2018
Impact of Delayed Addition of Anti-EGFR Monoclonal Antibodies on the Outcome of First-Line Therapy in Metastatic Colorectal Cancer Patients: a Retrospective Registry-Based Analysis
FIALA, Ondrej; Veronika VESKRNOVA; Renata CHLOUPKOVÁ; Alexandr POPRACH; Igor KISS et. al.Základní údaje
Originální název
Impact of Delayed Addition of Anti-EGFR Monoclonal Antibodies on the Outcome of First-Line Therapy in Metastatic Colorectal Cancer Patients: a Retrospective Registry-Based Analysis
Autoři
FIALA, Ondrej (203 Česká republika); Veronika VESKRNOVA (203 Česká republika); Renata CHLOUPKOVÁ (203 Česká republika, domácí); Alexandr POPRACH (203 Česká republika, domácí); Igor KISS (203 Česká republika, domácí); Katerina KOPECKOVA (203 Česká republika); Ladislav DUŠEK (203 Česká republika, domácí); Lubomir SLAVICEK (203 Česká republika); Milan KOHOUTEK (203 Česká republika); Jindrich FINEK; Marek SVOBODA (203 Česká republika, domácí); Lubos PETRUZELKA (203 Česká republika); Ludmila BOUBLIKOVA (203 Česká republika); Josef DVORAK (203 Česká republika); Bohuslav MELICHAR (203 Česká republika) a Tomas BUCHLER (203 Česká republika, garant)
Vydání
Targeted Oncology, Dordrecht, Springer, 2018, 1776-2596
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30204 Oncology
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 3.683
Kód RIV
RIV/00216224:14110/18:00105155
Organizační jednotka
Lékařská fakulta
UT WoS
000453659300007
EID Scopus
2-s2.0-85055685029
Klíčová slova anglicky
Anti-EGFR Monoclonal Antibodies; Colorectal Cancer
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 10. 2. 2019 13:57, Soňa Böhmová
Anotace
V originále
BackgroundThe addition of monoclonal antibodies targeting the epidermal growth factor receptor (anti-EGFR Abs) to chemotherapy for metastatic colorectal carcinoma (mCRC) is commonly delayed in the real-world clinical practice, usually because of late RAS testing results.ObjectiveTo determine whether delayed addition of anti-EGFR mAbs up to the fourth cycle of backbone chemotherapy adversely affected outcomes of mCRC patients treated with first-line regimens.Patients and MethodsClinical data of patients with histologically verified, RAS wild-type mCRC treated with first-line systemic therapy regimens containing anti-EGFR mAbs were retrospectively analysed from a national database. Patients were divided into three groups according to the timing of anti-EGFR mAbs addition to the chemotherapy backbone. Cohort A (n=401) included patients in whom anti-EGFR mAbs were added to chemotherapy from the first cycle, cohort B (n=71) patients with anti-EGFR mAbs added to chemotherapy from the second cycle, and cohort C (n=101) patients who had anti-EGFR mAbs added to chemotherapy from the third or fourth cycle.ResultsThree hundred and thirty-six (58.6%) patients received panitumumab and 237 (41.4%) patients received cetuximab. The median progression-free survival (PFS) of the whole cohort was 12.2months (95% confidence interval [CI] 10.9-13.5), and the median overall survival (OS) was 33.5months (95% CI 27.6-39.4). The median PFS and OS for patients treated with anti-EGFR mAbs added to chemotherapy were 12.9 (95% CI 11.5-14.3) and 30.6months (95% CI 25.2-36.1) for cohort A, 9.7 (95% CI 9.1-10.3) and not reached for cohort B, compared to 11.5 (95% CI 9.8-13.2) and 37.9months (95% CI 28.6-47.3) for cohort C, respectively.ConclusionsDelayed addition of anti-EGFR mAbs to first-line chemotherapy was not associated with inferior survival or response rates.