作者
Dave E. W. van der Kruijssen,Sjoerd G. Elias,Geraldine R. Vink,Karlijn L. van Rooijen,Jorine ‘t Lam-Boer,Linda Mol,Cornelis J. A. Punt,Johannes H. W. de Wilt,Miriam Koopman,Gijs J.D. van Acker,Rahim Altaf,Kees van Arkel,Coen I.M. Baeten,Sandra D. Bakker,Frank C den Boer,Marien O. den Boer,Koop Bosscha,Edwin A. van Breugel,Rebecca P. M. Brosens,Huib A. Cense,Esther C.J. Consten,Geert-Jan Creemers,Hester van Cruijsen,Wendy M. van der Deure,Joyce M. van Dodewaard,Anne-Lene G. Fromm,A.J. (Hans) Gelderblom,Michael F. Gerhards,Marie-José de Gier,Eelco J.R. de Graaf,W.M.U. (Helma) van Grevenstein,Jan Willem B. de Groot,Brigitte C.M. Haberkorn,Jamal Oulad Hadj,Paul Hamberg,Erwin van der Harst,Helgi H. Helgason,Mathijs P. Hendriks,Daniël A. Hess,Ignace H.J.T. de Hingh,R. Hoekstra,Joost A.B. van der Hoeven,M.J. van Hoogstraten,Henrik L. Jakobsen,Felix E. de Jongh,Emile D. Kerver,Monica L. Kjær,Bart C. Kuenen,Philomeen Kuijer,Sophie Kurk,Wouter K.G. Leclercq,Lobke L. van Leeuwen-Snoeks,Jeroen W.A Leijtens,Gabor I. Liposits,Olaf J.L. Loosveld,Martijn F. Lutke Holzik,Peter Nieboer,Jesper D. Nielsen,Koen C.M.J Peeters,Lone N. Petersen,Apollo Pronk,Bareld B. Pultrum,Koen Reijnders,J.M.G. H. (Anne-Marie) Van Riel,Ron C. Rietbroek,George P. van der Schelling,W.H. (Hermien) Schreurs,Nis H. Schlesinger,Heidi Schut,Michael Seiersen,Lieke H. J. Simkens,Dirkje W. Sommeijer,Pieter J. Tanis,Mehmet Temizkan,Marc W.A. van Tilburg,Marija Trajkovic,Anthony W.H van de Ven,Henk M.W. Verheul,Mareille Verseveld,Jeroen Vincent,Wouter J. Vles,F.J. (Jeroen) Vogelaar,Aad I. de Vos,Allert H. Vos,Ronald J.C.L.M. Vuylsteke,Wim A. Bleeker,Dareczka Wasowicz-Kemps,Johannes A. Wegdam,Henderik L. van Westreenen,Louise M. de Widt-Levert,A.J. (Yes) van de Wouw,Mette K Yilmaz,Peter van Duijvendijk
摘要
The role of primary tumor resection (PTR) in synchronous patients with metastatic colorectal cancer (mCRC) who had unresectable metastases and few or absent symptoms of their primary tumor is unclear. Studying subgroups with low postoperative mortality may identify patients who potentially benefit from PTR.To determine the difference in 60-day mortality between patients randomized to systemic treatment only vs PTR followed by systemic treatment, and to explore risk factors associated with 60-day mortality.CAIRO4 is a randomized phase 3 trial initiated in 2012 in which patients with mCRC were randomized to systemic treatment only or PTR followed by systemic treatment with palliative intent. This multicenter study was conducted by the Danish and Dutch Colorectal Cancer Group in general and academic hospitals in Denmark and the Netherlands. Patients included between August 2012 and December 2019 with histologically proven colorectal cancer, unresectable metastases, and a primary tumor with few or absent symptoms were eligible.Systemic treatment, consisting of fluoropyrimidine-based chemotherapy with bevacizumab vs PTR followed by fluoropyrimidine-based chemotherapy with bevacizumab.The aim of the current analysis was to compare 60-day mortality rates in both treatment arms. A secondary aim was the identification of risk factors for 60-day mortality in the treatment arms. These aims were not predefined in the study protocol.A total of 196 patients were included in the intention-to-treat analysis (112 [57%] men; median [IQR] age, 65 [59-70] years). Sixty-day mortality was 3% (95% CI, 1%-9%) in the systemic treatment arm and 11% (95% CI, 6%-19%) in the PTR arm (P = .03). In a per-protocol analysis, 60-day mortality was 2% (95% CI, 1%-7%) vs 10% (95% CI, 5%-18%; P = .048). Patients with elevated serum levels of lactate dehydrogenase, aspartate aminotransferase, alanine aminotransferase, and/or neutrophils who were randomized to PTR had a significantly higher 60-day mortality than patients without these characteristics.Patients with mCRC who were randomized to PTR followed by systemic treatment had a higher 60-day mortality than patients randomized to systemic treatment. Especially patients randomized to the PTR arm with elevated serum levels of lactate dehydrogenase, neutrophils, aspartate aminotransferase, and/or alanine aminotransferase were at high risk of postoperative mortality. Final study results on overall survival have to be awaited.ClinicalTrials.gov Identifier: NCT01606098.