI
  2. Sakamoto K, Honda G, Beppu T, Kotake K, Yamamoto M, Takahashi K, et al. Comprehensive data of 3,820 patients newly diagnosed with colorectal liver metastasis between 2005 and 2007: report of a nationwide survey in Japan. J Hepatobiliary Pancreat Sci 2018;25(2):115-123 View Article PubMed/NCBI
  3. Margonis GA, Sergentanis TN, Ntanasis-Stathopoulos I, Andreatos N, Tzanninis IG, Sasaki K, et al. Impact of Surgical Margin Width on Recurrence and Overall Survival Following R0 Hepatic Resection of Colorectal Metastases: A Systematic Review and Meta-analysis. Ann Surg 2018;267(6):1047-1055 View Article PubMed/NCBI
  4. Liu W, Sun Y, Zhang L, Xing BC. Negative surgical margin improved long-term survival of colorectal cancer liver metastases after hepatic resection: a systematic review and meta-analysis. Int J Colorectal Dis 2015;30(10):1365-1373 View Article PubMed/NCBI
  5. Cucchetti A, Ercolani G, Cescon M, Bigonzi E, Peri E, Ravaioli M, et al. Impact of subcentimeter margin on outcome after hepatic resection for colorectal metastases: a meta-regression approach. Surgery 2012;151(5):691-699 View Article PubMed/NCBI
  6. Dhir M, Lyden ER, Wang A, Smith LM, Ullrich F, Are C. Influence of margins on overall survival after hepatic resection for colorectal metastasis: a meta-analysis. Ann Surg 2011;254(2):234-242 View Article PubMed/NCBI
  7. Torzilli G, Adam R, Viganò L, Imai K, Goransky J, Fontana A, et al. Surgery of Colorectal Liver Metastases: Pushing the Limits. Liver Cancer 2016;6(1):80-89 View Article PubMed/NCBI
  8. Adam R, Laurent A, Azoulay D, Castaing D, Bismuth H. Two-stage hepatectomy: A planned strategy to treat irresectable liver tumors. Ann Surg 2000;232(6):777-785 View Article PubMed/NCBI
  9. Yamamoto M, Yoshida M, Furuse J, Sano K, Ohtsuka M, Yamashita S, et al. Clinical practice guidelines for the management of liver metastases from extrahepatic primary cancers 2021. J Hepatobiliary Pancreat Sci 2021;28(1):1-25 View Article PubMed/NCBI
  10. Donadon M, Cescon M, Cucchetti A, Cimino M, Costa G, Pesi B, et al. Parenchymal-Sparing Surgery for the Surgical Treatment of Multiple Colorectal Liver Metastases Is a Safer Approach than Major Hepatectomy Not Impairing Patients’ Prognosis: A Bi-Institutional Propensity Score-Matched Analysis. Dig Surg 2018;35(4):342-349 View Article PubMed/NCBI
  11. Memeo R, de Blasi V, Adam R, Goéré D, Azoulay D, Ayav A, et al. Parenchymal-sparing hepatectomies (PSH) for bilobar colorectal liver metastases are associated with a lower morbidity and similar oncological results: a propensity score matching analysis. HPB (Oxford) 2016;18(9):781-790 View Article PubMed/NCBI
  12. Lordan JT, Roberts JK, Hodson J, Isaac J, Muiesan P, Mirza DF, et al. Case-controlled study comparing peri-operative and cancer-related outcomes after major hepatectomy and parenchymal sparing hepatectomy for metastatic colorectal cancer. HPB (Oxford) 2017;19(8):688-694 View Article PubMed/NCBI
  13. Mise Y, Aloia TA, Brudvik KW, Schwarz L, Vauthey JN, Conrad C. Parenchymal-sparing Hepatectomy in Colorectal Liver Metastasis Improves Salvageability and Survival. Ann Surg 2016;263(1):146-152 View Article PubMed/NCBI
  14. de Haas RJ, Wicherts DA, Flores E, Azoulay D, Castaing D, Adam R. R1 resection by necessity for colorectal liver metastases: is it still a contraindication to surgery?. Ann Surg 2008;248(4):626-637 View Article PubMed/NCBI
  15. Angelsen JH, Horn A, Eide GE, Viste A. Surgery for colorectal liver metastases: the impact of resection margins on recurrence and overall survival. World J Surg Oncol 2014;12:127 View Article PubMed/NCBI
  16. Andreou A, Aloia TA, Brouquet A, Dickson PV, Zimmitti G, Maru DM, et al. Margin status remains an important determinant of survival after surgical resection of colorectal liver metastases in the era of modern chemotherapy. Ann Surg 2013;257(6):1079-1088 View Article PubMed/NCBI
  17. Brudvik KW, Mise Y, Chung MH, Chun YS, Kopetz SE, Passot G, et al. RAS Mutation Predicts Positive Resection Margins and Narrower Resection Margins in Patients Undergoing Resection of Colorectal Liver Metastases. Ann Surg Oncol 2016;23(8):2635-2643 View Article PubMed/NCBI
  18. Pawlik TM, Scoggins CR, Zorzi D, Abdalla EK, Andres A, Eng C, et al. Effect of surgical margin status on survival and site of recurrence after hepatic resection for colorectal metastases. Ann Surg 2005;241(5):715-724 View Article PubMed/NCBI
  19. Pandanaboyana S, White A, Pathak S, Hidalgo EL, Toogood G, Lodge JP, et al. Impact of margin status and neoadjuvant chemotherapy on survival, recurrence after liver resection for colorectal liver metastasis. Ann Surg Oncol 2015;22(1):173-179 View Article PubMed/NCBI
  20. Sasaki K, Margonis GA, Maitani K, Andreatos N, Wang J, Pikoulis E, et al. The Prognostic Impact of Determining Resection Margin Status for Multiple Colorectal Metastases According to the Margin of the Largest Lesion. Ann Surg Oncol 2017;24(9):2438-2446 View Article PubMed/NCBI
  21. Muratore A, Ribero D, Zimmitti G, Mellano A, Langella S, Capussotti L. Resection margin and recurrence-free survival after liver resection of colorectal metastases. Ann Surg Oncol 2010;17(5):1324-1329 View Article PubMed/NCBI
  22. Lordan JT, Karanjia ND. ‘Close shave’ in liver resection for colorectal liver metastases. Eur J Surg Oncol 2010;36(1):47-51 View Article PubMed/NCBI
  23. Laurent C, Adam JP, Denost Q, Smith D, Saric J, Chiche L. Significance of R1 Resection for Advanced Colorectal Liver Metastases in the Era of Modern Effective Chemotherapy. World J Surg 2016;40(5):1191-1199 View Article PubMed/NCBI
  24. Welsh FK, Tekkis PP, O’Rourke T, John TG, Rees M. Quantification of risk of a positive (R1) resection margin following hepatic resection for metastatic colorectal cancer: an aid to clinical decision-making. Surg Oncol 2008;17(1):3-13 View Article PubMed/NCBI
  25. Bodingbauer M, Tamandl D, Schmid K, Plank C, Schima W, Gruenberger T. Size of surgical margin does not influence recurrence rates after curative liver resection for colorectal cancer liver metastases. Br J Surg 2007;94(9):1133-1138 View Article PubMed/NCBI
  26. Truant S, Séquier C, Leteurtre E, Boleslawski E, Elamrani M, Huet G, et al. Tumour biology of colorectal liver metastasis is a more important factor in survival than surgical margin clearance in the era of modern chemotherapy regimens. HPB (Oxford) 2015;17(2):176-184 View Article PubMed/NCBI
  27. Takamoto T, Sugawara Y, Hashimoto T, Shimada K, Inoue K, Maruyama Y, et al. Two-dimensional assessment of submillimeter cancer-free margin area in colorectal liver metastases. Medicine (Baltimore) 2016;95(27):e4080 View Article PubMed/NCBI
  28. Xu D, Wang HW, Yan XL, Li J, Wang K, Xing BC. Sub-millimeter surgical margin is acceptable in patients with good tumor biology after liver resection for colorectal liver metastases. Eur J Surg Oncol 2019;45(9):1551-1558 View Article PubMed/NCBI
  29. Procopio F, Viganò L, Cimino M, Donadon M, Del Fabbro D, Torzilli G. Does KRAS mutation status impact the risk of local recurrence after R1 vascular resection for colorectal liver metastasis? An observational cohort study. Eur J Surg Oncol 2020;46(5):818-824 View Article PubMed/NCBI
  30. Ayez N, Lalmahomed ZS, Eggermont AM, Ijzermans JN, de Jonge J, van Montfort K, et al. Outcome of microscopic incomplete resection (R1) of colorectal liver metastases in the era of neoadjuvant chemotherapy. Ann Surg Oncol 2012;19(5):1618-1627 View Article PubMed/NCBI
  31. Nuzzo G, Giuliante F, Ardito F, Vellone M, Giovannini I, Federico B, et al. Influence of surgical margin on type of recurrence after liver resection for colorectal metastases: a single-center experience. Surgery 2008;143(3):384-393 View Article PubMed/NCBI
  32. Are C, Gonen M, Zazzali K, Dematteo RP, Jarnagin WR, Fong Y, et al. The impact of margins on outcome after hepatic resection for colorectal metastasis. Ann Surg 2007;246(2):295-300 View Article PubMed/NCBI
  33. Memeo R, de Blasi V, Adam R, Goéré D, Piardi T, Lermite E, et al. Margin Status is Still an Important Prognostic Factor in Hepatectomies for Colorectal Liver Metastases: A Propensity Score Matching Analysis. World J Surg 2018;42(3):892-901 View Article PubMed/NCBI
  34. Margonis GA, Sasaki K, Kim Y, Samaha M, Buettner S, Amini N, et al. Tumor Biology Rather Than Surgical Technique Dictates Prognosis in Colorectal Cancer Liver Metastases. J Gastrointest Surg 2016;20(11):1821-1829 View Article PubMed/NCBI
  35. Kokudo N, Miki Y, Sugai S, Yanagisawa A, Kato Y, Sakamoto Y, 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(7):833-840 View Article PubMed/NCBI
  36. Konopke R, Kersting S, Makowiec F, Gassmann P, Kuhlisch E, Senninger N, et al. Resection of colorectal liver metastases: is a resection margin of 3 mm enough: a multicenter analysis of the GAST Study Group. World J Surg 2008;32(9):2047-2056 View Article PubMed/NCBI
  37. Vandeweyer D, Neo EL, Chen JW, Maddern GJ, Wilson TG, Padbury RT. Influence of resection margin on survival in hepatic resections for colorectal liver metastases. HPB (Oxford) 2009;11(6):499-504 View Article PubMed/NCBI
  38. Hamady ZZ, Lodge JP, Welsh FK, Toogood GJ, White A, John T, et al. One-millimeter cancer-free margin is curative for colorectal liver metastases: a propensity score case-match approach. Ann Surg 2014;259(3):543-548 View Article PubMed/NCBI
  39. Postriganova N, Kazaryan AM, Røsok BI, Fretland Å, Barkhatov L, Edwin B. Margin status after laparoscopic resection of colorectal liver metastases: does a narrow resection margin have an influence on survival and local recurrence?. HPB (Oxford) 2014;16(9):822-829 View Article PubMed/NCBI
  40. Figueras J, Burdio F, Ramos E, Torras J, Llado L, Lopez-Ben S, 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(7):1190-1195 View Article PubMed/NCBI
  41. Viganò L, Procopio F, Cimino MM, Donadon M, Gatti A, Costa G, et al. Is Tumor Detachment from Vascular Structures Equivalent to R0 Resection in Surgery for Colorectal Liver Metastases? An Observational Cohort. Ann Surg Oncol 2016;23(4):1352-1360 View Article PubMed/NCBI
  42. Sadot E, Groot Koerkamp B, Leal JN, Shia J, Gonen M, Allen PJ, et al. Resection margin and survival in 2368 patients undergoing hepatic resection for metastatic colorectal cancer: surgical technique or biologic surrogate?. Ann Surg 2015;262(3):476-485 View Article PubMed/NCBI
  43. Hosokawa I, Allard MA, Gelli M, Ciacio O, Vibert E, Cherqui D, et al. Long-Term Survival Benefit and Potential for Cure after R1 Resection for Colorectal Liver Metastases. Ann Surg Oncol 2016;23(6):1897-1905 View Article PubMed/NCBI
  44. Hamady ZZ, Cameron IC, Wyatt J, Prasad RK, Toogood GJ, Lodge JP. Resection margin in patients undergoing hepatectomy for colorectal liver metastasis: a critical appraisal of the 1cm rule. Eur J Surg Oncol 2006;32(5):557-563 View Article PubMed/NCBI
  45. Poultsides GA, Schulick RD, Pawlik TM. Hepatic resection for colorectal metastases: the impact of surgical margin status on outcome. HPB (Oxford) 2010;12(1):43-49 View Article PubMed/NCBI
  46. Wakai T, Shirai Y, Sakata J, Valera VA, Korita PV, Akazawa K, et al. Appraisal of 1 cm hepatectomy margins for intrahepatic micrometastases in patients with colorectal carcinoma liver metastasis. Ann Surg Oncol 2008;15(9):2472-2481 View Article PubMed/NCBI
  47. Tanaka K, Nojiri K, Kumamoto T, Takeda K, Endo I. R1 resection for aggressive or advanced colorectal liver metastases is justified in combination with effective prehepatectomy chemotherapy. Eur J Surg Oncol 2011;37(4):336-343 View Article PubMed/NCBI
  48. Margonis GA, Spolverato G, Kim Y, Ejaz A, Pawlik TM. Intraoperative surgical margin re-resection for colorectal liver metastasis: is it worth the effort?. J Gastrointest Surg 2015;19(4):699-707 View Article PubMed/NCBI
  49. Torzilli G, Viganò L, Gatti A, Costa G, Cimino M, Procopio F, et al. Twelve-year experience of “radical but conservative” liver surgery for colorectal metastases: impact on surgical practice and oncologic efficacy. HPB (Oxford) 2017;19(9):775-784 View Article PubMed/NCBI
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Prognostic Impact of Surgical Margin Width in Hepatectomy for Colorectal Liver Metastasis

Katsunori Sakamoto, Toru Beppu, Kohei Ogawa, Kei Tamura, Masahiko Honjo, Naotake Funamizu, Yasutsugu Takada
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