Evidence map›Paper›PMID 40851424›Full record

ArticleCancer reports (Hoboken, N.J.)2025

Human Epidermal Growth Factor Receptor 2 [HER-2/neu] Amplification and Microsatellite Stable Status in Gastric and Gastroesophageal Adenocarcinoma: Assessing Frequency and Prognostic Implications at the Cancer Institute of Iran.

Samaneh Salarvand, Abbas Mohammadi, Reza Shahsiah, Farzaneh Bagheri, Mahsa Gholizadeh, Somayeh Jolany-Vangah, Ebrahim Esmati, Marzieh Lashkari, Vahid Soleymani, Seraj Zareh-Dehabadi and 6 more

Abstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

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

1 citing paper in PubMed.

  1. 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

16 authors.

Samaneh SalarvandDepartment of Clinical and Anatomical Pathology, Cancer Institute, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-1507-4494
Abbas MohammadiDepartment of Ophthalmology, School of Medicine, Ahvaz Joundishapur University of Medical Sciences, Ahvaz, Iran.ORCID 0000-0001-7295-8494
Reza ShahsiahDepartment of Clinical and Anatomical Pathology, Cancer Institute, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Farzaneh BagheriDepartment of Radiation Oncology, Cancer Institute, IKHC, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Mahsa GholizadehDepartment of Radiation Oncology, Cancer Institute, IKHC, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Somayeh Jolany-VangahDepartment of Radiation Oncology, Cancer Institute, IKHC, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Ebrahim EsmatiDepartment of Radiation Oncology, Cancer Institute, IKHC, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Marzieh LashkariRadiation Oncology Research Center, Cancer Research Institute, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0009-0009-3571-7611
Vahid SoleymaniDepartment of Clinical and Anatomical Pathology, Cancer Institute, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Seraj Zareh-DehabadiRadiation Oncology Research Center, Cancer Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
Vahid MehrtashDepartment of Clinical and Anatomical Pathology, Cancer Institute, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Amirmohsen JalaeefarDepartment of Oncosurgery, Cancer Institute, IKHC, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0002-9882-7828
Mohammad ShirkhodaDepartment of Oncosurgery, Cancer Institute, IKHC, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0001-8064-5623
Moones ToosangDepartment of Clinical and Anatomical Pathology, Cancer Institute, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Romina AbyanehRadiation Oncology Research Center, Cancer Research Institute, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-1948-8440
Reza GhalehtakiDepartment of Radiation Oncology, Cancer Institute, IKHC, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-1162-2019

Funding

Tehran University of Medical Sciences and Health Services 95-04-207-33772Tehran University of Medical Sciences and Health Services 97-01-207-38089Tehran University of Medical Sciences and Health Services 97-03-30-40246
6 · The paper itself

Abstract

backgroundMolecular targeted therapy and immunotherapy have shown promise in managing gastric adenocarcinoma. The amplified expression of Human epidermal growth factor receptor-2 (HER-2) and microsatellite stable (MSI) status serve as indicators of response to targeted therapy and immunotherapy, respectively.

aimsThis study assessed the frequency of MSI status and HER-2 expression in a pretreated sample of Iranian patients with gastric and gastroesophageal (GE) adenocarcinoma. METHODS AND

resultsWe conducted HER-2/neu expression and mismatch repair (MMR) system analyses on specimens from patients with gastric and GE adenocarcinoma at the Cancer Institute of Iran. Archival tissues from 135 mainly pre-treated surgical specimens of gastric adenocarcinoma cases were used for HER-2 analysis, and 66 specimens were used for MSI analysis. All specimens were tested for HER-2 amplification, revealing that 11 patients (8.1%) had HER-2 amplification, and three out of 66 examined patients exhibited MSI-H. Patients with HER-2 overexpressed specimens had a shorter median overall survival (OS) compared with HER-2 negative cases (21 months (95% CI: 1.4-40.6) vs. 31 months (95% CI: 22.9-39), p = 0.18). The median disease-free survival (DFS) for HER-2 positive and negative patients was 15 and 28 months, respectively (p = 0.25). The estimated median OS and DFS for patients with negative MSI were 26 and 20 months, respectively. However, none of the patients with MSI-positive status experienced recurrence, metastases, or death within the follow-up period; thus, MSI-H patients had a significantly improved OS and DFS (p = 0.018 and 0.020).

conclusionHER-2 expression, while less common in our Iranian population compared with North American or Western European countries, showed a nonsignificant trend toward poor outcomes in patients with gastric adenocarcinoma. MSI-H status was highly infrequent in our population, suggesting that immunotherapy may not be a beneficial treatment for a significant fraction of Iranian patients with gastric adenocarcinoma. However, a minority may still benefit from it. MSI-H was associated with reduced perineural invasion and improved OS and DFS. Therefore, this hypothesis warrants further investigation in clinical trials to underscore the prognostic significance of HER-2 and MSI status and the value of molecular profiling in guiding personalized treatment strategies.

Indexed as

AdenocarcinomaBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesEsophageal NeoplasmsMicrosatellite InstabilityStomach NeoplasmsAdultAgedAged, 80 and overEsophagogastric JunctionFemaleFollow-Up StudiesGene AmplificationHumansIranMaleBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesAdenocarcinomaDNA mismatch repairGastric neoplasmHER family receptor

Identifiers

PMID40851424
PMCPMC12375872

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