Initial experience of TAS-102 chemotherapy in Australian patients with Chemo-refractory metastatic colorectal cancer.
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Australia
Colonic Neoplasms
/ drug therapy
Colorectal Neoplasms
/ pathology
Drug Combinations
Humans
Middle Aged
Neoplasm Recurrence, Local
/ drug therapy
Pyrrolidines
Rectal Neoplasms
Retrospective Studies
Thymine
/ therapeutic use
Trifluridine
/ therapeutic use
Uracil
/ therapeutic use
Colorectal cancer
Metastatic
TAS-102
Trifluridine/Tipiracil
Journal
Current problems in cancer
ISSN: 1535-6345
Titre abrégé: Curr Probl Cancer
Pays: United States
ID NLM: 7702986
Informations de publication
Date de publication:
04 2022
04 2022
Historique:
received:
06
05
2021
revised:
09
08
2021
accepted:
20
08
2021
pubmed:
28
9
2021
medline:
19
4
2022
entrez:
27
9
2021
Statut:
ppublish
Résumé
For patients with refractory metastatic colorectal cancer (mCRC) treatment with Trifluridine/Tipiracil, also known as TAS-102, improves overall survival. This study aims to investigate the efficacy and safety of TAS-102 in a real-world population from Victoria, Australia. A retrospective analysis of prospectively collected data from the Treatment of Recurrent and Advanced Colorectal Cancer (TRACC) registry was undertaken. The characteristics and outcomes of patients receiving TAS-102 were assessed and compared to those enrolled in the registration study (RECOURSE). Across 13 sites, 107 patients were treated with TAS-102. The median age was 60 years (range: 31-83), compared to 63 for RECOURSE. Comparing registry TAS-102-treated and RECOURSE patients, 75% vs 100% were ECOG performance status 0-1, 74% vs 79% had initiated treatment more than 18 months from diagnosis of metastatic disease and 36% vs 49% were RAS wild-type. Median time on treatment was 10.4 weeks (range: 1.7-32). Median progression-free survival (PFS) was 3.3 months compared to 2 months in RECOURSE, while median overall survival was the same at 7.1 months. Two patients (2.3%) had febrile neutropenia and there were no treatment-related deaths, where TAS-102 dose at treatment initiation was at clinician discretion.TRACC registry patients treated with TAS-102 were younger than those from the RECOURSE trial, with similar overall survival observed. Less strict application of RECIST criteria and less frequent imaging may have contributed to an apparently longer PFS.
Identifiants
pubmed: 34565601
pii: S0147-0272(21)00110-0
doi: 10.1016/j.currproblcancer.2021.100793
pii:
doi:
Substances chimiques
Drug Combinations
0
Pyrrolidines
0
trifluridine tipiracil drug combination
0
Uracil
56HH86ZVCT
Thymine
QR26YLT7LT
Trifluridine
RMW9V5RW38
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
100793Informations de copyright
Copyright © 2021. Published by Elsevier Inc.