Evidence map›Paper›PMID 38935923›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2024

Adjuvant Trastuzumab Emtansine Versus Paclitaxel Plus Trastuzumab for Stage I Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer: 5-Year Results and Correlative Analyses From ATEMPT.

Paolo Tarantino, Nabihah Tayob, Guillermo Villacampa, Chau Dang, Denise A Yardley, Steven J Isakoff, Vicente Valero, Meredith Faggen, Therese Mulvey, Ron Bose and 42 more

Abstract readRandomized Controlled TrialClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 3 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

43 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Review
  7. Article
  8. Review
  9. Observational
  10. Article
  11. Headwinds in Breast Cancer Research: The Case for Pragmatic Radiotherapy De-escalation Studies.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article
  12. Article
  13. Article
  14. Associations of the HER2DX Genomic Test with Biological and Pathologic Features in HER2-Positive Breast Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

52 authors.

Paolo TarantinoMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0001-8686-0228
Nabihah TayobHarvard Medical School, Boston, MA.ORCID 0000-0001-6088-167X
Guillermo VillacampaSOLTI Breast Cancer Research Group, Barcelona, Spain.ORCID 0000-0003-4868-6585
Chau DangMemorial Sloan Kettering Cancer Center, New York, NY.
Denise A YardleySarah Cannon Research Institute and Tennessee Oncology, Nashville, TN.
Steven J IsakoffHarvard Medical School, Boston, MA.ORCID 0000-0002-6677-1014
Vicente ValeroMD Anderson Cancer Center, Houston, TX.
Meredith FaggenMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Therese MulveyHarvard Medical School, Boston, MA.ORCID 0000-0002-7364-2835
Ron BoseWashington University School of Medicine, St Louis, MO.ORCID 0000-0003-1977-8894
Douglas WecksteinNew Hampshire Oncology Hematology, Manchester, NH.
Antonio C WolffJohns Hopkins Sidney Kimmel Cancer Center, Washington, DC.ORCID 0000-0003-3734-1063
Katherine Reeder-HayesUniversity of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC.ORCID 0000-0001-6903-0177
Hope S RugoUniversity of California, San Francisco, CA.ORCID 0000-0001-6710-4814
Bhuvaneswari RamaswamyOhio State University Comprehensive Cancer Center, Columbus, OH.
Dan ZuckermanSt Luke's Mountain States Tumor Institute, Boise, ID.ORCID 0000-0002-4005-1764
Lowell HartWake Forest Baptist Health, Winston-Salem, NC.
Vijayakrishna K GadiUniversity of Illinois Cancer Center, Chicago, IL.ORCID 0000-0002-5427-7465
Michael ConstantineMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Kit ChengNorth Shore-LIJ Cancer Institute, Lake Success, NY.ORCID 0000-0003-0136-6912
Audrey Merrill GarrettNorthern Light Cancer Care, Brewer, ME.
P Kelly MarcomDuke University School of Medicine, Durham, NC.ORCID 0000-0001-5302-6368
Kathy AlbainLoyola University Medical Center, Maywood, IL.ORCID 0000-0002-2899-2473
Patricia DeFuscoHartford Healthcare Cancer Institute, Hartford, CT.
Nadine TungHarvard Medical School, Boston, MA.ORCID 0000-0003-1422-3734
Blair ArdmanLowell General Hospital, Lowell, MA.
Rita NandaUChicago Medicine, Chicago, IL.ORCID 0000-0001-5248-0876
Rachel C JankowitzPerelman Center for Advanced Medicine, Philadelphia, PA.ORCID 0000-0001-7691-2389
Mothaffar RimawiDan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX.ORCID 0000-0002-4284-5656
Vandana AbramsonVanderbilt-Ingram Cancer Center, Nashville, TN.ORCID 0000-0002-6855-1322
Paula R PohlmannMD Anderson Cancer Center, Houston, TX.
Catherine Van PoznakRogel Cancer Center, University of Michigan, Ann Arbor, MI.ORCID 0000-0001-5523-6908
Andres Forero-TorresKirklin UAB Hematology Oncology, Birmingham, AL.ORCID 0000-0001-5161-8319
Minetta C LiuNatera, Inc, Austin, TX.ORCID 0000-0002-8206-5232
Kathryn J RuddyMayo Clinic, Rochester, NY.ORCID 0000-0001-6298-332X
Adrienne G WaksMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Michelle DeMeoBreast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA.
Harold J BursteinMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0003-1963-8162
Ann H PartridgeMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-4722-4824
Patrizia Dell'OrtoIEO European Institute of Oncology, IRCCS, Milan, Italy.
Leila RussoIEO European Institute of Oncology, IRCCS, Milan, Italy.
Emma KrausePathAI, Boston, MA.ORCID 0000-0002-3296-3982
Daniel J NewhouseNanoString Technologies, Inc, Boston, MA.
Busem Binboğa KurtBreast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA.ORCID 0000-0002-7161-1496
Elizabeth A MittendorfBreast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA.ORCID 0000-0002-9762-8536
Bryan SchneiderIndiana University School of Medicine, Indianapolis, IN.ORCID 0000-0003-1868-7739
Aleix PratSOLTI Breast Cancer Research Group, Barcelona, Spain.ORCID 0000-0001-8686-0236
Eric P WinerMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-8819-1723
Ian E KropMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-6380-5944
Sara M TolaneyMedical Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-5940-8671
Consortium of the TBCRC Translational Investigators
TBCRC Translational Investigators

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Physician Scientist Training in Cancer ResearchT32CA009172 · NCI · DANA-FARBER CANCER INSTITUTE · PI Jennifer R Brown, James A. DeCaprio · 1985 to 2026
$17.1M
NCI NIH HHS P30 CA008748NCI NIH HHS T32 CA009172
6 · The paper itself

Abstract

purposeLong-term outcomes of patients with stage I human epidermal growth factor receptor 2 (HER2)-positive breast cancer receiving adjuvant trastuzumab emtansine (T-DM1) remain undefined, and prognostic predictors represent an unmet need.

methodsIn the ATEMPT phase II trial, patients with stage I centrally confirmed HER2-positive breast cancer were randomly assigned 3:1 to adjuvant T-DM1 for 1 year or paclitaxel plus trastuzumab (TH). Coprimary objectives were to compare the incidence of clinically relevant toxicities between arms and to evaluate invasive disease-free survival (iDFS) with T-DM1. Correlative analyses included the HER2DX genomic tool, multiomic evaluations of HER2 heterogeneity, and predictors of thrombocytopenia.

resultsAfter a median follow-up of 5.8 years, 11 iDFS events were observed in the T-DM1 arm, consistent with a 5-year iDFS of 97.0% (95% CI, 95.2 to 98.7). At 5 years, the recurrence-free interval (RFI) was 98.3% (95% CI, 97.0 to 99.7), the overall survival was 97.8% (95% CI, 96.3 to 99.3), and the breast cancer-specific survival was 99.4% (95% CI, 98.6 to 100). Comparable iDFS was observed with T-DM1 irrespective of tumor size, hormone receptor status, centrally determined HER2 immunohistochemical score, and receipt of T-DM1 for more or less than 6 months. Although ATEMPT was not powered for this end point, the 5-year iDFS in the TH arm was 91.1%. Among patients with sufficient tissue for HER2DX testing (n = 187), 5-year outcomes significantly differed according to HER2DX risk score, with better RFI (98.1%

conclusionAdjuvant T-DM1 for 1 year leads to outstanding long-term outcomes for patients with stage I HER2-positive breast cancer. A high HER2DX risk score predicted a higher risk of recurrence in ATEMPT.

Indexed as

Ado-Trastuzumab EmtansineAntineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesNeoplasm StagingPaclitaxelTrastuzumabAdultAgedChemotherapy, AdjuvantDisease-Free SurvivalFemaleHumansMiddle AgedAdo-Trastuzumab EmtansineERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesPaclitaxelTrastuzumab

Identifiers

PMID38935923
PMCPMC11527383

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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.