Efficacy and safety of trifluridine/tipiracil and bevacizumab (FTD/TPI+BEV) in patients with metastatic colorectal cancer (mCRC) in real-world practice.

N Nieves Martinez Lago (Department of Medical Oncology. Hospital Clínico Universitario e Instituto de Investigación Sanitaria de Santiago de Compostela, Santiago de Compostela, Spain) M Margarita Reboredo (Complejo Hospitalario Universitario La Coruña, La Coruña, Spain) B Borja Gonzalez Gomez (Hospital Universitario Lucus Augusti, Lugo, Spain) B Belén de Frutos González (Department of Medical Oncology, Ramón y Cajal University Hospital, IRYCIS, CIBERONC, Madrid, Spain) M Maria Carmen Riesco Martinez (Hospital Universitario 12 de Octubre, Madrid, Spain) P Paula Carla Antonilli (Hospital Universitario de Gran Canaria Dr. Negrin, Gran Canaria, Spain) A Ana Lopez Alfonso (Hospital Infanta Leonor, Madrid, Spain) E Elena Gallardo Martin (Medical Oncology Department, Hospital Álvaro Cunqueiro, Pontevedra, Spain) A Ana Fernandez Fernandez Montes (Department of Medical Oncology, Complejo Hospitalario Universitario de Ourense, Ourense, Spain) L Luis Cabezon-Gutierrez (Hospital Universitario de Torrejon, Torrejon De Ardoz, Spain) A Antia Cousillas Castiñeira (Complejo Hospitalario de Pontevedra, Pontevedra, Spain) R Reyes Ferreiro

Abstract

204 Background: In Sunlight trial, the combination of FTD/TPI + BEV showed a significant improvement in Overall Survival (OS) and Progression-Free Survival (PFS), along with better Objective Response Rate (ORR) and Disease Control Rate (DCR), compared to FTD/TPI alone, in patients with mCRC progressing after two chemotherapy regimens. The BeTAS trial aimed to evaluate the effectiveness and safety of the FTD/TPI + BEV combination in real-world practice. Methods: This was a retrospective, observational, multicenter study of mCRC patients treated with FTD/TPI+BEV in routine clinical practice across 11 Spanish university hospitals. It included patients with mCRC who were refractory or intolerant to standard therapies. Results: A total of 208 patients treated with FTD/TPI+BEV between July 2019 and December 2023 were included. The median age was 69 years (range 33 to 88 years), with 59.8% being male. 15.3% had an ECOG performance status of 2, 55.9% had RAS mutations, 30.3% had three or more metastatic sites, and 81.2% had liver metastases. Additionally, 19.8% had a time from diagnosis of first metastasis of less than 18 months, and 55.3% were categorized in Tabernero's Unfavorable Prognostic Subgroup. Most patients (81.3%) received FTD/TPI+BEV as third-line therapy, with 90.5% having previously received anti-VEGF therapy. The median number of treatment cycles was 4 (range 1 to 31 cycles). The ORR was 4.6%, and the DCR was 50%. The median PFS was 4.9 months (95% CI, 4.0-5.7 months), and the median OS was 11.1 months (95% CI, 9.5-12.8 months). The most common grade 3-4 toxicities included neutropenia (41.8%), asthenia (7.2%), and hepatic toxicity (5.5%). No treatment-related deaths were reported. Conclusions: Our series confirms the efficacy and safety of FTD/TPI + BEV in routine clinical practice, even in a population with poor prognosis and an extensive history of previous treatments.

Article Details

Volume / Issue Vol. 43, Issue 4_suppl
Published February 01, 2025
Pages 204-204
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (12)

N

Nieves Martinez Lago

Department of Medical Oncology. Hospital Clínico Universitario e Instituto de Investigación Sanitaria de Santiago de Compostela, Santiago de Compostela, Spain

M

Margarita Reboredo

Complejo Hospitalario Universitario La Coruña, La Coruña, Spain

B

Borja Gonzalez Gomez

Hospital Universitario Lucus Augusti, Lugo, Spain

B

Belén de Frutos González

Department of Medical Oncology, Ramón y Cajal University Hospital, IRYCIS, CIBERONC, Madrid, Spain

M

Maria Carmen Riesco Martinez

Hospital Universitario 12 de Octubre, Madrid, Spain

P

Paula Carla Antonilli

Hospital Universitario de Gran Canaria Dr. Negrin, Gran Canaria, Spain

A

Ana Lopez Alfonso

Hospital Infanta Leonor, Madrid, Spain

E

Elena Gallardo Martin

Medical Oncology Department, Hospital Álvaro Cunqueiro, Pontevedra, Spain

A

Ana Fernandez Fernandez Montes

Department of Medical Oncology, Complejo Hospitalario Universitario de Ourense, Ourense, Spain

L

Luis Cabezon-Gutierrez

Hospital Universitario de Torrejon, Torrejon De Ardoz, Spain

A

Antia Cousillas Castiñeira

Complejo Hospitalario de Pontevedra, Pontevedra, Spain

R

Reyes Ferreiro