Multidisciplinary clinic approach improves overall survival outcomes of patients with metastatic germ-cell tumors

被引:67
作者
Albany, C. [1 ]
Adra, N. [1 ]
Snavely, A. C. [2 ]
Cary, C. [3 ]
Masterson, T. A. [3 ]
Foster, R. S. [3 ]
Kesler, K. [4 ]
Ulbright, T. M. [5 ]
Cheng, L. [5 ]
Chovanec, M. [1 ,6 ,7 ]
Taza, F. [1 ]
Ku, K. [1 ,8 ]
Brames, M. J. [1 ]
Hanna, N. H. [1 ]
Einhorn, L. H. [1 ]
机构
[1] Indiana Univ Sch Med, Dept Med, Div Hematol & Med Oncol, 535 Barnhill Dr,RT 473, Indianapolis, IN 46202 USA
[2] PDstat, Chapel Hill, NC USA
[3] Indiana Univ Sch Med, Dept Urol, Indianapolis, IN 46202 USA
[4] Indiana Univ Sch Med, Thorac Div, Dept Surg, Indianapolis, IN 46202 USA
[5] Indiana Univ Sch Med, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
[6] Comenius Univ, Dept Oncol 2, Fac Med, Bratislava, Slovakia
[7] Natl Canc Inst, Bratislava, Slovakia
[8] Univ Wisconsin, Sch Med & Publ Hlth, Div Hematol & Med Oncol, Madison, WI USA
关键词
testicular cancer; germ-cell tumor; IGCCCG; multidisciplinary; SEER; HIGH-DOSE CHEMOTHERAPY; LYMPH-NODE DISSECTION; IFOSFAMIDE PLUS CISPLATIN; TESTICULAR CANCER; RANDOMIZED-TRIAL; SALVAGE THERAPY; BLEOMYCIN; VINBLASTINE; INSTITUTION; ETOPOSIDE;
D O I
10.1093/annonc/mdx731
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: To report our experience utilizing a multidisciplinary clinic (MDC) at Indiana University (IU) since the publication of the International Germ Cell Cancer Collaborative Group (IGCCCG), and to compare our overall survival (OS) to that of the National Cancer Institute (NCI) Surveillance, Epidemiology, and End Results (SEER) Program. Patients and methods: We conducted a retrospective analysis of all patients with metastatic germ-cell tumor (GCT) seen at IU from 1998 to 2014. A total of 1611 consecutive patients were identified, of whom 704 patients received an initial evaluation by our MDC (including medical oncology, pathology, urology and thoracic surgery) and started first-line chemotherapy at IU. These 704 patients were eligible for analysis. All patients in this cohort were treated with cisplatin-etoposide-based combination chemotherapy. We compared the progression-free survival (PFS) and OS of patients treated at IU with that of the published IGCCCG cohort. OS of the IU testis cancer primary cohort (n 1/4 622) was further compared with the SEER data of 1283 patients labeled with ` distant' disease. The Kaplan-Meier method was used to estimate PFS and OS. Results: With a median follow-up of 4.4 years, patients with good, intermediate, and poor risk disease by IGCCCG criteria treated at IU had 5-year PFS of 90%, 84%, and 54% and 5-year OS of 97%, 92%, and 73%, respectively. The 5-year PFS for all patients in the IU cohort was 79% [95% confidence interval (CI) 76% to 82%]. The 5-year OS for the IU cohort was 90% (95% CI 87% to 92%). IU testis cohort had 5-year OS 94% (95% CI 91% to 96%) versus 75% (95% CI 73% to 78%) for the SEER ` distant' cohort between 2000 and 2014, P-value< 0.0001. Conclusion: The MDC approach to GCT at high-volume cancer center associated with improved OS outcomes in this contemporary dataset. OS is significantly higher in the IU cohort compared with the IGCCCG and SEER ` distant' cohort.
引用
收藏
页码:341 / 346
页数:6
相关论文
共 28 条
[1]   Prognostic factors in patients with poor-risk germ-cell tumors: a retrospective analysis of the Indiana University experience from 1990 to 2014aEuro [J].
Adra, N. ;
Althouse, S. K. ;
Liu, H. ;
Brames, M. J. ;
Hanna, N. H. ;
Einhorn, L. H. ;
Albany, C. .
ANNALS OF ONCOLOGY, 2016, 27 (05) :875-879
[2]   Randomized phase III trial comparing retroperitoneal lymph node dissection with one course of bleomycin and etoposide plus cisplatin chemotherapy in the adjuvant treatment of clinical stage I nonseminomatous testicular germ cell tumors: AUO trial AH 01/94 by the German testicular cancer study group [J].
Albers, Peter ;
Siener, Roswitha ;
Krege, Susanne ;
Schmelz, Hans-Uwe ;
Dieckmann, Klaus-Peter ;
Heidenreich, Axel ;
Kwasny, Peter ;
Pechoel, Maik ;
Lehmann, Jan ;
Kliesch, Sabine ;
Koehrmann, Kai-Uwe ;
Fimmers, Rolf ;
Weissbach, Lothar ;
Loy, Volker ;
Wittekind, Christian ;
Hartmann, Michael .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (18) :2966-2972
[3]  
[Anonymous], 2014, J CLIN ONCOL S
[4]  
[Anonymous], RES DAT 1973 2014
[5]   A phase II trial of VP-16, ifosfamide, cisplatin, vinblastine, and bleomycin in advanced germ-cell tumors [J].
Blanke, C ;
Loehrer, PJ ;
Nichols, CR ;
Einhorn, LH .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1996, 19 (05) :487-491
[6]   Outcomes of Postchemotherapy Retroperitoneal Lymph Node Dissection Following High-Dose Chemotherapy With Stem Cell Transplantation [J].
Cary, Clint ;
Pedrosa, Jose A. ;
Jacob, Joseph ;
Beck, Stephen D. W. ;
Rice, Kevin R. ;
Einhorn, Lawrence H. ;
Foster, Richard S. .
CANCER, 2015, 121 (24) :4369-4375
[7]   Modified retroperitoneal lymph node dissection for post-chemotherapy residual tumour: a long-term update [J].
Cho, Jane S. ;
Kaimakliotis, Hristos Z. ;
Cary, Clint ;
Masterson, Timothy A. ;
Beck, Stephen ;
Foster, Richard .
BJU INTERNATIONAL, 2017, 120 (01) :104-108
[8]   Impact of the treating institution on survival of patients with "poor-prognosis" metastatic nonseminoma [J].
Collette, L ;
Sylvester, RJ ;
Stenning, SP ;
Fossa, SD ;
Mead, GM ;
de Wit, R ;
de Mulder, PHM ;
Neymark, N ;
Lallemand, E ;
Kaye, SB .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (10) :839-846
[9]   Refining the optimal chemotherapy regimen for good-risk metastatic nonseminomatous germ-cell tumors:: a randomized trial of the Genito-Urinary Group of the French Federation of Cancer Centers (GETUG T9313P) [J].
Culine, S. ;
Kerbrat, P. ;
Kramar, A. ;
Theodore, C. ;
ChevreauU, C. ;
Geoffrois, L. ;
Bui, N. B. ;
Peny, J. ;
Caty, A. ;
Delva, R. ;
Biron, P. ;
Fizazi, K. ;
Bouzy, J. ;
Droz, J. P. .
ANNALS OF ONCOLOGY, 2007, 18 (05) :917-924
[10]   Equivalence of three or four cycles of bleomycin, etoposide, and cisplatin chemotherapy and of a 3- or 5-day schedule in good-prognosis germ cell cancer:: A randomized study of the European organization for research and treatment of cancer genitourinary tract cancer cooperative group and the medical research council [J].
de Wit, R ;
Roberts, JT ;
Wilkinson, PM ;
de Mulder, PHM ;
Mead, GM ;
Fosså, SD ;
Cook, P ;
de Prijck, L ;
Stenning, S ;
Collette, L .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (06) :1629-1640