Table 3.
Agent | Response rate (%) | PFS (months) | OS (months) | Side effects | Comments |
---|---|---|---|---|---|
Pegylated liposomal doxorubicin61, 62 | 10–20 | 3–4 | 10–12 | Hand–foot syndrome; mucositis | Most frequently prescribed as every 4 weeks schedule |
Topotecan61, 63 | 12–18 | 3–4 | 10–12 mos. | Myelosuppression | Daily for 5 days or weekly administration used |
Docetaxel60 | 22 | 3.5 | 12.7 mos. | Myelosuppression | Single GOG trial with very good results |
Gemcitabine62, 103 | 15 | 4–5 | 11.8–12.7 mos. | Myelosuppression | Also data with platinums in resistant disease104; approved for platinum-sensitive disease with carboplatinum |
Pemetrexed105 | 15–21 | 2.9 | 11.4 mos. | Myelosuppression | Not approved in ovarian cancer |
Etoposide106, 107 | 6–27 | 4–5 | 10–11 mos. | Myelosuppression | Activity, dose and population dependent |
Paclitaxel64–67 | 10–30 | 4–6 | 13 mos. | Myelosuppression; Neuropathy | Usually administered weekly in this setting |
Nab-paclitaxel108 | 23 | 4–5 | 17.4 mos. | Myelosuppression; neuropathy | Not approved in ovarian cancer |
Bevacizumab79 | 21 | 4.7 | 17 | Hypertension; proteinuria; thrombosis | Not approved in ovarian cancer in the USA; pivotal phase II supporting phase III front-line and recurrence investigation |
Chemotherapy* +/−bevacizumab58 | 13 vs 31 | 3.4 vs 6.7 | Pending | Adding bevacizumab increased hypertension; proteinuria | OS pending; bevacizumab not approved in ovarian cancer |
Abbreviations: GOG, Gynecologic Oncology Group; PFS, Progression-free survival; OS, overall survival.
Allowable chemotherapy regimens in this study were paclitaxel (weekly), pegylated liposomal doxorubicin; topotecan (2 infusion styles: weekly, daily for 5 days).