Abstract | PURPOSE: We evaluated whether adding bevacizumab (Bev) to paclitaxel+carboplatin (TC) could improve outcomes, especially progression-free survival (PFS), in patients with platinum-sensitive recurrent ovarian cancer. PATIENTS AND METHODS: RESULTS: Nineteen patients received platinum-based chemotherapy and 13 patients received TC+Bev therapy. PFS (the primary endpoint) was 6.31 months in the platinum-based chemotherapy group versus 14.71 months in the TC+Bev group (hazard ratio: 0.304; 95% confidence interval: 0.114-0.8121; p=0.01752). The safety profile was similar to that expected. CONCLUSION: Adding Bev to TC prolonged PFS in patients with platinum-sensitive recurrent ovarian cancer and adverse effects were tolerable.
|
Authors | Takeshi Hirasawa, Hiroko Machida, Tetsuji Iida, Masae Ikeda, Masako Shida, Mikio Mikami |
Journal | The Tokai journal of experimental and clinical medicine
(Tokai J Exp Clin Med)
Vol. 43
Issue 3
Pg. 85-89
(Sep 20 2018)
ISSN: 2185-2243 [Electronic] Japan |
PMID | 30191541
(Publication Type: Journal Article, Observational Study)
|
Chemical References |
- Bevacizumab
- Carboplatin
- Paclitaxel
|
Topics |
- Adult
- Aged
- Aged, 80 and over
- Antineoplastic Combined Chemotherapy Protocols
(therapeutic use)
- Bevacizumab
(administration & dosage)
- Carboplatin
(administration & dosage)
- Carcinoma, Ovarian Epithelial
- Disease-Free Survival
- Drug Resistance, Neoplasm
- Female
- Humans
- Middle Aged
- Neoplasm Recurrence, Local
(drug therapy)
- Neoplasms, Glandular and Epithelial
(drug therapy)
- Ovarian Neoplasms
(drug therapy)
- Paclitaxel
(administration & dosage)
- Propensity Score
- Retrospective Studies
- Time Factors
- Treatment Outcome
|