Comparative analysis of mortality trends in acute versus chronic myeloid leukemia in the U.S. population with time series projection: A CDC WONDER–based study (1999–2023).

M Muhammad Saim (2Shiekh Zayed Medical College, Rahim Yar Khan, Pakistan) A Anid Hassan (HMH Jersey Shore University Medical Center, Neptune, NJ) S Sheraz Qasim (4Ameer-ud-Din Medical College, Lahore, Pakistan) A Amna Ghaffar (Azad Jammu and Kashmir Medical College, Muzafarabad, Pakistan) N Nagapratap Ganta (1JSUMC, Neptune, United States) S Samiul Haque (1JSUMC, Neptune, United States) G Ghazala Manan Manan (Quetta Institute of Medical Sciences, Quetta, Pakistan) S Safia Bibi (Quetta Institute of Medical Sciences, Quetta, Pakistan) A Ali Hassan M Mahnoor Fatima P Paula Gonzalez (Department of Biological Sciences, Wellesley College) B Brandon Nightingale (Jersey Shore University Medical Center, Neptune, NJ) M Michael J. Levitt (Atlantic Hematology Oncology Associates, Neptune, NJ) D David B. Greenberg (Atlantic Hematology Oncology Associates - Hackensack Meridian Health, Neptune, NJ) M Madhurima Anne (Hackensack Meridian Health Jersey Shore University Medical Center, Neptune, NJ) J Jennifer Hashem (Hackensack Meridian Health Jersey Shore University Medical Center, Neptune Township, NJ)

Abstract

e18501 Background: Myeloid leukemias (ML) pose a significant public health concern globally and in the United States, particularly affecting older adults. Acute (AML) and chronic (CML) forms differ in clinical behavior and outcomes. This study compares mortality trends of AML and CML among the U.S. population from 1999 to 2023 and uses an autoregressive integrated moving average (ARIMA) model for predicting future trends. Methods: Data retrieved from the CDC WONDER database (1999-2023) included individuals aged ≥45 years. Mortality trends among people diagnosed with AML (C92.0) and CML (C92.1) individually were analyzed. We performed a head-to-head comparison of both groups. Age-adjusted mortality rates (AAMRs) per 100,000 population stratified by age, sex, race, Hispanic origin, U.S. Census regions, and 2013 urbanization categories were analyzed. Joinpoint regression was used to estimate Annual Percent Changes (APCs) and corresponding 95% CI. p < 0.05 was considered significant. R Software (Version 4.5.0) was used for time-series projections performed using an ARIMA model based on historical trends. Results: Between 1999-2023, a total of 207,992 deaths were attributed to AML (AAMR: 6.87) while CML accounted for 27,199 deaths (AAMR: 0.93). In both AML and CML, males showed higher mortality rates than females contributing to 56.9% and 55.4% of total deaths respectively. From 1999 to 2001, males and non-Hispanics showed significant upward trends in AML mortality with APC of 5.66 (95% CI: 2.09-8.78) and 4.91 (95% CI: 2.13-7.11), respectively. While in CML, from 1999-2006 males and non-Hispanics showed a notable decline in mortality with APC of -9.23 (95% CI: -11.22 - -7.77) and -9.22 (95% CI: -12.81 - -7.15), respectively. Whites affected by AML exhibited significant rising trends in mortality from 1999-2010 with APC of 2.14 (95% CI: 0.84-7.21). For AML, the Northeast region reported the highest AAMR 6.90 whereas for CML, the highest AAMR (1.0) was observed in the Midwest. Among states, North Dakota showed the highest AAMR of 8.8 in AML-group while Wyoming recorded the highest AAMR for CML at 1.2. ARIMA-based forecasting through 2030 showed relatively stable AML rates at approximately 6.68 (95% prediction interval: 6.09–7.28), whereas CML rates declined from 0.71 to 0.57 with wider uncertainty (95% prediction interval in 2030: −0.17 to 1.32), highlighting persistent disparities. Conclusions: AML mortality rose sharply, then steadily increased before declining, whereas CML mortality fell rapidly and later plateaued. These distinct trends indicates the need for population specific interventions and evaluation of therapeutic strategies.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (16)

M

Muhammad Saim

2Shiekh Zayed Medical College, Rahim Yar Khan, Pakistan

A

Anid Hassan

HMH Jersey Shore University Medical Center, Neptune, NJ

S

Sheraz Qasim

4Ameer-ud-Din Medical College, Lahore, Pakistan

A

Amna Ghaffar

Azad Jammu and Kashmir Medical College, Muzafarabad, Pakistan

N

Nagapratap Ganta

1JSUMC, Neptune, United States

S

Samiul Haque

1JSUMC, Neptune, United States

G

Ghazala Manan Manan

Quetta Institute of Medical Sciences, Quetta, Pakistan

S

Safia Bibi

Quetta Institute of Medical Sciences, Quetta, Pakistan

A

Ali Hassan

M

Mahnoor Fatima

P

Paula Gonzalez

Department of Biological Sciences, Wellesley College

B

Brandon Nightingale

Jersey Shore University Medical Center, Neptune, NJ

M

Michael J. Levitt

Atlantic Hematology Oncology Associates, Neptune, NJ

D

David B. Greenberg

Atlantic Hematology Oncology Associates - Hackensack Meridian Health, Neptune, NJ

M

Madhurima Anne

Hackensack Meridian Health Jersey Shore University Medical Center, Neptune, NJ

J

Jennifer Hashem

Hackensack Meridian Health Jersey Shore University Medical Center, Neptune Township, NJ