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Unresolved issues and controversies surrounding the management of colorectal cancer liver metastasis
World Journal of Surgical Oncology volume 13, Article number: 61 (2015)
Ideally, tumors that might cause morbidity and mortality should be treated, preferably early, with proven, convincing, and effective therapy to prevent tumor progression or recurrence, while maintaining a favorable risk-benefit profile for the individual patient. For patients with colorectal cancer (CRC), this diagnostic, prognostic, and therapeutic precision is currently impossible. Despite significant improvements in diagnostic procedures, a sizable number of patients with CRC have liver metastases either at presentation or will subsequently develop it. And in many parts of the world, most cancer-related deaths are still due to metastases that are resistant to conventional therapy. Metastases to the liver occur in more than 50% of patients with CRC and represent the major determinant of outcome following curative treatment of the primary tumor. Liver resection offers the best chance of cure for metastases confined to the liver. However, due to a paucity of randomized controlled trials, its timing is controversial and a hotly debated topic. This article reviews some of the main controversies surrounding the surgical management of colorectal cancer liver metastases (CRLM).
Despite significant improvements in diagnostic procedures, surgical techniques, local and systemic treatment options, and general patient care, most cancer-related deaths are still due to metastases that are resistant to conventional therapies. Next to lymph nodes, the liver is the most common site of metastases from human solid tumors . Metastases to the liver occur in more than 50% of patients with CRC and represent the major determinant of outcome following curative treatment of the primary tumor . Indeed, for nearly one-third of patients with CRC the liver is the only site of metastatic disease . About 14% to 35% of patients with CRC have liver metastases at presentation, and another one-third will subsequently develop it [3-8]. Liver resection offers the only chance of cure for metastases confined to the liver with 5-year overall survival rates up to 58% [9-12]. Unfortunately, the majority of patients with CRLM are not amenable to surgery initially, and the reported rate of successful resection has ranged from 20% to 30% [13,14]. Some of the reasons for the low rate of successful liver resection are: disseminated disease with concomitant extrahepatic metastases, lack of a sufficient future remnant liver, and unfavorable anatomical location in the liver. These patients may become surgical candidates following conversion chemotherapy that downsize metastatic disease . In appropriately selected patients with primarily inoperable liver metastases, secondary resection after downstaging chemotherapy may afford long-term outcomes comparable to primary resection [15,16]. Overall, however, despite the advances made in the last decades, outcome after liver resection for CRLM as a primary or a two-stage resection is heterogeneous, and many patients still do poorly even after careful selection and a successful removal of the metastatic lesion . The main problem is that patients who actually undergo successful liver resection have a high risk of developing recurrent disease, either in the liver or elsewhere. This occurs in approximately 60% to 70% of patients after primary liver resection and roughly one-third of these patients die within 2 years of surgery for CRLM [18-20]. Patients with untreated liver metastases have a median survival of less than 12 months and a 5-year survival rate of almost zero [21-23]. Due to lack of convincing evidence, there are areas of controversies related to treatment protocols of patients with CRLM. Almost all studies regarding these controversial issues are nonrandomized studies with inherent limitations and representative data from prospective randomized trials is still missing. In this contribution, I focus on current controversies surrounding the management of CRLM (Table 1).
Simultaneous versus staged resection of colorectal cancer liver metastases
One of the controversial issues is the optimal timing of liver resection for resectable synchronous colorectal liver metastases (SCRLM). Traditionally, colorectal cancer and SCRLM have been approached with staged initial resection of the primary tumor followed by liver resection. But the paradigm for surgical management of SCRLM has begun to change, with authors reporting good results for simultaneous surgical removal of the primary tumor and the liver metastases [24-26]. In the simultaneous approach, the liver metastases and the primary tumor are resected at the same time. The main objective of this approach is cure thorough the removal of all cancer tissue during a single operation, thus, avoiding delay of surgical treatment of liver metastases. Some evidence suggests that patients with SCRLM who are treated with simultaneous resection of CRC and CRLM have similar long-term outcomes to those treated with a staged approach; and the simultaneous approach does not increase the morbidity or mortality associated with liver resection [27-33]. The major limitation of the simultaneous approach is that the mortality and morbidity of major liver resection, combined with bowel resection, are likely to be considerable; in some studies as high as 8% and 36% respectively [34-37]. In a large retrospective review, Reddy et al.  found that simultaneous colorectal and major liver resections increased morbidity and mortality by more than threefold compared with major liver resection alone and that the increased severe morbidity was maintained when compared with the added severe morbidity of staged colorectal plus liver resection. According to these authors, simultaneous procedures should only be pursued for minor liver resections with application to major liver resection on a selected basis. Furthermore, in agreement with others , these authors recommend avoiding the simultaneous approach in the following situations: 1) when SCRLM is noted on exploration for emergency situations such as colonic perforation (high risk of occult distant metastatic disease), bowel obstruction and bleeding; 2) in those patients with an extremely increased risk of postoperative liver failure, such as patients with liver cirrhosis or other long-standing chronic liver disease; and 3) in patients in whom the future remnant liver will provide inadequate hepatic function. A meta-analysis of 2,880 patients with SCRLM who were followed up for at least 36 months reported that simultaneous resection is as safe as delayed resection as long as patients were less than 70 years old and without severe coexisting disease . Similarly, in the study of Thelen et al. , patients with the simultaneous approach had far higher mortality than staged, which was associated with age >70 years and major hepatectomy. Furthermore, a time test approach has been suggested by some authors favoring the staged strategy to evaluate the biological behavior of the metastatic disease, to treat potentially occult disease, and to avoid liver resection in patients with rapidly progressing disease . And lastly, there is some evidence that the simultaneous approach has a negative effect on progression-free survival (PFS) [37,38,42]. Therefore, given the results of the above-mentioned studies (all nonrandomized retrospective) and other results [25,26,34,43] (Table 2), the simultaneous approach can be offered only in a highly selected subset of patients pending additional high-quality evidence. Currently, no randomized controlled trials on the relative merits of different therapeutic approaches are available; thus, there is no evidenced surgical practice that became as standard of care for resectable SCRLM. Thus, in evaluations of the utility of simultaneous resection of CRC and CRLM, surgeons should carefully consider the additional morbidity and mortality associated with the procedure, as well as the possible improvement in survival.
The role of chemotherapy in neoadjuvant setting
In cases of unresectable CRLM, there is no controversy as the only practical option is systemic chemotherapy. However, whether preoperative chemotherapy in patients with resectable CRLM confers a benefit in terms of decreased recurrence or improved survival is not clear. Thus, the balance between the risks and benefits of preoperative chemotherapy is a hotly debated topic . Some of these debates originated decades ago, yet are still ongoing despite interim advancements in other domains of oncology. The arguments in support of preoperative chemotherapy are based on the fact that this treatment modality decreases the magnitude of resection, eradicates micrometastases, increases R0 resection rates, and aids in the selection of adjuvant therapy based on assessments of responsiveness to a specific chemotherapy. It also identifies patients with aggressive tumor biology in whom liver resection may not be appropriate. In their retrospective study of 131 patients who underwent liver resection for CRLM, Adam et al.  found that patients whose metastatic lesions progressed during chemotherapy had a significantly poorer long-term prognosis (8% versus 37% 5-year survival). However, it can be equally argued that neoadjuvant chemotherapy (NC) delays liver resection and may increase the risk of tumor progression to an unresectable state if the patient does not respond to chemotherapy [8,46-49]. Moreover, in their series of 1,471 patients with resectable metachronous CRLM, Adam et al.  compared those who received NC with those treated by liver resection alone. The authors found that postoperative complications were significantly higher in the chemotherapy group, and more importantly, NC did not improve overall survival (OS). Thus, although NC may provide earlier control of disseminated disease, it induces histologic changes in the liver including steatohepatitis and vascular injury that may result in increased postoperative complications [50-55]. Others disagree with this view [56,57]. In a randomized controlled trial of 364 patients (European Organization for Research and Treatment of Cancer: EORTC 40983) with resectable CRLM, Nordlinger et al.  compared patients who received 12 cycles of FOLFOX (6 cycles before surgery and 6 cycles after) with patients treated by liver resection alone. Their result have not shown these harmful effects and showed a progression-free survival (PFS) of 36.2% at 3 years in the chemotherapy group compared to 28.1% (P = 0.041) in the surgery-alone group. However, at a median follow-up of 8.5 years, no significant improvement in OS had been observed in the chemotherapy group compared to surgery alone . Moreover, this study failed to prove whether the indicated benefit of PFS in the chemotherapy group related to neoadjuvant treatment, adjuvant treatment or a combination of both. In the series of Nanji et al. , a total of 284 out of 293 patients with resectable CRLM underwent liver resection without NC. These authors reported a 3-year PFS and a 5-year OS of 46.2% and 55%, respectively. These conflicting data have led many experts to dispute the necessity of administering preoperative chemotherapy for primarily resectable liver metastases altogether.
Given the benefit of PFS seen in the EORTC 40983, Nordlinger et al. [57,58] advocated the use of preoperative chemotherapy as the standard of care for patients with operable liver metastases. Conversely, others suggest surgery without preoperative chemotherapy for this population of patients, basing their argument on chemotherapy-induced liver injury with increased morbidity, the potential loss of that particular regimen of chemotherapy from future lines of treatment, and the nonbeneficial effect of chemotherapy on long-term survival [59-61] (Table 3).
In summary, the final decision on the timing of liver resection (upfront or after NC) should depend on the preference of the patient and of the interdisciplinary tumor board that includes the surgeon, the radiologist, the oncologist, the radiation therapist, and others working together. It should be made for the individual patient on the basis of the best available medical evidence in the context of the clinical situation.
Regarding adjuvant chemotherapy (AC) after liver resection, there are several studies that have demonstrated its benefit [19,62-66]. These positive results were taken by many as an answer to the benefit of AC after liver resection, and its use has become routine. However, the majority of these studies are retrospective. No randomized controlled trials have examined the benefit of AC after curative liver resection; any such trial would require a large sample size and prolonged follow-up. Two prospective randomized trials that intended to show the benefit of AC had to close prematurely because of slow accrual, thus lacking the statistical power to demonstrate the predefined difference in survival [67,68]. Therefore, the benefit of AC after liver resection for CRLM has not been rigorously validated in clinical trials.
Disappearing (no longer visible on imaging) liver metastases
Given recent therapeutic advances, the nihilism that decades ago often characterized the treatment of patients with CRLM has been replaced by a measure of excitement. Along with advances in operative technique and imaging that have clearly contributed to improvements in the management of patients with CRLM, recent therapeutic advances have been stimulated in part through identification of cellular processes characteristic of CRC that permit therapeutic targeting with favorable therapeutic index. Following the introduction of new, more effective cytotoxic agents, tumor response has improved significantly [69-74].
Disappearing liver metastases (DLM) refers to the complete response or disappearance of a liver metastasis on imaging after administration of preoperative chemotherapy . Depending on the quality and type of cross-sectional imaging, DLM occur in up to a quarter of patients who undergo preoperative systemic chemotherapy either in neoadjuvant setting for initially resectable liver metastases or as conversion chemotherapy for initially unresectable metastases in an attempt to bring patients to potentially curative resection [75-79]. Small size of the metastatic lesion (less than 2 cm) and prolonged duration of systemic chemotherapy may increase the likelihood of DLM [78,79]. The management of DLM is challenging because a complete response on imaging does not necessarily signify a complete clinical or pathological response. It can be the result of chemotherapy associated parenchymal changes to the liver such as steatosis and steatohepatitis that alter the imaging characteristics of the liver and lead to a reduction in the sensitivity of imaging during chemotherapy [80,81]. A durable clinical response for DLM occurs in about 20% to 50% of patients treated with systemic chemotherapy alone, leaving a subset of patients with undiagnosed microscopic liver metastases, which develop subsequent intrahepatic recurrence [75,79]. Study results regarding the outcome of DLM are discrepant and conflicting. In a report of Elias et al. , 27% of the DLMs were identified at laparotomy, whereas recurrence occurred in 20% of the studied patients. In the remaining 53%, follow-up showed no recurrence after 31 months. In their second series Elias et al.  reported that 10 (62%) out of 16 patients with DLM remained recurrence-free at 51 months. In the series of Auer et al. , 17 (44%) out of 39 patients with DLM developed an intrahepatic recurrence, 8 (21%) patients developed a recurrence at an extrahepatic site, and 17 (44%) patients remained recurrence-free at a median follow-up of 40 months. These authors found that the use of hepatic arterial chemotherapy, disappearance of the metastatic lesion on MRI and normalization of serum carcinoembryonic antigen (CEA) as independent predictors of a true response. By contrast, in the study of Benoist et al.  macroscopic residual disease was found in more than 25% of DLM during laparotomy at the site of liver metastases that were considered to have disappeared on imaging. Overall, these authors observed evidence of residual disease in 83% of DLMs.
To summarize, although the beneficial effect of resection of hepatic metastases on survival has been clear, the extent of primary surgery needed in DLM has not. Thus, controversy persists with regard to the extent of surgery required for patients with DLM. There are several proposed management strategies for this subset of patients. These include: resection of all initial sites of DLM when possible; surgical removal of residual macroscopic disease while leaving the disappeared lesions in situ if the resection would be too extensive, leaving insufficient remnant liver; resection followed by additional adjuvant chemotherapy; continuing systemic chemotherapy alone; and others. No strong evidence from randomized controlled trials exists to support any of these management options, particularly the routine use of risky and extensive liver resection in patients with DLM. For now, clinicians must use their best judgment taking a risk-benefit approach to establish the extent of surgical treatment. In the future, decision aids, such as one tested in a randomized controlled trial, might play a greater part in decision making about the treatment strategies of DLM.
The liver-first approach
Contrary to the classic bowel-first approach, the liver-first approach is the reverse of the classic approach and begins with systemic chemotherapy directed against the liver metastases, followed by liver resection, then chemoradiotherapy for patients with rectal cancer, and colorectal resection as the last surgical step. This approach has been proposed for patients with advanced synchronous CRLM, and in particular for those whom the primary is located in the rectum and is asymptomatic . In relation to chemotherapy, treatment after liver resection could be regarded as neoadjuvant for the primary disease, and adjuvant treatment is given after surgery for both liver metastases and colorectal cancer. Given the prognostic decisive role of liver metastases in long-term survival, the liver-first approach has a theoretical advantage. This new trend has been driven in part by efforts to improve survival. The option of giving systemic chemotherapy early in the treatment course provides a chance to evaluate a response and thereby define the tumor biology of the metastatic lesions. In addition the liver-first approach is the result of the assumption that it is the liver metastasis, rather than the primary tumor, that gives rise to systemic metastatic disease. It underlies the importance of prioritizing treatment of the most problematic component of the patient’s disease. Thus, considering the time needed for neoadjuvant chemoradiation and resection of rectal cancer, which is longer than 3 months , addressing the liver first may avoid the risk for progression of CRLM while the patient is being treated for the primary tumor, which is a concern in the classic approach. This view has been supported by some studies (all nonrandomized) that showed a median survival up to 44 months and 3-year survival rates as high as 83% [8,46-48]. Data to support this argument is limited, and there is a counterevidence to suggest that it is the primary tumor that produces systemic effects promoting angiogenesis in the liver and thus favoring the spread of metastatic disease [85,86]. Moreover, despite apparently similar treatment protocols used in those few studies, the variations in survival rates of the liver-first approach are wide [47,48]. This makes its comparison with other treatment protocols, such as the bowel-first approach or the combined strategy, difficult. An adequately powered randomized controlled trial examining the effect of the liver-first approach on recurrence and long-term survival might be logistically challenging, because of the need for a large sample size. Thus, to date, no randomized, controlled studies have assessed the benefits of this modern strategy or its effects on recurrence and long-term survival of patients with CRLM.
Unresectable liver metastases and asymptomatic primary tumor
Historically, the common treatment strategy in patients with asymptomatic primary tumor with synchronous unresectable liver metastases is surgical removal of the primary tumor followed by systemic chemotherapy. The theoretical basis that supports this approach is that the growth of the primary tumor is the main cause of major complications such as intestinal obstruction, perforation and hemorrhage, so resection should be more likely to prevent these complications while achieving best palliation in terms of quality of life [87-89]. Further, resection of the primary tumor reduces the risk of the growth of additional metastatic disease that may influence long-term outcomes. Results of retrospective studies show that with an estimated survival advantage of 6 months, primarily resected patients live significantly longer than non-resected patients [90-93]. Moreover, patients put on initial systemic chemotherapy tended to have more major complications that mandated surgical intervention and termination of chemotherapy. Bowel obstruction is the most frequently encountered complication during chemotherapy with a rate ranging from 5.6% to 29% followed by bleeding from the primary tumor that was experienced by 3% to 5% of the patients [90,93-95].
On the other side, results of comparative studies demonstrate that most patients with widely metastatic disease will not experience a complication resulting from an non-resected primary tumor, and that the rate of intestinal obstruction due to subsequent growth of the primary tumor is similar to that caused by adhesions after colorectal resection . Initial systemic therapy is safe and patients put on this treatment modality showed an overall response rate as high as 70% [18,92,97]. According to one report, 93% of patients initially treated by systemic chemotherapy never required emergency surgery . Overall morbidity and mortality after resection for advanced metastatic colorectal cancer were as high as 21% and 16%, respectively [99,100]. This figure is significantly higher than that of colorectal cancer in general [100,101]. Moreover, experimental data show that resection of the primary tumor may enhance the growth and proliferation of metastatic cells [89,102,103]. The underlying mechanism is thought to be lack of a circulating anti-angiogenic factor, normally produced by the primary tumor that leads to suppression of angiogenesis and enhanced apoptosis and hence inhibiting metastatic progression. All this suggests that any benefit to preventing the growth of additional metastases by resection of the primary tumor does not influence long-term outcome.
In summary, studies examining the effect of primary surgery on long-term outcomes in patients with asymptomatic CRC and unresectable CRLM have limitations, and the routine use of surgery in all patients in this group might not be justified. Therefore, surgery is no longer routinely considered as an initial therapeutic intervention, and the appropriateness of resection has been questioned in this setting. Thus, recently resection is hesitantly offered as an alternative with ill-defined indications and mixed results.
The classic, combined, and reverse strategies are associated with similar outcomes. While some authors argue that the mortality and morbidity of major liver resection, combined with bowel resection, are likely to be considerable, with some studies showing an increase of more than threefold, others disagree with this view. Despite experiences reported by some authors, there is no consensus as yet for the role of the liver-first strategy in improving long-term survival in patients with CRLM. The benefit of chemotherapy in neoadjuvant or adjuvant setting for resectable CRLM has not been rigorously validated in clinical trials. There are several proposed management strategies for patients with disappearing liver metastases. However, no strong evidence from randomized controlled trials exists to support either of these management options.
All these controversies surrounding the management of CRLM underscore the need for large-scale, multicenter randomized trials to better define effective therapeutic strategies for clinically meaningful long-term outcomes. In the absence of high-quality evidence, disease management of CRLM needs to be personalized, balancing potential risks and benefits of treatment (and related uncertainties) with risk of the disease (Figure 1).
Colorectal cancer liver metastases
Disappearing liver metastases
European Organisation for Research and Treatment of Cancer
Synchronous colorectal liver metastases
Weiss L, Grundmann E, Torhost J, Hartveit F, Moberg I, Eder M, et al. Haematogenous metastatic patterns in colonic carcinoma: an analysis of 1541 necropsies. J Pathol. 1986;150:195–203.
Bramhall SR, Gur U, Coldham C, Gunson BK, Mayer AD, McMaster P, et al. Liver resection for colorectal metastases. Ann R Coll Surg Engl. 2003;85:334–9.
Fegiz G, Ramacciato G, Gennari L, Doci R, Pezzuoli G, Leggeri A, et al. Hepatic resections for colorectal metastases: the Italian multicenter experience. J Surg Oncol Suppl. 1991;2:144–54.
Jatzko GR, Lisborg PH, Stettner HM, Klimpfinger MG. Hepatic resection for Metastases from colorectal carcinoma: a survival analysis. Eur J Cancer. 1995;31A:41–6.
Leporrier J, Maurel J, Chiche L, Bara S, Segol P, Launoy G. A population-based study of the incidence, management and prognosis of hepatic metastases from colorectal cancer. Br J Surg. 2006;93:465–74.
Manfred S, Lepage C, Hatem C, Coatmeur O, Faivre J, Couveir AM. Epidemiology and management of colorectal liver metastases from colorectal cancer. Ann Surg. 2006;244:254–9.
Small R, Lubezky N, Ben-Haim M. Current controversies in the surgical management of colorectal cancer metastases to the liver. Isr Med Assoc J. 2007;9:742–7.
Brouquet A, Mortenson MM, Vauthey JN, Rodriguez-Bigas MA, Overman MJ, Chang GJ, et al. Surgical strategies for synchronous colorectal liver metastases in 156 consecutive patients: classical, combined or reverse strategy? J Am Coll Surg. 2010;210(6):934–41.
Lise M, Da Pian PP, Nitti D, Pilati PL. Colorectal metastases to the liver: present results and future strategies. J Surg Oncol Suppl. 1991;2:69–73.
Tayler M, Forster J, Langer B, Tayler BR, Greig PD, Mahut C. A study of prognostic factors for hepatic resection for colorectal metastases. Am J Surg. 1997;173:467–71.
Choti MA, Sitzmann JV, Tiburi MF, Sumetchotimetha W, Rangsin R, Schulick RD, et al. Trends in long-term survival following liver resection for hepatic colorectal metastases. Ann Surg. 2002;235:759–66.
Fedorowicz Z, Lodge M, Al-asfoor A, Carter B. Resection versus no intervention or other surgical interventions for colorectal cancer liver metastases. Cochrane database of systematic reviews 2008, issue 2. Art. No.: CD006039. doi:10.1002/14651858.CD006039.pub4
Scheele J, Stange R, Altendorf-Hofmann A, Paul M. Resection of colorectal liver metastases. World J Surg. 1995;19:59–71.
Van Nordlinger B, Custem E, Rougier P, Köhne CH, Ychou M, Sobrero A, et al. Does chemotherapy prior to liver resection increase the potential for cure in patients with metastatic colorectal cancer? A report from the European colorectal metastases treatment group. Eur J Cancer. 2007;43:2037–45.
Alberts SR. Update on the optimal management of patients with colorectal liver metastases. Crit Rev Oncol Hematol. 2012;84:59–70.
Folprecht G, Gruenberger T, Bechstein WO, Raab HR, Lordick F, Hartmann JT, et al. Tumor response and secondary resectability of colorectal liver metastases following neoadjuvant chemotherapy with cetuximab: the CELIM randomised phase 2 trail. Lancet Oncol. 2010;11:38–47.
Cardona K, Mastrodomenico P, D’Amico F, Shia J, Gönen M, Weiser MR, et al. Detailed pathologic characteristics of the primary colorectal tumor independently predict outcome after hepatectomy for metastases. Ann Surg Oncol. 2013;20:148–54.
Kopetz S, Chang GJ, Overman MJ, Eng C, Sargent DJ, Larson DW, et al. Improved survival in metastatic colorectal cancer is associated with adoption of hepatic resection and improved chemotherapy. J Clin Oncol. 2009;27:3677–83.
de Jong MC, Pulitano C, Ribero D, Strub J, Mentha G, Schulick RD, et al. Rates and patterns of recurrence following curative intent surgery for colorectal liver metastases: an international multi-institutional analysis of 1669 patients. Ann Surg. 2009;250:440–8.
Jones RP, Jackson R, Dunne DFJ, Malik HZ, Fenwick SW, Poston GJ, et al. Systematic review and meta-analysis of follow-up after hepatectomy for colorectal liver metastases. Br J Surg. 2012;99:477–86.
Scheele J, Stangl R, Altendorf-Hofmann A. Hepatic metastases from colorectal carcinoma: impact of surgical resection on the natural history. Br J Surg. 1990;77:1241–6.
Kavolius J, Fong Y, Blumgart LH. Surgical resection of metastatic liver tumors. Surg Oncol Clin North Am. 1996;5:337–52.
Lam VWT, Pang T, Laurence JM, Johnston E, Hollands MJ, Pleass HCC, et al. A systemic review of repeat hepatectomy for recurrent colorectal liver metastases. J Gastrointest Surg. 2013;17:1312–21.
Elias D, Detroz B, Lasser P, Plaud B, Jerbi G. Is simultaneous hepatectomy and intestinal anastomosis safe? Am J Surg. 1995;169:254–60.
Lyass S, Zamir G, Matot I, Goitein D, Eid A, Jurim O. Combined colon and hepatic resection for synchronous colorectal liver metastases. J Surg Oncol. 2001;78:17–21.
Martin R, Paty P, Fong Y, Grace A, Cohen A, DeMatteo R, et al. Simultaneous liver and colorectal resections are safe for synchronous colorectal liver metastasis. J Am Coll Surg. 2003;197:233–41.
Simmonds PC, Primrose JN, Colquitt JL, Garden OJ, Poston GJ, Rees M. Surgical resection of hepatic metastases from colorectal cancer: a systematic review of published studies. Br J Cancer. 2006;94:982–99.
Capussotti L, Vigano L, Ferrero A, Lo Tesoriere R, Ribero D, Polastri R. Timing of resection of liver metastases synchronous to colorectal tumor: proposal for prognosis-based decisional model. Ann Surg Oncol. 2007;14:1143–50.
Capussotti L, Ferrero A, Vigano L, Ribero D, Lo Tesoriere R, Polastri R. Major liver resections synchronous with colorectal surgery. Ann Surg Oncol. 2007;14:195–201.
Vassiliou I, Arkadopoulos N, Theodosopoulos T, Fragulidis G, Marinis A, Kondi-Paphiti A, et al. Surgical approaches of resectable synchronous colorectal liver metastases: timing considerations. World J Gastroenterol. 2007;13:1431–4.
Bipat S, van Leeuwen MS, Ijzermans JN, Comans EF, Planting AS, Bossuyt PM, et al. Evidence-base guideline on management of colorectal liver metastases in the Netherlands. Neth J Med. 2007;65:5–14.
Turrini O, Viret F, Guiramand J, Lelong B, Bège T, Delpero JR. Strategies for the treatment of synchronous liver metastasis. Eur J Surg Oncol. 2007;33:735–40.
Martin 2nd RC, Augenstein V, Reuter NP, Scoggins CR, McMasters KM. Simultaneous versus staged resection for synchronous colorectal cancer liver metastases. J Am Coll Surg. 2009;208:842–50.
Nordlinger B, Guiguet M, Vaillant JC, Balladur P, Boudjema K, Bachellier P, et al. Surgical resection of colorectal carcinoma metastases to the liver. Cancer. 1996;77:1254–62.
Bolton JS, Fuhrman GM. Survival after resection of multiple bilobar hepatic metastases from colorectal carcinoma. Ann Surg. 2000;231:743–51.
Tanaka K, Shimada H, Matsuo K, Nagano Y, Endo I, Sekido H, et al. Outcome after simultaneous colorectal and hepatic resection for colorectal cancer with synchronous metastases. Surgery. 2004;136:650–9.
Reddy SK, Pawlik TM, Torzi D, Gleisner AL, Ribero D, Assumpcao L, et al. Simultaneous resections of colorectal cancer and synchronous liver metastases: a multi-institutional analysis. Ann Surg Oncol. 2007;14:3481–91.
Adam R. Colorectal cancer with synchronous liver metastases. Br J Surg. 2007;94:129–31.
Yin Z, Liu C, Chen Y, Bai Y, Shang C, Yin R, et al. Timing of hepatectomy in resectable synchronous colorectal liver metastases (SCRLM): simultaneous or delayed? Hepatology. 2013;57:2346–57.
Thelen A, Jonas S, Benckert C, Spinelli A, Lopez-Hänninen E, Rudolph B, et al. Simultaneous versus staged liver resection of synchronous liver metastases from colorectal cancer. Int J Colorectal Dis. 2007;22:1269–76.
Lambert LA, Colacchio TA, Barth Jr RJ. Intrval hepatic resection of colorectal metastases improves patient selection. Arch Surg. 2000;135:473–9.
de Haas RJ, Adam R, Wicherts DA, Azoulay D, Bismuth H, Vibert E, et al. Comparison of simultaneous or delayed liver surgery for limited synchronous colorectal metastases. Br J Surg. 2010;97:1279–89.
Weber JC, Bachellier P, Oussoultzoglou E, Jaeck D. Simultaneous resection of colorectal primary tumour and synchronous liver metastases. Br J Surg. 2003;90:956–62.
Vauthey JN, Nordlinger B, Kopetz S, Poston G. Sequenced chemotherapy and surgery for potentially resectable colorectal liver metastases: a debate over goals of research and an approach while the jury remains out. Ann Surg Oncol. 2010;17:1983–6.
Adam R, Pascal G, Castaing D, Azoulay D, Delvart V, Paule B, et al. Tumor progression while on chemotherapy: a contraindication to liver resection for multiple colorectal metastases? Ann Surg. 2004;240:1052–61.
Mentha G, Roth AD, Terraz S, Giostra E, Gervaz P, Andres A, et al. ‘Liver first’ approach in the treatment of colorectal cancer with synchronous liver metastases. Dig Surg. 2008;25:430–5.
Verhoef C, van der Pool AE, Nuyttens JJ, Planting AS, Eggermont AM, de Wilt JH. The “liver-first approach” for patients with locally advanced rectal cancer and synchronous liver metastases. Dis Colon Rectum. 2009;52:23–30.
de Jong MC, van Dam RM, Maas M, Bemelmans MH, Olde Damink SW, Beets GL, et al. The liver-first approach for synchronous colorectal liver metastasis: a 5-year single-centre experience. HPB (Oxford). 2011;13:745–52.
Lehmann K, Rickenbacher A, Weber A, Pestalozzi BC, Clavien PA. Chemotherapy before liver resection of colorectal metastases: friend or foe? Ann Surg. 2012;255:237–47.
Adam R, Bhangui P, Poston G, Mirza D, Nuzzo G, Barroso E, et al. Is perioperative chemotherapy useful for solitary, metachronous, colorectal liver metastases? Ann Surg. 2010;252:774–87.
Rubbia-Brandt L, Audard V, Sartoretti P, Roth AD, Brezault C, Le Charpentier M, et al. Severe hepatic sinusoidal obstruction associated with oxaliplatin-based chemotherapy in patients with metastatic colorectal cancer. Ann Oncol. 2004;15:460–6.
Vauthey JN, Pawlik TM, Ribero D, Wu TT, Zorzi D, Hoff PM, et al. Chemotherapy regimen predicts steatohepatitis and an increase in 90-day mortality after surgery for hepatic colorectal metastases. J Clin Oncol. 2006;24:2065–72.
Pawlik TM, Olino K, Gleisner AL, Torbenson M, Schulick R, Choti MA. Preoperative chemotherapy for colorectal liver metastases: impact on hepatic histology and postoperative outcome. J Gastrointest Surg. 2007;11:860–8.
Mehta NN, Ravikumar R, Coldham CA, Buckels JA, Hubscher SG, Bramhall SR, et al. Effect of preoperative chemotherapy on liver resection for colorectal liver metastases. Eur J Surg Oncol. 2008;34:782–6.
Scoggins CR, Campbell ML, Landry CS, Slomiany BA, Woodall CE, McMasters KM, et al. Preoperative chemotherapy does not increase morbidity or mortality of hepatic resection for colorectal cancer metastases. Ann Surg Oncol. 2009;16:35–41.
Welsh FK, Tilney HS, Tekkis PP, John TG, Rees M. Safe liver resection following chemotherapy for colorectal metastases is a matter of timing. Br J Cancer. 2007;96:1037–42.
Nordlinger B, Sorbye H, Glimelius B, Poston GJ, Schlag PM, Rougier P, 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;371:1007–16.
Nordlinger B, Sorbye H, Glimelius B, Poston GJ, Schlang PM, Rougier P, et al. Perioperativ FOLFOX4 chemotherapy and surgery versus surgery alone for resectable liver metastases from colorectal cancer (EORTC 40983): long-term results of a randomized, controlled, phase 3 trial. Lancet. 2013;14:1208–15.
Nanji S, Cleary S, Ryan P, Guindi M, Selvarajah S, Grieg P, et al. Up-front hepatic resection for metastatic colorectal cancer results in favorable long-term survival. Ann Surg Oncol. 2013;20:295–304.
Jones RP, Malik HZ, Fenwick SW, Poston GJ. Perioperative chemotherapy for resectable colorectal liver metastases: Where now? EJSO. 2013;39:807–11.
Reddy SK, Zorzi D, Lum YW, Barbas AS, Pawlik TM, Ribero D, et al. Timing of multimodality therapy for resectable synchronous colorectal liver metastases: a retrospective multi-institutional analysis. Ann Surg Oncol. 2009;16:1809–19.
Figueras J, Valls C, Rafecas A, Fabregat J, Ramos E, Jaurrieta E. Resection rate and effect of postoperative chemotherapy on survival after surgery for colorectal liver metastases. Br J Surg. 2001;88:980–5.
Figueras J, Torras J, Valls C, Llado L, Ramos E, Marti-Ragué J, et al. Surgical resection of colorectal liver metastases in patients with expanded indications: a single-center experience with 501 patients. Dis Colon Rectum. 2007;50:478–88.
Parks R, Gonen M, Kemeny N, Jarnagin W, D’Angelica M, DeMatteo R, et al. Adjuvant chemotherapy improves survival after resection of hepatic colorectal metastases: analysis of data from two continents. J Am Col Surg. 2007;204:753–61.
Kornprat P, Jarnagin WR, Gonen M, DeMatteo RP, Fong Y, Blumgart LH, et al. Outcome after hepatectomy for multiple (four or more) colorectal metastases in the era of effective chemotherapy. Ann Surg Oncol. 2007;14:1151–60.
Mitry E, Fields ALA, Bleiberg H, Labianca R, Portier G, Tu D, et al. Adjuvant chemotherapy after potentially curative resection of metastases from colorectal cancer: a pooled analysis of two randomized trials. J Clin Oncol. 2008;26:4906–11.
Langer B, Bleiberg H, Labianca R. Fluorouracil (FU) plus I-leukovorin (I-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 (abstract). Proc Am Soc Clin Oncol. 2002;21(Suppl):592.
Portier G, Elias D, Bouche O, Rougier P, Bosset JF, Saric J, 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;24:4976–82.
Giacchetti S, Perpoint B, Zidani R, Le Bail N, Faffiuolo R, Focan C, et al. Phase III multicenter randomized trial of oxaliplatin added to chronomodulated fluorouracil-leucovorin as first-line treatment of metastatic colorectal cancer. J Clin Oncol. 2000;18:136–47.
de Gramont A, Figer A, Seymour M, Homerin M, Hmissi A, Cassidy J, et al. Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer. J Clin Oncol. 2000;18:2938–47.
Douillard JY, Cunningham D, Roth AD, Navarro M, James RD, Karasek P, et al. Irinotecan combined with fluoraouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: a multicenter randomized trial. Lancet. 2000;355:1041–7.
Hoff PM, Ansari R, Batist G, Cox J, Kocha W, Kuperminc M, et al. Comparison of oral capcitabine versus intravenous fluorouracil plus leucovorin as first-line treatment in 605 patients with metastatic colorectal cancer: results of a randomized phase III study. J Clin Oncol. 2001;19:2282–92.
Tournigand C, Andre T, Achille E, Lledo G, Flesh M, Mery-Mignard D, et al. FOLFIRI followed by FOLFOX6 or the reverse sequence in advanced colorectal cancer: a randomized GERCOR study. J Clin Oncol. 2004;22:229–37.
Fuchs CS, Marshall J, Barrueco J. Randomized, controlled trial of irinotecan plus infusional, bolus, or oral fluoropyrimidines in first-line treatment of metastatic colorectal cancer: updated results from the BICC-C study. J Clin Oncol. 2008;26:689–90.
Bischof DA, Clary BM, Maithel SK, Pawlik TM. Surgical management of disappearing colorectal liver metastases. Br J Surg. 2013;100:1414–20.
Benoist S, Brouquet A, Penna C, Julié C, El Hajjam M, Chagnon S, et al. Complete response of colorectal liver metastases after chemotherapy: does it mean cure? J Clin Oncol. 2006;24:3939–45.
Elias D, Goere D, Boige V, Kohneh-Sharhi N, Malka D, Tomasic G, et al. Outcome of posthepatectomy-missing colorectal liver metastases after complete response to chemotherypy: impact of adjuvant intra-arterial hepatic oxaliplatin. Ann Surg Oncol. 2007;14:3188–94.
Auer RC, White RR, Kemeny NE, Schwartz LH, Shia J, Blumgart LH, et al. Predictors of a true complete response among disappearing liver metastases from colorectal cancer after chemotherapy. Cancer. 2010;116:1502–9.
van Vledder MG, de Jong MC, Pawlik TM, Schulick RD, Diaz LA, Choti MA. Disappearing colorectal liver metastases after chemotherapy: Should we be concerned? J Gastrointest Surg. 2010;14:1691–700.
Zorzi D, Laurent A, Pawlik TM, Lauwers GY, Vauthey JN, Abdalla EK. Chemotherapy-associated hepatotoxicity and surgery for colorectal liver metastases. Br J Surg. 2007;94:274–86.
Oliva MR, Mortele KJ, Segatto E, Glickman JN, Erturk SM, Ros PR, et al. Computed tomography features of nonalcoholic steatohepatitis with histopathologic correlation. J Comput Assist Tomogr. 2006;30:37–43.
Elias D, Youssef O, Sideris L, Dromain C, Baton O, Boige V, et al. Evaluation of missing colorectal liver metastases Following Inductive Chemotherapy and hepatectomy. J Surg Oncol. 2004;86:4–9.
Mentha G, Majno PE, Andres A, Rubbia-Brandt L, Morel P, Roth AD. Neoadjuvant chemotherapy and resection of advanced synchronous liver metastases before treatment of the colorectal primary. Br J Surg. 2006;93:872–8.
Bosset JF, Collette L, Calais G, Mineur L, Maingon P, Radosevic-Jelic L, et al. Chemotherapy with preoperative radiotherapy in rectal cancer. N Engl J Med. 2006;355:1114–23.
van der Wal GE, Gouw ASH, Kamps JAAM, Bulthuis ML, Molema G, de Jong KP. Angiogenesis in synchronous and metachronous colorectal liver metastases: the liver as a permissive soil. Ann Surg. 2012;255:86–94.
Jegatheeswaran S, Mason JM, Hancock HC, Siriwardena AK. The liver-first approach to the management of colorectal cancer with synchronous hepatic metastases. JAMA Surg. 2013;148:385–91.
Millikan KW, Staren ED, Doolsa A. Invasive therapy of metastatic colorectal cancer to the liver. Surg Clin North Am. 1997;77:27–48.
Reddy SK, Barbas AS, Clary BM. Synchronous colorectal liver metastases: is it time to reconsider traditional paradigms of management? Ann Surg Oncol. 2009;16:2395–410.
Ruers TJM, Hagendoom J. Treatment dilemmas in patients with synchronous colorectal liver metastases. Recent Results Cancer Res. 2012;196:37–49.
Ruo L, Gougoutas C, Paty PB, Guillem JG, Cohen AM, Wong WD. Elective bowel resection for incurable stage IV colorectal cancer: prognostic variables for asymptomatic patients. J Am Coll Surg. 2003;196:722–8.
Galizia G, Lieto E, Orditura M, Castellano P, Imperatore V, Pinto M, et al. First-line chemotherapy vs bowel tumor resection plus chemotherapy for patients with unresectable synchronous colorectal hepatic metastases. Arch Surg. 2008;143:352–8.
Karoui M, Koubaa W, Delbaldo C, Charachon A, Laurent A, Piedbois P, et al. Chemotherapy has also an effect on primary tumor in colon carcinoma. Ann Surg Oncol. 2008;15:3440–6.
Stillwell AP, Buettner PG, Ho YH. Meta-analysis of survival of patients with stage IV colorectal cancer managed with surgical resection versus chemotherapy alone. World J Surg. 2010;34:797–807.
Muratore A, Zorzi D, Bouzari H, Amisano M, Massucco P, Sperti E, et al. Asymptomatic colorectal cancer with unresectable liver metastases: immediate colorectal resection or up-front systemic chemotherapy? Ann Surg Oncol. 2007;14:766–70.
Scheer MG, Sloots CE, van der Wilt GJ, Ruers TJ. Management of patients with asymptomatic colorectal cancer and synchronous irresectable metastases. Ann Oncol. 2008;19:1829–35.
Tebbutt NC, Norman AR, Cunningham D, Hill ME, Tait D, Oates J, et al. Intestinal complications after chemotherapy for patients with unresected primary colorectal cancer and synchronous metastases. Gut. 2003;52:568–73.
Benoist S, Pautrat K, Mitry E, Rougier P, Penna C, Nordlinger B. Treatment strategy for patients with colorectal cancer and synchronous irresectable liver metastases. Br J Surg. 2005;92:1155–60.
Poultsides GA, Servais EL, Saltz LB, Patil S, Kemeny NE, Guillem JG, et al. Outcome of primary tumor in patients with synchronous stage IV colorectal cancer receiving combination chemotherapy without surgery as initial treatment. J Clin Oncol. 2009;27:3379–84.
Michel P, Roque I, Di FF, Langlois S, Scotte M, Tenière P, et al. Colorectal cancer with non-resectable synchronous metastases: should the primary tumor be resected? Gastroenterol Clin Biol. 2004;28:434–7.
Evans MD, Escofet S, Karandikar SS, Stamatakis JD. Outcomes of resection and non-resection strategies in management of patients with advanced colorectal cancer. World J Surg Oncol. 2009;7:28.
Eisenberger A, Whelan RL, Neugut AI. Survival and symptomatic benefit from palliative primary tumor resection in patients with metastatic colorectal cancer: a review. Int J Colorectal Dis. 2008;23:559–68.
Peeters CF, Westphal JR, de Waal RM, Ruiter DJ, Wobbes T, Ruers TJ. Vascular density in colorectal liver metastases increases after removal of the primary tumor in human cancer patients. Int J Cancer. 2004;112:554–9.
Peeters CF, de Waal RM, Wobbes T, Westphal JR, Ruers TJ. Outgrowth of human liver metastases after resection of the primary colorectal tumor: a shift in the balance between apoptosis and proliferation. Int J Cancer. 2006;119:1249–53.
I acknowledge support from the German Research Foundation (DFG) and Leipzig University within the program of Open Access Publishing.
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Kassahun, W.T. Unresolved issues and controversies surrounding the management of colorectal cancer liver metastasis. World J Surg Onc 13, 61 (2015). https://doi.org/10.1186/s12957-014-0420-6
- Colorectal cancer
- Colorectal cancer liver metastases
- Liver resection
- Timing of liver resection