Adra N, Althouse S K, Liu H, Brames M J, Hanna N H, Einhorn L H, Albany C
Division of Hematology/Oncology and Biostatistics, Melvin & Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, USA.
Division of Hematology/Oncology and Biostatistics, Melvin & Bren Simon Cancer Center, Indiana University School of Medicine, Indianapolis, USA
Ann Oncol. 2016 May;27(5):875-9. doi: 10.1093/annonc/mdw045. Epub 2016 Feb 9.
Based on the risk stratification from the International Germ Cell Cancer Collaborative Group (IGCCCG), only 14% of patients with metastatic germ-cell tumors (GCT) had poor-risk disease with a 5-year progression-free survival (PFS) rate of 41% and a 5-year overall survival (OS) rate of only 48%. This analysis attempts to identify prognostic factors for patients with poor-risk disease.
We conducted a retrospective analysis of all patients with GCT diagnosed and treated at Indiana University from 1990 to 2014. Clinical and pathological characteristics were available for all patients and all of them were treated with cisplatin-etoposide-based chemotherapy. Cox proportional hazards models were used to target significant predictors of disease progression and mortality. A significance level of 5% was used in the analysis.
We identified 273 consecutive patients with poor-risk GCT (PRGCT). Median follow-up time was 8 years (range 0.03-24.5). The 5-year PFS and OS rates were 58% [95% confidence interval (CI) 51% to 63%] and 73% (95% CI 67% to 78%), respectively. In multivariate survival analyses, multiple risk factors were associated with disease progression, including liver metastasis, brain metastasis, primary mediastinal nonseminomatous GCT (PMNSGCT), and elevation in logarithmic β-hCG. Significant predictors of mortality were PMNSGCT [hazard ratio (HR) 4.63, 95% CI 2.25-9.56; P < 0.001], brain metastasis (HR 3.30, 95% CI 1.74-6.23; P < 0.001), and increasing age (HR 1.03, 95% CI 1.01-1.06; P = 0.02).
Patients with PMNSGCT, brain metastasis, or with increasing age are at higher risk of death than their counterparts. This contemporary cohort (1990-2014) of 273 patients with PRGCT had improved PFS and OS outcomes than those from the historical IGCCCG group of patients (1975-1990).
根据国际生殖细胞癌协作组(IGCCCG)的风险分层,只有14%的转移性生殖细胞肿瘤(GCT)患者具有高风险疾病,其5年无进展生存率(PFS)为41%,5年总生存率(OS)仅为48%。本分析旨在确定高风险疾病患者的预后因素。
我们对1990年至2014年在印第安纳大学诊断和治疗的所有GCT患者进行了回顾性分析。所有患者均有临床和病理特征,且均接受了以顺铂-依托泊苷为基础的化疗。采用Cox比例风险模型来确定疾病进展和死亡的显著预测因素。分析中使用的显著性水平为5%。
我们确定了273例连续的高风险GCT(PRGCT)患者。中位随访时间为8年(范围0.03 - 24.5年)。5年PFS率和OS率分别为58%[95%置信区间(CI)51%至63%]和73%(95%CI 67%至78%)。在多因素生存分析中,多种风险因素与疾病进展相关,包括肝转移、脑转移、原发性纵隔非精原细胞瘤(PMNSGCT)以及对数β-hCG升高。死亡的显著预测因素为PMNSGCT[风险比(HR)4.63,95%CI 2.25 - 9.56;P < 0.001]、脑转移(HR 3.30,95%CI 1.74 - 6.23;P < 0.001)以及年龄增长(HR 1.03,95%CI 1.01 - 1.06;P = 0.02)。
患有PMNSGCT、脑转移或年龄增长的患者比其他患者死亡风险更高。与历史IGCCCG组患者(1975 - 1990年)相比,这一由273例PRGCT患者组成的当代队列(1990 - 2014年)的PFS和OS结局有所改善。