Tas-102 for Refractory Metastatic Colorectal Cancer: A Multicenter Retrospective Cohort Study

Author:

Conti Matteo1,Bolzacchini Elena1ORCID,Luchena Giovanna1ORCID,Bertu’ Lorenza2,Tagliabue Paola3,Aglione Stefania3,Ardizzoia Antonio4,Arnoffi Jessica4,Guida Francesco Maria4,Bertolini Alessandro5,Pastorini Alessandro5,Duro Maria6,Bettega Donato7,Roda’ Giovambattista8,Artale Salvatore3,Squizzato Alessandro29ORCID,Giordano Monica1

Affiliation:

1. Oncology Unit, Sant’Anna Hospital, ASST Lariana, 22042 San Fermo della Battaglia, Italy

2. Department of Medicine and Surgery, University of Insubria, 21100 Varese, Italy

3. Oncology Unit, Vimercate Hospital, ASST della Brianza, 20871 Vimercate, Italy

4. Oncology Unit, Alessandro Manzoni Hospital, ASST Lecco, 23900 Lecco, Italy

5. Oncology Unit, Ospedale Civile di Sondrio, ASST Valtellinese, 23100 Sondrio, Italy

6. Oncology Unit, Valduce Hospital, 22100 Como, Italy

7. Oncology Unit, Sacra Famiglia Hospital, 22036 Erba, Italy

8. Oncology Unit, Istituto Clinico Humanitas Mater Domini, 21100 Castellanza, Italy

9. Department of Internal Medicine, Ospedale Sant’Anna, ASST Lariana, 22100 Como, Italy

Abstract

Trifluridine/tipiracil (TAS-102) is an oral chemotherapy approved for the treatment of metastatic colorectal cancer. The efficacy and tolerability of TAS-102 were shown in phase II-III clinical trials and in several real-life studies. The elderly and other special subgroups are underrepresented in published literature. We conducted a retrospective multicenter study to assess the effectiveness and safety of TAS-102 in consecutive patients with pretreated mCRC. In particular, we estimated the effectiveness and safety of TAS-102 in elderly patients (aged ≥70, ≥75 and ≥80 years) and in special subgroups, e.g., patients with concomitant heart disease. One hundred and sixty patients were enrolled. In particular, 71 patients (44%) were 70 years of age or older, 50 (31%) were 75 years of age or older, and 23 (14%) were 80 years of age or older. 19 patients (12%) had a concomitant chronic heart disease, three (2%) patients were HIV positive, and one (<1%) patient had a DPYD gene polymorphism. In 115 (72%) cases TAS-102 was administered as a third-line treatment. The median overall survival (OS) in the overall population was 8 months (95% confidence interval [CI], 6–9), while the median progression-free survival (PFS) was 3 months (95% CI, 3–4). No significant age-related reduction in effectiveness was observed in the subpopulations of elderly patients included. The toxicity profile was acceptable in both the whole and subgroups’ population. Our study confirms the effectiveness and safety of TAS-102 in patients with pretreated mCRC, suggesting a similar risk-benefit profile in the elderly.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

Reference27 articles.

1. (2023, April 01). Cancer Today 2022. Available online: https://gco.iarc.fr/today/online-analysis-pie?v=2020&mode=cancer&mode_population=continents&population=900&populations=900&key=total&sex=0&cancer=39&type=2&statistic=5&prevalence=1&population_group=0&ages_group%5B%5D=0&ages_group%5B%5D=17&nb_items=7&group_cancer=1&include_nmsc=1&include_nmsc_other=1&half_pie=0&donut=0#collapse-group-0-4.

2. ESMO consensus guidelines for the management of patients with metastatic colorectal cancer;Cervantes;Ann. Oncol.,2016

3. TAS-102, a novel antitumor agent: A review of the mechanism of action;Lenz;Cancer Treat. Rev.,2015

4. Randomized Trial of TAS-102 for Refractory Metastatic Colorectal Cancer;Mayer;New Engl. J. Med.,2015

5. Petrelli, F., Barni, S., Bertocchi, P., and Zaniboni, A. (2016). TAS-102, the first “cardio-gentle” fluoropyrimidine in the colorectal cancer landscape?. BMC Cancer, 16.

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