Incidence of Disease Recurrence in Patients With Colon and Upper Rectum Adenocarcinoma Stage II and III Receiving Adjuvant Capecitabine Monotherapy: Do Number of Chemotherapy Cycles and Relative Dose Intensity of the Drug Play a Role?


Journal

Clinical colorectal cancer
ISSN: 1938-0674
Titre abrégé: Clin Colorectal Cancer
Pays: United States
ID NLM: 101120693

Informations de publication

Date de publication:
06 2023
Historique:
received: 09 09 2022
revised: 26 02 2023
accepted: 28 02 2023
medline: 26 5 2023
pubmed: 27 3 2023
entrez: 26 3 2023
Statut: ppublish

Résumé

Adjuvant capecitabine monotherapy is an option for colon and upper rectum adenocarcinoma patients, providing they have stage II disease with an intermediate risk of recurrence, or stage III but they are above 70's or they have comorbidities. We wanted to examine whether the number of chemotherapy cycles and the relative dose intensity (RDI) of capecitabine monotherapy in the adjuvant setting are affecting disease recurrence. We included patients with completely resected stage II and III colon and upper rectum cancer who received adjuvant capecitabine monotherapy, from 2003 until May 2020. Patients with early relapse, i.e. during chemotherapy or within 6 months after the completion of adjuvant chemotherapy, and those with rectal cancer who received radiotherapy were excluded. Patients were divided into 3 groups based on the number of chemotherapy cycles received and the RDI. Group A included patients with ≤4 cycles of chemotherapy, group B patients with >4 cycles of chemotherapy and RDI ≤80%, and group C patients with >4 cycles of chemotherapy and RDI >80%. Study's endpoint, was recurrence free survival (RFS). Two hundred twenty six patients with stage II and III disease (164 and 62 respectively) were included. Sixteen, 166 and 44 were included in groups A, B and C respectively. After a median follow-up of 41 months, 21 patients (9,3%) had relapsed. Patients belonging to group C were found to have a trend for lower relapse rate compared to patients belonging to group A or group B. Number of adjuvant capecitabine cycles and RDI might play a role in RFS in patients with stage II and III colon and upper rectum adenocarcinoma.

Sections du résumé

INTRODUCTION/BACKGROUND
Adjuvant capecitabine monotherapy is an option for colon and upper rectum adenocarcinoma patients, providing they have stage II disease with an intermediate risk of recurrence, or stage III but they are above 70's or they have comorbidities. We wanted to examine whether the number of chemotherapy cycles and the relative dose intensity (RDI) of capecitabine monotherapy in the adjuvant setting are affecting disease recurrence.
PATIENTS AND METHODS
We included patients with completely resected stage II and III colon and upper rectum cancer who received adjuvant capecitabine monotherapy, from 2003 until May 2020. Patients with early relapse, i.e. during chemotherapy or within 6 months after the completion of adjuvant chemotherapy, and those with rectal cancer who received radiotherapy were excluded. Patients were divided into 3 groups based on the number of chemotherapy cycles received and the RDI. Group A included patients with ≤4 cycles of chemotherapy, group B patients with >4 cycles of chemotherapy and RDI ≤80%, and group C patients with >4 cycles of chemotherapy and RDI >80%. Study's endpoint, was recurrence free survival (RFS).
RESULTS
Two hundred twenty six patients with stage II and III disease (164 and 62 respectively) were included. Sixteen, 166 and 44 were included in groups A, B and C respectively. After a median follow-up of 41 months, 21 patients (9,3%) had relapsed. Patients belonging to group C were found to have a trend for lower relapse rate compared to patients belonging to group A or group B.
CONCLUSION
Number of adjuvant capecitabine cycles and RDI might play a role in RFS in patients with stage II and III colon and upper rectum adenocarcinoma.

Identifiants

pubmed: 36967268
pii: S1533-0028(23)00024-5
doi: 10.1016/j.clcc.2023.02.007
pii:
doi:

Substances chimiques

Capecitabine 6804DJ8Z9U
Fluorouracil U3P01618RT

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

238-244

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Auteurs

Joseph Sgouros (J)

Third Department of Medical Oncology, "Agii Anargiri"General Hospital and Cancer Center, Athens, Greece. Electronic address: josephsgouros@yahoo.co.uk.

Stefania Gkoura (S)

Third Department of Medical Oncology, "Agii Anargiri"General Hospital and Cancer Center, Athens, Greece; Department of Medical Oncology, University Hospital of Ioannina, Ioannina, Greece.

Nikolaos Spathas (N)

Third Department of Medical Oncology, "Agii Anargiri"General Hospital and Cancer Center, Athens, Greece.

Fotios Tzoudas (F)

Third Department of Medical Oncology, "Agii Anargiri"General Hospital and Cancer Center, Athens, Greece.

Konstantinos Karampinos (K)

Department of Hygiene, Epidemiology and Medical Statistics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

Nikolaos Miaris (N)

Third Department of Medical Oncology, "Agii Anargiri"General Hospital and Cancer Center, Athens, Greece.

Anastasios Visvikis (A)

Third Department of Medical Oncology, "Agii Anargiri"General Hospital and Cancer Center, Athens, Greece.

Nick Dessypris (N)

Department of Hygiene, Epidemiology and Medical Statistics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

Davide Mauri (D)

Department of Medical Oncology, University Hospital of Ioannina, Ioannina, Greece.

Gerasimos Aravantinos (G)

Second Department of Medical Oncology, "Agii Anargiri" General Hospital and Cancer Center, Athens, Greece.

Ilias Theodoropoulos (I)

Third Department of Medical Oncology, "Agii Anargiri"General Hospital and Cancer Center, Athens, Greece.

George Stamoulis (G)

Third Department of Medical Oncology, "Agii Anargiri"General Hospital and Cancer Center, Athens, Greece.

Epaminondas Samantas (E)

Third Department of Medical Oncology, "Agii Anargiri"General Hospital and Cancer Center, Athens, Greece.

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Classifications MeSH