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霍奇金淋巴瘤患者综合治疗后的第二原发性肿瘤——耶鲁大学的经验

Second neoplasms in patients with Hodgkin's disease following combined modality therapy--the Yale experience.

作者信息

Koletsky A J, Bertino J R, Farber L R, Prosnitz L R, Kapp D S, Fischer D, Portlock C S

出版信息

J Clin Oncol. 1986 Mar;4(3):311-7. doi: 10.1200/JCO.1986.4.3.311.

Abstract

From 1969 to 1982, 183 patients with previously untreated stages IIIB and IV Hodgkin's disease and relapsing Hodgkin's disease after radiation therapy were treated with combination chemotherapy plus low-dose irradiation (CRT). One hundred fifty patients who achieved a complete response (CR) were analyzed for risk of developing a second neoplasm. Median follow-up has been 8.3 years. Actuarial survival of all patients is 74% at 10 years with a relapse-free survival of 68%. An additional 24 patients with stage IIIA disease were also treated with CRT. There were 22 CRs at risk who were analyzed. Median follow-up has been 3+ years with an actuarial survival of 90% at five years and a relapse-free survival of 83%. Second neoplasms have developed in 14 of 172 patients at risk: acute nonlymphocytic leukemia (ANLL; five patients); aggressive histology non-Hodgkin's lymphoma (NHL; three patients); and a variety of solid neoplasms (six patients). Time to second neoplasm diagnosis after initial treatment ranged from 12 to 141 months. Five patients were older than 40 years. At the time of diagnosis of the second malignancy, 11 patients were free of Hodgkin's disease (for 36 to 141 months) and three were receiving therapy for recurrent Hodgkin's disease. The 10-year actuarial risk (%) of developing ANLL was 5.9 +/- 2.8; for NHL, the risk was 3.5 +/- 2.4, and for solid neoplasms, 5.8 +/- 3.0. Our results suggest that combination chemotherapy plus low-dose irradiation does not appear to significantly increase the risk of developing second neoplasms above that already reported for combination chemotherapy when administered as either initial or salvage treatment of Hodgkin's disease.

摘要

1969年至1982年期间,183例先前未经治疗的ⅢB期和Ⅳ期霍奇金病患者以及放疗后复发的霍奇金病患者接受了联合化疗加低剂量照射(CRT)。对150例获得完全缓解(CR)的患者进行了发生第二种肿瘤风险的分析。中位随访时间为8.3年。所有患者10年的精算生存率为74%,无复发生存率为68%。另外24例ⅢA期疾病患者也接受了CRT治疗。对22例有风险的CR患者进行了分析。中位随访时间为3年以上,5年精算生存率为90%,无复发生存率为83%。172例有风险的患者中有14例发生了第二种肿瘤:急性非淋巴细胞白血病(ANLL;5例);侵袭性组织学非霍奇金淋巴瘤(NHL;3例);以及多种实体瘤(6例)。初次治疗后至第二种肿瘤诊断的时间为12至141个月。5例患者年龄超过40岁。在诊断第二种恶性肿瘤时,11例患者无霍奇金病(36至141个月),3例正在接受复发性霍奇金病的治疗。发生ANLL的10年精算风险(%)为5.9±2.8;NHL的风险为3.5±2.4,实体瘤的风险为5.8±3.0。我们的结果表明,联合化疗加低剂量照射作为霍奇金病的初始或挽救治疗时,似乎不会比联合化疗已报道的风险显著增加发生第二种肿瘤的风险。

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