Bokemeyer C, Nowak P, Haupt A, Metzner B, Köhne H, Hartmann J T, Kanz L, Schmoll H J
Department of Hematology/Oncology, Hannover University Medical School, Germany.
J Clin Oncol. 1997 Apr;15(4):1449-54. doi: 10.1200/JCO.1997.15.4.1449.
Despite improved cure rates for patients with metastatic testicular cancer with cisplatin-based combination chemotherapy, patients who develop brain metastases are generally considered to possess a poor prognosis. This report summarizes the long-term results in 44 patients with brain metastases from testicular cancer treated between 1978 and 1995 at Hannover University Medical School.
Histologically, 42 patients (95%) had a nonseminomatous germ cell cancer and two patients (5%) a seminoma. Thirty-nine patients (89%) had lung metastases and 37 (84%) fulfilled the criteria for advanced disease according to the Indiana University classification even without considering the brain metastases. Eighteen patients (41%) presented with brain metastases at primary diagnosis (group 1), four (9%) developed brain metastases at relapse after a previous favorable response to combination chemotherapy (group 2), and 22 (50%) developed brain metastases during or directly after cisplatin-based chemotherapy. Chemotherapy consisted of cisplatin-based combination treatment and radiotherapy was given as whole-brain irradiation of 30 to 40 Gy and in single cases combined with a boost of 10 Gy to single lesions.
Overall, 10 patients achieved long-term survival (23%; 95% confidence interval [CI], 10.1% to 35.4%). The prognosis was significantly better for patients in groups 1 and 2, with six of 18 (33%) and three of four (75%) patients alive, compared with only one of 22 (5%) in group 3 (P < .01). Patients treated with either chemotherapy or radiotherapy alone did not achieve long-term survival, while nine of 28 (32%) who received treatment with both modalities with or without surgery achieved sustained long-term survival. During univariate analysis, patients with the diagnosis of brain metastases at first presentation (P < .01), patients with a single brain lesion (P < .02), and patients who received combined chemotherapy and radiotherapy (P < .03) had a significantly improved outcome.
Long-term survival can be achieved in approximately 25% of patients with brain metastases from testicular cancer by combined treatment with brain irradiation and aggressive cisplatin-based chemotherapy. Patients who develop brain metastases during systemic treatment should receive only palliative radiation therapy, since sustained survival will not be reached.
尽管基于顺铂的联合化疗使转移性睾丸癌患者的治愈率有所提高,但发生脑转移的患者通常预后较差。本报告总结了1978年至1995年间在汉诺威大学医学院接受治疗的44例睾丸癌脑转移患者的长期治疗结果。
组织学检查显示,42例患者(95%)为非精原细胞性生殖细胞癌,2例患者(5%)为精原细胞瘤。39例患者(89%)有肺转移,37例(84%)即使不考虑脑转移,也符合印第安纳大学晚期疾病分类标准。18例患者(41%)在初次诊断时出现脑转移(第1组),4例(9%)在先前对联合化疗有良好反应后的复发时出现脑转移(第2组),22例(50%)在基于顺铂的化疗期间或化疗刚结束后出现脑转移。化疗采用基于顺铂的联合治疗,放疗采用全脑照射30至40 Gy,个别病例对单个病灶加量照射10 Gy。
总体而言,10例患者实现了长期生存(23%;95%置信区间[CI],10.1%至35.4%)。第1组和第2组患者的预后明显较好,18例中有6例(33%)、4例中有3例(75%)存活,而第3组22例中只有1例(5%)存活(P<.01)。单独接受化疗或放疗的患者未实现长期生存,而28例接受了两种治疗方式(无论是否手术)的患者中有9例(32%)实现了持续长期生存。在单因素分析中,初次就诊时诊断为脑转移的患者(P<.01)、单个脑病灶的患者(P<.02)以及接受联合化疗和放疗的患者(P<.03)预后明显改善。
通过脑照射和积极的基于顺铂的联合化疗,约25%的睾丸癌脑转移患者可实现长期生存。在全身治疗期间发生脑转移的患者应仅接受姑息性放射治疗,因为无法实现持续生存。