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EMBARK 和 PSMA PET 成像时代的生化复发前列腺癌:一切都变了,除了患者。

Biochemically recurrent prostate cancer in the era of EMBARK and PSMA PET imaging: everything has changed, except the patients.

机构信息

Beth Israel Deaconess Medical Center, Boston, Massachusetts.

Inova Schar Cancer Institute, Fairfax, Virginia.

出版信息

Curr Opin Oncol. 2024 May 1;36(3):164-168. doi: 10.1097/CCO.0000000000001030. Epub 2024 Feb 23.

DOI:10.1097/CCO.0000000000001030
PMID:38573205
Abstract

PURPOSE OF REVIEW

Patients with biochemically recurrent prostate cancer (BCR) after unsuccessful curative therapies frequently have an indolent and asymptomatic disease course for years. There are no prospective data showing that treating BCR improves overall survival despite new imaging strategies and emerging therapeutic data. Managing BCR requires a unique perspective in oncology that balances toxicities and disease kinetics.

RECENT FINDINGS

Prostate specific membrane antigen (PSMA) imaging is now widely available and can define subclinical disease in patients with BCR who otherwise have negative CT and bone scans, but limited data exists showing that treating PSMA-positive disease has long term impact. A phase 3 trial demonstrated that the androgen receptor pathway inhibitor enzalutamide either alone or with androgen deprivation therapy (ADT) was superior in delaying metastasis, relative to ADT alone. Survival benefits from this study remain unknown.

SUMMARY

BCR is a heterogeneous population where overtreatment may present greater risk to patients than a disease course that is often indolent. Management of BCR should be individualized based on disease kinetics. Given the unique biology of BCR, future therapeutic research should emphasize an approach that alters disease trajectory without accompanying side effects and should explore options beyond ADT-based strategies.

摘要

目的综述

经过不成功的根治性治疗后出现生化复发的前列腺癌(BCR)患者,其疾病多年来通常处于惰性和无症状状态。尽管有新的影像学策略和新兴治疗数据,但尚无前瞻性数据表明治疗 BCR 可改善总体生存率。管理 BCR 需要肿瘤学的独特视角,平衡毒性和疾病动力学。

最新发现

前列腺特异性膜抗原(PSMA)成像现在广泛可用,可在 CT 和骨扫描阴性的 BCR 患者中定义亚临床疾病,但有限的数据表明,治疗 PSMA 阳性疾病具有长期影响。一项 3 期试验表明,与单独 ADT 相比,雄激素受体通路抑制剂恩扎鲁胺单独或与 ADT 联合使用可延迟转移。该研究的生存获益尚不清楚。

总结

BCR 是一个异质性人群,过度治疗可能比通常惰性的疾病过程对患者的风险更大。BCR 的管理应根据疾病动力学个体化。鉴于 BCR 的独特生物学特性,未来的治疗研究应强调一种改变疾病轨迹而不伴随副作用的方法,并应探索除 ADT 策略之外的选择。

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