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Prognostic value of liver metastases in colorectal cancer treated by systemic therapy: An ARCAD pooled analysis.
Cohen, Romain; Raeisi, Morteza; Chibaudel, Benoist; Shi, Qian; Yoshino, Takayuki; Zalcberg, John R; Adams, Richard; Cremolini, Chiara; Van Cutsem, Eric; Heinemann, Volker; Tabernero, Josep; Punt, Cornelis J A; Arnold, Dirk; Hurwitz, Herbert I; Douillard, Jean-Yves; Venook, Alan P; Saltz, Leonard B; Maughan, Timothy S; Kabbinavar, Fairooz; Bokemeyer, Carsten; Grothey, Axel; Mayer, Robert J; Kaplan, Richard; Tebbutt, Niall C; Randolph Hecht, J; Giantonio, Bruce J; Díaz-Rubio, Eduardo; Sobrero, Alberto F; Peeters, Marc; Koopman, Miriam; Goldberg, Richard M; Andre, Thierry; de Gramont, Aimery.
Afiliación
  • Cohen R; Sorbonne University, Department of Medical Oncology, Hôpital Saint-Antoine, AP-HP, and INSERM UMRS 938, Équipe Instabilité des Microsatellites et Cancer, Équipe Labellisée par la Ligue Nationale Contre le Cancer, SIRIC CURAMUS, Centre de recherche Saint Antoine, Paris, France.
  • Raeisi M; Statistical Unit, ARCAD Foundation, Paris, France. Electronic address: morteza.raeisi@fondationarcad.org.
  • Chibaudel B; Department of Medical Oncology, Franco-British Hospital, Fondation Cognacq-Jay, Levallois-Perret, France.
  • Shi Q; Department of Quantitative Health Science, Mayo Clinic, Rochester, USA.
  • Yoshino T; Department of Gastroenterology and Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
  • Zalcberg JR; Monash University School of Public Health and Preventive Medicine and Department of Medical Oncology, Alfred Health, Melbourne, VIC, Australia.
  • Adams R; Cardiff University and Velindre Cancer Centre, Cardiff, United Kingdom.
  • Cremolini C; Department of Translational Research and New Technologies, University of Pisa, Pisa, Italy.
  • Van Cutsem E; Department of Gastrointestinal and Liver Diseases, Digestive Oncology Unit, University Hospitals Leuven and KU Leuven, Leuven, Belgium.
  • Heinemann V; Department of Medical Oncology, LMU Hospital, University of Munich, Munich, Germany.
  • Tabernero J; Vall d'Hebron University Hospital and Vall d'Hebron Institute of Oncology (VHIO), IOB-Quiron, Barcelona, Spain.
  • Punt CJA; University Medical Center Utrecht, Utrecht, the Netherlands.
  • Arnold D; Asklepios Tumorzentrum Hamburg, Asklepios Klinik Altona, Hamburg, Germany.
  • Hurwitz HI; Duke University, Durham, NC, USA.
  • Douillard JY; Medical Oncology Department, Integrated Centers for Oncology Nantes, Nantes, France.
  • Venook AP; Department of Medicine, The University of California San Francisco, San Francisco, CA, USA.
  • Saltz LB; Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Maughan TS; University of Liverpool, Liverpool, United Kingdom.
  • Kabbinavar F; Cardiff Oncology, San Diego, USA.
  • Bokemeyer C; Department of Oncology and Hematology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Grothey A; West Cancer Center, Germantown, TN, USA.
  • Mayer RJ; Dana-Farber Cancer Institute, Boston, MA, USA.
  • Kaplan R; MRC Clinical Trials Unit at UCL, London, UK.
  • Tebbutt NC; Department of Medical Oncology, Olivia Newton-John Cancer, Wellness and Research Centre, Austin Health, Heidelberg, VIC, Australia.
  • Randolph Hecht J; David Geffen School of Medicine at UCLA, University of California at Los Angeles, Los Angeles, USA.
  • Giantonio BJ; Massachusetts General Hospital, Boston, MA, USA.
  • Díaz-Rubio E; Hospital Clínico San Carlos, Prof. Martín Lagos, 28040 Madrid, Spain.
  • Sobrero AF; Department of Medical Oncology, Ospedale San Martino, Genoa, Italy.
  • Peeters M; University Hospital Ghent, Ghent, Belgium.
  • Koopman M; University Medical Center Utrecht, Utrecht, the Netherlands.
  • Goldberg RM; Department of Medicine, West Virginia University Cancer Institute, Morgantown, USA.
  • Andre T; Sorbonne University, Department of Medical Oncology, Hôpital Saint-Antoine, AP-HP, and INSERM UMRS 938, Équipe Instabilité des Microsatellites et Cancer, Équipe Labellisée par la Ligue Nationale Contre le Cancer, SIRIC CURAMUS, Centre de recherche Saint Antoine, Paris, France; ARCAD Foundation, Pari
  • de Gramont A; ARCAD Foundation, Paris, France; Department of Medical Oncology, Franco-British Hospital, Levallois-Perret, France.
Eur J Cancer ; 207: 114160, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38896997
ABSTRACT

BACKGROUND:

The liver is the most frequent site of metastases in colorectal cancer (CRC). This study aimed to assess the response rate and survival outcomes in metastatic CRC patients with non-liver metastases (NLM) compared to those with liver metastases (LM) across different lines of treatment.

METHODS:

A total of 17,924 mCRC patients included in 26 trials from the ARCAD CRC database were analyzed. The analysis was conducted based on the presence or absence of LM across different treatment groups chemotherapy (CT) alone, CT + anti-VEGF, CT + anti-EGFR in KRAS wild-type tumors, within the first-line (1 L) and second-line (2 L), and patients enrolled in third-line (≥3 L) trials treated with trifluridine/tipiracil or regorafenib or placebo. The endpoints were overall survival (OS), progression-free survival (PFS), and overall response rate (ORR).

RESULTS:

Out of the 17,924 patients, 14,066 had LM (30.6 % with only liver involvement and 69.4 % with liver and other metastatic sites), while 3858 patients had NLM. In the CT alone and CT + anti-VEGF subgroups, NLM patients showed better OS and PFS in the 1 L and 2 L settings. However, in the CT + anti-EGFR 1 L and 2 L subgroups, there was no significant difference in OS and PFS between NLM and LM patients. In the ≥ 3 L subgroups, better OS and PFS were observed in NLM patients. ORRs were higher in LM patients than in NLM patients across all cohorts treated in the 1 L and only in the anti-EGFR cohort in the 2 L.

CONCLUSION:

LM is a poor prognostic factor for mCRC increasing from 1 L to ≥ 3 L except for patients in 1 L and 2 L receiving CT+anti-EGFR. These data justify using LM as a stratification factor in future trials for patients with unresectable mCRC.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Hepáticas Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Cancer Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Hepáticas Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Cancer Año: 2024 Tipo del documento: Article País de afiliación: Francia
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