Detailed Information on Publication Record
2020
Sequential Treatment with Bevacizumab and Aflibercept for Metastatic Colorectal Cancer in Real-World Clinical Practice
BUCHLER, Tomas, Igor KISS, Jana HORNOVA, Ondrej FIALA, Marketa WIESNEROVA et. al.Basic information
Original name
Sequential Treatment with Bevacizumab and Aflibercept for Metastatic Colorectal Cancer in Real-World Clinical Practice
Authors
BUCHLER, Tomas (203 Czech Republic, guarantor), Igor KISS (203 Czech Republic, belonging to the institution), Jana HORNOVA (203 Czech Republic), Ondrej FIALA (203 Czech Republic), Marketa WIESNEROVA (203 Czech Republic), Michal SVOBODA (203 Czech Republic), Jiri SILAR (203 Czech Republic), Katerina KOPECKOVA (203 Czech Republic), Alexandr POPRACH (203 Czech Republic, belonging to the institution), Jindrich FINEK (203 Czech Republic), Lubos PETRUZELKA (203 Czech Republic) and Bohuslav MELICHAR (203 Czech Republic)
Edition
Targeted Oncology, Dordrecht, Springer, 2020, 1776-2596
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30204 Oncology
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 4.493
RIV identification code
RIV/00216224:14110/20:00116027
Organization unit
Faculty of Medicine
UT WoS
000513061300001
Keywords in English
SIAN PATIENTS; SAFETY; FLUOROURACIL; COMBINATION; LEUCOVORIN; IRINOTECAN; EFFICACY
Tags
International impact, Reviewed
Změněno: 17/7/2020 10:07, Mgr. Tereza Miškechová
Abstract
V originále
Background Bevacizumab and aflibercept are currently the mainstay of antiangiogenic therapy for metastatic colorectal carcinoma (mCRC). They are often used in sequence with first- and second-line chemotherapy, especially in patients with RAS-mutated tumours. Objective The aim of the present study was to investigate the outcomes of patients with mCRC treated with the bevacizumab-aflibercept sequence in real-world clinical practice. Patients and Methods Data from a national clinical registry of targeted therapies for mCRC were analysed retrospectively. Overall, there were 366 patients with valid data who received first-line treatment with bevacizumab and chemotherapy followed by aflibercept with chemotherapy. The majority of the patients (n = 296, 80.8%) had RAS mutated tumours. Results Median cumulative progression-free survival (PFS) from the start of the bevacizumab-containing regimen to progression on aflibercept was 18.2 months (95% CI 16.8-19.5). Median PFS for bevacizumab and aflibercept was 10.6 months (95% CI 9.5-11.7) and 5.6 months (95% CI 5.1-6.1), respectively. Longer PFS on aflibercept was associated with metachronous metastatic disease and longer PFS on bevacizumab. Median overall survival (OS) from the start of first-line bevacizumab was 32.0 months (95% CI 26.6-37.5). The presence of metastatic disease at diagnosis was associated with worse OS. Conclusions Patients treated with aflibercept in real-world clinical practice achieved similar survival outcomes as those treated within randomised trials. Cumulative survival data provide a benchmark for future studies and enable indirect comparisons with other treatment sequences used in mCRC.