National trends in infection-related mortality among US cancer decedents in the immunotherapy era (1999-2023).

Authors

Lu Jiang, Jundan Wang, Xuefei Yang, Ting Huang, Heran Zhou

Published in

Medicine. Volume 105. Issue 41. Pages e51069. Oct 09, 2026.

Abstract

While immune checkpoint inhibitors (ICIs) have reshaped cancer care, population-level patterns of infection-related involvement at death among cancer decedents remain incompletely characterized. We analyzed >25 million US cancer deaths recorded in Centers for Disease Control and Prevention Wide-Ranging Online Data for Epidemiologic Research (CDC WONDER; 1999-2023), excluding deaths with COVID-19 as the underlying cause. Infection-related involvement was defined using infection-related multiple-cause-of-death codes among decedents with cancer as the underlying cause. To approximate treatment context at the population level, malignancies were grouped by tumor-site-based likelihood of ICI exposure (a proxy rather than observed receipt), and temporal changes were evaluated using Joinpoint regression and interrupted time-series (ITS) models anchored to 2015, corresponding to the period of broad clinical adoption of ICIs. The proportion of cancer-underlying-cause deaths with infection-related multiple causes increased from 7.98% in 2009-2013 to 8.65% in 2017-2019 (+0.67 percentage points) in the prespecified period comparison. Joinpoint analysis identified a 2015 inflection, shifting from a pre-2015 decline to a sustained post-2015 increase (APC, +1.42% through 2023). Post-2015, cancers in the high-ICI-likelihood group (including melanoma, kidney, lung, and stomach cancers) showed a larger relative increase in infection-related multiple causes than low-ICI-likelihood cancers (+16.2% vs +6.7%), and ITS models supported a steeper post-2015 slope after accounting for the pandemic period. These findings indicate that infection-related conditions listed on death certificates among US cancer decedents have increased since 2015, with larger rises observed in tumor sites more likely to be treated with ICIs. Further work using patient-level treatment data is needed to determine whether these temporal patterns reflect immunotherapy exposure, shifts in case mix, or changes in certification and coding practices.

PMID:
42854069
Bibliographic data and abstract were imported from PubMed on 10 Oct 2026.

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