Evidence map›Paper›PMID 37936380›Full record

ArticleJournal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners2024

Impact of relative dose intensity on pathologic complete response in human epidermal growth factor receptor 2 positive breast cancer patients receiving neoadjuvant TCHP.

Kaylyn Collette, Cassandra L Perkey, Val Adams, Brent J Shelton, Lauren S Corum, Allison Butts

Abstract read
In one paragraph

Article in Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Kaylyn ColletteDepartment of Pharmacy Services, UK HealthCare Albert B. Chandler Medical Center, Lexington, KY, USA.ORCID 0000-0003-1187-6932
Cassandra L PerkeyAmerican Oncology Network, Fort Myers, FL, USA.
Val AdamsUniversity of Kentucky College of Pharmacy, Lexington, KY, USA.
Brent J SheltonMarkey Cancer Center, UK HealthCare Albert B. Chandler Medical Center, Lexington, KY, USA.
Lauren S CorumMarkey Cancer Center, UK HealthCare Albert B. Chandler Medical Center, Lexington, KY, USA.
Allison ButtsDepartment of Pharmacy Services, UK HealthCare Albert B. Chandler Medical Center, Lexington, KY, USA.ORCID 0000-0002-4208-7656

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI KATHLEEN L. O'CONNOR · 2013 to 2026
$38.3M
Oncology Research Training for Surgeon-ScientistsT32CA160003 · NCI · UNIVERSITY OF KENTUCKY · PI Bernard Mark Evers, Pamela Carmen Hull · 2011 to 2026
$3.2M
NCI NIH HHS P30 CA177558NCI NIH HHS T32 CA160003
6 · The paper itself

Abstract

purposeThe standard of care for locally advanced, human epidermal growth factor receptor 2 positive (HER2+) breast cancer includes neoadjuvant chemotherapy with docetaxel, carboplatin, trastuzumab, and pertuzumab (TCHP). Many patients do not receive the full course of therapy due to various complications, possibly affecting the potential to achieve a pathologic complete response (pCR). The amount of therapy received is typically measured by relative dose intensity (RDI). This study aimed to evaluate pCR rates in patients receiving optimal and suboptimal RDI TCHP.

methodsThis study was a retrospective chart review of patients treated between 2014 and 2021 at UK HealthCare. Patients included were 18 years of age or older with HER2+ breast cancer and received at least one cycle of neoadjuvant TCHP. The primary objective compared pCR rates in patients receiving ≥ 85% RDI or <85% RDI. Secondary objectives included pCR rates based on clinical stage, age, body mass index, or hormone receptor status; factors leading to discontinuation or delay in treatment; and impact of dose reductions and delays on pCR.

resultsA total of 101 patients were included and divided into two cohorts: 54 patients received ≥ 85% RDI and 47 patients received <85% RDI. Patients who received ≥ 85% total RDI had an approximate increase of 17% in pCR rates (59.3% vs 42.6%,

conclusionsPatients who received ≥ 85% RDI had increased pCR rates compared to patients receiving <85% RDI. A larger patient population is needed to formulate definitive conclusions on the impact of RDI and pCR rates.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsCarboplatinDocetaxelErb-b2 Receptor Tyrosine KinasesNeoadjuvant TherapyTrastuzumabAdultAgedAntibodies, Monoclonal, HumanizedDose-Response Relationship, DrugFemaleHumansMiddle AgedPathologic Complete ResponseRetrospective StudiesAntibodies, Monoclonal, HumanizedCarboplatinDocetaxelERBB2 protein, humanErb-b2 Receptor Tyrosine KinasespertuzumabTrastuzumabchemotherapyHER2+ breast cancermonoclonal antibodyrelative dose intensity

Identifiers

PMID37936380
PMCPMC11972010

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Registered trials

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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.