Second-line FOLFIRI plus ramucirumab with or without prior bevacizumab for patients with metastatic colorectal cancer.
Adult
Aged
Aged, 80 and over
Antibodies, Monoclonal, Humanized
/ pharmacology
Antineoplastic Combined Chemotherapy Protocols
/ pharmacology
Bevacizumab
/ pharmacology
Camptothecin
/ analogs & derivatives
Cohort Studies
Colorectal Neoplasms
/ drug therapy
Female
Fluorouracil
/ pharmacology
Humans
Leucovorin
/ pharmacology
Male
Middle Aged
Neoplasm Metastasis
Retrospective Studies
Ramucirumab
Anti-VEGF
Bevacizumab-naïve
Colorectal cancer
EGFR
RAM
Journal
Cancer chemotherapy and pharmacology
ISSN: 1432-0843
Titre abrégé: Cancer Chemother Pharmacol
Pays: Germany
ID NLM: 7806519
Informations de publication
Date de publication:
08 2019
08 2019
Historique:
received:
13
02
2019
accepted:
02
05
2019
pubmed:
9
5
2019
medline:
22
4
2020
entrez:
9
5
2019
Statut:
ppublish
Résumé
Few data of folinic acid, fluorouracil, and irinotecan (FOLFIRI) plus ramucirumab (RAM) obtained in bevacizumab-naïve patients in clinical trials or routine clinical practice are available. The purpose of this retrospective study was to report the results of FOLFIRI plus RAM treatment as second-line chemotherapy for metastatic colorectal cancer (mCRC). Seventy-four patients with mCRC who received second-line FOLFIRI + RAM mCRC therapy were stratified by previous first-line therapy to groups that had (PB) or had not (NPB) been given bevacizumab. The overall survival (OS), progression-free survival (PFS), and objective response were evaluated. The overall median PFS was 6.2 months (95% CI 4.6-9.3) and median OS was 17.0 months (95% CI 11.6-NA). Median PFS was 8.0 months (95% CI 4.9-11.2) in NPB patients and 5.0 months (95% CI 3.1-7.3) in PB patients (hazard ratio = 0.72, 95% CI 0.40-1.30, p = 0.28). The response rates were 23% and 3% in NPB and PB patients, respectively. The disease control rates were 85% and 69% in NPB and PB patients, respectively. The effectiveness of FOLFIRI + RAM as a second-line chemotherapy in patients with mCRC was in line with that reported in the previous RAISE phase III trial. The response was better in bevacizumab-naïve patients than those with first-line treatment that had included bevacizumab.
Identifiants
pubmed: 31065729
doi: 10.1007/s00280-019-03855-w
pii: 10.1007/s00280-019-03855-w
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
Bevacizumab
2S9ZZM9Q9V
Leucovorin
Q573I9DVLP
Fluorouracil
U3P01618RT
Camptothecin
XT3Z54Z28A
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM