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聚乙二醇化脂质体阿霉素单药治疗及联合卡铂治疗韩国复发性卵巢癌、输卵管癌或原发性腹膜癌患者的疗效和安全性:单机构经验

The efficacy and safety of pegylated liposomal doxorubicin monotherapy and combination therapy with carboplatin in Korean patients with recurrent ovarian, fallopian tube, or primary peritoneal cancer: a single-institution experience.

作者信息

Lee Young-Jae, Kim Yong-Man, Kim Hyun Jin, Choi Sung Wook, Lee Shin-Wha, Park Jeong-Yeol, Kim Dae-Yeon, Suh Dae-Shik, Kim Jong-Hyeok, Kim Young-Tak, Nam Joo-Hyun

机构信息

Department of Obstetrics and Gynecology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.

出版信息

Obstet Gynecol Sci. 2017 Sep;60(5):433-439. doi: 10.5468/ogs.2017.60.5.433. Epub 2017 Sep 18.

Abstract

OBJECTIVE

This study aimed to evaluate the efficacy and safety of pegylated liposomal doxorubicin (PLD) with or without carboplatin in Korean patients with recurrent ovarian cancer (ROC), fallopian tube, or primary peritoneal cancer.

METHODS

This retrospective study included 52 patients with ROC, fallopian tube, or primary peritoneal cancer who received PLD (50 mg/m) between 1 December 2014 and 31 July 2016.

RESULTS

The mean number of chemotherapy cycles was 3.8 (range, 2 to 9) in the PLD monotherapy group and 7 (range, 2 to 13) in the PLD combined with carboplatin (PLD-C) group. In overall response rates and clinical beneficial rates, PLD monotherapy group shows 5.0% and 17.5%, and PLD-C group shows 33.3% and 75.0%. The mean progression-free survival (PFS) was 5 and 13 months in the PLD monotherapy and PLD-C groups, respectively. At 6 months after treatment initiation, absence of disease progression was confirmed in 6 (15%) and 10 (83.3%) patients in the PLD monotherapy and PLD-C groups. Hematological adverse events (e.g., neutropenia and thrombocytopenia) were more common in the PLD-C group (<0.001, =0.004). The incidence of anemia and non-hematological adverse events, including mucositis, hand-foot syndrome, and allergic reactions, was similar in both groups.

CONCLUSION

This study demonstrated the efficacy and safety of PLD monotherapy and PLD-C combination in Korean patients with ROC. This study would be helpful to consider the degree of worry about side effects and treatment expectations after treatment. Further retrospective studies with larger samples are required to confirm the efficacy of PLD monotherapy in Asian patients with platinum-resistant ROC.

摘要

目的

本研究旨在评估聚乙二醇化脂质体阿霉素(PLD)联合或不联合卡铂治疗韩国复发性卵巢癌(ROC)、输卵管癌或原发性腹膜癌患者的疗效和安全性。

方法

这项回顾性研究纳入了2014年12月1日至2016年7月31日期间接受PLD(50mg/m)治疗的52例ROC、输卵管癌或原发性腹膜癌患者。

结果

PLD单药治疗组的化疗周期数平均为3.8个(范围2至9个),PLD联合卡铂(PLD-C)组为7个(范围2至13个)。在总缓解率和临床获益率方面,PLD单药治疗组分别为5.0%和17.5%,PLD-C组分别为33.3%和75.0%。PLD单药治疗组和PLD-C组的平均无进展生存期(PFS)分别为5个月和13个月。在开始治疗6个月后,PLD单药治疗组和PLD-C组分别有6例(15%)和10例(83.3%)患者确认无疾病进展。血液学不良事件(如中性粒细胞减少和血小板减少)在PLD-C组更为常见(<0.001,=0.004)。两组贫血及包括粘膜炎、手足综合征和过敏反应在内的非血液学不良事件的发生率相似。

结论

本研究证明了PLD单药治疗和PLD-C联合治疗韩国ROC患者的疗效和安全性。本研究有助于考虑治疗后对副作用的担忧程度和治疗期望。需要进一步进行更大样本量的回顾性研究,以证实PLD单药治疗对亚洲铂耐药ROC患者的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d724/5621072/ba47fc6ffda5/ogs-60-433-g001.jpg

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