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大剂量化疗联合自体造血干细胞移植治疗复发/难治性霍奇金淋巴瘤的长期疗效。

Long-term outcomes after high dose therapy and autologous haematopoietic cell rescue for refractory/relapsed Hodgkin lymphoma.

机构信息

Department of Radiation Oncology, Stanford University, Palo Alto, CA, USA.

出版信息

Br J Haematol. 2012 Nov;159(3):329-39. doi: 10.1111/bjh.12038. Epub 2012 Sep 12.

Abstract

The standard treatment for patients with refractory or relapsed Hodgkin lymphoma (HL) is high-dose chemotherapy and/or radiation with autologous haematopoietic cell rescue (AHCR). In this study, we assessed quality of life and evaluated the risk of late morbidity and mortality for HL patients who underwent AHCR. One hundred and fifty-four patients who underwent AHCR at Stanford University from 1988 to 2002 and survived ≥2 years were evaluated. Median follow-up was 10·2 years. There were 54 deaths, 34 from HL, 20 from other causes. The 10-year cumulative incidence of death from HL or other causes was 21·7% and 12·7%, respectively. Thirteen deaths were from second malignancies. The risk ratio of second malignancies was 8·0 [95% confidence interval (CI), 4·7-12·6] compared with the general population, and 3·0 (95% CI, 1·8-4·8) compared with HL patients not undergoing AHCR. The risk ratio of second malignancies was 1·5 (95% CI, 0·9-2·4) compared with HL patients receiving non-AHCR therapy. Overall quality of life did not differ from the general population, but AHCR survivors did note reduced functioning and some worse symptoms. AHCR survivors may be at increased risk of death from HL and other causes compared with the general population, but not compared with the HL population as a whole.

摘要

对于难治性或复发性霍奇金淋巴瘤 (HL) 患者,标准治疗方法是大剂量化疗和/或放疗联合自体造血细胞移植 (AHCR)。本研究评估了接受 AHCR 的 HL 患者的生活质量,并评估了迟发性发病和死亡的风险。斯坦福大学 1988 年至 2002 年间接受 AHCR 治疗且存活时间≥2 年的 154 例患者纳入研究。中位随访时间为 10.2 年。共发生 54 例死亡,其中 34 例死于 HL,20 例死于其他原因。HL 或其他原因导致的 10 年累积死亡率分别为 21.7%和 12.7%。13 例死亡是由第二恶性肿瘤引起的。与普通人群相比,第二恶性肿瘤的风险比为 8.0(95%置信区间,4.7-12.6),与未接受 AHCR 治疗的 HL 患者相比,风险比为 3.0(95%置信区间,1.8-4.8)。与接受非 AHCR 治疗的 HL 患者相比,第二恶性肿瘤的风险比为 1.5(95%置信区间,0.9-2.4)。总体生活质量与普通人群无差异,但 AHCR 幸存者注意到功能下降和一些症状恶化。与普通人群相比,AHCR 幸存者 HL 相关死亡和其他原因导致的死亡风险可能增加,但与整个 HL 人群相比,这种风险并未增加。

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