Evidence map›Paper›PMID 35313558›Full record

ArticleBreast cancer (Dove Medical Press)2022

Weekly vs Every-3-Week Carboplatin with Weekly Paclitaxel in Neoadjuvant Chemotherapy for Triple-Negative Breast Cancer: A Retrospective Analysis.

Kara K Landry, Jessica L Lyon, Kitty E Victoria, P Nick Changizzadeh, Bernard F Cole, Bhargavi Pulluri, William M Sikov, Marie E Wood

Open access · goldAbstract read
In one paragraph

Article in Breast cancer (Dove Medical Press), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 52% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

8 authors at 5 institutions in 1 country.

Kara K LandryDivision of Hematology and Oncology, Department of Medicine, University of Vermont Medical Center, Burlington, VT, USA.ORCID 0000-0002-1912-739X
Jessica L LyonLarner College of Medicine at the University of Vermont, Burlington, VA, USA.
Kitty E VictoriaDivision of Hematology and Oncology, Department of Medicine, University of Vermont Medical Center, Burlington, VT, USA.
P Nick ChangizzadehHematology and Oncology, Eastern Connecticut Hematology and Oncology, Norwich, CT, USA.
Bernard F ColeCollege of Engineering and Mathematical Sciences, University of Vermont, Burlington, VA, USA.
Bhargavi PulluriDivision of Hematology and Oncology, Saint Agnes Hospital, Baltimore, MD, USA.ORCID 0000-0002-4170-1706
William M SikovWomen and Infants Hospital of Rhode Island, Program in Women's Oncology, and Warren Alpert Medical School of Brown University, Providence, RI, USA.ORCID 0000-0001-5451-6449
Marie E WoodDivision of Hematology and Oncology, Department of Medicine, University of Vermont Medical Center, Burlington, VT, USA.
University of Vermont Medical Center · USUniversity of Vermont · USBrown University · USEastern Connecticut Hematology and Oncology Associates · USSaint Agnes Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Adding carboplatin to weekly paclitaxel as part of neoadjuvant chemotherapy (NACT) for stage II-III triple negative breast cancer (TNBC) has been shown to significantly increase the pathologic complete response (pCR) rate. Hematologic toxicities associated with every 3-week dosing of carboplatin have led some oncologists to explore weekly dosing as an alternative, but there are little published data comparing the two dosing schedules. Methods: We performed a retrospective analysis of patients who received paclitaxel and carboplatin, usually followed by AC, as initial NACT for TNBC at two academic cancer centers between 2008 and 2018 for whom pathologic results and post-operative follow-up were available. We recorded pCR, defined as ypT0/isN0, treatment delivery and disease-free survival, censored as of the patient's last follow-up visit. Results: A total of 76 patients were identified (median age 49 years). A total of 47 received weekly carboplatin, of whom 83% received at least 11 of 12 planned doses, and 29 received every 3-week carboplatin, of whom 90% received all 4 planned doses. pCR rates were similar, 53% with weekly and 55% with every 3-week carboplatin dosing. At median follow-up of 18 months (range <1-118), 93% of patients who achieved pCR were alive and free from recurrence, compared to 74% of those who did not. Conclusion: pCR rates were similar between patients receiving weekly or every 3-week carboplatin and were similar to those reported in prior trials with carboplatin. These data suggest that providers can choose either weekly or every 3-week carboplatin dosing without compromising the likelihood of achieving pCR.

Indexed as

carboplatin dosingchemotherapyneoadjuvant treatmenttriple negative breast cancer

Identifiers

PMID35313558
PMCPMC8934152
OpenAlexW4220677166

What OpenQuestion holds

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LicenceCC BY-NC
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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.