Partnering bevacizumab with irinotecan as first line-therapy of metastatic colorectal cancer improves progression free survival-A retrospective analysis.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 01 06 2020
accepted: 08 03 2021
entrez: 28 4 2021
pubmed: 29 4 2021
medline: 16 9 2021
Statut: epublish

Résumé

Colorectal cancer remains one of the most frequent malignancies (third place at both genders) worldwide in the last decade, owing to significant changes in modern dietary habits. Approximately half of the patients develop metastases during the course of their disease. The available therapeutic armamentarium is constantly evolving, raising questions regarding the best approach for improving survival. Bevacizumab remains one of the most widely used therapies for treating metastatic colorectal cancer and can be used after progression. This study aimed to identify the best chemotherapy partner for bevacizumab after progression. We performed a retrospective analysis of patients with metastatic colorectal cancer who were treated with bevacizumab as first- and second-line chemotherapy. Data were collected for 151 patients, 40 of whom were treated with double-dose bevacizumab after the first progression. The two standard chemotherapy regimens combined with bevacizumab were FOLFIRI/CAPIRI and FOLFOX4/CAPEOX. The initiation of first-line treatment with irinotecan-based chemotherapy improved progression-free survival and time to treatment failure but not overall survival. After the first progression, retreatment with the same regimen as that used in the induction phase was the best approach for improving overall survival (median overall survival: 46.5 vs. 27.0 months for the same vs. switched strategy, respectively). No correlations were observed between the dose intensity of irinotecan, oxaliplatin, 5-fluorouracil, or bevacizumab and the overall survival, progression-free survival in the first-/second-line treatment, and time to treatment failure. Interaction between an irinotecan-based regimen as a second-line treatment and double-dose bevacizumab after progression was associated with an improved overall survival (p = 0.06). Initiating systemic treatment with an irinotecan-based regimen in combination with bevacizumab improved the progression-free survival in the first-line treatment and time to treatment failure. In terms of overall survival, bevacizumab treatment after the first progression is better partnered with the same regimen as that used in the induction phase.

Identifiants

pubmed: 33909622
doi: 10.1371/journal.pone.0248922
pii: PONE-D-20-16569
pmc: PMC8081186
doi:

Substances chimiques

Antineoplastic Agents 0
Bevacizumab 2S9ZZM9Q9V
Irinotecan 7673326042

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0248922

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Calin Cainap (C)

Ion Chiricuta Institute of Oncology, Cluj-Napoca, Romania.
Department of Oncology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Rodica Ana Ungur (RA)

Department of Medical Specialties, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Ovidiu-Vasile Bochis (OV)

Ion Chiricuta Institute of Oncology, Cluj-Napoca, Romania.

Patriciu Achimas (P)

Ion Chiricuta Institute of Oncology, Cluj-Napoca, Romania.
Department of Oncology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Catalin Vlad (C)

Ion Chiricuta Institute of Oncology, Cluj-Napoca, Romania.
Department of Oncology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Andrei Havasi (A)

Ion Chiricuta Institute of Oncology, Cluj-Napoca, Romania.

Andreea Vidrean (A)

Ion Chiricuta Institute of Oncology, Cluj-Napoca, Romania.

Anca Farcas (A)

Department of Medical Specialties, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Tiberiu Tat (T)

Ion Chiricuta Institute of Oncology, Cluj-Napoca, Romania.

Alexandra Gherman (A)

Ion Chiricuta Institute of Oncology, Cluj-Napoca, Romania.
Department of Oncology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Andra Piciu (A)

Ion Chiricuta Institute of Oncology, Cluj-Napoca, Romania.
Department of Oncology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Madalina Bota (M)

Department of Mother and Child, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Anne-Marie Constantin (AM)

Department of Morphological Sciences, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Laura Ancuta Pop (LA)

Department of Molecular Sciences, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Dana Maniu (D)

Faculty of Physics, Babes-Bolyai University, Cluj-Napoca, Romania.

Ovidiu Crisan (O)

Faculty of Pharmacy, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Cosmin Vasile Cioban (CV)

Faculty of Dental Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Ovidiu Balacescu (O)

Ion Chiricuta Institute of Oncology, Cluj-Napoca, Romania.

Ovidiu Coza (O)

Ion Chiricuta Institute of Oncology, Cluj-Napoca, Romania.
Department of Oncology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Loredana Balacescu (L)

Ion Chiricuta Institute of Oncology, Cluj-Napoca, Romania.

Monica Mihaela Marta (MM)

Department of Medical Education, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Eleonora Dronca (E)

Department of Molecular Sciences, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

Simona Cainap (S)

Department of Mother and Child, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.

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