Evidence map›Paper›PMID 37167571›Full record

ArticleJCO oncology practice2023

Real-World First-Line Use of Pertuzumab With Different Taxanes for Human Epidermal Growth Factor Receptor 2-Positive Metastatic Breast Cancer: A Comparative Effectiveness Study Using US Electronic Health Records.

Letizia Polito, Jinjoo Shim, Sara A Hurvitz, Chau T Dang, Adam Knott, Yolande Du Toit, Eleonora Restuccia, Thibaut Sanglier, Sandra M Swain

Open access · hybridAbstract read
In one paragraph

Article in JCO oncology practice, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Observational
  3. Article
  4. Article
  5. 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

9 authors at 5 institutions in 3 countries.

Letizia PolitoProduct Development Data Science, F. Hoffmann-La Roche Ltd, Basel, Switzerland.ORCID 0000-0001-7014-9677
Jinjoo ShimProduct Development Data Science, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Sara A HurvitzDavid Geffen School of Medicine, University of California, Los Angeles, CA.ORCID 0000-0001-7808-7191
Chau T DangDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Adam KnottProduct Development Oncology, Roche Products Limited, Welwyn, United Kingdom.
Yolande Du ToitUS Medical Affairs, Genentech, Inc., South San Francisco, CA.ORCID 0000-0002-2526-9503
Eleonora RestucciaProduct Development Oncology, F. Hoffmann-La Roche Ltd, Basel, Switzerland.ORCID 0000-0001-5751-094X
Thibaut SanglierProduct Development Data Science, F. Hoffmann-La Roche Ltd, Basel, Switzerland.ORCID 0000-0003-0740-2048
Sandra M SwainGeorgetown University Medical Center, Lombardi Comprehensive Cancer Center, MedStar Health, Washington, DC.ORCID 0000-0002-1320-3830
Roche (Switzerland) · CHGeorgetown University · USMemorial Sloan Kettering Cancer Center · USRoche (United Kingdom) · GBUniversity of California, Los Angeles · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeOn the basis of the results from CLEOPATRA, pertuzumab plus trastuzumab and chemotherapy is the first-line standard of care for human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer (MBC). However, discrepancies have been reported between clinical trial and real-world outcomes. We report real-world outcomes for patients with HER2-positive MBC treated with first-line pertuzumab plus trastuzumab and a taxane in routine clinical practice in the United States.

methodsA retrospective analysis was conducted using electronic health record-derived deidentified data from the Flatiron Health database. Patients were grouped according to the first taxane received (paclitaxel/nab-paclitaxel or docetaxel). Median real-world progression-free survival (rwPFS) and overall survival (rwOS) was estimated using Kaplan-Meier methodology. Subgroup analyses were conducted in patients treated with docetaxel who met CLEOPATRA's key eligibility criteria.

resultsWe included 1,065 patients; 313 patients received paclitaxel/nab-paclitaxel and 752 received docetaxel. Patients who received paclitaxel/nab-paclitaxel were older, had a worse Eastern Cooperative Oncology Group Performance Status, and had more recurrent metastatic disease compared with the docetaxel group. After adjustment for potential confounders, similar median rwPFS (inverse probability of treatment weighted average treatment effect for the treated [IPTW-ATT] hazard ratio [HR], 1.09; 95% CI, 0.9 to 1.3;

conclusionThere was no statistically significant difference in real-world outcomes between patients treated with paclitaxel/nab-paclitaxel and those treated with docetaxel. Selecting patients using key CLEOPATRA eligibility criteria resulted in rwPFS and rwOS similar to those observed in CLEOPATRA, highlighting the importance of ensuring similar patient populations when comparing clinical trial and real-world data.

Indexed as

Breast NeoplasmsAntibodies, Monoclonal, HumanizedBridged-Ring CompoundsDocetaxelElectronic Health RecordsErb-b2 Receptor Tyrosine KinasesFemaleHumansPaclitaxelRetrospective StudiesTaxoidsTrastuzumabAntibodies, Monoclonal, HumanizedBridged-Ring CompoundsDocetaxelERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesPaclitaxelpertuzumabtaxaneTaxoidsTrastuzumab

Identifiers

PMID37167571
PMCPMC10337715
OpenAlexW4376224000

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.