Long-term Surveillance of Patients with Complete Response Following Chemotherapy for Metastatic Nonseminomatous Germ Cell Tumor

被引:13
|
作者
Nason, Gregory J. [1 ]
Jewett, Michael A. S. [1 ]
Bostrom, Peter J. [1 ]
Goldberg, Hanan [1 ]
Hansen, Aaron R. [2 ]
Bedard, Philippe L. [2 ]
Sturgeon, Jeremy [2 ]
Warde, Padraig [3 ]
Chung, Peter [3 ]
Anson-Cartwright, Lynn [1 ]
Sweet, Joan [4 ]
Atenafu, Eshetu G. [5 ]
O'Malley, Martin [6 ]
Hamilton, Robert J. [1 ]
机构
[1] Princess Margaret Canc Ctr, Dept Surg, Div Urol, 600 Univ Ave, Toronto, ON M5G 1X5, Canada
[2] Princess Margaret Canc Ctr, Div Med Oncol & Hematol, Toronto, ON, Canada
[3] Princess Margaret Canc Ctr, Dept Radiat Oncol, Toronto, ON, Canada
[4] Univ Toronto, Univ Hlth Network, Dept Pathol & Lab Med, Toronto, ON, Canada
[5] Princess Margaret Canc Ctr, Dept Biostat, Toronto, ON, Canada
[6] Univ Toronto, Univ Hlth Network, Joint Dept Med Imaging, Div Abdominal Imaging, Toronto, ON, Canada
来源
EUROPEAN UROLOGY ONCOLOGY | 2021年 / 4卷 / 02期
关键词
Testis neoplasm; Retroperitoneal lymph node; dissection; Surveillance; Relapse; Survival; LYMPH-NODE DISSECTION; POSTCHEMOTHERAPY RETROPERITONEAL SURGERY; TESTICULAR CANCER; RESIDUAL TUMOR; COMBINATION CHEMOTHERAPY; CISPLATIN; CLASSIFICATION; COMPLICATIONS; TERATOMA;
D O I
10.1016/j.euo.2020.08.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: There is controversy regarding the management of patients with normal markers and residual masses (<= 1 cm) after chemotherapy for nonseminomatous germ cell tumors (NSGCTs). Objective: To determine long-term outcomes of a surveillance strategy in such patients. Design, setting, and participants: A retrospective review of our multidisciplinary testicular cancer database was performed. All patients who underwent primary chemotherapy for metastatic NSGCTs were identified between 1981 and 2016. A complete response (CR) was defined as normalization of serum tumor markers and a <= 1 cm residual mass in the largest axial dimension following chemotherapy. All such patients were surveilled. Outcome measurements and statistical analysis: Outcome variables of interest were time to death, time to cancer-specific survival, and time to relapse. Overall survival and relapse-free survival were calculated using the Kaplan-Meier method, and the cumulative incidence of cause-specific survival rates was calculated using competing risk analysis. The impact of risk group and chemotherapy regimen on relapse-free survival was assessed using log-rank test. Results and limitations: During the study period, 1429 metastatic germ cell tumor patients were treated with primary chemotherapy. CR was achieved in 191 (18.5%) NSGCT patients. The median age at diagnosis was 27.4 yr, with a median follow-up of 81.1 mo. The majority had American Joint Committee on Cancer stage II at diagnosis (I: 23.8%; II: 49.2%; III: 27%) and International Germ Cell Cancer Collaborative Group good-risk disease (good: 78%; intermediate: 17.8%; poor: 4.2%). Of the 191 patients with a CR, 175 (91.6%) never relapsed and remain disease free. Sixteen (8.4%) patients relapsed after a median of 11.3 mo (range 1-332 mo), with over half (nine patients; 4.7%) relapsing in the retroperitoneum only and salvaged success-fully with postchemotherapy retroperitoneal lymph node dissection (PC-RPLND) alone. Of these nine patients, only two (1%) had viable disease in the PC-RPLND specimen. The remaining seven patients had relapses outside the retroperitoneum and received salvage chemotherapy +/- postchemotherapy resection. Overall, nine (4.7%) patients have died, but only four (2.1%) from testis cancer. Conclusions: Our data, the largest series to date, confirm that surveillance is safe and effective for men who achieve a CR following chemotherapy for metastatic NSGCTs. Patient summary: Surveillance is a safe strategy for patients who achieve a complete response following chemotherapy for metastatic testis cancer. (c) 2020 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:289 / 296
页数:8
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