Genitourinary Oncology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Cancer. 2013 Jul 15;119(14):2574-81. doi: 10.1002/cncr.28025. Epub 2013 Apr 19.
Germ cell tumors (GCTs) primarily affect adolescent and young adult men. Detailed clinical and treatment characteristics in older men are lacking.
Patients with GCT seen over a 20-year period at Memorial Sloan-Kettering Cancer Center were identified. Primary tumor site and histology were compared for patients aged ≥ 50 years at diagnosis versus younger men. For patients aged ≥ 50, individual chart review was performed and treatment delays, changes, and toxicities were recorded for those treated with first-line chemotherapy.
Of 4235 diagnoses of GCT, 3999 (94.4%) were made at age < 50 versus 236 (5.6%) at age ≥ 50. Compared with patients diagnosed before age 50, older men more frequently had seminoma (62.7% versus 36.7%) and less frequently, nonseminoma (34.7% versus 63.2%) (P < .0001). Predominant histology switched from nonseminoma to seminoma around age 35. Distribution of primary sites also differed for older versus younger men (testis: 89.4% versus 92.9%; retroperitoneal: 3.8% versus 0.7%; CNS 0% versus 1.7%) except for mediastinal primary tumors, which remained constant across age groups. Fifty patients age ≥ 50 received first-line platinum-based chemotherapy; 30 experienced complications leading to treatment discontinuation, delay ≥ 7 days, or regimen change. Twenty-two (44%) patients experienced neutropenic fever, 6 despite prophylactic growth factor support. Estimated 5-year survival for chemotherapy-treated patients was 84.9%.
Men aged ≥ 50 years comprise less than 10% of GCT diagnoses and have distinct clinical and histological characteristics as compared with younger patients. Although complications from chemotherapy occur frequently in older men, prognosis remains excellent when risk-directed treatment is administered with curative intent.
生殖细胞肿瘤(GCT)主要影响青少年和青年男性。目前缺乏关于老年男性的详细临床和治疗特征。
在纪念斯隆-凯特琳癌症中心(Memorial Sloan-Kettering Cancer Center),我们对 20 年来的 GCT 患者进行了研究。我们比较了诊断时年龄≥50 岁的患者与年轻男性的原发肿瘤部位和组织学特征。对于年龄≥50 岁的患者,我们进行了个体病历回顾,并记录了接受一线化疗治疗的患者的治疗延迟、改变和毒性。
在 4235 例 GCT 诊断中,3999 例(94.4%)发生在年龄<50 岁,236 例(5.6%)发生在年龄≥50 岁。与 50 岁前诊断的患者相比,老年男性更常患有精原细胞瘤(62.7%比 36.7%),而非精原细胞瘤(34.7%比 63.2%)较少(P<0.0001)。精原细胞瘤的主要组织学类型在 35 岁左右从非精原细胞瘤转变为精原细胞瘤。原发部位的分布也因年龄不同而不同,老年男性比年轻男性更常发生睾丸(89.4%比 92.9%)和较少发生腹膜后(3.8%比 0.7%),中枢神经系统(0%比 1.7%),而纵隔原发肿瘤在各年龄组之间保持不变。50 名年龄≥50 岁的患者接受了一线铂类化疗;30 名患者因并发症导致治疗中断、延迟≥7 天或方案改变。22 名(44%)患者发生中性粒细胞减少性发热,其中 6 名患者尽管接受了预防性生长因子支持。接受化疗的患者的 5 年生存率为 84.9%。
年龄≥50 岁的男性占 GCT 诊断的不到 10%,与年轻患者相比,他们具有明显的临床和组织学特征。尽管老年男性化疗相关并发症较为常见,但当给予有治愈意图的风险导向治疗时,预后仍然良好。