Evidence map›Paper›PMID 38913986›Full record

ArticleThe oncologist2024

Dose delay, dose reduction, and early treatment discontinuation in Black and White women receiving chemotherapy for nonmetastatic breast cancer.

Moriah Forster, Allison M Deal, Annie Page, Sanah Vohra, Alexis C Wardell, Joyce Pak, Jennifer L Lund, Kirsten A Nyrop, Hyman B Muss

Abstract read
In one paragraph

Article in The oncologist, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

9 authors.

Moriah ForsterDivision of Hematology and Oncology, Department of Medicine, Vanderbilt University, Nashville, TN 37232, United States.ORCID 0000-0002-6108-1727
Allison M DealLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC 27599, United States.ORCID 0000-0003-3526-3938
Annie PageDepartment of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC 27599, United States.ORCID 0000-0001-6279-529X
Sanah VohraLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC 27599, United States.ORCID 0000-0003-4461-5157
Alexis C WardellLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC 27599, United States.
Joyce PakDepartment of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC 27599, United States.ORCID 0000-0003-2443-7971
Jennifer L LundLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC 27599, United States.
Kirsten A NyropLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC 27599, United States.ORCID 0000-0002-2974-480X
Hyman B MussLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC 27599, United States.ORCID 0000-0003-2862-9970

Funding

Breast Cancer Research Foundation BCRF-21-114
6 · The paper itself

Abstract

backgroundTo describe reasons for deviations from planned chemotherapy treatments in women with nonmetastatic breast cancer that contribute to less-than-planned receipt of chemotherapy.

methodsElectronic medical records for patients receiving chemotherapy were reviewed for adverse events and treatment modifications. Log-binomial regression models were used to estimate relative risks (RRs) with 95% CIs to examine associations between chemotherapy modifications, patient characteristics, and treatment modalities.

resultsDelays in chemotherapy initiation (7%) were for surgical complications (58%), personal reasons (16%), and other (26%; port malfunction, infections, and obtaining extra imaging). Delays during chemotherapy (38%) were for infections (20%), neutropenia (13%), and personal reasons (13%). Dose reductions (38%) were for neuropathy (36%), unknown causes (9%), anemia (9%), and neutropenia (8%). Early treatment discontinuations (23%) were for neuropathy (29%). Patients receiving paclitaxel/nab-paclitaxel (RR 2.05; 95% CI, 1.47-2.87) and an anthracycline (RR 1.89; 95% CI, 1.39-2.57) reported more dose delays during chemotherapy. Black race (RR 1.46; 95% CI, 1.07-2.00), stage 3 (RR 1.79; 95% CI, 1.09-2.93), and paclitaxel/nab-paclitaxel receipt (RR 1.39; 95% CI, 1.02-1.90) increased the likelihood of dose reduction. Both Black race (RR 2.06; 95% CI, 1.35-3.15) and receipt of paclitaxel/nab-paclitaxel (RR 1.93; 95% CI, 1.19-3.13) increased the likelihood of early discontinuation. Patients receiving anthracyclines had higher rates of hospitalizations during chemotherapy (RR: 1.79; 95% CI, 1.11-2.89).

conclusionToxicities are the most common reason for treatment modifications and need close monitoring in high-risk groups for timely intervention. Dose reductions and early treatment discontinuations occurred more for Black patients and need further study.

Indexed as

Breast NeoplasmsAdultAgedAntineoplastic Combined Chemotherapy ProtocolsBlack or African AmericanFemaleHumansMiddle AgedPaclitaxelTreatment DelayWhitePaclitaxelbreast cancerchemotherapyracetoxicity

Identifiers

PMID38913986
PMCPMC11449010

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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.