首页> 外文期刊>British Journal of Haematology >Long-term outcomes after high dose therapy and autologous haematopoietic cell rescue for refractory/relapsed Hodgkin lymphoma
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Long-term outcomes after high dose therapy and autologous haematopoietic cell rescue for refractory/relapsed Hodgkin lymphoma

机译:大剂量治疗和自体造血细胞抢救治疗难治性/复发性霍奇金淋巴瘤后的长期结果

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摘要

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.
机译:难治性或复发性霍奇金淋巴瘤(HL)患者的标准治疗方法是大剂量化疗和/或放射治疗并自体造血细胞抢救(AHCR)。在这项研究中,我们评估了接受AHCR的HL患者的生活质量并评估了其晚期发病和死亡风险。对1988年至2002年在斯坦福大学接受AHCR且生存≥2年的154例患者进行了评估。中位随访时间为10·2年。死亡54例,HL死亡34例,其他原因死亡20例。 HL或其他原因导致的10年累计死亡发生率分别为21·7%和12·7%。 13例死于第二次恶性肿瘤。与一般人群相比,第二恶性肿瘤的风险比为8·0 [95%置信区间(CI),4·7-12·6],而3·0(95%CI,1·8-4·8)与未接受AHCR的HL患者相比。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%CI,0·9-2·4)。总体生活质量与普通人群没有区别,但是AHCR幸存者确实注意到功能下降和一些较差的症状。与普通人群相比,AHCR幸存者死于HL和其他原因的死亡风险可能更高,但与整个HL人群相比却没有。

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