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在 Gleason 10 前列腺癌中,雄激素剥夺疗法联合多西他赛治疗取得了卓越的病理完全缓解。

Exceptional pathologic complete response achieved with androgen deprivation and docetaxel therapy in Gleason 10 prostate cancer.

作者信息

Vaishampayan Ulka, Shi Dongping, Abdulfatah Eman, Aoun Hussein, Wynberg Jason

机构信息

Department of Oncology, Wayne State University/Karmanos Cancer Institute, Detroit, MI, USA.

Department of Pathology, Wayne State University/Karmanos Cancer Institute, Detroit, MI, USA.

出版信息

Urol Case Rep. 2019 Jan 28;23:103-105. doi: 10.1016/j.eucr.2019.01.018. eCollection 2019 Mar.

DOI:10.1016/j.eucr.2019.01.018
PMID:30740311
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6357690/
Abstract

Pathologic complete response is an exceptionally rare occurrence in prostate cancer, especially in the setting of poorly differentiated cancer, with high risk and poor prognostic features. Patient reviewed and signed an informed consent. The case details were collected. Patient had PSA of 52.6 ng/dl and Gleason score 5 + 5 = 10 prostate adenocarcinoma with focal signet ring cell pattern. Genomic testing revealed pathogenic p53 and SPOP mutations. The patient received androgen deprivation therapy and six cycles of docetaxel. His PSA declined to undetectable, and radical prostatectomy (RP) showed no evidence of malignancy. The patient has discontinued all therapy and continues in remission 12 months after surgery.

摘要

病理完全缓解在前列腺癌中极为罕见,尤其是在分化差的癌症情况下,这类癌症具有高风险和不良预后特征。患者已审阅并签署知情同意书。收集了病例详细信息。患者前列腺特异性抗原(PSA)为52.6 ng/dl, Gleason评分5 + 5 = 10,患有局灶印戒细胞型前列腺腺癌。基因检测显示p53和SPOP基因发生致病性突变。该患者接受了雄激素剥夺治疗和六个周期的多西他赛治疗。其PSA降至检测不到的水平,根治性前列腺切除术(RP)未发现恶性肿瘤迹象。患者已停止所有治疗,术后12个月仍处于缓解状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f8/6357690/3cb39b754fb1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f8/6357690/bfb932457e34/gr1a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f8/6357690/269588290981/gr1b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f8/6357690/3cb39b754fb1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f8/6357690/bfb932457e34/gr1a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f8/6357690/269588290981/gr1b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f8/6357690/3cb39b754fb1/gr2.jpg

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引用本文的文献

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本文引用的文献

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Therapy of Advanced Prostate Cancer: Targeting the Androgen Receptor Axis in Earlier Lines of Treatment.晚期前列腺癌的治疗:在早期治疗线中靶向雄激素受体轴。
Target Oncol. 2018 Dec;13(6):679-689. doi: 10.1007/s11523-018-0611-0.
2
Impact of Therapy on Genomics and Transcriptomics in High-Risk Prostate Cancer Treated with Neoadjuvant Docetaxel and Androgen Deprivation Therapy.新辅助多西他赛和雄激素剥夺治疗高危前列腺癌的基因组学和转录组学治疗影响。
Clin Cancer Res. 2017 Nov 15;23(22):6802-6811. doi: 10.1158/1078-0432.CCR-17-1034. Epub 2017 Aug 25.
3
SPOP Mutation Drives Prostate Tumorigenesis In Vivo through Coordinate Regulation of PI3K/mTOR and AR Signaling.
SPOP突变通过协调调控PI3K/mTOR和AR信号通路在体内驱动前列腺肿瘤发生。
Cancer Cell. 2017 Mar 13;31(3):436-451. doi: 10.1016/j.ccell.2017.02.004.
4
Improvements in Radiographic Progression-Free Survival Stratified by ERG Gene Status in Metastatic Castration-Resistant Prostate Cancer Patients Treated with Abiraterone Acetate.在接受醋酸阿比特龙治疗的转移性去势抵抗性前列腺癌患者中,按ERG基因状态分层的影像学无进展生存期的改善情况。
Clin Cancer Res. 2015 Apr 1;21(7):1621-7. doi: 10.1158/1078-0432.CCR-14-1961. Epub 2015 Jan 15.
5
Rationale for and review of neoadjuvant therapy prior to radical prostatectomy for patients with high-risk prostate cancer.高危前列腺癌患者根治性前列腺切除术前新辅助治疗的理由和评价。
Drugs. 2013 Sep;73(13):1417-30. doi: 10.1007/s40265-013-0107-2.