Feldman Darren R, Lorch Anja, Kramar Andrew, Albany Costantine, Einhorn Lawrence H, Giannatempo Patrizia, Necchi Andrea, Flechon Aude, Boyle Helen, Chung Peter, Huddart Robert A, Bokemeyer Carsten, Tryakin Alexey, Sava Teodoro, Winquist Eric William, De Giorgi Ugo, Aparicio Jorge, Sweeney Christopher J, Cohn Cedermark Gabriella, Beyer Jörg, Powles Thomas
Darren R. Feldman, Memorial Sloan-Kettering Cancer Center and Weill Medical College of Cornell University, New York, NY; Anja Lorch, University Hospital Düsseldorf, Düsseldorf; Carsten Bokemeyer, University Hospital Eppendorf, Hamburg, Germany; Andrew Kramar, Centre Oscar Lambret, Lille; Aude Flechon and Helen Boyle, Centre Léon Bérard, Lyon, France; Costantine Albany and Lawrence H. Einhorn, Indiana University, Bloomington, IN; Patrizia Giannatempo and Andrea Necchi, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico Istituto Nazionale dei Tumori, Milano; Teodoro Sava, Azienda Ospedaliera Universitaria Integrata di Verona, Verona; Ugo De Giorgi, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori, Istituto di Ricovero e Cura a Carattere Scientifico, Meldola, Italy; Peter Chung, Princess Margaret Cancer Centre, University of Toronto, Toronto; Eric William Winquist, London Health Sciences Center, London, Ontario, Canada; Robert A. Huddart, Royal Marsden Hospital; Thomas Powles, St Bartholomew's Hospital, London, United Kingdom; Alexey Tryakin, Blokhin's Russian Cancer Research Center, Moscow, Russia; Jorge Aparicio, University Hospital Le Fe, Valencia, Spain; Christopher J. Sweeney, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA; Gabriella Cohn Cedermark, Karolinska Institute and Karolinska University Hospital, Stockholm, Sweden; and Jörg Beyer, UniversitätsSpital Zürich, Zürich, Switzerland.
J Clin Oncol. 2016 Feb 1;34(4):345-51. doi: 10.1200/JCO.2015.62.7000. Epub 2015 Oct 12.
To define characteristics, treatment response, and outcomes of men with brain metastases (BM) from germ cell tumors (GCT).
Data from 523 men with BM from GCT were collected retrospectively from 46 centers in 13 countries by using standardized questionnaires. Clinical features were correlated with overall survival (OS) as the primary end point.
BM were present at initial diagnosis in 228 men (group A) and at relapse in 295 men (group B). OS at 3 years (3-year OS) was superior in group A versus group B (48% v 27%; P < .001). Multiple BM and the presence of liver or bone metastasis were independent adverse prognostic factors in both groups; primary mediastinal nonseminoma (group A) and elevations of α-fetoprotein of 100 ng/mL or greater or of human chorionic gonadotropin of 5,000 U/L or greater (group B) were additional independent adverse prognostic factors. Depending on these factors, the 3-year OS ranged from 0% to 70% in group A and from 6% to 52% in group B. In group A, 99% of patients received chemotherapy; multimodality treatment or high-dose chemotherapy was not associated with statistically improved survival in multivariable analysis. In group B, only 54% of patients received chemotherapy; multimodality treatment was associated with improved survival compared with single-modality therapy (hazard ratio, 0.51; 95% CI, 0.36 to 0.73; P < .001), as was high-dose compared with conventional-dose chemotherapy (hazard ratio, 0.41; 95% CI, 0.24 to 0.70; P = .001).
Men with BM from GCT have poor OS, particularly if additional risk factors are present. High-dose chemotherapy and multimodality treatment seemed to improve survival probabilities in men with BM at relapse.
明确患有生殖细胞肿瘤(GCT)脑转移(BM)男性患者的特征、治疗反应及预后。
通过标准化问卷,对来自13个国家46个中心的523例患有GCT脑转移的男性患者的数据进行回顾性收集。将临床特征与作为主要终点的总生存期(OS)进行关联分析。
228例男性患者(A组)在初次诊断时即存在脑转移,295例男性患者(B组)在复发时出现脑转移。A组3年总生存期(3年OS)优于B组(48%对27%;P <.001)。两组中,多发脑转移以及存在肝或骨转移均为独立的不良预后因素;原发性纵隔非精原细胞瘤(A组)以及甲胎蛋白升高至100 ng/mL或更高或人绒毛膜促性腺激素升高至5000 U/L或更高(B组)是额外的独立不良预后因素。根据这些因素,A组3年OS范围为0%至70%,B组为6%至52%。A组中,99%的患者接受了化疗;在多变量分析中,多模式治疗或大剂量化疗与生存改善无统计学关联。B组中,仅54%的患者接受了化疗;与单模式治疗相比,多模式治疗与生存改善相关(风险比,0.51;95%可信区间,0.36至0.73;P <.001),与常规剂量化疗相比,大剂量化疗也与生存改善相关(风险比,0.41;95%可信区间,0.24至0.70;P =.001)。
患有GCT脑转移的男性患者总生存期较差,尤其是存在其他危险因素时。大剂量化疗和多模式治疗似乎可提高复发时患有脑转移男性患者的生存概率。