Evidence map›Paper›PMID 42688229›Full record

ArticleFrontiers in immunology2026

Unlocking HER2 as a target in KRAS-mutated rectal cancer: a case of significant response to zanidatamab-based regimen.

Kexun Zhou, Yu Yang

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Kexun ZhouDivision of Abdominal Cancer, Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Yu YangDivision of Abdominal Cancer, Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Colorectal cancer (CRC) with human epidermal growth factor receptor 2 (HER2) overexpression and RAS mutations is often associated with poor response to conventional treatments, presenting substantial therapeutic challenges. This report describes a remarkable response in a patient with HER2-amplified, KRAS-mutated metastatic rectal cancer, who was treated with a zanidatamab-based combination regimen. Case presentation: A 54-year-old male was admitted to our hospital complaining of hematochezia and was diagnosed with rectal adenocarcinoma via biopsy. Baseline imaging revealed extensive, unresectable liver metastases. Next-generation sequencing identified a KRAS G12D mutation alongside HER2 amplification. Although the combination of chemotherapy and bevacizumab yielded promising efficacy, but tumor markers still remained high. When the anti-HER2 bispecific antibody zanidatamab was added, after three cycles of this triplet therapy, the liver metastases exhibited radiographic regression, and tumor markers showed substantial decline. The patient achieved sufficient downstaging and subsequently underwent successful hepatic resection. Pathological examination confirmed negative surgical margins. Conclusion: This case underscores the potential of HER2 inhibition as an effective therapeutic strategy in KRAS-mutated CRC. It also highlights zanidatamab's promise as part of a conversion therapy approach in patients with historically refractory disease.

Indexed as

AdenocarcinomaAntineoplastic Combined Chemotherapy ProtocolsErb-b2 Receptor Tyrosine KinasesMutationProto-Oncogene Proteins p21(ras)Rectal NeoplasmsAntibodies, BispecificBiomarkers, TumorHumansLiver NeoplasmsMaleMiddle AgedTreatment OutcomeAntibodies, BispecificBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesKRAS protein, humanProto-Oncogene Proteins p21(ras)zanidatamabbiomarker-guided treatmentcolorectal cancerhuman epidermal growth factor receptor 2KRAS mutationzanidatamab

Identifiers

PMID42688229
PMCPMC13533939

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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.