Evidence map›Paper›PMID 41543393›Full record

ArticleCancer research communications2026

ctDNA Detected after Neoadjuvant Therapy for HER2-Positive Breast Cancer Is Associated with Inferior Outcomes and May Inform Adjuvant Therapy.

Po-Han Lin, Li-Wei Tsai, Chiao Lo, Sung-Hsin Kuo, Chia-Chun Ni, Chih-Hao Yu, Chiun-Sheng Huang

Registry-linked trialAbstract read
In one paragraph

Article in Cancer research communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07565324 (Phase II Study of Ultrasound and ctDNA Guided Neoadjuvant Systemic Therapy for Patients With HER2-positive Early Breast Cancer), which is not on this map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

NCT07565324 phase2not yet recruitingnot on this map

Phase II Study of Ultrasound and ctDNA Guided Neoadjuvant Systemic Therapy for Patients With HER2-positive Early Breast Cancer

TypeinterventionalSponsorNational Taiwan University HospitalRan2026 to 2032Enrolled54ConditionsHER-2 Positive Breast CancerArmsLipo-Dox®, Cyclophosphamide, Trastuzumab (Herceptin), Pertuzumab
3 · Its place in the literature

Who cites it

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

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. MRI-guided de-escalation in HER2-positive early breast cancer: precision progress with necessary prudence.Translational breast cancer research : a journal focusing on translational research in breast cancer · 2026
    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

7 authors.

Po-Han LinDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.ORCID 0000-0001-6066-398X
Li-Wei TsaiDepartment of Surgery, National Taiwan University Hospital and Medical College of the National Taiwan University, Taipei, Taiwan.ORCID 0000-0002-6877-0138
Chiao LoDepartment of Surgery, National Taiwan University Hospital and Medical College of the National Taiwan University, Taipei, Taiwan.ORCID 0000-0002-5779-9234
Sung-Hsin KuoDepartment of Oncology, National Taiwan University Hospital and Medical College of the National Taiwan University, Taipei, Taiwan.ORCID 0000-0003-0054-887X
Chia-Chun NiDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.ORCID 0009-0005-3390-561X
Chih-Hao YuDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.ORCID 0009-0002-3710-552X
Chiun-Sheng HuangDepartment of Surgery, National Taiwan University Hospital and Medical College of the National Taiwan University, Taipei, Taiwan.ORCID 0000-0002-6557-211X

Funding

National Science and Technology Council (NSTC) 113-2314-B-002-006National Science and Technology Council (NSTC) 113-2314-B-002-096National Taiwan University Hospital (NTUH) NTUH. 110-005105
6 · The paper itself

Abstract

ctDNA has been reported as a predictor of the progression of metastatic breast cancer and recurrence in early breast cancer (EBC). This study explored whether ctDNA persistence in patients with HER2-positive (HER2+) EBC who achieved pathologic complete response (pCR) after neoadjuvant therapy (NAT) indicates a poor prognosis and the need for adjuvant T-DM1. Of the 117 patients enrolled, 25 patients achieved pCR after NAT and 92 patients did not. Six of the 25 pCR patients showed positive ctDNA after NAT, whereas 26 of the 92 non-pCR patients were ctDNA-positive. Eighteen patients received adjuvant T-DM1, whereas 99 patients did not. Among the non-T-DM1 group, ctDNA positivity after NAT independently predicted recurrence (HR, 5.505; 95% confidence interval, 1.950-15.540; P = 0.001). pCR patients with ctDNA positivity experienced a shorter recurrence-free survival (RFS) compared with pCR and ctDNA-negative patients after NAT(P = 0.008), whereas non-pCR patients with ctDNA-negative tumors had a better RFS compared with non-pCR patients with ctDNA-positive status (P = 0.001). In the 79 patients who were ctDNA-positive before NAT, clearance of ctDNA by NAT was associated with significantly better RFS than nonclearance (P < 0.001). Adjuvant T-DM1 also significantly improved the ctDNA clearance rate (P = 0.035) compared with non-T-DM1 therapy in patients with ctDNA positivity after NAT during serial tests. We classified the 117 patients as T-DM1/non-T-DM1 and ctDNA-positive/negative, and a significantly shorter RFS was observed in patients with ctDNA-positive/non-T-DM1 (P = 0.029) than in the other three patient groups. In conclusion, the presence of ctDNA after NAT in patients with HER2+ EBC is associated with a poor prognosis and may indicate adjuvant T-DM1. SIGNIFICANCE: Adjuvant T-DM1 can improve the survival of HER2+ EBC patients who don't achieve pCR. Our study showed that ctDNA positivity after NAT was associated with decreased RFS. ctDNA-positive status after NAT can be switched to ctDNA-negative status in patients treated with T-DM1. Patients who were ctDNA-positive and treated with T-DM1 had a similar RFS to those who were ctDNA-negative, indicating that "ctDNA positivity" could be a marker determining adjuvant T-DM1 therapy.

Indexed as

Biomarkers, TumorBreast NeoplasmsCirculating Tumor DNAErb-b2 Receptor Tyrosine KinasesAdo-Trastuzumab EmtansineAdultAgedChemotherapy, AdjuvantDisease-Free SurvivalFemaleHumansMiddle AgedNeoadjuvant TherapyNeoplasm Recurrence, LocalPathologic Complete ResponsePrognosisAdo-Trastuzumab EmtansineBiomarkers, TumorCirculating Tumor DNAERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesTrastuzumab

Identifiers

PMID41543393
PMCPMC12802552

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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.