[安罗替尼联合尼拉帕利治疗铂类耐药复发性卵巢癌患者的有效性和安全性]。

M Yang, J J Wang, S Q Deng, S S Liang, L Sun
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引用次数: 0

摘要

研究目的研究安罗替尼联合尼拉帕利治疗铂类耐药卵巢癌患者的有效性和安全性。方法35名病理确诊的铂类耐药卵巢癌患者在接受至少两线标准治疗后病情出现进展。他们均在2019年9月至2021年10月期间接受了安罗替尼联合尼拉帕利的治疗。主要终点是无进展生存期(PFS)。第二终点包括总生存期、客观反应率(ORR)、疾病控制率(DCR)和安全性。生存期分析采用卡普兰-梅耶法和对数秩检验,影响因素分析采用考克斯比例风险回归模型。结果最佳总反应显示,14 名患者出现部分反应,13 名患者病情稳定,8 名患者病情进展。因此,这35名患者的ORR和DCR分别为40.0%(95% CI:22.9%-57.1%)和77.1%(95% CI:62.9%-91.4%)。中位随访时间为18.9个月(6.9-32.2个月)。中位 PFS 为 6.5 个月(95% CI:5.35-7.66)。PFS的多变量Cox回归分析表明,年龄、东部合作肿瘤学组表现状态(ECOG PS)评分、国际妇产科联盟(FIGO)分期和BRCA突变状态是影响PFS的独立因素(P<0.05)。此外,从未接受过PARP抑制剂治疗的BRCA突变患者的PFS明显长于既往接受过PARPi治疗的无BRCA突变患者(15.0个月 vs 6.0个月,P=0.029)。最常见的治疗相关不良反应是疲劳(85.7%)、血液毒性(85.7%)和高血压(74.3%)。无治疗相关死亡病例。结论安罗替尼联合尼拉帕利治疗铂耐药ROC患者具有良好的疗效和可耐受的安全性。
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[The efficacy and safety of anlotinib combined with niraparib in treating patients with platinum-resistant recurrent ovarian cancer].

Objectives: To investigate the efficacy and safety of anlotinib combined with niraparib in treating patients with platinum-resistant ovarian cancer. Methods: Thirty-five patients with pathological confirmed platinum-resistant ovarian cancer who experienced progression after receiving at least two lines of standard treatment were eligible. All of them were treated with anlotinib combined with niraparib between September 2019 and October 2021. The primary endpoint was progression-free survival (PFS). The second endpoints included overall survival, objective response rate (ORR), disease control rate (DCR) and safety. Survival analysis was performed using the Kaplan-Meier method and Log-rank test, and influence factor analysis was performed using Cox proportional risk regression models. Results: The best overall response showed that partial response was observed in 14 patients, stable disease was noted within 13 patients, and progressive disease was found in 8 patients. Therefore, the ORR and DCR of these 35 patients were 40.0% (95% CI:22.9%-57.1%) and 77.1% (95% CI:62.9%-91.4%), respectively. The median follow-up duration was 18.9 months (6.9-32.2). The median PFS was 6.5 months (95% CI:5.35-7.66). Multivariate Cox regression analysis for PFS indicated that age, Eastern Cooperative Oncology Group performance status (ECOG PS) score, International Federation of Gynecology and Obstetrics (FIGO) stage, and BRCA mutation status were independent factors influencing PFS (P<0.05). Additionally, the PFS in patients with BRCA mutation who have never received PARP inhibitor treatment was significantly longer than that in patients without BRCA mutation who have been exposed to prior PARPi treatment (15.0 vs 6.0 month, P=0.029). The most common treatment-related adverse reactions were fatigue (85.7%), hematologic toxic (85.7%) and hypertension (74.3%). There were no treatment-related deaths. Conclusion: Anlotinib combined with niraparib shows a promising efficacy and tolerable safety in platinum-resistant ROC patients.

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来源期刊
中华肿瘤杂志
中华肿瘤杂志 Medicine-Medicine (all)
CiteScore
1.40
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0.00%
发文量
10433
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