Integrating geriatric assessment and genetic profiling to personalize therapy selection in older adults with acute myeloid leukemia

被引:17
作者
Bhatt, Vijaya R. [1 ,2 ,8 ]
Wichman, Christopher [3 ]
Al-Kadhimi, Zaid S. [1 ,2 ]
Koll, Thuy T. [4 ]
Fisher, Alfred L. [4 ]
Mahato, Ram I. [5 ]
Hyde, R. Katherine [2 ,6 ]
Berger, Ann [7 ]
Armitage, James O. [1 ,2 ]
Holstein, Sarah A. [1 ,2 ]
Maness, Lori J. [1 ,2 ]
Gundabolu, Krishna [1 ,2 ]
机构
[1] Univ Nebraska Med Ctr, Dept Internal Med, Div Hematol Oncol, Omaha, NE USA
[2] Univ Nebraska Med Ctr, Fred & Pamela Buffett Canc Ctr, Omaha, NE USA
[3] Univ Nebraska Med Ctr, Dept Biostat, Omaha, NE USA
[4] Univ Nebraska Med Ctr, Dept Internal Med, Div Geriatr Gerontol & Palliat Med, Omaha, NE USA
[5] Univ Nebraska Med Ctr, Coll Pharm, Dept Pharmaceut Sci, Omaha, NE USA
[6] Univ Nebraska Med Ctr, Dept Biochem & Mol Biol, Omaha, NE USA
[7] Univ Nebraska Med Ctr, Coll Nursing, Omaha Div, Omaha, NE USA
[8] Univ Nebraska Med Ctr, Nebraska Med Ctr 986840, Omaha, NE 68198 USA
关键词
Acute myeloid leukemia; Geriatric assessment; Precision; -oncology; Clinical trial; Chemotherapy; AZACITIDINE; SURVIVAL; CARE;
D O I
10.1016/j.jgo.2022.04.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Survival benefit associated with intensive over low-intensity chemotherapy in older adults with acute myeloid leukemia (AML) is controversial. Geriatric assessment and genetic risk categories correlate with survival following intensive chemotherapy in older adults with AML and can guide treatment selection.Materials and methods: In a single-center trial, we integrated both geriatric assessment, and genetic risk catego-ries to personalize selection of intensive versus low-intensity chemotherapy in older adults >= 60 years with AML (NCT03226418). In the present report, we demonstrate feasibility of this approach.Results: Broad eligibility criteria and co-management of patients with community oncologists allowed enroll-ment of 45% of all patients with AML treated at our center during the study period. The median time from enroll-ment to therapy initiation was two days (range 0-9). Over half of the trial patients had a score of >= 3 on hematopoietic cell transplantation comorbidity index, impairment in physical function (Short Physical Perfor-mance Battery), and Montreal Cognitive Assessment. Three fit patients received intensive chemotherapy, whereas other patients received low-intensity chemotherapy. Mortality at 30 days from diagnosis was 3.7% (95% confidence interval [CI] 0.7-18.3%) and at 90 days was 29.6% (95% CI 15.9-48.5%). One-year overall survival was 66% (95% CI 60-87%). Discussion: Our data demonstrate the feasibility of integrating geriatric assessment in precision oncology trials to define fitness for intensive chemotherapy. Broad eligibility criteria and academic-community collaboration can expand access to clinical trials.(c) 2022 Elsevier Ltd. All rights reserved.
引用
收藏
页码:871 / 874
页数:4
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