Evidence map›Paper›PMID 41732900›Full record

ArticleCancer2026

Initial chemotherapy dose reductions and subsequent treatment delivery in stage I-IIIA breast cancer.

Maria J Monroy-Iglesias, Kelli O'Connell, Jenna Bhimani, Victoria S Blinder, Rachael P Burganowski-Doud, Isaac J Ergas, Grace B Gallagher, Jennifer J Griggs, Narre Heon, Tatjana Kolevska and 15 more

Abstract read
In one paragraph

Article in Cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

25 authors.

Maria J Monroy-IglesiasDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID https://orcid.org/0000-0003-2417-3275
Kelli O'ConnellDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Jenna BhimaniDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Victoria S BlinderDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Rachael P Burganowski-DoudKaiser Permanente Washington Health Research Institute, Kaiser Permanente Washington, Seattle, Washington, USA.
Isaac J ErgasDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, USA.ORCID https://orcid.org/0000-0002-3187-9754
Grace B GallagherDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID https://orcid.org/0009-0004-9277-5002
Jennifer J GriggsDivision of Hematology/Oncology, Department of Medicine, Department of Health Management and Policy, University of Michigan, Ann Arbor, Michigan, USA.
Narre HeonDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Tatjana KolevskaDepartment of Oncology, Kaiser Permanente Medical Center, Vallejo, California, USA.
Yuriy KotsurovskyyDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Candyce H KroenkeDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, USA.ORCID https://orcid.org/0000-0002-6128-3118
Cecile A LaurentDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, USA.
Raymond LiuDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, USA.
Kanichi G NakataKaiser Permanente Washington Health Research Institute, Kaiser Permanente Washington, Seattle, Washington, USA.
Sonia PersaudDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Janise M RohDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, USA.
Yashasvini SampathkumarDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID https://orcid.org/0009-0007-2120-2620
Sara TabatabaiDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Emily ValiceDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, USA.
Peng WangDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Erin J Aiello BowlesKaiser Permanente Washington Health Research Institute, Kaiser Permanente Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0001-6287-7391
Elisa V BanderaCancer Epidemiology and Health Outcomes, Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.
Lawrence H KushiDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, USA.
Elizabeth D KantorDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID https://orcid.org/0000-0002-9124-5323

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Risk-based Imaging Strategies to Improve Breast Cancer Surveillance OutcomesP01CA154292 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Diana L Miglioretti · 2011 to 2026
$52.9M
Infrastructure for Pathways, a Prospective Study of Breast Cancer SurvivorshipU01CA195565 · NCI · KAISER FOUNDATION RESEARCH INSTITUTE · PI AMBROSONE, CHRISTINE B., KUSHI, LAWRENCE H · 2016 to 2025
$18.8M
CRN4: Cancer Research Resources & Collaboration in Integrated Health Care SystemsU24CA171524 · NCI · KAISER FOUNDATION RESEARCH INSTITUTE · PI KUSHI, LAWRENCE H · 2012 to 2016
$16.0M
Obesity, chemotherapy dosing, and breast cancer outcomesR37CA222793 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI KANTOR, ELIZABETH DAVID · 2018 to 2024
$4.0M
Oncology-focused Postdoctoral Training in Care Delivery and Symptom Science (OPTICS)T32CA275764 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI JONINE L. BERNSTEIN, JUN J MAO · 2023 to 2026
$1.8M
Group Health Cancer Research Program Research Specialist AwardR50CA211115 · NCI · KAISER FOUNDATION RESEARCH INSTITUTE · PI BOWLES, ERIN JANELLE AIELLO · 2017 to 2021
$919k
Geoffrey Beene Cancer Research CenterNCI NIH HHS P01 CA154292NCI NIH HHS P01CA154292NCI NIH HHS P30 CA008748NCI NIH HHS P30CA008748NCI NIH HHS R37 CA222793NCI NIH HHS R37CA222793NCI NIH HHS R50 CA211115NCI NIH HHS R50CA211115NCI NIH HHS T32 CA275764NCI NIH HHS T32CA275764NCI NIH HHS U01 CA195565NCI NIH HHS U01CA195565NCI NIH HHS U24 CA171524NCI NIH HHS U24CA171524
6 · The paper itself

Abstract

backgroundFor most cytotoxic drugs, guidelines recommend body-surface-area-based dosing, yet some patients start with reduced doses, potentially reflecting tolerability concerns. The relationship between first-cycle dose reductions and subsequent delivery is unclear.

methodsThe authors analyzed data from women with stage I-IIIA breast cancer treated with adjuvant chemotherapy. Sankey diagrams illustrated trajectories from first-cycle dose proportion (FCDP) to average relative dose intensity (ARDI, ratio of received to expected dose intensity across the regimen), and cumulative dose proportion (CDP, ratio of total received to expected dose). Poisson regression estimated adjusted prevalence ratios for reduced FCDP (<95% vs. ≥95%) and three outcomes: ARDI reduction beyond initial FCDP, receiving fewer cycles, and CDP reduction beyond initial FCDP. Analyses assessed effect modification by age, body mass index (BMI), and comorbidities. Dosing was analyzed for cytotoxic and HER2-targeted therapy.

resultsA total of 8772 (90.8%) patients started with FCDP ≥95%; most maintained ARDI ≥95% (65.1%) and CDP ≥95% (79.9%). In multi-variable models, FCDP <95% was not significantly associated with further ARDI or CDP reductions or receipt of fewer cycles. BMI modified these associations (p-interaction = .004 for fewer cycles; p-interaction = .03 for CDP), with positive associations among overweight but not obese or normal-weight patients. FCDP <95% was linked to a lower likelihood of further ARDI reductions for both therapy types and lower likelihood of cumulative dose reduction in HER2-targeted therapy.

conclusionsEarly dosing decisions shaped subsequent chemotherapy delivery. Most patients who began at full dose maintained consistent dosing, whereas early reductions did not stave off subsequent changes, underscoring the need to balance safety with adequate dose intensity.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsDrug TaperingAdultAgedBody Mass IndexChemotherapy, AdjuvantDose-Response Relationship, DrugErb-b2 Receptor Tyrosine KinasesFemaleHumansMiddle AgedNeoplasm StagingErb-b2 Receptor Tyrosine Kinasesadjuvant chemotherapybreast cancerchemotherapy dose reductionstreatment delivery

Identifiers

PMID41732900
PMCPMC13179111

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