Evidence map›Paper›PMID 26984450›Full record

Trial reportThe oncologist2016

Cardiac Safety of Paclitaxel Plus Trastuzumab and Pertuzumab in Patients With HER2-Positive Metastatic Breast Cancer.

Anthony F Yu, Carlos Manrique, Shawn Pun, Jennifer E Liu, Elton Mara, Martin Fleisher, Sujata Patil, Lee W Jones, Richard M Steingart, Clifford A Hudis and 1 more

Open access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in The oncologist, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 56 citations in OpenAlex.

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  18. Circulating Biomarkers for Cardiotoxicity Risk Prediction.Current treatment options in oncology · 2021
    Review
  19. Cardiotoxicity of chemotherapy and targeted agents.American journal of cancer research · 2021
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Anthony F YuDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA yua3@mskcc.org.
Carlos ManriqueDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Shawn PunDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Jennifer E LiuDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Elton MaraDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Martin FleisherDepartment of Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Sujata PatilDepartment of Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Lee W JonesDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Richard M SteingartDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Clifford A HudisDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Chau T DangDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Memorial Sloan Kettering Cancer Center · US

Funding

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

Abstract

introductionMyocardial strain imaging and blood biomarkers have been proposed as adjuncts to left ventricular ejection fraction (LVEF) monitoring for the early detection of cardiotoxicity during cancer therapy. We report the results of a preplanned cardiac safety analysis of global longitudinal strain (GLS), and troponin-I (TnI) and brain natriuretic peptide (BNP) levels in the phase II study of paclitaxel, trastuzumab, and pertuzumab (THP) for metastatic HER2-positive breast cancer. PATIENTS AND

methodsPatients with 0-1 lines of prior therapy were treated with weekly paclitaxel (80 mg/m(2)) plus trastuzumab (8 mg/kg loading dose followed by 6 mg/kg) and pertuzumab (840 mg loading dose followed by 420 mg) every 3 weeks. Exploratory endpoints were GLS measured with speckle-tracking echocardiography every 3 months and TnI and BNP levels measured every 6 weeks (immediately pre- and postchemotherapy infusion) at 6 time points.

resultsSixty-seven of 69 enrolled patients were treated with THP: 19 (28%) had hypertension, 8 (12%) had diabetes, 11 (16%) had hyperlipidemia, and 26 (38%) had smoking history. After a median follow-up of 21 months (range: 3-38 months), no patients developed symptomatic heart failure. Two patients (3.0%) experienced asymptomatic LVEF decline (grade 2). The mean GLS (±SD) was 19% ± 2% (baseline), 19% ± 2% (month 6), and 19% ± 3% (month 12). Detectable TnI (>0.06 ng/mL) and elevated BNP (>100 pg/mL) levels were observed in 3 (4.3%) and 2 (3.0%) patients, respectively, but were not associated with LVEF decline.

conclusionThe absence of any significant changes in GLS and cardiac biomarkers (TnI and BNP) further support the cardiac safety of THP in patients with metastatic HER2-positive breast cancer. IMPLICATIONS FOR PRACTICE: Dual anti-HER2 therapy with trastuzumab and pertuzumab in combination with taxane-based chemotherapy improves overall survival in patients with metastatic HER2-positive breast cancer. There is a critical need to investigate the potential cardiotoxicity of dual anti-HER2 blockade, given the importance of HER2 signaling in cardiac homeostasis and stress response. Global longitudinal strain and cardiac biomarkers have been proposed as adjuncts to left ventricular ejection fraction for the early detection of cardiotoxicity. In this phase II study of combination trastuzumab and pertuzumab with paclitaxel, no clinically significant change was observed in global longitudinal strain or cardiac biomarkers. These results further support the cardiac safety of dual anti-HER2 blockade previously reported in the CLEOPATRA study. The findings in the current study also call into question the role of intensive cardiac monitoring among patients treated with anti-HER2 therapy in the absence of anthracyclines. Less frequent cardiac assessments could lead to a reduction in unnecessary treatment interruption and is an important consideration given the rise in medical expenditures, but this requires further investigation.

Indexed as

AdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedBreast NeoplasmsCardiotoxicityErb-b2 Receptor Tyrosine KinasesFemaleHumansMiddle AgedNatriuretic Peptide, BrainNeoplasm MetastasisPaclitaxelTrastuzumabTroponin IVentricular Function, LeftAntibodies, Monoclonal, HumanizedErb-b2 Receptor Tyrosine KinasesNatriuretic Peptide, BrainPaclitaxelpertuzumabTrastuzumabTroponin IBiomarkersCardiotoxicityHeart failureImagingPertuzumabTrastuzumab

Identifiers

PMID26984450
PMCPMC4828117
OpenAlexW2302127666

What OpenQuestion holds

Textmetadata
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.