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Significance of postoperative adjuvant chemotherapy with an oxaliplatin-based regimen after simultaneous curative resection for colorectal cancer and synchronous colorectal liver metastasis: a propensity score matching analysis

BMC Surgery volume 21, Article number: 188 (2021) Cite this article

A Correction to this article was published on 26 April 2021

This article has been updated

Abstract

Background

Expansion of the indication for liver resection and new regimens for systemic chemotherapy have improved postoperative outcomes for synchronous colorectal liver metastases (CRLM). However, such cases can still have a high recurrence rate, even after curative resection. Therefore, there is a need for postoperative adjuvant chemotherapy (POAC) after liver resection in patients with CRLM. There are few studies of the efficacy of POAC with an oxaliplatin-based regimen after simultaneous resection for colorectal cancer and CRLM with curative intent. The goal of the study was to compare POAC with oxaliplatin-based and fluoropyrimidine regimens using propensity score (PS) matching analysis.

Methods

The subjects were 94 patients who received POAC after simultaneous resection for colorectal cancer and synchronous CRLM, and were enrolled retrospectively. The patients were placed in a L-OHP (+) group (POAC with an oxaliplatin-based regimen, n = 47) and a L-OHP (−) group (POAC with a fluoropyrimidine regimen, n = 47). Recurrence-free (RFS), cancer-specific (CSS), unresectable recurrence-free (URRFS), remnant liver recurrence-free (RLRFS), and extrahepatic recurrence-free (EHRFS) survival were analyzed.

Results

Before PS matching, the L-OHP (+) and (−) groups had no significant differences in RFS, CSS, URRFS, RLRFS, and EHRFS. Univariate analysis indicated significant differences in age, preoperative serum CEA (≤ 30.0 ng/mL/ > 30.0 ng/mL), differentiation of primary tumor (differentiated/undifferentiated), T classification (T1–3/T4), number of hepatic lesions and maximum diameter of the hepatic lesion between the L-OHP (+) and (−) groups. After PS matching using these confounders, RFS was significantly better among patients in the L-OHP (+) group compared with the L-OHP (−) group (HR 0.40, 95% CI 0.17–0.96, p = 0.04). In addition, there was a trend towards better RLRFS among patients in the L-OHP (+) group compared with the L-OHP (−) group (HR 0.42, 95% CI 0.17–1.02, p = 0.055). However, there were no significant differences in CSS, URRFS and EHRFS between the L-OHP (+) and (−) groups.

Conclusions

PS matching analysis demonstrated the efficacy of POAC with an oxaliplatin-based regimen in RFS and RLRFS.

Peer Review reports

Background

Colorectal cancer is a global cause of death and an increasingly common disease in Japan [1, 2]. Expansion of the indication for liver resection and new regimens for systemic chemotherapy have altered therapeutic strategies and improved postoperative outcomes for synchronous colorectal liver metastases (CRLM) [3]. In cases with resectable CRLM, treatment with liver resection is now thought to be the best strategy [4,5,6]. However, such cases can still have a high recurrence rate, even after curative resection [7]. Therefore, there is a need for postoperative adjuvant chemotherapy (POAC) after liver resection in patients with CRLM. A randomized controlled trial has shown that POAC with oral uracil-tegafur with leucovorin (UFT/LV) prolongs recurrence-free survival (RFS) after liver resection for synchronous CRLM compared with surgery alone [8]. In contrast, the guidelines of the National Comprehensive Cancer Network (NCCN) [9] and those of the European Society for Medical Oncology (ESMO) [10] suggest that an oxaliplatin-based regimen (FOLFOX or CapeOX) is preferred after synchronous colectomy and liver resection, as well as a fluoropyrimidine regimen (capecitabine or 5-FU/leucovorin).

The superiority of an oxaliplatin-based regimen over a fluoropyrimidine regimen for synchronous CRLM is uncertain. The European Organisation for Research and Treatment of Cancer (EORTC) intergroup trial 40,983 [11] demonstrated a progression-free survival (PFS) benefit with perioperative FOLFOX over surgery alone, but no effect on overall survival (OS) in resectable CRLM. However, this study did not include comparisons between an oxaliplatin-based regimen and a fluoropyrimidine regimens. Moreover, this study evaluated perioperative treatment in resectable CRLM. Therefore, currently, there is no evidence of a better clinical outcome after POAC with an oxaliplatin-based regimen over a fluoropyrimidine regimen. Therefore, this study was conducted to compare POAC with oxaliplatin-based and fluoropyrimidine regimens using propensity score (PS) matching analysis.

Materials and methods

Patient selection

The scheme of the study is shown in Fig. 1. Of 3248, 1412 and 922 consecutive patients with colorectal cancer who were treated surgically at Juntendo University Hospital between 2002 and 2018, at Juntendo University Nerima Hospital between 2007 and 2019, and at Juntendo University Shizuoka Hospital between 2011 and 2018, respectively, 274 (8.4%), 89 (6.3%) and 57 (6.2%) presented with synchronous CRLM. Among these respective patients, 105, 6 and 14 underwent simultaneous resection for colorectal cancer and synchronous CRLM with curative intent. Finally, 78, 4 and 12 patients, who received POAC after simultaneous resection with curative intent for colorectal cancer and synchronous CRLM, were enrolled retrospectively in the study. The patients were divided into a L-OHP (+) group (POAC with an oxaliplatin-based regimen, n = 47) and a L-OHP (−) group (POAC with a fluoropyrimidine regimen, n = 47). Patients who underwent POAC with molecular-targeted agents were excluded from the study because these agents were not widely used during the study period [12]. Data were collected in a retrospective review of a database and medical records. Synchronous metastases were defined as liver metastatic disease at presentation in this study. Liver resection was indicated for liver metastases for cases in which (1) curative resection was possible for a primary tumor, liver metastases and extrahepatic distant metastases; (2) there was likely to be an acceptable liver functional reserve after liver resection; and (3) the patient could tolerate surgery. The study was conducted in accordance with the Declaration of Helsinki. The study was approved by the institutional review board (IRB) of Juntendo University Hospital (No. 19-140), Juntendo University Nerima Hospital (No.2020-14) and Juntendo University Shizuoka Hospital (No. 776). The requirement for formal informed consent was waived because of the study’s retrospective design.

Fig. 1
figure 1

Study scheme. Of 3248, 1412 and 922 consecutive patients with colorectal cancer who were treated surgically at Juntendo University Hospital between 2002 and 2018, at Juntendo University Nerima Hospital between 2007 and 2019, and at Juntendo University Shizuoka Hospital between 2011 and 2018, respectively, 274 (8.4%), 89 (6.3%) and 57 (6.2%) presented with synchronous CRLM. Among these respective patients, 105, 6 and 14 underwent simultaneous resection for colorectal cancer and synchronous CRLM with curative intent. Finally, 78, 4 and 12 patients, who received POAC after simultaneous resection with curative intent for colorectal cancer and synchronous CRLM, were enrolled retrospectively in the study. The patients were divided into a L-OHP (+) group (POAC with an oxaliplatin-based regimen, n = 47) and a L-OHP (−) group (POAC with a fluoropyrimidine regimen, n = 47). A total of 21 patients in each group were matched in one-on-one pair PS matching analysis

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Surgical strategies for colorectal cancer and synchronous CRLM

Colorectal cancer was resected with lymph node dissection at the root of the main vessels (ileocolic, middle colic, inferior mesenteric arteries and veins) with curative intent [13]. The principle of radical surgery for colorectal cancer was complete mesocolic excision (CME) or total mesorectal excision (TME) [13]. Open or laparoscopic surgery was indicated based on tumor-related factors (tumor site and extent of cancer progression) and patient-related factors (obesity, history of abdominal surgery). We note that these indications changed to some extent over the period of the study.

Preoperative evaluation using enhanced computed tomography (CT) and/or magnetic resonance imaging (MRI) was performed, as we have previously described for CRLM [14]. Occult tumors that were not detected by preoperative imaging or by inspection or palpation in laparotomy were identified by routine intraoperative ultrasound (IOUS). Relationships of tumors with vasculo-biliary structures were also shown on IOUS. Anatomical or non-anatomical IOUS-guided resection of tumors was performed to give a tumor-free margin.

Postoperative adjuvant chemotherapy (POAC)

The POAC regimen was selected based on age and clinicopathological factors. The regimen for each case was finally decided based on a discussion between the physician and patient. POAC was started 4–8 weeks postoperatively.

Clinicopathological analysis

Clinicopathological factors (age, gender, location in the colon or rectum, preoperative and postoperative serum carcinoembryonic antigen (CEA), differentiation of primary tumor, T classification, N classification, number of hepatic lesions, maximum diameter of hepatic lesion, presence or absence of synchronous extrahepatic metastasis, partial or anatomical liver resection, negative or positive surgical margin of a hepatic lesion), and survival were analyzed in this study. Since serum CEA has been reported to be a critical predictive factor for perioperative FOLFOX for resectable CRLM [15], it was analyzed as a categorical variable (≤ 30.0 ng/mL/ > 30.0 ng/mL, ≤ 5.0 ng/mL/ > 5.0 ng/mL), as well as a continuous variable. Postoperative serum CEA was measured once between simultaneous resection of colorectal cancer and synchronous CRLM, and the initiation of POAC. Based on International Union Against Cancer guidelines [16], negative and positive surgical margins were defined as a microscopically negative margin ≥ 1 mm, and a tumor free margin < 1 mm with microscopic tumor invasion of the resection margin, respectively.

Follow-up

Postoperative follow-up procedures included clinical assessment and serum CEA measurements every 3 months, chest CT and abdominal ultrasonography or CT every 3–6 months.

Propensity score (PS) matching analysis

Differences in clinicopathological severity between the L-OHP (+) and (−) groups were adjusted by PS matching analysis. The PS was estimated, and the log odds of the probability of treatment of a patient using POAC with an oxaliplatin-based regimen (L-OHP (+) group) was modeled with potential confounders of patient background factors and tumor characteristics with p < 0.05 in univariate analyses between the L-OHP (+) and (−) groups. The confounders for PS matching analysis were selected based on the factors that were mainly used to select the regimen. The c-statistic was calculated to determine the propensity model discrimination. One-on-one pair PS matching analysis with calipers < 0.05 was performed in JMP 14 (SAS Institute Inc., Cary, NC, USA).

Statistical analysis

Recurrence-free (RFS: time from initial surgery for colorectal cancer and synchronous CRLM until first recurrence of the disease), cancer-specific (CSS: time from surgery until cancer-related death), unresectable recurrence-free (URRFS: time from surgery until first unresectable recurrence), remnant liver recurrence-free (RLRFS: time from surgery until first recurrence in the remnant liver), and extrahepatic recurrence-free (EHRFS: time from surgery until first extrahepatic recurrence) survival were determined with the Kaplan–Meier method, and significance was evaluated by univariate analyses using a log-rank test. The concept of URRFS is the same as the time to surgical failure (TSF), which could be a suitable endpoint for CRLM overall management [17]. Discrete and continuous variables were compared by Fisher exact test and Mann–Whitney U-test, respectively. JMP 14 was used for all analyses, with differences considered significant at p < 0.05. Values are shown as median (minimum–maximum).

Results

POAC regimens

The common regimens in the L-OHP (+) group were CapeOX (n = 25 patients, 26.6%) and FOLFOX (n = 22, 23.4%), and those in the L-OHP(-) group were UFT/LV (n = 38, 40.4%), S-1 (n = 7, 7.4%) and capecitabine (n = 2, 2.1%) (Table 1). The median numbers of cycles in each regimen in the L-OHP (+) group were 8 for CapeOX and 12 for FOLFOX. The median periods for each regimen in the L-OHP(-) group were 6 months for UFT/LV, 12 months for S-1 and 11 months for capecitabine (including discontinuation due to recurrence or adverse events).

Table 1 Details of the regimens of postoperative adjuvant chemotherapy (POAC)
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RFS, CSS, URRFS, RLRFS and EHRFS in the whole cohort

The median observation period was 64.5 months (range: 7.5–163.1 months) for recurrence-free surviving patients. The L-OHP (+) and (−) groups had no significant differences in RFS [hazard ratio (HR) 0.80, 95% confidence interval (CI) 0.48–1.32, p = 0.38], CSS (HR 1.16, 95% CI 0.63–2.16, p = 0.63), URRFS (HR: 1.09, 95% CI 0.63–1.89, p = 0.77), RLRFS (HR 0.77, 95% CI 0.43–1.35, p = 0.36), and EHRFS (HR 0.98, 95% CI 0.55–1.76, p = 0.96) (Fig. 2).

Fig. 2
figure 2

Comparisons of recurrence-free (RFS), cancer-specific (CSS), unresectable recurrence-free (URRFS), remnant liver recurrence-free (RLRFS), and extrahepatic recurrence-free (EHRFS) survival in the entire cohort. The L-OHP (+) and (−) groups had no significant differences in RFS (hazard ratio (HR): 0.80, 95% confidence interval (CI): 0.48–1.32, p = 0.38), CSS (HR 1.16, 95% CI 0.63–2.16, p = 0.63), URRFS (HR 1.09, 95% CI 0.63–1.89, p = 0.77), RLRFS (HR 0.77, 95% CI 0.43–1.35, p = 0.36), and EHRFS (HR 0.98, 95% CI 0.55–1.76, p = 0.96)

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Clinicopathological factors in the L-OHP (+) and (−) groups

Univariate analysis indicated that age, preoperative serum CEA (≤ 30.0 ng/mL/ > 30.0 ng/mL), differentiation of primary tumor (differentiated/undifferentiated), T classification (T1-3/T4), number of hepatic lesions and maximum diameter of the hepatic lesion differed significantly between the L-OHP (+) and (−) groups. Patients in the L-OHP (+) group were younger (p = 0.02); more frequently had preoperative serum CEA > 30.0 ng/mL (p = 0.04), an undifferentiated primary tumor (p = 0.03) and a T1–T3 primary tumor (p = 0.046); and had more (p = 0.04) and larger (p = 0.03) hepatic lesions (Table 2). There were no significant differences in other clinicopathological factors between the two groups.

Table 2 Clinicopathological factors in the L-OHP (+) and (−) groups before and after propensity score matching
Full size table

The PS was estimated with potential confounders of age, preoperative serum CEA, differentiation of primary tumor, T classification, number of hepatic lesions, and maximum diameter of hepatic lesions. The median PS was 0.72 (0.04–1.00) in the L-OHP (+) group and 0.32 (0.04–0.77) in the L-OHP (−) group (p < 0.001). The c-statistic of 0.82 (95% CI 0.73–0.91, p < 0.001) showed satisfactory discrimination. A total of 21 patients in each group were matched in one-on-one pair PS matching analysis (Fig. 1). There were no significant differences in univariate analysis of clinicopathological factors between the L-OHP (+) and (−) groups after PS matching (Table 2).

RFS, CSS, URRFS, RLRFS and EHRFS in the propensity-matched cohort

RFS was significantly better among patients in the L-OHP (+) group compared with the L-OHP (−) group (HR 0.40, 95% CI 0.17–0.96, p = 0.04). In addition, there was a trend towards better RLRFS among patients in the L-OHP (+) group compared with the L-OHP (−) group (HR 0.42, 95% CI 0.17–1.02, p = 0.055). CSS (HR 0.62, 95% CI 0.23–1.68, p = 0.35), URRFS (HR 0.63, 95% CI 0.26–1.55, p = 0.32), and EHRFS (HR 0.66, 95% CI 0.25–1.73, p = 0.40) did not differ significantly between the two groups (Fig. 3).

Fig. 3
figure 3

Comparisons of recurrence-free (RFS), cancer-specific (CSS), unresectable recurrence-free (URRFS), remnant liver recurrence-free (RLRFS), and extrahepatic recurrence-free (EHRFS) survival in the propensity-matched cohort. RFS was significantly better among patients in the L-OHP (+) group compared with the L-OHP (−) group (HR 0.40, 95% CI 0.17–0.96, p = 0.04). In addition, there was a trend towards better RLRFS among patients in the L-OHP (+) group compared with the L-OHP (−) group (HR 0.42, 95% CI 0.17–1.02, p = 0.055). CSS (HR: 0.62, 95% CI 0.23–1.68, p = 0.35), URRFS (HR 0.63, 95% CI 0.26–1.55, p = 0.32), and EHRFS (HR 0.66, 95% CI 0.25–1.73, p = 0.40) did not differ significantly between the two groups

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Discussion

Synchronous CRLM is found in about 20% of cases of colorectal cancer [12, 18]. Synchronous CRLM has less favorable cancer biology, and the 5-year survival rate after curative resection is only 39% [19]. Patients with recurrence of synchronous CRLM are thought to have had residual undetectable micrometastases when synchronous CRLM is initially resected. Therefore, use of POAC in this setting may be helpful [12, 19], but the role of POAC is still controversial.

In a study of the efficacy of POAC with an oxaliplatin-based regimen compared to a fluoropyrimidine regimen, Kim et al. [20] found that this regimen gave significantly better disease-free survival (DFS) compared to cases treated with a fluoropyrimidine regimen, but without a significant difference in OS between these groups. Hsu et al. [21] also reported that POAC with an oxaliplatin-based regimen resulted in favorable RFS compared with a fluoropyrimidine regimen, but not OS, in multivariate analysis. However, the backgrounds of the groups were not balanced, and there were trends (not significant) in the number and maximum size of synchronous CRLM between the two groups. Therefore, these differences require adjustment.

Age, preoperative serum CEA (≤ 30.0 ng/mL/ > 30.0 ng/mL), differentiation of primary tumor (differentiated/undifferentiated), T classification (T1-3/T4), and the number and maximum diameter of synchronous CRLM differed significantly between the L-OHP (+) and (−) groups in our study. Therefore, the efficacy of POAC with an oxaliplatin-based regimen was examined using PS matching analysis. The PS reflects the treatment assignment probability based on baseline covariables [22], and there is increasing use of PS methods to counter the effects of confounding factors in observational studies of the effects of treatment on outcomes [23]. There may be significant differences between patients treated with POAC with oxaliplatin-based and fluoropyrimidine regimens in clinical practice, particularly for age, tumor aggressiveness, and patient status. Therefore, we accounted for the selection bias and non-random treatment groups through use of PS matching analysis.

Baseline data in the whole cohort indicated more use of POAC with an oxaliplatin-based regimen for younger cases with more severe tumor aggressiveness, but one-on-one pair PS matching balanced these factors between the L-OHP (+) and (−) groups. We believe that this is the first use of PS matching analysis to examine the efficacy of POAC with an oxaliplatin-based regimen after simultaneous resection of colorectal cancer and synchronous CRLM. Our results indicate that the oxaliplatin-based regimen has limited efficacy in these patients. RFS was significantly better among patients in the L-OHP (+) group compared with the L-OHP (−) group. In addition, there was a trend towards better RLRFS among patients in the L-OHP (+) group compared with the L-OHP (−) group. However, there was no difference in CSS between the two groups. The absence of a difference in CSS may be because the patients in the L-OHP (−) group underwent systemic chemotherapy with an oxaliplatin-based regimen after recurrence, which may have prolonged CSS in the L-OHP (−) group. These results are similar to those in the two earlier studies [20, 21], which did not balance patient backgrounds between the groups. This indicates that cases who undergo simultaneous resection of colorectal cancer and synchronous CRLM may not require an oxaliplatin-based regimen immediately after the initial surgery. Such POAC may not be necessary until recurrence, in order to avoid oxaliplatin-related adverse events especially in elderly patients.

There are some limitations in this study. First, data were collected only for a small number of patients. Second, the POAC regimens were not constant over the study period. Third, since the oxaliplatin-based regimen was introduced more recently than the fluoropyrimidine regimen, there was a difference in study periods between the L-OHP (+) and (−) groups. This might have affected better RFS and RLRFS in the L-OHP (+) group after PS matching analysis because preoperative imaging with CT and MRI has also become more sophisticated. Fourth, data for adverse events in both regimens were not available. Finally, the RAS gene mutation status was not available in all cases, and this status affects the risk of recurrence of CRLM [24, 25].

Conclusions

RFS was significantly better among patients in the L-OHP (+) group compared with the L-OHP (−) group. In addition, there was a trend towards better RLRFS among patients in the L-OHP (+) group compared with the L-OHP (−) group. However, there was no difference in CSS between the two groups. Therefore, the efficacy of POAC with an oxaliplatin-based regimen after simultaneous resection of colorectal cancer and synchronous CRLM is limited.

Availability of data and materials

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

Change history

Abbreviations

CRLM:

Colorectal liver metastases

POAC:

Postoperative adjuvant chemotherapy

UFT/LV:

Uracil-tegafur with leucovorin

RFS:

Recurrence-free survival

NCCN:

National Comprehensive Cancer Network

ESMO:

European Society for Medical Oncology

EORTC:

European Organisation for Research and Treatment of Cancer

OS:

Overall survival

PS:

Propensity score

L-OHP:

Oxaliplatin

IRB:

Institutional review board

CME:

Complete mesocolic excision

TME:

Total mesorectal excision

CT:

Computed tomography

MRI:

Magnetic resonance imaging

IOUS:

Intraoperative ultrasound

CEA:

Carcinoembryonic antigen

CSS:

Cancer-specific survival

URRFS:

Unresectable recurrence-free survival

RLRFS:

Remnant liver recurrence-free survival

EHFRS:

Extrahepatic recurrence-free survival

TSF:

Time to surgical failure

References

  1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2019. CA Cancer J Clin. 2019;69:7–34.

    Article  Google Scholar 

  2. Carioli G, Malvezzi M, Bertuccio P, Hashim D, Waxman S, Negri E, et al. Cancer mortality in the elderly in 11 countries worldwide, 1970–2015. Ann Oncol. 2019;30:1344–55.

    Article  CAS  Google Scholar 

  3. Schiergens TS, von Einem J, Thomas MN, Albertsmeier M, Giessen-Jung C, Dörsch M, et al. Multidisciplinary treatment of colorectal liver metastases. Minerva Med. 2017;108:527–46.

    Article  Google Scholar 

  4. Martin RC 2nd, Augenstein V, Reuter NP, Scoggins CR, McMasters KM. Simultaneous versus staged resection for synchronous colorectal cancer liver metastases. J Am Coll Surg. 2009;208:842–52.

    Article  Google Scholar 

  5. Feng Q, Wei Y, Zhu D, Ye L, Lin Q, Li W, et al. Timing of hepatectomy for resectable synchronous colorectal liver metastases: for whom simultaneous resection is more suitable–a meta-analysis. PLoS ONE. 2014;9:e104348.

    Article  Google Scholar 

  6. Ferretti S, Tranchart H, Buell JF, Eretta C, Patriti A, Spampinato MG, et al. Laparoscopic simultaneous resection of colorectal primary tumor and liver metastases: results of a multicenter international study. World J Surg. 2015;39:2052–60.

    Article  Google Scholar 

  7. Fonseca GM, Herman P, Faraj SF, Kruger JAP, Coelho FF, Jeismann VB, et al. Pathological factors and prognosis of resected liver metastases of colorectal carcinoma: implications and proposal for a pathological reporting protocol. Histopathology. 2018;72:377–90.

    Article  Google Scholar 

  8. Hasegawa K, Saiura A, Takayama T, Miyagawa S, Yamamoto J, Ijichi M, et al. Adjuvant oral uracil-tegafur with leucovorin for colorectal cancer liver metastases: a randomized controlled trial. PLoS ONE. 2016;11:e0162400.

    Article  Google Scholar 

  9. NCCN: NCCN Guidelines. Colon Cancer Version 4. 2020. http://www.nccn.org/. Assessed 22 Jun 2020.

  10. Van Cutsem E, Cervantes A, Adam R, Sobrero A, Van Krieken JH, Aderka D, et al. ESMO consensus guidelines for the management of patients with metastatic colorectal cancer. Ann Oncol. 2016;27:1386–422.

    Article  Google Scholar 

  11. Nordlinger B, Sorbye H, Glimelius B, Poston GJ, Schlag PM, Rougier P, et al. Perioperative FOLFOX4 chemotherapy and surgery versus surgery alone for resectable liver metastases from colorectal cancer (EORTC 40983): long-term results of a randomised, controlled, phase 3 trial. Lancet Oncol. 2013;14:1208–15.

    Article  CAS  Google Scholar 

  12. Chow FC, Chok KS. Colorectal liver metastases: an update on multidisciplinary approach. World J Hepatol. 2019;11:150–72.

    Article  Google Scholar 

  13. Hashiguchi Y, Muro K, Saito Y, Ito Y, Ajioka Y, Hamaguchi T, et al. Japanese Society for Cancer of the Colon and Rectum (JSCCR) guidelines 2019 for the treatment of colorectal cancer. Int J Clin Oncol. 2020;25:1–42.

    Article  Google Scholar 

  14. Oguro S, Imamura H, Yoshimoto J, Ishizaki Y, Kawasaki S. Liver metastases from gastric cancer represent systemic disease in comparison with those from colorectal cancer. J Hepatobiliary Pancreat Sci. 2016;23:324–32.

    Article  Google Scholar 

  15. Sorbye H, Mauer M, Gruenberger T, Glimelius B, Poston GJ, Schlag PM, et al. Predictive factors for the benefit of perioperative FOLFOX for resectable liver metastasis in colorectal cancer patients (EORTC Intergroup Trial 40983). Ann Surg. 2012;255:534–9.

    Article  Google Scholar 

  16. Brierley JD, Gospodarowicz MK, Wittekind C. TNM classification of malignant tumours. 8th ed. Hoboken: John Wiley & Sons; 2017.

    Google Scholar 

  17. Oba M, Hasegawa K, Matsuyama Y, Shindoh J, Mise Y, Aoki T, et al. Discrepancy between recurrence-free survival and overall survival in patients with resectable colorectal liver metastases: a potential surrogate endpoint for time to surgical failure. Ann Surg Oncol. 2014;21:1817–24.

    Article  Google Scholar 

  18. van der Geest LG, Lam-Boer J, Koopman M, Verhoef C, Elferink MA, de Wilt JH. Nationwide trends in incidence, treatment and survival of colorectal cancer patients with synchronous metastases. Clin Exp Metastasis. 2015;32:457–65.

    Article  Google Scholar 

  19. Adam R, de Gramont A, Figueras J, Kokudo N, Kunstlinger F, Loyer E, et al. Managing synchronous liver metastases from colorectal cancer: a multidisciplinary international consensus. Cancer Treat Rev. 2015;41:729–41.

    Article  Google Scholar 

  20. Kim SY, Kim HJ, Hong YS, Jung KH, Park JW, Choi HS, et al. Resected colorectal liver metastases: does the survival differ according to postoperative chemotherapy regimen? J Surg Oncol. 2009;100:713–8.

    Article  CAS  Google Scholar 

  21. Hsu HC, Chou WC, Shen WC, Wu CE, Chen JS, Liau CT, et al. Efficacy of postoperative oxaliplatin- or irinotecan-based chemotherapy after curative resection of synchronous liver metastases from colorectal cancer. Anticancer Res. 2013;33:3317–25.

    CAS  PubMed  Google Scholar 

  22. Rosenbaum PR, Rubin DB. The central role of the propensity score in observational studies for causal effects. Biometrika. 1983;70:41–55.

    Article  Google Scholar 

  23. Austin PC. The performance of different propensity score methods for estimating marginal hazard ratios. Stat Med. 2013;32:2837–49.

    Article  Google Scholar 

  24. Passiglia F, Bronte G, Bazan V, Galvano A, Vincenzi B, Russo A. Can KRAS and BRAF mutations limit the benefit of liver resection in metastatic colorectal cancer patients? A systematic review and meta-analysis. Crit Rev Oncol Hematol. 2016;99:150–7.

    Article  Google Scholar 

  25. Tsilimigras DI, Ntanasis-Stathopoulos I, Bagante F, Moris D, Cloyd J, Spartalis E, et al. Clinical significance and prognostic relevance of KRAS, BRAF, PI3K and TP53 genetic mutation analysis for resectable and unresectable colorectal liver metastases: a systematic review of the current evidence. Surg Oncol. 2018;27:280–8.

    Article  Google Scholar 

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Acknowledgements

We are especially grateful to all members of the Department of Coloproctological Surgery, Juntendo University Faculty of Medicine for useful discussions and technical support.

Funding

The authors have no financial support.

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Authors and Affiliations

  1. Department of Coloproctological Surgery, Juntendo University Faculty of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan

    Kiichi Sugimoto, Kazuhiro Sakamoto, Shinya Munakata, Makoto Takahashi, Yutaka Kojima & Yuichi Tomiki

  2. Department of General Surgery, Juntendo University Nerima Hospital, Tokyo, Japan

    Yuki Ii, Kota Amemiya & Hiroyuki Sugo

  3. Department of Surgery, Juntendo University Shizuoka Hospital, Shizuoka, Japan

    Tomoaki Ito & Koichi Sato

  4. Department of Hepatobiliary-Pancreatic Surgery, Juntendo University Faculty of Medicine, Tokyo, Japan

    Akio Saiura & Seiji Kawasaki

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  12. Akio Saiura
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  13. Seiji Kawasaki
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Contributions

Sugimoto K and Sakamoto K developed the concept of the study and drafted the article. Sugimoto K, YI, KA, TI and SM performed the patient survey and analyzed data. HS, MT, YK, YT, Sato K, AS and SK recruited patients, and YK and YT matched patient survey data with medical records in revision of the article. Sugimoto K, Sakamoto K, TI and HS obtained IRB approval for the protocol of the study. The article was revised and has been approved by all authors. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Kiichi Sugimoto.

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Ethics approval and consent to participate

The study was approved by the institutional review board (IRB) of Juntendo University Hospital (No. 19-140), Juntendo University Nerima Hospital (No.2020-14) and Juntendo University Shizuoka Hospital (No. 776). The institutional review board (IRB) of Juntendo University Hospital, Juntendo University Nerima Hospital and Juntendo University Shizuoka Hospital waived the need of informed consent because of the study’s retrospective design.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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The original online version of this article was revised: Following the publication of the original article, the authors have notified us of a mistake in the Legend for Figure 1, in the lowest column of the study scheme: Incorrect line: L-OHP (+) group (n=26), L-OHP (-) group (n=26) Corrected line: L-OHP (+) group (n=21), L-OHP (-) group (n=21).

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Sugimoto, K., Sakamoto, K., Ii, Y. et al. Significance of postoperative adjuvant chemotherapy with an oxaliplatin-based regimen after simultaneous curative resection for colorectal cancer and synchronous colorectal liver metastasis: a propensity score matching analysis. BMC Surg 21, 188 (2021). https://doi.org/10.1186/s12893-021-01193-4

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Keywords

BMC Surgery

ISSN: 1471-2482

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