Centro Hospitalar Universitário de São João, Porto, Portugal.
Centro Hospitalar Vila Nova de Gaia/Espinho, Vila Nova de Gaia, Portugal.
Adv Ther. 2022 Nov;39(11):5289-5299. doi: 10.1007/s12325-022-02259-2. Epub 2022 Sep 5.
Ovarian cancer is a leading cause of death among women with gynecologic malignancies. The relapse rate is high after platinum-based therapy, with the effectiveness of subsequent treatment lines decreasing over time. Recent data suggest the benefit of maintenance therapy with niraparib in platinum-sensitive recurrent disease.
We report a case series of five women with advanced ovarian cancer and BRCAness phenotype who responded favorably, and in some cases with long-term response, to maintenance therapy with niraparib. Toxicities were as expected and generally manageable. Two patients developed grade 2/3 hematological toxicity, which resolved with treatment suspension and subsequent dose reductions, and one patient reported a rare skin toxicity while responding to full-dose niraparib treatment, which was controlled with photoprotection and sunscreen.
This case series highlights the role of PARP1/2 inhibitors as a new standard of care as maintenance therapy for recurrent platinum-sensitive high-grade ovarian cancer, irrespective of BRCA status.
卵巢癌是妇科恶性肿瘤患者死亡的主要原因之一。铂类药物治疗后复发率高,随着时间的推移,后续治疗线的疗效逐渐降低。最近的数据表明,尼拉帕利维持治疗对铂类敏感复发性疾病有益。
我们报告了五例晚期卵巢癌和 BRCA 表型的女性病例,这些患者对尼拉帕利维持治疗反应良好,在某些情况下长期反应良好。毒性与预期相符,通常可管理。两名患者出现 2/3 级血液学毒性,经暂停治疗和随后减少剂量后得到缓解,一名患者在接受尼拉帕利全剂量治疗时出现罕见皮肤毒性,但通过光保护和防晒霜得到控制。
本病例系列强调了 PARP1/2 抑制剂作为一种新的标准治疗方法,作为复发性铂类敏感高级别卵巢癌的维持治疗,无论 BRCA 状态如何。