Efficacy and toxicity of prolonged pegylated liposomal doxorubicin use in women with recurrent epithelial ovarian cancer

被引:2
|
作者
Chambers, Laura M. [1 ]
Pendlebury, Adam [2 ]
Rose, Peter G. [1 ]
Yao, Meng [3 ]
DeBernardo, Robert [1 ]
机构
[1] Cleveland Clin, Div Gynecol Oncol, Obstet Gynecol & Womens Hlth Inst, Desk A81,9500 Euclid Ave, Cleveland, OH 44195 USA
[2] Mercy Hosp Women, Dept Gynecol Oncol, 163 Studley Rd, Heidelberg, Vic 3058, Australia
[3] Cleveland Clin, Quantitat Hlth Sci, JJ Bldg,9500 Euclid Ave, Cleveland, OH 44195 USA
关键词
Recurrent ovarian cancer; Pegylated liposomal doxorubicin; SQUAMOUS-CELL CARCINOMA; PHASE-II TRIAL; PLATINUM-SENSITIVE OVARIAN; LONG-TERM USE; EVERY; WEEKS; CARDIAC SURVEILLANCE; RESISTANT OVARIAN; WEEKLY PACLITAXEL; ORAL-CAVITY; CARBOPLATIN;
D O I
10.1016/j.ygyno.2020.04.708
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. To evaluate the efficacy and toxicity of extended duration pegylated liposomal doxorubicin (PLD) in women with recurrent epithelial ovarian carcinoma (rEOC). Methods. Women with rEOC who received >7 cycles of PLD were retrospectively identified. Response was determined by RECIST 1.1. Progression free survival (PFS) and overall survival (OS) were calculated from PLD initiation. Toxicity was assessed by CTCAE v5.0. Kaplan Meier estimates and Cox proportional hazards were used to evaluate differences in time to recurrence or survival. Results. 69 patients with rEOC received a median of 11.0 cycles (range, 7-115) at a median cumulative dose of 400 mg/m(2) (range, 210-4600 mg/m(2)); 29.0% (n = 20) had platinum sensitive and 71.0% (n = 49) had platinum resistant disease. Of the observed grade 3/4 toxicities (31.9%; n = 22), dermatologic were most frequent (n = 13; 18.8%). 41 women (59.4%) experienced clinical benefit; complete response in 17.4% (n = 12), partial response in 13.0% (n = 9) and stable disease in 29.0% (n = 20). Median PFS for all patients was 13.0 months (95% CI, 10.7, 15.2); there were no significant differences between platinum sensitive versus resistant disease (15.9 months vs. 12.3 months; HR 1.15, 95% CI, 0.66, 2.00; p = .61). With extended duration PLD, median OS was 40.2 months (95% CI 30.0, 49.0); no significant differences were noted for platinum sensitive versus resistant disease (44.7 months vs. 33.3 months; HR 1.85, 95% CI, 0.91, 3.78; p = .07). Four cases (5.8%) of oral squamous cell carcinoma occurred during treatment. Conclusions. Among women with both platinum sensitive and resistant rEOC who received >7 cycles of PLD, approximately one-half experienced sustained clinical benefit with acceptable toxicity. PLD may be considered for extended usage and maintenance in initially responding women with rEOC at least stable disease. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:309 / 315
页数:7
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