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EAU-ESTRO-SIOG 前列腺癌诊治指南。第二部分:复发、转移和去势抵抗性前列腺癌的治疗。

EAU-ESTRO-SIOG Guidelines on Prostate Cancer. Part II: Treatment of Relapsing, Metastatic, and Castration-Resistant Prostate Cancer.

机构信息

Royal Liverpool and Broadgreen Hospitals NHS Trust, Liverpool, UK.

Bladder Cancer Center, Dana-Farber Cancer Institute, Boston, MA, USA; Harvard Medical School, Boston, MA, USA.

出版信息

Eur Urol. 2017 Apr;71(4):630-642. doi: 10.1016/j.eururo.2016.08.002. Epub 2016 Aug 31.

Abstract

OBJECTIVE

To present a summary of the 2016 version of the European Association of Urology (EAU) - European Society for Radiotherapy & Oncology (ESTRO) - International Society of Geriatric Oncology (SIOG) Guidelines on the treatment of relapsing, metastatic, and castration-resistant prostate cancer (CRPC).

EVIDENCE ACQUISITION

The working panel performed a literature review of the new data (2013-2015). The guidelines were updated, and the levels of evidence and/or grades of recommendation were added based on a systematic review of the literature.

EVIDENCE SYNTHESIS

Relapse after local therapy is defined by a rising prostate-specific antigen (PSA) level >0.2ng/ml following radical prostatectomy (RP) and >2ng/ml above the nadir after radiation therapy (RT). C-choline positron emission tomography/computed tomography is of limited importance if PSA is <1.0ng/ml; bone scans and computed tomography can be omitted unless PSA is >10ng/ml. Multiparametric magnetic resonance imaging and biopsy are important to assess biochemical failure following RT. Therapy for PSA relapse after RP includes salvage RT at PSA levels <0.5ng/ml and salvage RP, high-intensity focused ultrasound, cryosurgical ablation or salvage brachytherapy of the prostate in radiation failures. Androgen deprivation therapy (ADT) remains the basis for treatment of men with metastatic prostate cancer (PCa). However, docetaxel combined with ADT should be considered the standard of care for men with metastases at first presentation, provided they are fit enough to receive the drug. Follow-up of ADT should include analysis of PSA, testosterone levels, and screening for cardiovascular disease and metabolic syndrome. Level 1 evidence for the treatment of metastatic CRPC (mCRPC) includes, abiraterone acetate plus prednisone (AA/P), enzalutamide, radium 223 (Ra 223), docetaxel at 75 mg/m every 3 wk and sipuleucel-T. Cabazitaxel, AA/P, enzalutamide, and radium are approved for second-line treatment of CRPC following docetaxel. Zoledronic acid and denosumab can be used in men with mCRPC and osseous metastases to prevent skeletal-related complications.

CONCLUSIONS

The knowledge in the field of advanced and metastatic PCa and CRPC is changing rapidly. The 2016 EAU-ESTRO-SIOG Guidelines on PCa summarise the most recent findings and advice for use in clinical practice. These PCa guidelines are the first endorsed by the European Society for Therapeutic Radiology and Oncology and the International Society of Geriatric Oncology and reflect the multidisciplinary nature of PCa management. A full version is available from the EAU office or online (http://uroweb.org/guideline/prostate-cancer/).

PATIENT SUMMARY

In men with a rise in their PSA levels after prior local treatment for prostate cancer only, it is important to balance overtreatment against further progression of the disease since survival and quality of life may never be affected in many of these patients. For patients diagnosed with metastatic castrate-resistant prostate cancer, several new drugs have become available which may provide a clear survival benefit but the optimal choice will have to be made on an individual basis.

摘要

目的

总结 2016 年版欧洲泌尿外科学会(EAU)-欧洲放射肿瘤学会(ESTRO)-国际老年肿瘤学会(SIOG)关于复发性、转移性和去势抵抗性前列腺癌(CRPC)治疗的指南。

证据获取

工作组对新数据(2013-2015 年)进行了文献回顾。根据文献系统评价,更新了指南,并添加了证据水平和/或推荐等级。

证据综合

局部治疗后复发定义为根治性前列腺切除术(RP)后前列腺特异性抗原(PSA)水平>0.2ng/ml 升高,放射治疗(RT)后高于最低点>2ng/ml。如果 PSA<1.0ng/ml,则胆碱 C 正电子发射断层扫描/计算机断层扫描的重要性有限;如果 PSA>10ng/ml,则可以省略骨扫描和计算机断层扫描。多参数磁共振成像和活检对于评估 RT 后的生化失败很重要。RP 后 PSA 复发的治疗包括 PSA<0.5ng/ml 时进行挽救性 RT,PSA 失败时进行挽救性 RP、高强度聚焦超声、冷冻手术消融或前列腺近距离治疗。雄激素剥夺治疗(ADT)仍然是治疗转移性前列腺癌(PCa)患者的基础。然而,对于首次出现转移的患者,如果身体状况足以接受该药物,应考虑多西他赛联合 ADT 作为标准治疗。ADT 的随访应包括 PSA、睾酮水平的分析,以及心血管疾病和代谢综合征的筛查。转移性 CRPC(mCRPC)治疗的 1 级证据包括醋酸阿比特龙加泼尼松(AA/P)、恩扎鲁胺、镭 223(Ra 223)、每 3 周 75mg/m 的多西他赛和树突细胞疫苗。卡巴他赛、AA/P、恩扎鲁胺和镭已获准用于多西他赛治疗后 CRPC 的二线治疗。唑来膦酸和地舒单抗可用于有 mCRPC 和骨转移的男性,以预防骨骼相关并发症。

结论

晚期和转移性 PCa 和 CRPC 领域的知识正在迅速变化。2016 年 EAU-ESTRO-SIOG 前列腺癌指南总结了最近的发现和在临床实践中的应用建议。这些前列腺癌指南是第一个得到欧洲放射治疗和肿瘤学会以及国际老年肿瘤学会认可的指南,反映了前列腺癌管理的多学科性质。完整版本可从 EAU 办公室或在线获得(http://uroweb.org/guideline/prostate-cancer/)。

患者总结

对于仅在先前局部治疗前列腺癌后 PSA 水平升高的男性,重要的是要平衡过度治疗与疾病的进一步进展,因为许多此类患者的生存和生活质量可能永远不会受到影响。对于诊断为转移性去势抵抗性前列腺癌的患者,已有几种新的药物可供使用,这些药物可能会带来明确的生存获益,但最佳选择将需要根据个体情况做出。

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