Platinum-based adjuvant chemotherapy for early-stage epithelial ovarian cancer: single or combination chemotherapy?
Article first published online: 18 JUN 2010
© 2010 The Authors Journal compilation © RCOG 2010 BJOG An International Journal of Obstetrics and Gynaecology
BJOG: An International Journal of Obstetrics & Gynaecology
Volume 117, Issue 12, pages 1459–1467, November 2010
How to Cite
Adams, G., Zekri, J., Wong, H., Walking, J. and Green, J. (2010), Platinum-based adjuvant chemotherapy for early-stage epithelial ovarian cancer: single or combination chemotherapy?. BJOG: An International Journal of Obstetrics & Gynaecology, 117: 1459–1467. doi: 10.1111/j.1471-0528.2010.02635.x
- Issue published online: 18 JUN 2010
- Article first published online: 18 JUN 2010
- Accepted 9 May 2010. Published Online 18 June 2010.
- Adjuvant chemotherapy;
- early epithelial ovarian cancer;
Please cite this paper as: Adams G, Zekri J, Wong H, Walking J, Green J. Platinum-based adjuvant chemotherapy for early-stage epithelial ovarian cancer: single or combination chemotherapy? BJOG 2010;117:1459–1467.
Objective To evaluate the clinical benefit and toxicity of two regimens; single agent carboplatin (C) and a carboplatin/paclitaxel (CP) combination in early epithelial ovarian cancer.
Design A retrospective review.
Setting Single cancer centre serving a population of 2.1 million in the northwest of England.
Population All women treated with adjuvant chemotherapy for International Federation of Obstetrics and Gynecology stage Ia–IIc ovarian cancer between 2002 and 2005.
Methods Case and operation notes were reviewed. Details of the surgery performed, performance status (PS), tumour histology, stage, grade, intended chemotherapy, chemotherapy received, acute and late toxicity, relapse and death were all recorded.
Main outcome measures Overall survival (OS), relapse-free survival (RFS), acute and late toxicity.
Results Sixty women received CP and 35 received C. Younger women (P < 0.0001) and those with a better performance status (P = 0.045) were more likely to receive CP. Median follow up was 38 months (range 0–70). Five-year OS was 62% (95% CI 44–81%) for C and 73% (95% CI 61–85%) for CP P = 0.316. For the subgroup with stage I disease and good PS (0/1) 5-year OS was 80% (59–100%) for C and 79% (63–95%) for CP; P = 1.0. For those with stage 2 disease, 5-year OS was 29% (95% CI 0–62%) for C and 63% (95% CI 44–82%) for CP; P = 0.025. Subgroup analyses by grade or histology showed no difference in OS. P was discontinued prematurely in nine (15%) women on account of toxicity, whereas C was not stopped early. P-related neuropathy (G1/2) was reported in ten (17%) women at 6 months and in two (3%) at 1 year.
Conclusions Combination therapy is administered more often than carboplatin; especially in those with younger age, better PS and nonmucinous histology. Recurrence and death rates were similar with both treatments. Well-designed trials are needed to identify the optimum chemotherapy regimen in this group.