Evidence map›Paper›PMID 39186271›Full record

Trial reportJAMA network open2024

Long-Term Outcomes of Adjuvant Trastuzumab for 9 Weeks or 1 Year for ERBB2-Positive Breast Cancer: A Secondary Analysis of the SOLD Randomized Clinical Trial.

Heikki Joensuu, Judith Fraser, Hans Wildiers, Riikka Huovinen, Päivi Auvinen, Meri Utriainen, Kenneth K Villman, Päivi Halonen, Helena Granstam-Björneklett, Minna Tanner and 9 more

Registry-linked trialAbstract readRandomized Controlled TrialMulticenter StudyEquivalence Trial
In one paragraph

Trial report in JAMA network open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00593697 (A Randomized Phase III Study Comparing Trastuzumab Plus Docetaxel), which is not on this 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.

NCT00593697 phase3completednot on this map

A Randomized Phase III Study Comparing Trastuzumab Plus Docetaxel (HT) Followed by 5-FU, Epirubicin, and Cyclophosphamide (FEC) to the Same Regimen Followed by Single-agent Trastuzumab as Adjuvant Treatments for Early Breast Cancer

TypeinterventionalSponsorFinnish Breast Cancer GroupRan2008 to 2014Enrolled2,168ConditionsBreast NeoplasmsArmstrastuzumab (9 weeks) + docetaxel, trastuzumab (9 weeks) + docetaxel + CEF + trastuzumab (up to 51 weeks)
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Computationally Derived Spatial Immune Signature Identifies Trastuzumab Responders in HER2+ Breast Cancer: NSABP B-41 Clinical Trial Validation.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Trial
  2. Review
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

19 authors.

Heikki JoensuuDepartment of Oncology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Judith FraserBeatson West of Scotland Cancer Centre, Glasgow, United Kingdom.
Hans WildiersMultidisciplinary Breast Centre, University Hospitals Leuven, Leuven, Belgium.
Riikka HuovinenTurku University Hospital, Turku, Finland.
Päivi AuvinenDepartment of Oncology, Kuopio University Hospital, Kuopio, Finland.
Meri UtriainenDepartment of Oncology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Kenneth K VillmanÖrebro University Hospital, Örebro, Sweden.
Päivi HalonenDepartment of Oncology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Helena Granstam-BjörneklettVästerås Central Hospital, Västerås, Sweden.
Minna TannerDepartment of Oncology, Tampere University Hospital and Tampere University, Tampere, Finland.
Liisa SailasVaasa Central Hospital, Vaasa, Finland.
Taina Turpeenniemi-HujanenDepartment of Oncology and Radiotherapy, Oulu University Hospital, Oulu, Finland.
Jeffrey YachninCenter for Clinical Cancer Studies, Karolinska University Hospital, Stockholm, Sweden.
Teppo HuttunenEstiMates Ltd, Turku, Finland.
Patrick NevenMultidisciplinary Breast Centre, University Hospitals Leuven, Leuven, Belgium.
Peter CanneyBeatson West of Scotland Cancer Centre, Glasgow, United Kingdom.
Vernon J HarveyAuckland City Hospital, Auckland, New Zealand.
Pirkko-Liisa Kellokumpu-LehtinenDepartment of Oncology, Tampere University Hospital and Tampere University, Tampere, Finland.
Henrik LindmanDepartment of Immunology, Genetics and Pathology, Uppsala University Hospital, Uppsala, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: The standard adjuvant treatment for patients with ERRB2-positive breast cancer is chemotherapy plus 1 year of trastuzumab. Shorter durations of trastuzumab administration improve cardiac safety, but more information is needed about their effect on survival. Objective: To compare survival outcomes after 9-week vs 1-year administration of trastuzumab with the same adjuvant chemotherapy. Design, Setting, and Participants: This post hoc secondary analysis of an open-label, multicenter, noninferiority-design randomized clinical trial included women aged 18 years or older with early ERBB2-positive, axillary node-negative or axillary node-positive breast cancer who were enrolled from January 3, 2008, to December 16, 2014, at 65 centers in 7 European countries. The current exploratory analysis was conducted after achieving the maximum attainable follow-up data when the last patient enrolled had completed the last scheduled visit in December 2022. Intervention: Chemotherapy consisted of 3 cycles of docetaxel administered at 3-week intervals followed by 3 cycles of fluorouracil, epirubicin, and cyclophosphamide at 3-week intervals. Trastuzumab was administered in both groups for 9 weeks concomitantly with docetaxel. In the 9-week group, no further trastuzumab was administered after chemotherapy, whereas in the 1-year group, trastuzumab was continued after chemotherapy to complete 1 year of administration. Main Outcomes and Measures: The primary objective was disease-free survival (DFS). Distant DFS and OS were secondary objectives. Survival between groups was compared using the Kaplan-Meier method and log-rank test or univariable Cox proportional hazards regression. Results: Among the 2174 women analyzed, median age was 56 years (IQR, 48-64 years). The median follow-up time was 8.1 years (IQR, 8.0-8.9 years); 357 DFS events and 176 deaths occurred. Trastuzumab for 9 weeks was associated with shorter DFS compared with trastuzumab for 1 year (hazard ratio [HR], 1.36; 90% CI, 1.14-1.62); 10-year DFS was 80.3% in the 1-year group vs 78.6% in the 9-week group. The 5-year and 10-year OS rates were comparable between the 9-week and 1-year groups (95.0% vs 95.9% and 89.1% vs 88.2%, respectively; HR for all time points, 1.20; 90% CI, 0.94-1.54). In multivariable analyses, 9-week treatment was associated with shorter DFS compared with 1-year treatment (HR for recurrence or death, 1.36; 95% CI, 1.10-1.68; P = .005), but there was no between-group difference in OS (HR, 1.22; 95% CI, 0.90-1.64; P = .20). Only 4 patients (0.2%) died of a cardiac cause. Conclusions and Relevance: In this secondary analysis of a randomized clinical trial, 1-year vs 9-week adjuvant trastuzumab was associated with improved DFS among patients with ERRB2-positive breast cancer receiving chemotherapy, but there was no significant difference in OS between the groups. Trial Registration: ClinicalTrials.gov Identifier: NCT00593697.

Indexed as

Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesTrastuzumabAdultAgedAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsChemotherapy, AdjuvantCyclophosphamideDisease-Free SurvivalDocetaxelDrug Administration ScheduleEpirubicinFemaleFluorouracilHumansAntineoplastic Agents, ImmunologicalCyclophosphamideDocetaxelEpirubicinERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesFluorouracilTrastuzumab

Identifiers

PMID39186271
PMCPMC12507463

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Registered trials

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.