Study | Intervention | No.of participants | Age,years Median (range) | Type of trial | Patient characteristics | Pretreatment status | Main outcomes | ||
---|---|---|---|---|---|---|---|---|---|
Pujade-Lauraine 2010 [13] | carbo(AUC5) + PLD 30 mg/m2 q4wks | 466 | 60.5 (24–82) | phase III randomized multicenter, open-label trial | PS ROC | After first-or second-line Platinum and taxane-based | PFS, OS, Toxicity | ||
carbo(AUC5) + PAC 175 mg/m2 q3wks | 509 | 61 (27–82) | |||||||
Gladieff2012 [14] | carbo(AUC5) + PLD 30 mg/m2 q4wks | 161 | 60 (24–82) | phase III randomized non-inferiority trial | PS ROC | After first- or second-line platinum- and taxane-based | PFS, Toxicity | ||
carbo(AUC5) + PAC 175 mg/m2 q3wks | 183 | 60 (30–80) | |||||||
Mahner2014 [15] | carbo(AUC5) + PLD 30 mg/m2 q4wks | 131 | 60 (30–80) | phase III randomized multicenter trial | PS ROC | Platinum and taxane-pretreated | PFS, OS, Toxicity | ||
carbo(AUC5) + PAC 175 mg/m2 q3wks | 128 | 63 (27–82) | |||||||
Bafaloukos2010 [16] | carbo(AUC5) + PLD 45 mg/m2 q4wks | 93 | 62 (38–89) | phase II randomized multicenter | PS ROC | One cycle or more Of platinum-based | ORR, OS, Toxicity | ||
carbo(AUC5) + PAC 175 mg/m2 q3wks | 96 | 63 (37–81) | |||||||
Mutch2007 [17] | PLD 50 mg/m2 IVI q4wks | 96 | 62 (28–83) | phase III randomized multicenter open-label | PS ROC | Prior platinum-based ≤ 2 prior regimens allowed | PFS, OS, Toxicity | ||
Gemcitabine 1000 mg/m2 D1,8 q3wks | 99 | 59 (38–85) | |||||||
Ferrandina2008 [18] | PLD 40 mg/m2 IVI q4wks | 76 | 63 (28–80) | phase III randomized multicenter | Partial PS and PR ROC | Failed first-line Platinum or paclitaxel | OS, Toxicity | ||
Gemcitabine 1000 mg/m2 D1,5,8,15 q4wks | 77 | 63 (39–79) | |||||||
Vergote2009I [19] | PLD 50 mg/m2 IVI q4wks | 130 | 60 (30–82) | phase III randomized multicenter | platinum-refractory or PR ROC | Failed one second-Line therapy with either topotecan or PLD | Toxicity | ||
Canfosfamide 1000 mg/m2 q3wks | 231 | 60 (26–85) | |||||||
Vergote2009II [19] | PLD 50 mg/m2 IVI q4wks | 130 | 60 (30–82) | phase III randomized multicenter | platinum-refractory or PR ROC | Failed one second-Line therapy with either topotecan or PLD | Toxicity | ||
Topotecan 1.5 mg/m2 D1–5 q3wks | 87 | 60 (30–82) | |||||||
Colombo2012 [20] | PLD 50 mg/m2 IVI q4wks | 417 | 59 (23–84) | phase III randomized open-label | PR ROC | Failed≥4 cycles of platinum-based or discontinued | PFS, OS, Toxicity | ||
Patupilone 10 mg/m2 IVI q3wks | 412 | 59 (25–87) | |||||||
Banerjee2018 [21] | PLD 40 mg/m2 IVI q4wks | 48 | 62 (52–86) | phase II randomized open-label | PR ROC | Progressed or relapsed < 6 months with a platinum-based | PFS, Toxicity | ||
LIFA 2.4 mg/kg q3wks | 47 | 62 (43–83) | |||||||
Kaye2012I [22] | PLD 50 mg/m2 IVI q4wks | 33 | 53 (43–81) | phase II open-label randomized Multicenter | Partial PS and PR ROC | Recurred or progressed < 12 months with platinum-based | PFS, OS, Toxicity | ||
Olaparib 200 mg bid continuously | 32 | 58.5 (45–77) | |||||||
Kaye2012II [22] | PLD 50 mg/m2 IVI q4wks | 33 | 53 (43–81) | phase II open-label randomized Multicenter | Partial PS and PR ROC | Recurred or progressed < 12 months with platinum-based | PFS,OS, Toxicity | ||
Olaparib 400 mg bid continuously | 32 | 53.5 (35–76) |