Polypharmacy, drug–drug interactions and adverse drug reactions in older Chinese cancer patients: evidence from CHARLS

To (i) quantify the prevalence of polypharmacy and clinically significant DDIs, (ii) examine their independent and combined associations with ADRs, and (iii) explore whether depression and cognition modify these relationships among older Chinese adults with cancer among older Chinese adults diagnose...

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Published inFrontiers in pharmacology Vol. 16; p. 1579023
Main Authors Yan, Zijun, Fan, Ke-qin, Yu, Ting, Su, Ning, Zou, Yan, Xia, Liangjing
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 29.05.2025
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ISSN1663-9812
1663-9812
DOI10.3389/fphar.2025.1579023

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Abstract To (i) quantify the prevalence of polypharmacy and clinically significant DDIs, (ii) examine their independent and combined associations with ADRs, and (iii) explore whether depression and cognition modify these relationships among older Chinese adults with cancer among older Chinese adults diagnosed with cancer. A total of 408 participants aged ≥60 years completed both the 2011 baseline and 2013 follow-up surveys, forming the analytic cohort. This analysis used data from the China Health and Retirement Longitudinal Study (CHARLS; 2011-2013). Eligible participants were community-dwelling adults aged ≥60 years who answered "yes" to the CHARLS question "Has a doctor ever told you that you had a malignant tumour or cancer?" (variable DAOO7-4, mapped to ICD-10 C00-C97). The most frequently reported sites were lung, stomach, colorectal, liver and breast cancers, yielding an analytic cohort of 408 individuals. Polypharmacy (≥5 medications/day) was determined through face-to-face interviews, and DDIs were identified using standardized reference compendia. ADRs were confirmed by self-reports corroborated with medical records. Depression and cognition were measured using validated scales. Logistic regression models adjusted for sociodemographic and clinical factors were used to evaluate associations. At baseline, 36.0% of participants reported polypharmacy, rising to 38.0% at follow-up. Clinically significant DDIs increased from 20.1% to 23.0%, while ADRs grew from 6.9% to 8.1%. In adjusted models, both polypharmacy (OR = 2.21, 95% CI = 1.14-4.30) and DDIs (OR = 3.28, 95% CI = 1.54-6.99) independently heightened ADR risk. Elevated depression scores were also linked to increased odds of ADRs, particularly among older women. Polypharmacy and DDIs substantially magnify the risk of ADRs in older Chinese adults with cancer, with depression further compounding vulnerability. Targeted medication management, careful DDI monitoring, and attention to psychosocial well-being may reduce preventable harms and improve outcomes in this rapidly expanding geriatric oncology population.
AbstractList ObjectiveTo (i) quantify the prevalence of polypharmacy and clinically significant DDIs, (ii) examine their independent and combined associations with ADRs, and (iii) explore whether depression and cognition modify these relationships among older Chinese adults with cancer among older Chinese adults diagnosed with cancer. A total of 408 participants aged ≥60 years completed both the 2011 baseline and 2013 follow-up surveys, forming the analytic cohort.MethodsThis analysis used data from the China Health and Retirement Longitudinal Study (CHARLS; 2011–2013). Eligible participants were community-dwelling adults aged ≥60 years who answered “yes” to the CHARLS question “Has a doctor ever told you that you had a malignant tumour or cancer?” (variable DAOO7-4, mapped to ICD-10 C00–C97). The most frequently reported sites were lung, stomach, colorectal, liver and breast cancers, yielding an analytic cohort of 408 individuals. Polypharmacy (≥5 medications/day) was determined through face-to-face interviews, and DDIs were identified using standardized reference compendia. ADRs were confirmed by self-reports corroborated with medical records. Depression and cognition were measured using validated scales. Logistic regression models adjusted for sociodemographic and clinical factors were used to evaluate associations.ResultsAt baseline, 36.0% of participants reported polypharmacy, rising to 38.0% at follow-up. Clinically significant DDIs increased from 20.1% to 23.0%, while ADRs grew from 6.9% to 8.1%. In adjusted models, both polypharmacy (OR = 2.21, 95% CI = 1.14–4.30) and DDIs (OR = 3.28, 95% CI = 1.54–6.99) independently heightened ADR risk. Elevated depression scores were also linked to increased odds of ADRs, particularly among older women.ConclusionPolypharmacy and DDIs substantially magnify the risk of ADRs in older Chinese adults with cancer, with depression further compounding vulnerability. Targeted medication management, careful DDI monitoring, and attention to psychosocial well-being may reduce preventable harms and improve outcomes in this rapidly expanding geriatric oncology population.
To (i) quantify the prevalence of polypharmacy and clinically significant DDIs, (ii) examine their independent and combined associations with ADRs, and (iii) explore whether depression and cognition modify these relationships among older Chinese adults with cancer among older Chinese adults diagnosed with cancer. A total of 408 participants aged ≥60 years completed both the 2011 baseline and 2013 follow-up surveys, forming the analytic cohort.ObjectiveTo (i) quantify the prevalence of polypharmacy and clinically significant DDIs, (ii) examine their independent and combined associations with ADRs, and (iii) explore whether depression and cognition modify these relationships among older Chinese adults with cancer among older Chinese adults diagnosed with cancer. A total of 408 participants aged ≥60 years completed both the 2011 baseline and 2013 follow-up surveys, forming the analytic cohort.This analysis used data from the China Health and Retirement Longitudinal Study (CHARLS; 2011-2013). Eligible participants were community-dwelling adults aged ≥60 years who answered "yes" to the CHARLS question "Has a doctor ever told you that you had a malignant tumour or cancer?" (variable DAOO7-4, mapped to ICD-10 C00-C97). The most frequently reported sites were lung, stomach, colorectal, liver and breast cancers, yielding an analytic cohort of 408 individuals. Polypharmacy (≥5 medications/day) was determined through face-to-face interviews, and DDIs were identified using standardized reference compendia. ADRs were confirmed by self-reports corroborated with medical records. Depression and cognition were measured using validated scales. Logistic regression models adjusted for sociodemographic and clinical factors were used to evaluate associations.MethodsThis analysis used data from the China Health and Retirement Longitudinal Study (CHARLS; 2011-2013). Eligible participants were community-dwelling adults aged ≥60 years who answered "yes" to the CHARLS question "Has a doctor ever told you that you had a malignant tumour or cancer?" (variable DAOO7-4, mapped to ICD-10 C00-C97). The most frequently reported sites were lung, stomach, colorectal, liver and breast cancers, yielding an analytic cohort of 408 individuals. Polypharmacy (≥5 medications/day) was determined through face-to-face interviews, and DDIs were identified using standardized reference compendia. ADRs were confirmed by self-reports corroborated with medical records. Depression and cognition were measured using validated scales. Logistic regression models adjusted for sociodemographic and clinical factors were used to evaluate associations.At baseline, 36.0% of participants reported polypharmacy, rising to 38.0% at follow-up. Clinically significant DDIs increased from 20.1% to 23.0%, while ADRs grew from 6.9% to 8.1%. In adjusted models, both polypharmacy (OR = 2.21, 95% CI = 1.14-4.30) and DDIs (OR = 3.28, 95% CI = 1.54-6.99) independently heightened ADR risk. Elevated depression scores were also linked to increased odds of ADRs, particularly among older women.ResultsAt baseline, 36.0% of participants reported polypharmacy, rising to 38.0% at follow-up. Clinically significant DDIs increased from 20.1% to 23.0%, while ADRs grew from 6.9% to 8.1%. In adjusted models, both polypharmacy (OR = 2.21, 95% CI = 1.14-4.30) and DDIs (OR = 3.28, 95% CI = 1.54-6.99) independently heightened ADR risk. Elevated depression scores were also linked to increased odds of ADRs, particularly among older women.Polypharmacy and DDIs substantially magnify the risk of ADRs in older Chinese adults with cancer, with depression further compounding vulnerability. Targeted medication management, careful DDI monitoring, and attention to psychosocial well-being may reduce preventable harms and improve outcomes in this rapidly expanding geriatric oncology population.ConclusionPolypharmacy and DDIs substantially magnify the risk of ADRs in older Chinese adults with cancer, with depression further compounding vulnerability. Targeted medication management, careful DDI monitoring, and attention to psychosocial well-being may reduce preventable harms and improve outcomes in this rapidly expanding geriatric oncology population.
To (i) quantify the prevalence of polypharmacy and clinically significant DDIs, (ii) examine their independent and combined associations with ADRs, and (iii) explore whether depression and cognition modify these relationships among older Chinese adults with cancer among older Chinese adults diagnosed with cancer. A total of 408 participants aged ≥60 years completed both the 2011 baseline and 2013 follow-up surveys, forming the analytic cohort. This analysis used data from the China Health and Retirement Longitudinal Study (CHARLS; 2011-2013). Eligible participants were community-dwelling adults aged ≥60 years who answered "yes" to the CHARLS question "Has a doctor ever told you that you had a malignant tumour or cancer?" (variable DAOO7-4, mapped to ICD-10 C00-C97). The most frequently reported sites were lung, stomach, colorectal, liver and breast cancers, yielding an analytic cohort of 408 individuals. Polypharmacy (≥5 medications/day) was determined through face-to-face interviews, and DDIs were identified using standardized reference compendia. ADRs were confirmed by self-reports corroborated with medical records. Depression and cognition were measured using validated scales. Logistic regression models adjusted for sociodemographic and clinical factors were used to evaluate associations. At baseline, 36.0% of participants reported polypharmacy, rising to 38.0% at follow-up. Clinically significant DDIs increased from 20.1% to 23.0%, while ADRs grew from 6.9% to 8.1%. In adjusted models, both polypharmacy (OR = 2.21, 95% CI = 1.14-4.30) and DDIs (OR = 3.28, 95% CI = 1.54-6.99) independently heightened ADR risk. Elevated depression scores were also linked to increased odds of ADRs, particularly among older women. Polypharmacy and DDIs substantially magnify the risk of ADRs in older Chinese adults with cancer, with depression further compounding vulnerability. Targeted medication management, careful DDI monitoring, and attention to psychosocial well-being may reduce preventable harms and improve outcomes in this rapidly expanding geriatric oncology population.
Author Yan, Zijun
Zou, Yan
Fan, Ke-qin
Xia, Liangjing
Su, Ning
Yu, Ting
AuthorAffiliation Department of Pharmacy , Panzhihua Central Hospital , Panzhihua , Sichuan , China
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Keywords adverse drug reactions
drug-drug interactions
geriatric oncology
medication safety
pharmacological interactions
polypharmacy
Language English
License Copyright © 2025 Yan, Fan, Yu, Su, Zou and Xia.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
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Xiaochen Li, Shandong University, China
Guangzhu Cao, Kunming University of Science and Technology, China
These authors have contributed equally to this work
Edited by: Shangke Huang, Southwest Medical University, China
Reviewed by: Uday Venkat Mateti, Nitte (Deemed to be University), India
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Snippet To (i) quantify the prevalence of polypharmacy and clinically significant DDIs, (ii) examine their independent and combined associations with ADRs, and (iii)...
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SubjectTerms adverse drug reactions
drug-drug interactions
geriatric oncology
medication safety
pharmacological interactions
Pharmacology
polypharmacy
Title Polypharmacy, drug–drug interactions and adverse drug reactions in older Chinese cancer patients: evidence from CHARLS
URI https://www.ncbi.nlm.nih.gov/pubmed/40510418
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