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复发性卵巢癌奥拉帕利治疗期间患者咨询及症状管理

Patient Counseling and Management of Symptoms During Olaparib Therapy for Recurrent Ovarian Cancer.

作者信息

Moore Kathleen N, Monk Bradley J

机构信息

Stephenson Cancer Center, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, USA

Department of Obstetrics and Gynecology, University of Arizona Cancer Center-Phoenix, Creighton University School of Medicine at Dignity Health, St. Joseph's Hospital and Medical Center, Phoenix, Arizona, USA.

出版信息

Oncologist. 2016 Aug;21(8):954-63. doi: 10.1634/theoncologist.2015-0268. Epub 2016 Jun 2.

Abstract

UNLABELLED

: Our primary objective is to review the safety and tolerability profile of olaparib, a novel anticancer therapy, and to discuss key considerations for symptom management in patients with advanced ovarian cancer. Olaparib is the first of a new class of anticancer therapies, poly (ADP-ribose) polymerase (PARP) inhibitors that target tumors that have deficits in homologous recombination repair (such as BRCA mutations) by a process known as synthetic lethality. Through this process, neither the deficiency in homologous recombination repair nor PARP inhibition alone is cytotoxic, but the combination of these two conditions leads to cell death. In December 2014, olaparib received accelerated approval by the U.S. Food and Drug Administration (FDA) as monotherapy for patients with known or suspected deleterious germline BRCA-mutated (as detected by an FDA-approved test) advanced ovarian cancer who had been treated with at least three lines of chemotherapy. Most adverse events (AEs) reported during olaparib clinical trials conducted in patients with recurrent ovarian cancer and measurable disease were of grade 2 or less severity according to the National Cancer Institute's Common Terminology Criteria for Adverse Events. Fatigue and gastrointestinal AEs are among the most common in ovarian cancer clinical trials and can be particularly bothersome to patients. We focus on interventions to address these AEs in patients who are candidates for treatment with olaparib and allow them to remain on therapy for as long as clinically indicated.

IMPLICATIONS FOR PRACTICE

Olaparib therapy represents a new approach to treating recurrent ovarian cancer. Some associated adverse events can have a substantial effect on quality of life. It is therefore important for patients, caregivers, and health care providers to have realistic expectations and a thorough understanding of the safety and tolerability profile of olaparib to prevent or alleviate key symptoms so that therapy can continue uninterrupted if possible. This report summarizes a practical approach to supportive care for patients receiving olaparib therapy.

摘要

未标记

我们的主要目标是回顾新型抗癌疗法奥拉帕利的安全性和耐受性概况,并讨论晚期卵巢癌患者症状管理的关键注意事项。奥拉帕利是一类新型抗癌疗法中的首个药物,即聚(ADP - 核糖)聚合酶(PARP)抑制剂,它通过一种称为合成致死的过程靶向同源重组修复存在缺陷的肿瘤(如BRCA突变)。通过这个过程,单独的同源重组修复缺陷或PARP抑制都不具有细胞毒性,但这两种情况的结合会导致细胞死亡。2014年12月,奥拉帕利获得美国食品药品监督管理局(FDA)加速批准,作为单药疗法用于治疗已知或疑似有害种系BRCA突变(通过FDA批准的检测方法检测)的晚期卵巢癌患者,这些患者至少接受过三线化疗。根据美国国立癌症研究所的不良事件通用术语标准,在复发性卵巢癌和可测量疾病患者中进行的奥拉帕利临床试验期间报告的大多数不良事件(AE)严重程度为2级或更低。疲劳和胃肠道不良事件是卵巢癌临床试验中最常见的,对患者可能特别困扰。我们专注于针对这些不良事件的干预措施,以治疗适合使用奥拉帕利的患者,并允许他们在临床指征允许的情况下尽可能长时间继续治疗。

对实践的启示

奥拉帕利疗法代表了一种治疗复发性卵巢癌的新方法。一些相关的不良事件可能对生活质量产生重大影响。因此,对于患者、护理人员和医疗保健提供者来说,拥有现实的期望并全面了解奥拉帕利的安全性和耐受性概况非常重要,以便预防或减轻关键症状,从而在可能的情况下使治疗能够持续不间断。本报告总结了一种对接受奥拉帕利治疗患者的支持性护理实用方法。

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