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First-line chemotherapy with raltitrexed in metastatic colorectal cancer: an Association des Gastro-entérologues Oncologues (AGEO) multicentre study.
Gallois, Claire; Hafliger, Emilie; Auclin, Edouard; Perret, Audrey; Coutzac, Clélia; Turpin, Anthony; Pellat, Anna; Randrian, Violaine; Basile, Debora; Faroux, Roger; Pernot, Simon; Locher, Christophe; Hautefeuille, Vincent; Dubreuil, Olivier; Palmieri, Lola-Jade; Dior, Marie; Artru, Pascal; Taieb, Julien.
Afiliação
  • Gallois C; Paris University, Assistance Publique-Hôpitaux de Paris, Department of Gastroenterology and Digestive Oncology, Hôpital Européen Georges Pompidou, Paris, France.
  • Hafliger E; Department of Gastroenterology and Digestive Oncology, Hôpital privé Jean Mermoz, Lyon, France.
  • Auclin E; Paris University, Assistance Publique-Hôpitaux de Paris, Department of Medical Oncology, Hôpital Européen Georges Pompidou, Paris, France.
  • Perret A; Department of Cancer Medicine, Gustave Roussy Cancer Institute, Villejuif, France.
  • Coutzac C; Centre Léon Bérard, Cancer Research Center of Lyon (CRCL), Lyon, France.
  • Turpin A; Univ. Lille, CNRS UMR9020, Inserm UMR-S 1277 - Canther - Cancer Heterogeneity, Plasticity and Resistance to Therapies, CHU Lille, Department of Medical Oncology, Lille, France.
  • Pellat A; Sorbonne University, Department of Digestive Oncology, Hôpital Saint-Antoine, Paris, France.
  • Randrian V; Department of Hepato-gastroenterology, Centre Hospitalier Universitaire de Poitiers, Poitiers University, Poitiers, France.
  • Basile D; Department of Medicine (DAME), University of Udine, Udine, Italy.
  • Faroux R; Department of Hepato-gastroenterology, Hôpital de La Roche-sur-Yon, La Roche-sur-Yon, France.
  • Pernot S; Department of Medical Oncology, Institut Bergonié, Bordeaux, France.
  • Locher C; Department of Hepato-gastroenterology, Centre Hospitalier de Meaux, Meaux, France.
  • Hautefeuille V; Department of Hepato-gastroenterology and Digestive Oncology, Centre Hospitalier Universitaire d'Amiens, Amiens, France.
  • Dubreuil O; Department of Digestive Oncology, Groupe hospitalier Diaconesses Croix Saint Simon, Paris, France.
  • Palmieri LJ; Paris University, Department of Hepato-gastroenterology, Hôpital Cochin, Paris, France.
  • Dior M; Department of Hepato-gastroenterology, Hôpital Louis Mourier, Colombes, France.
  • Artru P; Department of Gastroenterology and Digestive Oncology, Hôpital privé Jean Mermoz, Lyon, France.
  • Taieb J; Paris University, Assistance Publique-Hôpitaux de Paris, Department of Gastroenterology and Digestive Oncology, Hôpital Européen Georges Pompidou, Paris, France. Electronic address: jtaieb75@gmail.com.
Dig Liver Dis ; 54(5): 684-691, 2022 05.
Article em En | MEDLINE | ID: mdl-34470724
ABSTRACT

BACKGROUND:

In case of contraindication or intolerance to fluoropyrimidines, raltitrexed is a validated alternative in metastatic colorectal cancer (mCRC), associated or not with oxaliplatin. Little is known about the outcomes of raltitrexed combined with irinotecan or targeted therapies.

METHODS:

This retrospective multicentre study enroled mCRC patients treated with first-line raltitrexed-based chemotherapy. Treatment-related toxicities were recorded. Progression-free survival (PFS) and overall survival (OS) were calculated from treatment start.

RESULTS:

75 patients were treated with raltitrexed alone, TOMOX, or TOMIRI with or without bevacizumab. Grade 3-4 adverse events were seen in 31% of patients, without significant difference between the different treatment schedules. amongst the 36 patients with a history of fluoropyrimidine-induced cardiac toxicity, none developed cardiovascular events on raltitrexed. Median PFS and OS were 10.6 (95% CI 8.2 - 13.1) and 27.4 months (95% CI 24.1-38.1), respectively. Considering the chemotherapy regimen, TOMOX was significantly associated with better PFS and OS compared to TOMIRI and raltitrexed alone.

CONCLUSIONS:

In patients with mCRC not eligible for fluoropyrimidines, first-line raltitrexed-based chemotherapy had an acceptable safety profile. PFS and OS were consistent with usual survival data in mCRC, and significantly better in patients treated with TOMOX, independently of associated targeted therapies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Retais / Neoplasias Colorretais / Neoplasias do Colo Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Retais / Neoplasias Colorretais / Neoplasias do Colo Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article