Bevacizumab Plus Pemetrexed Versus Pemetrexed Alone as Maintenance Therapy for Patients With Advanced Nonsquamous Non-Small-cell Lung Cancer: Update From the Swiss Group for Clinical Cancer Research (SAKK) 19/09 Trial.

Détails

ID Serval
serval:BIB_5A81368FB843
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Bevacizumab Plus Pemetrexed Versus Pemetrexed Alone as Maintenance Therapy for Patients With Advanced Nonsquamous Non-Small-cell Lung Cancer: Update From the Swiss Group for Clinical Cancer Research (SAKK) 19/09 Trial.
Périodique
Clinical lung cancer
Auteur⸱e⸱s
Gautschi O., Rothschild S.I., Li Q., Matter-Walstra K., Zippelius A., Betticher D.C., Früh M., Stahel R.A., Cathomas R., Rauch D., Pless M., Peters S., Froesch P., Zander T., Schneider M., Biaggi C., Mach N., Ochsenbein A.F.
Collaborateur⸱rice⸱s
Swiss Group for Clinical Cancer Research
ISSN
1938-0690 (Electronic)
ISSN-L
1525-7304
Statut éditorial
Publié
Date de publication
05/2017
Peer-reviewed
Oui
Volume
18
Numéro
3
Pages
303-309
Langue
anglais
Notes
Publication types: Clinical Trial, Phase II ; Journal Article ; Multicenter Study
Publication Status: ppublish
Résumé
Pemetrexed and bevacizumab as single agents have been approved for maintenance therapy after platinum-based induction in patients with advanced nonsquamous non-small-cell lung cancer. It is currently unknown whether bevacizumab plus pemetrexed is superior to pemetrexed alone.
We conducted a nonrandomized phase II trial with 2 sequential cohorts. In the first cohort, 77 patients were treated with 4 cycles of cisplatin, bevacizumab, and pemetrexed every 3 weeks, followed by bevacizumab plus pemetrexed maintenance until progression. In the second cohort, we treated 52 patients without bevacizumab, using maintenance with pemetrexed alone. Progression-free survival (PFS), overall survival (OS), overall response rate (ORR), adverse events, and the treatment costs of the 2 cohorts were compared.
The median PFS from the time of registration was 6.9 months in cohort 1 and 5.6 months in cohort 2. The ORR was 62.3% in cohort 1% and 44.2% in cohort 2. The PFS (hazard ratio, 0.7; 95% confidence interval [CI], 0.5-1.0; P = .041) and ORR (odds ratio, 2.1; 95% CI, 1.0-4.3; P = .049) were better in cohort 1 than in cohort 2. No OS difference was found (hazard ratio, 1.0; 95% CI, 0.7-1.6; P = .890) after a median follow-up period of 47 months for cohort 1 and 27 months for cohort 2. The rate of grade ≥ 3 adverse events was greater in cohort 1. The treatment costs per patient were on average 1.4 times greater for cohort 1.
The addition of bevacizumab increased the ORR and PFS, but not OS, in our nonrandomized trial. Furthermore, the addition of bevacizumab was associated with greater toxicity and higher costs.

Mots-clé
Adult, Aged, Antineoplastic Combined Chemotherapy Protocols/economics, Antineoplastic Combined Chemotherapy Protocols/therapeutic use, Bevacizumab/therapeutic use, Carcinoma, Non-Small-Cell Lung/drug therapy, Carcinoma, Non-Small-Cell Lung/mortality, Carcinoma, Non-Small-Cell Lung/pathology, Cohort Studies, Cost-Benefit Analysis, Female, Follow-Up Studies, Humans, Lung Neoplasms/drug therapy, Lung Neoplasms/mortality, Lung Neoplasms/pathology, Male, Middle Aged, Neoplasm Staging, Pemetrexed/therapeutic use, Survival Analysis, Switzerland, Treatment Outcome, Bevacizumab, Chemotherapy, Lung cancer, Maintenance therapy, Pemetrexed
Pubmed
Web of science
Création de la notice
29/12/2016 9:58
Dernière modification de la notice
20/08/2019 15:13
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