Evidence map›Paper›PMID 40066239›Full record

ArticleBiologics : targets & therapy2025

Dual Anti-HER2 Therapy Vs Trastuzumab Alone with Neoadjuvant Anthracycline and Taxane in HER2-Positive Early-Stage Breast Cancer: Real-World Insights.

Baha Sharaf, Faris Tamimi, Haneen Al-Abdallat, Suhaib Khater, Osama Salama, Anas Zayed, Osama El Khatib, Assem Qaddoumi, Malek Horani, Yosra Al-Masri and 4 more

Abstract read
In one paragraph

Article in Biologics : targets & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

14 authors.

Baha SharafKing Hussein Cancer Center, Amman, Jordan.ORCID 0000-0003-4368-1224
Faris TamimiKing Hussein Cancer Center, Amman, Jordan.ORCID 0000-0002-9337-6618
Haneen Al-AbdallatSchool of Medicine, The University of Jordan, Amman, Jordan.ORCID 0000-0002-6264-3306
Suhaib KhaterKing Hussein Cancer Center, Amman, Jordan.
Osama SalamaKing Hussein Cancer Center, Amman, Jordan.
Anas ZayedKing Hussein Cancer Center, Amman, Jordan.
Osama El KhatibKing Hussein Cancer Center, Amman, Jordan.
Assem QaddoumiKing Hussein Cancer Center, Amman, Jordan.
Malek HoraniKing Hussein Cancer Center, Amman, Jordan.
Yosra Al-MasriKing Hussein Cancer Center, Amman, Jordan.
Wafa AshaKing Hussein Cancer Center, Amman, Jordan.
Bayan Altalla'King Hussein Cancer Center, Amman, Jordan.
Hira Bani HaniKing Hussein Cancer Center, Amman, Jordan.
Hikmat Abdel-RazeqKing Hussein Cancer Center, Amman, Jordan.ORCID 0000-0003-2833-6051

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The integration of anti-HER2 targeted therapy with chemotherapy has demonstrated an increase in pathologic complete response rates (pCR) in patients with HER2-positive early-stage breast cancer (EBC). This study presents real-world data on the use of trastuzumab with or without pertuzumab, in combination with anthracycline and taxanes-based chemotherapy regimen. Methods: We conducted a retrospective analysis of patients with HER2-positive EBC who underwent neoadjuvant chemotherapy (NACT), treated between January 2014 and September 2021. The regimen included four cycles of doxorubicin and cyclophosphamide (AC), followed by four cycles of docetaxel every three weeks, with anti-HER2 therapy administered alongside docetaxel. Outcomes assessed included pCR, 3-year disease-free survival (DFS), and surgical outcomes. Results: During the study period, 484 consecutive patients with HER2-positive EBC, median age of 47 (range, 21-80) years, were enrolled. (64.7%) of patients received dual anti-HER2 therapy, while 35.3% received single-agent trastuzumab. The overall pCR rate was 44.2%, with a higher rate (55.6%) in hormone receptor (HR)-negative patients compared to HR-positive patients (39.8%), p=0.002. Although dual therapy resulted in a higher pCR rate (46.6%) compared to trastuzumab alone (39.8%), the difference was not statistically significant (p=0.15). The estimated 3-year DFS was 86.1% with dual therapy and 83.1% with trastuzumab alone (p=0.37). Further stratification revealed superior 3-year DFS in node-negative disease (96.4%) compared to node-positive disease (82.3%), p=0.0021. Patients who achieved pCR had a significantly better 3-year DFS (89.3%) compared to those with residual disease (82.2%), p=0.0177. Rate of breast conserving surgery (BCS) was lower (15.2%) among patients who received trastuzumab alone, compared to 26.5% among those who received dual anti-HER2 [Odds Ratio (OR)= 0.50, 95% Confidence Interval (CI), 0.30-0.80, p=0.005]. Conclusion: Dual anti-HER2 therapy did not significantly enhance DFS but was associated with higher BCS rates, highlighting its potential to improve surgical outcomes.

Indexed as

breast cancerdual anti-HER2 regimenneoadjuvantpertuzumabtrastuzumab

Identifiers

PMID40066239
PMCPMC11892743

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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.