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      Second and third look laparoscopy in pT4 colon cancer patients for early detection of peritoneal metastases; the COLOPEC 2 randomized multicentre trial

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          Abstract

          Background

          Approximately 20–30% of patients with pT4 colon cancer develop metachronous peritoneal metastases (PM). Due to restricted accuracy of imaging modalities and absence of early symptoms, PM are often detected at a stage in which only a quarter of patients are eligible for curative intent treatment. Preliminary findings of the COLOPEC trial (NCT02231086) revealed that PM were already detected during surgical re-exploration within two months after primary resection in 9% of patients with pT4 colon cancer. Therefore, second look diagnostic laparoscopy (DLS) to detect PM at a subclinical stage may be considered an essential component of early follow-up in these patients, although this needs confirmation in a larger patient cohort. Furthermore, a third look DLS after a negative second look DLS might be beneficial for detection of PM occurring at a later stage.

          Methods

          The aim of this study is to determine the yield of second look DLS and added value of third look DLS after negative second look DLS in detecting occult PM in pT4N0-2 M0 colon cancer patients after completion of primary treatment. Patients will undergo an abdominal CT at 6 months postoperative, followed by a second look DLS within 1 month if no PM or other metastases not amenable for local treatment are detected. Patients without PM will subsequently be randomized between routine follow-up including 18 months abdominal CT, or an experimental arm with a third look DLS provided that PM or incurable metastases are absent at the 18 months abdominal CT. Primary endpoint is the proportion of PM detected after a negative second look DLS and will be determined at 20 months postoperative.

          Discussion

          Second look DLS is supposed to result in 10% occult PM, and third look DLS after negative second look DLS is expected to detect an additional 10% of PM compared to routine follow-up alone in patients with pT4 colon cancer. Detection of PM at an early stage will likely increase the proportion of patients eligible for curative intent treatment and subsequently improve survival, given the uniformly reported direct association between the extent of peritoneal disease and survival.

          Trial registration

          ClinicalTrials.gov: NCT03413254, January 2018.

          Electronic supplementary material

          The online version of this article (10.1186/s12885-019-5408-8) contains supplementary material, which is available to authorized users.

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          Most cited references33

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          Peritoneal colorectal carcinomatosis treated with surgery and perioperative intraperitoneal chemotherapy: retrospective analysis of 523 patients from a multicentric French study.

          PURPOSE Peritoneal carcinomatosis (PC) from colorectal cancer traditionally is considered a terminal condition. Approaches that combine cytoreductive surgery (CRS) and perioperative intraperitoneal chemotherapy (PIC) have been developed recently. The purpose of this study was to assess early and long-term survival in patients treated with that strategy. PATIENTS AND METHODS A retrospective-cohort, multicentric study from French-speaking countries was performed. All consecutive patients with PC from colorectal cancer who were treated with CRS and PIC (with or without hyperthermia) were included. Patients with PC of appendiceal origin were excluded. Results The study included 523 patients from 23 centers in four French-speaking countries who underwent operation between 1990 and 2007. The median follow-up was 45 months. Mortality and grades 3 to 4 morbidity at 30 days were 3% and 31%, respectively. Overall median survival was 30.1 months. Five-year overall survival was 27%, and five-year disease-free survival was 10%. Complete CRS was performed in 84% of the patients, and median survival was 33 months. Positive independent prognostic factors identified in the multivariate analysis were complete CRS, PC that was limited in extent, no invaded lymph nodes, and the use of adjuvant chemotherapy. Neither the grade of disease nor the presence of liver metastases had a significant prognostic impact. CONCLUSION This combined treatment approach against PC achieved low postoperative morbidity and mortality, and it provided good long-term survival in patients with peritoneal scores lower than 20. These results should improve in the future, because the different teams involved will gain experience. This approach, when feasible, is now considered the gold standard in the French guidelines.
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            Cytoreductive surgery combined with perioperative intraperitoneal chemotherapy for the management of peritoneal carcinomatosis from colorectal cancer: a multi-institutional study.

            The three principal studies dedicated to the natural history of peritoneal carcinomatosis (PC) from colorectal cancer consistently showed median survival ranging between 6 and 8 months. New approaches combining cytoreductive surgery and perioperative intraperitoneal chemotherapy suggest improved survival. A retrospective multicenter study was performed to evaluate the international experience with this combined treatment and to identify the principal prognostic indicators. All patients had cytoreductive surgery and perioperative intraperitoneal chemotherapy (intraperitoneal chemohyperthermia and/or immediate postoperative intraperitoneal chemotherapy). PC from appendiceal origin was excluded. The study included 506 patients from 28 institutions operated between May 1987 and December 2002. Their median age was 51 years. The median follow-up was 53 months. The morbidity and mortality rates were 22.9% and 4%, respectively. The overall median survival was 19.2 months. Patients in whom cytoreductive surgery was complete had a median survival of 32.4 months, compared with 8.4 months for patients in whom complete cytoreductive surgery was not possible (P <.001). Positive independent prognostic indicators by multivariate analysis were complete cytoreduction, treatment by a second procedure, limited extent of PC, age less than 65 years, and use of adjuvant chemotherapy. The use of neoadjuvant chemotherapy, lymph node involvement, presence of liver metastasis, and poor histologic differentiation were negative independent prognostic indicators. The therapeutic approach combining cytoreductive surgery with perioperative intraperitoneal chemotherapy achieved long-term survival in a selected group of patients with PC from colorectal origin with acceptable morbidity and mortality. The complete cytoreductive surgery was the most important prognostic indicator.
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              Complete cytoreductive surgery plus intraperitoneal chemohyperthermia with oxaliplatin for peritoneal carcinomatosis of colorectal origin.

              To compare the long-term survival of patients with isolated and resectable peritoneal carcinomatosis (PC) in comparable groups of patients treated with systemic chemotherapy containing oxaliplatin or irinotecan or by cytoreductive surgery plus hyperthermic intraperitoneal chemotherapy (HIPEC). All patients with gross PC from colorectal adenocarcinoma who had undergone cytoreductive surgery plus HIPEC from 1998 to 2003 were evaluated. The standard group was constituted by selecting patients with colorectal PC treated with palliative chemotherapy during the same period, but who had not benefited from HIPEC because the technique was unavailable in the center at that time. Forty-eight patients were retrospectively included in the standard group and were compared with 48 patients who had undergone HIPEC and were evaluated prospectively. All characteristics were comparable except age and tumor differentiation. There was no difference in systemic chemotherapy, with a mean of 2.3 lines per patient. Median follow-up was 95.7 months in the standard group versus 63 months in the HIPEC group. Two-year and 5-year overall survival rates were 81% and 51% for the HIPEC group, respectively, and 65% and 13% for the standard group, respectively. Median survival was 23.9 months in the standard group versus 62.7 months in the HIPEC group (P < .05, log-rank test). Patients with isolated, resectable PC achieve a median survival of 24 months with modern chemotherapies, but only surgical cytoreduction plus HIPEC is able to prolong median survival to roughly 63 months, with a 5-year survival rate of 51%.
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                Author and article information

                Contributors
                v.p.bastiaenen@amc.nl
                c.e.klaver@amc.nl
                n.kok@nki.nl
                hans.dewilt@radboudumc.nl
                ignace.d.hingh@catharinaziekenhuis.nl
                a.aalbers@nki.nl
                d.boerma@antoniusziekenhuis.nl
                andre.bremers@radboudumc.nl
                pim.burger@catharinaziekenhuis.nl
                e.vanduyn@mst.nl
                p.evers@nfk.nl
                w.m.u.vangrevenstein@umcutrecht.nl
                p.h.j.hemmer@umcg.nl
                e.madsen@erasmusmc.nl
                p.snaebjornsson@nki.nl
                j.tuynman@vumc.nl
                r.wiezer@antoniusziekenhuis.nl
                m.g.dijkgraaf@amc.nl
                jvdbilt@flevoziekenhuis.nl
                p.j.tanis@amc.nl
                Journal
                BMC Cancer
                BMC Cancer
                BMC Cancer
                BioMed Central (London )
                1471-2407
                21 March 2019
                21 March 2019
                2019
                : 19
                : 254
                Affiliations
                [1 ]ISNI 0000000084992262, GRID grid.7177.6, Department of Surgery, Amsterdam UMC, , University of Amsterdam, Cancer Center Amsterdam, ; PO Box 22660, 1105 AZ Amsterdam, the Netherlands
                [2 ]GRID grid.430814.a, Department of Surgery, , the Netherlands Cancer Institute, ; Amsterdam, the Netherlands
                [3 ]ISNI 0000 0004 0444 9382, GRID grid.10417.33, Department of Surgery, , Radboud University Medical Centre, ; Nijmegen, the Netherlands
                [4 ]ISNI 0000 0004 0398 8384, GRID grid.413532.2, Department of Surgery, , Catharina Hospital, ; Eindhoven, the Netherlands
                [5 ]ISNI 0000 0004 0622 1269, GRID grid.415960.f, Department of Surgery, , St. Antonius Hospital, ; Nieuwegein, the Netherlands
                [6 ]ISNI 0000 0004 0399 8347, GRID grid.415214.7, Department of Surgery, , Medisch Spectrum Twente, ; Enschede, the Netherlands
                [7 ]Dutch Federation of Cancer Patient Organizations (NFK), Utrecht, the Netherlands
                [8 ]ISNI 0000000120346234, GRID grid.5477.1, Department of Surgery, University Medical Centre Utrecht, , Utrecht University, ; Utrecht, the Netherlands
                [9 ]ISNI 0000 0004 0407 1981, GRID grid.4830.f, Department of Surgery, University Medical Centre Groningen, , University of Groningen, ; Groningen, the Netherlands
                [10 ]ISNI 000000040459992X, GRID grid.5645.2, Department of Surgery, Erasmus MC, ; Rotterdam, the Netherlands
                [11 ]GRID grid.430814.a, Department of Pathology, , the Netherlands Cancer Institute, ; Amsterdam, the Netherlands
                [12 ]ISNI 0000 0004 1754 9227, GRID grid.12380.38, Department of Surgery, Amsterdam UMC, , Vrije Universiteit Amsterdam, Cancer Center Amsterdam, ; Amsterdam, the Netherlands
                [13 ]ISNI 0000000084992262, GRID grid.7177.6, Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Amsterdam UMC, , University of Amsterdam, ; Amsterdam, the Netherlands
                [14 ]GRID grid.440159.d, Department of Surgery, , Flevo hospital, ; Almere, the Netherlands
                Author information
                http://orcid.org/0000-0002-8711-9383
                Article
                5408
                10.1186/s12885-019-5408-8
                6429794
                30898098
                31f1c7a9-a4e3-4a93-a3b1-e6f8c329b756
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 17 January 2019
                : 25 February 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100004622, KWF Kankerbestrijding;
                Award ID: 11543
                Award Recipient :
                Categories
                Study Protocol
                Custom metadata
                © The Author(s) 2019

                Oncology & Radiotherapy
                t4 colon cancer,peritoneal metastases,early detection,diagnostic laparoscopy,second/third look surgery

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