du Bois A, Pfisterer J, Burchardi N, Loibl S, Huober J, Wimberger P, Burges A, Stähle A, Jackisch C, Kölbl H
Department of Gynecology and Gynecologic Oncology, Dr. Horst Schmidt Klinik, Ludwig-Erhard-Str. 100, 65185 Wiesbaden, Germany.
Gynecol Oncol. 2007 Dec;107(3):518-25. doi: 10.1016/j.ygyno.2007.08.008. Epub 2007 Oct 25.
A multicenter non-randomized phase II study was initiated to evaluate tolerability and efficacy of pegylated liposomal doxorubicin (PLD) in combination with carboplatin in gynecologic malignancies.
One hundred forty women with recurrent or advanced endometrial (n=31), cervical or vaginal cancer (n=31), uterine sarcomas (n=11), or recurrent platinum-sensitive ovarian cancer (n=67) received six courses of PLD 40 mg/m2 and carboplatin (AUC 6) every 28 days.
Hematological toxicities with NCI-CTC grade 3/4 were anemia in 8%, thrombocytopenia in 14%, neutropenia in 24%, and febrile neutropenia in 2% of 652 cycles. Grade 3/4 non-hematological toxicities included fatigue (14% of patients), pain (10%), dyspnea (9%), palmar-plantar erythrodysesthesia (7%), and nausea/vomiting (7%). Dose intensity reached 87.2% for PLD and 88.2% for carboplatin. Seventy-four percent of all non-progressive patients received at least 5 cycles. Overall response rates were (116 patients evaluable for response): ovarian cancer (n=54) 68%, endometrial cancer (n=27) 44%, uterine sarcomas (n=9) 33%, and cervical/vaginal cancer (n=26) 12%. Median progression-free survival was 11.6 months (95%CI 9.6-14.1) for ovarian cancer and 9.5 months (95%CI 6.6-12.6) for endometrial cancer. Median overall survival was 23.8 months (95%CI 19.0-30.2) and 21.4 months (95%CI 11.9-), respectively.
The combination of PLD and carboplatin was well tolerated and feasible in patients with gynecologic malignancies. Efficacy was low in cervical/vaginal cancer, but promising in patients with endometrial cancer. Efficacy was within the expected range in recurrent platinum-sensitive ovarian cancer and is currently under further investigation in a prospective randomized phase III trial comparing PLD/carboplatin with paclitaxel/carboplatin (CALYPSO-trial; AGO-OVAR 2.9).
开展一项多中心非随机II期研究,以评估聚乙二醇化脂质体阿霉素(PLD)联合卡铂治疗妇科恶性肿瘤的耐受性和疗效。
140例复发性或晚期子宫内膜癌(n = 31)、宫颈癌或阴道癌(n = 31)、子宫肉瘤(n = 11)或铂类敏感的复发性卵巢癌(n = 67)患者,每28天接受6个疗程的PLD 40 mg/m²联合卡铂(AUC 6)治疗。
在652个疗程中,美国国立癌症研究所常见毒性标准(NCI-CTC)3/4级血液学毒性包括:贫血8%、血小板减少14%、中性粒细胞减少24%、发热性中性粒细胞减少2%。3/4级非血液学毒性包括:疲劳(14%的患者)、疼痛(10%)、呼吸困难(9%)、手足红斑性感觉异常(7%)、恶心/呕吐(7%)。PLD和卡铂的剂量强度分别达到87.2%和88.2%。所有病情未进展的患者中,74%接受了至少5个疗程的治疗。总体缓解率为(116例可评估缓解情况的患者):卵巢癌(n = 54)68%、子宫内膜癌(n = 27)44%、子宫肉瘤(n = 9)33%、宫颈癌/阴道癌(n = 26)12%。卵巢癌的中位无进展生存期为11.6个月(95%CI 9.6 - 14.1),子宫内膜癌为9.5个月(95%CI 6.6 - 12.6)。中位总生存期分别为23.8个月(95%CI 19.0 - 30.2)和21.4个月(95%CI 11.9 -)。
PLD联合卡铂在妇科恶性肿瘤患者中耐受性良好且可行。在宫颈癌/阴道癌中疗效较低,但在子宫内膜癌患者中前景良好。在铂类敏感的复发性卵巢癌中,疗效在预期范围内,目前正在一项前瞻性随机III期试验中进一步研究,该试验比较PLD/卡铂与紫杉醇/卡铂(CALYPSO试验;AGO-OVAR 2.9)。