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首页> 外文期刊>Journal of Clinical Oncology >Low-dose interleukin-2 immunotherapy does not improve outcome of patients age 60 years and older with acute myeloid leukemia in first complete remission: Cancer and Leukemia Group B Study 9720.
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Low-dose interleukin-2 immunotherapy does not improve outcome of patients age 60 years and older with acute myeloid leukemia in first complete remission: Cancer and Leukemia Group B Study 9720.

机译:低剂量白细胞介素2免疫疗法不能改善首次完全缓解的60岁及以上的急性髓样白血病患者的预后:癌症和白血病B组研究9720。

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PURPOSE: Cancer and Leukemia Group B (CALGB) 9720 evaluated subcutaneous low-dose recombinant interleukin-2 (rIL-2) maintenance immunotherapy as a strategy for prolonging remission in older patients with acute myeloid leukemia (AML). PATIENTS AND METHODS: AML patients age 60 years and older in first complete remission after induction and consolidation chemotherapy were randomly assigned to no further therapy or a 90-day regimen of 14-day cycles of low-dose rIL-2, aimed at expanding natural killer (NK) cells, followed by 3-day higher doses aimed at activating cytotoxicity of expanded NK cells to lyse residual AML cells. All randomly assigned patients were included in an intention-to-treat analysis. RESULTS: A total of 163 (64%) of 254 patients who completed induction and consolidation chemotherapy on CALGB 9720 were randomly assigned to rIL-2 (n = 81) or no further therapy (n = 82); the most common reasons for lack of random assignment were patient refusal and relapse. Fifteen patients randomly assignedto rIL-2 never initiated it because of refusal, intercurrent medical problems, or relapse, and 24 patients initiated rIL-2 but stopped early because of toxicity or relapse. Grade 4 toxicities during rIL-2 therapy included thrombocytopenia (65%) and neutropenia (64%), and grade 3 toxicities included anemia (33%), infection (24%) and malaise/fatigue (14%). Forty-two patients (52%) randomly assigned to rIL-2 completed the full 90-day course. Patients in both arms had similar distributions of both disease-free (combined median = 6.1 months; P = .47) and overall survival (combined median = 14.7 months; P = .61) after random assignment. Moreover, the 42 patients who completed all planned therapy did not show prolongation of disease-free or overall survival. CONCLUSION: Low-dose rIL-2 maintenance immunotherapy is not a successful strategy in older AML patients.
机译:目的:癌症和白血病B组(CALGB)9720评估了皮下低​​剂量重组白介素2(rIL-2)维持免疫疗法,作为延长老年急性髓细胞白血病(AML)患者缓解的策略。患者和方法:年龄在60岁及以上的AML患者在诱导和巩固化疗后首次完全缓解后,被随机分配为不进行进一步治疗或低剂量rIL-2的14天周期90天治疗方案,旨在扩大自然杀伤(NK)细胞,随后3天更高剂量旨在激活扩增的NK细胞的细胞毒性,以裂解残留的AML细胞。所有随机分配的患者均纳入意向治疗分析。结果:在254名根据CALGB 9720完成诱导和巩固化疗的患者中,共有163名(64%)被随机分配至rIL-2(n = 81)或无进一步治疗(n = 82);缺乏随机分配的最常见原因是患者拒绝和复发。随机分配给rIL-2的15名患者由于拒绝,并发医疗问题或复发而从未启动过rIL-2,而24名患者因rIL-2的毒性或复发而未启动rIL-2。 rIL-2治疗期间的4级毒性包括血小板减少症(65%)和中性粒细胞减少症(64%),而3级毒性包括贫血(33%),感染(24%)和不适/疲劳(14%)。随机分配给rIL-2的42例患者(52%)完成了整个90天的疗程。随机分配后,两组患者的无病(中位数= 6.1个月; P = 0.47)和总生存期(中位数= 14.7个月; P = 0.61)的分布相似。此外,完成所有计划治疗的42例患者未显示无病或总体生存期延长。结论:低剂量的rIL-2维持免疫疗法在老年AML患者中不是成功的策略。

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