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低负担敏感寡转移前列腺癌患者前列腺和寡转移病灶放疗疗效和安全性评估方案:一项开放、探索性的临床试验。

Protocol for Evaluating the Efficacy and Safety of Radiotherapy for Prostate and Oligometastatic Lesions in Patients With Low-Burden Sensitive Oligometastatic Prostate Cancer: An Open, Exploratory Pilot Clinical Trial.

机构信息

Department of Radiation Oncology, The First Affiliated Hospital of Naval Medical University, Shanghai, China.

Department of Radiation Oncology, Tongji Hospital,School of Medicine, Tongji University, Shanghai, China.

出版信息

Cancer Control. 2024 Jan-Dec;31:10732748241274595. doi: 10.1177/10732748241274595.

Abstract

INTRODUCTION

The existing large prospective study demonstrates the benefits of primary radiotherapy in patients with low-volume oligometastatic prostate cancer (OMPC), and there is additional evidence of the benefits of local metastasis-directed therapy (MDT) for metastatic lesions. However, there are no results from a prospective study to demonstrate the efficacy of radiotherapy for prostate and oligometastases. Therefore, the aim of the protocol is to illustrate the efficacy of radiotherapy for prostate and oligometastatic lesions in patients with low-volume de novo hormone-sensitive OMPC.

METHODS AND ANALYSIS

This study involves a prospective, single-center, limited-sample, single-arm exploration of radiotherapy for prostate and oligometastatic lesions in patients diagnosed with low-volume hormone-sensitive OMPC. Eligible participants undergo thorough assessments and treatment involving endocrine therapy alongside radiation targeting metastatic lesions and the pelvic region. The primary site is treated with volumetric modulated arc therapy (VMAT), while metastatic sites are treated with either VMAT or stereotactic body radiation therapy (SBRT) depending on their location. All patients received radiation therapy for both the primary and metastatic lesions combined with endocrine therapy. Endocrine therapy with an antiandrogen (bicalutamide, for 4 weeks) androgen deprivation therapy combined with novel hormonal agents (acetate abiraterone) will be continued for 2 years. The primary objective is to evaluate progression-free survival-2 (PFS-2), while secondary endpoints include androgen deprivation therapy (ADT)-free survival, quality of life (QoL), overall survival, time to castration-resistant prostate cancer (CRPC), radiation-related complications, and endocrine therapy-related adverse events.

ETHICS AND DISSEMINATION

Approval was obtained from the ethics committee of the First Affiliated Hospital of Naval Medical University (CHEC2023-220). This is a single-arm exploration pilot trial evaluating radiotherapy for prostate and oligometastatic lesions in patients with OMPC. It aims to disseminate its findings through peer-reviewed journals and relevant medical conferences, with the intention of publication and presentation at these events.

TRIAL REGISTRATION NUMBERS

Clinicaltrials.gov identifier NCT06198387.

摘要

简介

现有的大型前瞻性研究表明,对于低容量寡转移前列腺癌(OMPC)患者,原发放疗具有益处,而对于转移灶,局部转移导向治疗(MDT)也具有额外益处。然而,目前尚无前瞻性研究结果表明放疗对前列腺和寡转移灶的疗效。因此,本方案的目的是阐明放疗对低容量初治激素敏感 OMPC 患者前列腺和寡转移灶的疗效。

方法和分析

这是一项前瞻性、单中心、小样本、单臂研究,旨在探索放疗对低容量初治激素敏感 OMPC 患者前列腺和寡转移灶的疗效。符合条件的患者接受全面评估和治疗,包括内分泌治疗联合针对转移灶和盆腔的放疗。原发灶采用容积旋转调强放疗(VMAT),转移灶采用 VMAT 或立体定向体部放疗(SBRT),具体取决于转移灶位置。所有患者均接受原发灶和转移灶的联合放疗及内分泌治疗。内分泌治疗采用抗雄激素(比卡鲁胺,4 周)联合新型激素药物(醋酸阿比特龙)进行雄激素剥夺治疗,持续 2 年。主要终点是评估无进展生存期 2(PFS-2),次要终点包括雄激素剥夺治疗(ADT)无进展生存期、生活质量(QoL)、总生存期、去势抵抗性前列腺癌(CRPC)时间、放疗相关并发症和内分泌治疗相关不良反应。

伦理和传播

本研究已获得海军军医大学第一附属医院伦理委员会的批准(CHEC2023-220)。这是一项评估 OMPC 患者前列腺和寡转移灶放疗的单臂探索性试验,旨在通过同行评议期刊和相关医学会议传播研究结果,计划在这些会议上发表和展示。

临床试验注册编号

Clinicaltrials.gov 标识符 NCT06198387。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dce9/11344251/72a84beb6c0b/10.1177_10732748241274595-fig1.jpg

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