Evidence map›Paper›PMID 36762832›Full record

ArticleJournal of the National Cancer Institute2023

Toxicity risk score and clinical decline after adjuvant chemotherapy in older breast cancer survivors.

Jingran Ji, Can-Lan Sun, Harvey J Cohen, Hyman B Muss, Marie Bae, Mina S Sedrak

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Jingran JiDepartment of Medical Oncology, City of Hope National Medical Center, Duarte, CA, USA.ORCID 0000-0002-7284-0709
Can-Lan SunDepartment of Medical Oncology, City of Hope National Medical Center, Duarte, CA, USA.
Harvey J CohenDepartment of Medicine, Duke University Medical Center, Durham, NC, USA.
Hyman B MussDepartment of Medicine, UNC Lineberger Comprehensive Cancer Center, Chapel Hill, NC, USA.
Marie BaeDepartment of Medical Oncology, City of Hope National Medical Center, Duarte, CA, USA.
Mina S SedrakDepartment of Medical Oncology, City of Hope National Medical Center, Duarte, CA, USA.ORCID 0000-0002-8379-391X
City Of Hope National Medical Center · USDuke Medical Center · USUNC Lineberger Comprehensive Cancer Center

Funding

Oncology Research Career Development ProgramK12CA001727 · NCI · CITY OF HOPE NATIONAL MEDICAL CENTER · PI MORTIMER, JOANNE E. · 1992 to 2024
$14.6M
Biomarkers of Molecular Age to Predict the Toxicity of Cancer ChemotherapyR01CA203023 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MUSS, HYMAN · 2016 to 2020
$2.5M
Clinical and Biological Predictors of Chemotherapy Toxicity in Older AdultsR01AG037037 · NIA · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI HURRIA, ARTI · 2011 to 2015
$2.4M
Targeting Senescence to Improve Frailty in Older Cancer SurvivorsK76AG074918 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SEDRAK, MINA S · 2022 to 2024
$729k
Using Senolytics to Improve Physical Function in Older Breast Cancer SurvivorsR21CA277660 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SEDRAK, MINA S · 2023 to 2024
$422k
Improving Clinical Trial Participation of Older Adults with CancerR03AG064377 · NIA · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI SEDRAK, MINA S · 2019 to 2020
$260k
NCI NIH HHS K12 CA001727NCI NIH HHS K12CA001727NCI NIH HHS R01 CA203023NCI NIH HHS R21 CA277660NIA NIH HHS K76 AG074918NIA NIH HHS K76AG074918NIA NIH HHS NIA R01 AG037037NIA NIH HHS R01 AG037037NIA NIH HHS R03 AG064377
6 · The paper itself

Abstract

backgroundChemotoxicity risk scores were developed to predict grade 3-5 chemotherapy toxicity in older women with early breast cancer. However, whether these toxicity risk scores are associated with clinically meaningful decline in patient health remains unknown.

methodsIn a prospective study of women aged 65 years and older with stage I-III breast cancer treated with chemotherapy, we assessed chemotoxicity risk using the Cancer and Aging Research Group-Breast Cancer (CARG-BC) score (categorized as low, intermediate, and high). We measured patient health status before (T1) and after (T2) chemotherapy using a clinical frailty index (Deficit Accumulation Index, categorized as robust, prefrail, and frail). The population of interest was robust women at T1. The primary outcome was decline in health status after chemotherapy, defined as a decline in Deficit Accumulation Index from robust at T1 to prefrail or frail at T2. Multivariable logistic regression was used to examine the association between T1 CARG-BC score and decline in health status, adjusted for sociodemographic and clinical characteristics.

resultsOf the 348 robust women at T1, 83 (24%) experienced declining health status after chemotherapy, of whom 63% had intermediate or high CARG-BC scores. After adjusting for sociodemographic and clinical characteristics, women with intermediate (odds ratio = 3.14, 95% confidence interval = 1.60 to 6.14, P < .001) or high (odds ratio = 3.80, 95% confidence interval = 1.35 to 10.67, P = .01) CARG-BC scores had greater odds of decline in health status compared with women with low scores.

conclusionsIn this cohort of older women with early breast cancer, higher CARG-BC scores before chemotherapy were associated with decline in health status after chemotherapy independent of sociodemographic and clinical risk factors.

Indexed as

Breast NeoplasmsCancer SurvivorsAgedChemotherapy, AdjuvantFemaleHumansProspective StudiesRisk Factors

Identifiers

PMID36762832
PMCPMC10165485
OpenAlexW4319827647

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.