TY - JOUR
T1 - Survival of Older Adults With Newly Diagnosed Acute Myeloid Leukemia
T2 - Effect of Using Multiagent Versus Single-agent Chemotherapy
AU - Bhatt, Vijaya R.
AU - Shostrom, Valerie
AU - Holstein, Sarah A.
AU - Al-Kadhimi, Zaid S.
AU - Maness, Lori J.
AU - Berger, Ann
AU - Armitage, James O.
AU - Gundabolu, Krishna
N1 - Funding Information:
V. R. Bhatt reports serving as a consultant for Abbvie, Partner Therapeutics, Omeros, CSL Behring, Agios, Takeda and Incyte and has received research funding from Jazz Pharmaceuticals, Incyte, Tolero, and the National Marrow Donor Program. S. Holstein reports serving as a consultant for Celgene, Takeda, Adaptive Biotechnologies, Sorrento, and GlaxoSmithKline. J. O. Armitage reports serving as a consultant for Conatus – IDMC, Samus Therapeutics, and Ascentage and is on Board of Director's for Tesaro Bio, Inc. K. Gundabolu reports serving as a consultant for Jazz Pharmaceuticals, Pfizer, and Novartis. The remaining authors have stated that they have no conflicts of interest.The present project was supported by the National Institute of General Medical Sciences (grant 1U54GM115458-01). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The National Cancer Database (NCDB) is a joint project of the Commission on Cancer of the American College of Surgeons and the American Cancer Society. The data used in the study were derived from a de-identified NCDB file. The American College of Surgeons and the Commission on Cancer have not verified and are not responsible for the analytic or statistical methods used or the conclusions drawn from these data by the investigators.
Funding Information:
V. R. Bhatt reports serving as a consultant for Abbvie, Partner Therapeutics, Omeros, CSL Behring, Agios, Takeda and Incyte and has received research funding from Jazz Pharmaceuticals, Incyte , Tolero , and the National Marrow Donor Program . S. Holstein reports serving as a consultant for Celgene, Takeda, Adaptive Biotechnologies, Sorrento, and GlaxoSmithKline. J. O. Armitage reports serving as a consultant for Conatus – IDMC, Samus Therapeutics, and Ascentage and is on Board of Director’s for Tesaro Bio, Inc. K. Gundabolu reports serving as a consultant for Jazz Pharmaceuticals, Pfizer, and Novartis. The remaining authors have stated that they have no conflicts of interest.
Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2020/5
Y1 - 2020/5
N2 - Background: Controversy exists regarding the optimal chemotherapy regimen for older adults with acute myeloid leukemia (AML). Patients and Methods: We analyzed data from the US National Cancer Data Base of 25,621 patients aged 60 to 79 years, with a diagnosis of AML from 2004 to 2014, who had received single-agent versus multiagent chemotherapy. A Cox proportional hazard model was used for overall survival (OS) analysis for the entire study cohort and separately for patients who had received single-agent (n = 6743) versus multiagent (n = 6743) chemotherapy, matched for age, Charlson comorbidity index, and AML subtype. Results: The use of multiagent chemotherapy was high overall (70%) but declined with factors, such as increasing age, Charlson comorbidity index, AML subtype other than good risk, academic center, lower rate of high school graduation, and more recent year of diagnosis. Patients treated with multiagent chemotherapy had greater 1-year OS (43% vs. 28%), especially for patients aged 60 to 69 years and those with good-risk AML or Charlson comorbidity index of 0 to 1. OS (hazard ratio, 1.32; 95% confidence interval, 1.28-1.36) remained more favorable for the multiagent chemotherapy group on multivariable analysis. This was confirmed in a matched cohort analysis. Conclusions: To the best of our knowledge, this is the largest real-world study that has demonstrated an association between factors such as age, comorbidity, and AML subtype and the use of multiagent chemotherapy. The use of multiagent chemotherapy was associated with improved OS, especially for patients aged <70 years, those with good-risk AML, and those with a low Charlson comorbidity index.
AB - Background: Controversy exists regarding the optimal chemotherapy regimen for older adults with acute myeloid leukemia (AML). Patients and Methods: We analyzed data from the US National Cancer Data Base of 25,621 patients aged 60 to 79 years, with a diagnosis of AML from 2004 to 2014, who had received single-agent versus multiagent chemotherapy. A Cox proportional hazard model was used for overall survival (OS) analysis for the entire study cohort and separately for patients who had received single-agent (n = 6743) versus multiagent (n = 6743) chemotherapy, matched for age, Charlson comorbidity index, and AML subtype. Results: The use of multiagent chemotherapy was high overall (70%) but declined with factors, such as increasing age, Charlson comorbidity index, AML subtype other than good risk, academic center, lower rate of high school graduation, and more recent year of diagnosis. Patients treated with multiagent chemotherapy had greater 1-year OS (43% vs. 28%), especially for patients aged 60 to 69 years and those with good-risk AML or Charlson comorbidity index of 0 to 1. OS (hazard ratio, 1.32; 95% confidence interval, 1.28-1.36) remained more favorable for the multiagent chemotherapy group on multivariable analysis. This was confirmed in a matched cohort analysis. Conclusions: To the best of our knowledge, this is the largest real-world study that has demonstrated an association between factors such as age, comorbidity, and AML subtype and the use of multiagent chemotherapy. The use of multiagent chemotherapy was associated with improved OS, especially for patients aged <70 years, those with good-risk AML, and those with a low Charlson comorbidity index.
KW - AML
KW - Database study
KW - Early mortality
KW - Older adult
KW - Survival
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U2 - 10.1016/j.clml.2020.01.015
DO - 10.1016/j.clml.2020.01.015
M3 - Article
C2 - 32111572
AN - SCOPUS:85080026989
SN - 2152-2669
VL - 20
SP - e239-e258
JO - Clinical Lymphoma, Myeloma and Leukemia
JF - Clinical Lymphoma, Myeloma and Leukemia
IS - 5
ER -