Neoadjuvant Chemotherapy for Newly Diagnosed, Advanced Ovarian Cancer: ASCO Guideline Update.

IF 41.9 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2025-03-01 Epub Date: 2025-01-22 DOI:10.1200/JCO-24-02589
Stéphanie Gaillard, Christina Lacchetti, Deborah K Armstrong, William A Cliby, Mitchell I Edelson, Agustin A Garcia, Rahel G Ghebre, Gregory M Gressel, Jamie L Lesnock, Larissa A Meyer, Kathleen N Moore, Roisin E O'Cearbhaill, Alexander B Olawaiye, Ritu Salani, Dee Sparacio, Willemien J van Driel, William P Tew
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Abstract

Purpose: To provide updated guidance regarding neoadjuvant chemotherapy (NACT) and primary cytoreductive surgery (PCS) among patients with stage III-IV epithelial ovarian, fallopian tube, or primary peritoneal cancer (epithelial ovarian cancer [EOC]).

Methods: A multidisciplinary Expert Panel convened and updated the systematic review.

Results: Sixty-one studies form the evidence base.

Recommendations: Patients with suspected stage III-IV EOC should be evaluated by a gynecologic oncologist, with cancer antigen 125, computed tomography of the abdomen and pelvis, and chest imaging included. All patients with EOC should be offered germline genetic and somatic testing at diagnosis. For patients with newly diagnosed advanced EOC who are fit for surgery and have a high likelihood of achieving complete cytoreduction, PCS is recommended. For patients fit for PCS but deemed unlikely to have complete cytoreduction, NACT is recommended. Patients with newly diagnosed advanced EOC and a high perioperative risk profile should receive NACT. Before NACT, patients should have histologic confirmation of invasive ovarian cancer. For NACT, a platinum-taxane doublet is recommended. Interval cytoreductive surgery (ICS) should be performed after ≤four cycles of NACT for patients with a response to chemotherapy or stable disease. For patients with stage III disease, good performance status, and adequate renal function treated with NACT, hyperthermic intraperitoneal chemotherapy may be offered during ICS. After ICS, chemotherapy should continue to complete a six-cycle treatment plan with the optional addition of bevacizumab. Patients with EOC should be offered US Food and Drug Administration-approved maintenance treatments. Patients with progressive disease on NACT should have diagnosis reconfirmed via tissue biopsy. Patients without previous comprehensive genetic or molecular profiling should be offered testing. Treatment options include alternative chemotherapy regimens, clinical trials, and/or initiation of end-of-life care.Additional information is available at www.asco.org/gynecologic-cancer-guidelines.This guideline has been endorsed by the Society of Gynecologic Oncology.

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新诊断晚期卵巢癌的新辅助化疗:ASCO指南更新。
目的:为III-IV期上皮性卵巢癌、输卵管癌或原发性腹膜癌(上皮性卵巢癌[EOC])患者提供新辅助化疗(NACT)和原发性细胞减少手术(PCS)的最新指导。方法:多学科专家小组召集并更新系统评价。结果:61项研究形成了证据基础。建议:疑似III-IV期EOC的患者应由妇科肿瘤科医生进行评估,包括癌抗原125、腹部和骨盆计算机断层扫描以及胸部影像学检查。所有EOC患者在诊断时都应进行生殖系遗传和体细胞检测。对于新诊断为晚期EOC的患者,适合手术并且有很高的可能性实现完全的细胞减少,推荐使用PCS。对于适合PCS但被认为不太可能完全细胞减少的患者,建议使用NACT。新诊断的晚期EOC和围手术期高风险的患者应接受NACT治疗。在行NACT前,患者应有浸润性卵巢癌的组织学证实。对于NACT,建议使用铂-紫杉烷双重衬里。对于对化疗有反应或病情稳定的患者,应在≤4个NACT周期后进行间隔细胞减少手术(ICS)。对于接受NACT治疗的III期疾病患者,良好的运动状态和足够的肾功能,可以在ICS期间提供温热腹腔内化疗。ICS后,化疗应继续完成6个周期的治疗计划,并可选择添加贝伐单抗。EOC患者应接受美国食品和药物管理局批准的维持治疗。NACT治疗进展性疾病的患者应通过组织活检重新确诊。以前没有全面遗传或分子谱分析的患者应提供检测。治疗方案包括替代化疗方案、临床试验和/或开始临终关怀。更多信息可在www.asco.org/gynecologic-cancer-guidelines.This上获得,指南已得到妇科肿瘤学会的认可。
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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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