Clinical Outcomes Following Trifluridine/Tipiracil Treatment for Patients With Metastatic Colorectal Cancer Ineligible for Regorafenib Treatment.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 10 02 2021
revised: 24 02 2021
accepted: 25 02 2021
entrez: 4 4 2021
pubmed: 5 4 2021
medline: 10 4 2021
Statut: ppublish

Résumé

In later-line treatment of metastatic colorectal cancer (mCRC), trifluridine/tipiracil is often selected because regorafenib is difficult to use in patients with comorbidities such as thrombosis, hemorrhage, or cardiac events. However, the safety and efficacy of trifluridine/tipiracil in these patients is not clear. The clinical outcomes of trifluridine/tipiracil were retrospectively investigated in patients who were ineligible for regorafenib because of comorbidities. Among the 27 patients who received trifluridine/tipiracil, many had comorbidities of deep venous thrombosis or hemorrhage. The median overall survival was 12.4 months, and the median progression-free survival was 2.8 months. The median overall survival was 7.7 months in 19 patients without subsequent regorafenib. Grade 3 or higher toxicities were found in 51% of patients. No treatment discontinuation because of comorbidities was observed. Trifluridine/tipiracil can be safely administered while maintaining efficacy in patients who were ineligible for regorafenib.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
In later-line treatment of metastatic colorectal cancer (mCRC), trifluridine/tipiracil is often selected because regorafenib is difficult to use in patients with comorbidities such as thrombosis, hemorrhage, or cardiac events. However, the safety and efficacy of trifluridine/tipiracil in these patients is not clear.
PATIENTS AND METHODS METHODS
The clinical outcomes of trifluridine/tipiracil were retrospectively investigated in patients who were ineligible for regorafenib because of comorbidities.
RESULTS RESULTS
Among the 27 patients who received trifluridine/tipiracil, many had comorbidities of deep venous thrombosis or hemorrhage. The median overall survival was 12.4 months, and the median progression-free survival was 2.8 months. The median overall survival was 7.7 months in 19 patients without subsequent regorafenib. Grade 3 or higher toxicities were found in 51% of patients. No treatment discontinuation because of comorbidities was observed.
CONCLUSION CONCLUSIONS
Trifluridine/tipiracil can be safely administered while maintaining efficacy in patients who were ineligible for regorafenib.

Identifiants

pubmed: 33813435
pii: 41/4/2203
doi: 10.21873/anticanres.14996
doi:

Substances chimiques

Drug Combinations 0
Phenylurea Compounds 0
Pyridines 0
Pyrrolidines 0
trifluridine tipiracil drug combination 0
regorafenib 24T2A1DOYB
Thymine QR26YLT7LT
Trifluridine RMW9V5RW38

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2203-2207

Informations de copyright

Copyright © 2021 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Yusuke Niisato (Y)

Department of Gastroenterology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan.

Toshikazu Moriwaki (T)

Department of Gastroenterology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan; tmoriwak@gmail.com.

Shota Fukuoka (S)

Division of Experimental Therapeutics, National Cancer Center, Kashiwa, Japan.

Toshiki Masuishi (T)

Department of Clinical Oncology, Aichi Cancer Center Hospital, Aichi, Japan.

Atsuo Takashima (A)

Gastrointestinal Medical Oncology Division, National Cancer Center Hospital, Tokyo, Japan.

Yosuke Kumekawa (Y)

Department of Gastroenterology, Saitama Cancer Center, Saitama, Japan.

Takeshi Kajiwara (T)

Department of Gastrointestinal Medical Oncology, National Hospital Organization Shikoku Cancer Center, Ehime, Japan.

Kentaro Yamazaki (K)

Division of Gastrointestinal Oncology, Shizuoka Cancer Center, Shizuoka, Japan.

Taito Esaki (T)

Department of Gastrointestinal and Medical Oncology, National Kyushu Cancer Center, Fukuoka, Japan.

Akitaka Makiyama (A)

Department of Hematology/Oncology, Japan Community Healthcare Organization Kyushu Hospital, Kitakyushu, Japan.

Tadamichi Denda (T)

Division of Gastroenterology, Chiba Cancer Center, Chiba, Japan.

Yukimasa Hatachi (Y)

Division of Oncology, Kobe City Medical Center General Hospital, Hyogo, Japan.

Takeshi Suto (T)

Department of Gastroenterological Surgery, Yamagata Prefectural Central Hospital, Yamagata, Japan.

Naotoshi Sugimoto (N)

Department of Medical Oncology, Osaka International Cancer Institute, Osaka, Japan.

Yasuhiro Shimada (Y)

Clinical Oncology Division, Kochi Health Sciences Center, Kochi, Japan.

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Classifications MeSH