Evidence map›Paper›PMID 40025472›Full record

ReviewBMC cancer2025

Exploring Zanidatamab's efficacy across HER2-positive Malignancies: a narrative review.

Warisha Kanwal, Kaneez Narjis, Sarah Musani, Fnu Nancy, Laiba Qureshi, Muhammad Mudasir, Rohma Naseem, Fnu Tooba, Juvairia Yousuf, Kanza Farhan and 2 more

Abstract readReview
In one paragraph

Review in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Fighting HER2 in Gastric Cancer: Current Approaches and Future Landscapes.International journal of molecular sciences · 2025
    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

12 authors.

Warisha KanwalKarachi Medical and Dental College, Karachi, Pakistan.
Kaneez NarjisIsra University of Medical Sciences, Hyderabad, Pakistan.
Sarah MusaniDow University of Health Sciences, Karachi, Pakistan.
Fnu NancyJinnah Sindh Medical University, Karachi, Pakistan.
Laiba QureshiIsra University of Medical Sciences, Hyderabad, Pakistan.
Muhammad MudasirLiaquat University of Medical and Health Sciences, Jamshoro, Pakistan.
Rohma NaseemLiaquat National Hospital and Medical College, Karachi, Pakistan.
Fnu ToobaHamdard University, Karachi, Pakistan.
Juvairia YousufDow University of Health Sciences, Karachi, Pakistan.
Kanza FarhanJinnah Sindh Medical University, Karachi, Pakistan.
Hadiya JavedDow University of Health Sciences, Karachi, Pakistan.
Mohammed Mahmmoud Fadelallah EljackCommunity Department , University of Bakhtalruda, Ad Duwaym, 1131, Sudan. m.mahmmoud96@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHER2-positive cancers involve amplification or overexpression of the HER2 gene, leading to aggressive tumor growth across several cancer types, including breast, gastric, ovarian, and pancreatic cancers. Detection methods such as immunohistochemistry, next-generation sequencing, and fluorescence in situ hybridization are used, with new advancements like biosensors and circulating tumor DNA offering improved diagnostic potential. Treatment strategies have evolved, including anti-HER2 drugs like trastuzumab and newer agents like zanidatamab, which show promise against HER2-positive malignancies.

methodsA comprehensive search of the following academic databases was performed including PubMed, Cochrane Library, and clinicaltrials.gov. A detailed search string was made. Studies were selected based on whether they contained the keywords and if they reported the details of treatment for zanidatamab. A total of 16 studies were selected. Abstracts were independently examined by one author and critically reviewed by another and if there were any conflicting viewpoints they were discussed until consensus was reached. DISCUSSION: Zanidatamab has shown promising clinical outcomes in several HER2-positive cancers, including biliary tract, breast, gastric, and lung cancers, with high disease control rates and progression-free survival. Although it is not yet FDA-approved, it has received priority review for HER2-positive biliary tract cancer, with an FDA decision expected in November 2024. The safety profile of zanidatamab has been well-studied. The most common side effects include diarrhea, infusion reactions, and other mild to moderate treatment-related adverse events. In combination with Palbociclib for HER2-positive breast cancer, more severe side effects were observed, resulting in some patients discontinuing treatment. However, no treatment-related deaths have been reported across trials. While its anticancer efficacy and manageable safety profile are promising, long-term safety and efficacy data are still needed. Early clinical trials demonstrate strong efficacy, though some side effects, such as diarrhea and decreased ejection fraction, were noted. Future research should focus on understanding potential resistance mechanisms and establishing zanidatamab's broader role in the treatment landscape of HER2-positive cancers.

conclusionIn summary, zanidatamab has shown significant tumor response, progression-free survival, disease control, and improved quality of life in early trials, however, the lack of long-term safety and efficacy data remains a key limitation, requiring further research.

Indexed as

Antineoplastic AgentsErb-b2 Receptor Tyrosine KinasesNeoplasmsAntibodies, BispecificBreast NeoplasmsFemaleHumansAntibodies, BispecificAntineoplastic AgentsERBB2 protein, humanErb-b2 Receptor Tyrosine KinaseszanidatamabBispecific antibodyEfficacyHER2MalignanciesOutcomeTargeted therapyZanidatamab

Identifiers

PMID40025472
PMCPMC11871714

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.