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局部前列腺及转移灶定向放疗在寡转移前列腺癌治疗中的作用

The Role of Local Prostate and Metastasis-Directed Radiotherapy in the Treatment of Oligometastatic Prostate Cancer.

作者信息

Choi Seo Hee, Beom Seung-Hoon, Choi Young Deuk, Ham Won Sik, Han Hyunho, Han Woong Kyu, Jang Won Sik, Lee Seung Hwan, Cho Jaeho

机构信息

Department of Radiation Oncology, Yonsei Cancer Center, Heavy Ion Therapy Research Institute, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.

Department of Internal Medicine, Division of Medical Oncology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.

出版信息

Cancers (Basel). 2024 Sep 14;16(18):3159. doi: 10.3390/cancers16183159.

DOI:10.3390/cancers16183159
PMID:39335131
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11429795/
Abstract

Oligometastatic prostate cancer (OMPC) represents an early stage of metastatic disease characterized by a limited number of lesions. Recent advancements in imaging and treatment have revived interest in personalized therapies, including metastasis-directed radiotherapy (OMDRT) and primary prostate radiotherapy (PPR). This study evaluates the impact of OMDRT timing and the role of PPR on survival outcomes in OMPC patients; In this retrospective cohort study, 82 patients with OMPC who underwent OMDRT between 2010 and 2019 were analyzed. Patients were classified based on OMDRT timing (early vs. late) and disease type (synchronous vs. metachronous). Progression-free survival (PFS) and overall survival (OS) were the primary endpoints, assessed via Kaplan-Meier analysis and Cox proportional hazards models; Among the patients, 36 (43.9%) had synchronous and 46 (56.1%) had metachronous OMD. With a median follow-up of 32 months, the 5-year PFS and OS rates were 77.5% and 88.5%, respectively. Early OMDRT significantly improved PFS (HR 0.461, 95% CI: 0.257-0.826, = 0.009) and OS (HR 0.219, 95% CI: 0.080-0.603, = 0.003). Subgroup analysis showed the most favorable outcomes for synchronous OMD patients receiving early OMDRT, with a median PFS of 22.2 months and a 5-year survival rate of 42.1%. The treatment of the primary prostate provided a survival benefit in the OS of synchronous OMD patients (5-year 83.1% vs. 50%, = 0.025), and there was a further improvement in OS after PPR (5-year 87.7% vs. 50%, = 0.015). Early OMDRT significantly enhances survival outcomes in OMPC, in both synchronous and metachronous cases. The integration of PPR can further improve results, emphasizing the importance of early intervention and personalized treatment strategies. To more definitively clarify our findings across various clinical situations, further studies with larger cohorts or prospective designs are necessary.

摘要

寡转移前列腺癌(OMPC)是转移性疾病的早期阶段,其特征为转移病灶数量有限。影像学和治疗方面的最新进展重新激发了人们对个性化治疗的兴趣,包括转移灶定向放疗(OMDRT)和前列腺原发灶放疗(PPR)。本研究评估了OMDRT时机的影响以及PPR在OMPC患者生存结局中的作用;在这项回顾性队列研究中,分析了2010年至2019年间接受OMDRT的82例OMPC患者。根据OMDRT时机(早期与晚期)和疾病类型(同时性与异时性)对患者进行分类。无进展生存期(PFS)和总生存期(OS)是主要终点,通过Kaplan-Meier分析和Cox比例风险模型进行评估;在这些患者中,36例(43.9%)为同时性OMPC,46例(56.1%)为异时性OMPC。中位随访32个月,5年PFS率和OS率分别为77.5%和88.5%。早期OMDRT显著改善了PFS(风险比[HR]0.461,95%置信区间[CI]:0.257 - 0.826,P = 0.009)和OS(HR 0.219,95% CI:0.080 - 0.603,P = 0.003)。亚组分析显示,对于接受早期OMDRT的同时性OMPC患者,结局最为有利,中位PFS为22.2个月,5年生存率为42.1%。前列腺原发灶的治疗对同时性OMPC患者的OS有生存获益(5年生存率83.1%对50%,P = 0.025),PPR后OS进一步改善(5年生存率87.7%对50%,P = 0.015)。早期OMDRT显著提高了OMPC患者(包括同时性和异时性病例)的生存结局。PPR的整合可进一步改善结果,强调了早期干预和个性化治疗策略的重要性。为了更明确地阐明我们在各种临床情况下的研究结果,有必要进行更大样本队列或前瞻性设计的进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b606/11429795/20cf59ce98ba/cancers-16-03159-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b606/11429795/561d91d9d6bc/cancers-16-03159-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b606/11429795/8e4e6b7b7aeb/cancers-16-03159-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b606/11429795/fe01409a0468/cancers-16-03159-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b606/11429795/d9562eba02aa/cancers-16-03159-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b606/11429795/20cf59ce98ba/cancers-16-03159-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b606/11429795/561d91d9d6bc/cancers-16-03159-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b606/11429795/8e4e6b7b7aeb/cancers-16-03159-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b606/11429795/fe01409a0468/cancers-16-03159-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b606/11429795/d9562eba02aa/cancers-16-03159-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b606/11429795/20cf59ce98ba/cancers-16-03159-g005.jpg

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