Detailed Information on Publication Record
2019
Sequential therapy with bevacizumab and EGFR inhibitors for metastatic colorectal carcinoma: a national registry-based analysis
BUCHLER, Tomas, Renata CHLOUPKOVÁ, Alexandr POPRACH, Ondrej FIALA, Igor KISS et. al.Basic information
Original name
Sequential therapy with bevacizumab and EGFR inhibitors for metastatic colorectal carcinoma: a national registry-based analysis
Authors
BUCHLER, Tomas (203 Czech Republic, guarantor), Renata CHLOUPKOVÁ (203 Czech Republic, belonging to the institution), Alexandr POPRACH (203 Czech Republic, belonging to the institution), Ondrej FIALA (203 Czech Republic), Igor KISS (203 Czech Republic, belonging to the institution), Katerina KOPECKOVA (203 Czech Republic), Ladislav DUŠEK (203 Czech Republic, belonging to the institution), Veronika VESKRNOVA (203 Czech Republic), Lubomir SLAVICEK (203 Czech Republic), Milan KOHOUTEK (203 Czech Republic), Jindrich FINEK (203 Czech Republic), Marek SVOBODA (203 Czech Republic, belonging to the institution), Lubos PETRUZELKA (203 Czech Republic) and Bohuslav MELICHAR (203 Czech Republic)
Edition
CANCER MANAGEMENT AND RESEARCH, ALBANY, DOVE MEDICAL PRESS LTD, 2019, 1179-1322
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30204 Oncology
Country of publisher
New Zealand
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.886
RIV identification code
RIV/00216224:14110/19:00109476
Organization unit
Faculty of Medicine
UT WoS
000454529000001
Keywords in English
colorectal carcinoma; bevacizumab; panitumumab; cetuximab; sequence
Tags
International impact, Reviewed
Změněno: 11/5/2020 09:12, Mgr. Tereza Miškechová
Abstract
V originále
Purpose: Although inhibitors of vascular endothelial growth factor and inhibitors of epidermal growth factor receptor (EGFRi) are commonly used for the treatment of metastatic colorectal cancer (mCRC), the optimal sequencing of the agents is currently unclear. Methods: A national registry of targeted therapies was used to analyze baseline characteristics and outcomes of patients with mCRC and wild-type KRAS exon 2 status who received bevacizumab and EGFRi (cetuximab or panitumumab) as a part of first- and second-line treatment in either sequence. Results: The cohort included 490 patients (181 patients treated with first-line EGFRi and second-line bevacizumab and 309 patients treated with first-line bevacizumab and second-line EGFRi). Median overall survival (OS) from the initiation on first-line therapy was similar for patients treated with either sequence, reaching 31.8 (95% CI 27.5-36.1) vs 31.4 months (95% CI 27.8-35.0) for EGFRi -> bevacizumab vs bevacizumab -> EGFRi cohort, respectively. Time from first-line initiation to progression on the second-line therapy [progression-free survival (PFS)] was 21.1 (95% CI 19.3-23.0) vs 19.3 months (95% CI 17.3-21.3) for bevacizumab -> EGFRi vs EGFRi -> bevacizumab cohort, respectively (P=0.016). Conclusion: This retrospective analysis of real-world data of patients with wild-type KRAS exon 2 mCRC showed no differences in OS between cohorts treated with bevacizumab -> EGFRi vs the reverse sequence while combined PFS favored the bevacizumab -> EGFRi sequence.