Evidence map›Paper›PMID 41426155›Full record

ArticleSouth Asian journal of cancer2025

A Study of Molecular Subtypes (Profile) of Colorectal Cancer and Their Correlation with Clinical and Pathological Profile in a Tertiary Care Center in India.

Srujana Joga, Sumit Goyal, Anurag Mehta, Manish Sharma, Venkata Pradeep Babu Koyyala, Pankaj Goyal, Chaturbhuj Aggarwal, M Shiv Shankara Swamy, Amrith B Patel, Shrinidhi Nathany and 8 more

Abstract read
In one paragraph

Article in South Asian journal of cancer, 2025. 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

18 authors.

Srujana JogaDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.ORCID 0000-0001-9083-7100
Sumit GoyalDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.
Anurag MehtaDepartment of Histopathology, Molecular Diagnostics and Research, RGCIRC, Rohini, Delhi, India.
Manish SharmaDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.
Venkata Pradeep Babu KoyyalaDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.ORCID 0000-0002-3968-8354
Pankaj GoyalDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.
Chaturbhuj AggarwalDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.
M Shiv Shankara SwamyDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.
Amrith B PatelDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.ORCID 0000-0002-7066-0173
Shrinidhi NathanyDepartment of Pathology and Molecular Diagnostics, RGCIRC, Rohini, Delhi, India.
Moushumi SuryavanshiMolecular Diagnostics and Cell Biology, RGCIRC, Rohini, Delhi, India.
Anurag SharmaDepartment of Research, RGCIRC, Rohini, Delhi, India.
Satya Narayan SaraswatDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.
Satyajeet SoniDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.ORCID 0000-0003-2564-2619
Arpit JainDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.ORCID 0000-0002-3916-4411
Pallavi RedhuDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.
Vineet TalwarDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.ORCID 0000-0001-9149-6969
D C DovalDepartment of Medical Oncology, RGCIRC, Rohini, Delhi, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Colorectal cancer (CRC) is a heterogeneous disease morphologically, histologically, and molecularly. Most of the studies are on this molecular heterogeneity and their clinicopathological correlation from the western world. Very few studies have been done in India. Objectives: The aims of this study were to evaluate the clinical and pathological profile of CRCs, to determine the frequency of molecular subtypes of CRCs, to correlate between the molecular subtypes and their clinicopathological features, and to determine the association between different molecular subtypes of CRC. Materials and Methods: A prospective noninvasive interventional study was done on 50 patients (both outpatients and inpatients) with newly diagnosed CRCs presenting to the Rajiv Gandhi Cancer Institute and Research Centre, Rohini, Delhi, from February 2019 to March 2020. Clinical and histopathological data were collected from case sheets as per the study proforma: history and physical examination, noninvasive and invasive imaging, and histopathological reports. Patients in whom tissue was insufficient or not available for testing for at least three of five molecular markers (KRAS, NRAS, BRAF, MSI, and MLH1 methylation) were excluded. The results were analyzed with SSPS 23.0 software. For comparison of the frequencies among groups, the chi-squared test and the Fisher exact test were used. A Results: The median age was 53 years. The majority of the males (54%) had CRC and 44% were right-sided colon tumors. Of the 50 patients with CRC, 40, 0, 4, and 4% had KRAS mutation, NRAS and BRAF mutation, and deficient mismatch repair (dMMR), respectively. KRAS mutation was significantly associated with upfront liver metastases ( Conclusion: In conclusion, this is a prospective study evaluating the correlations between RAS/BRAF mutation and dMMR status with clinicopathological characteristics in Indian CRC patients, which is slightly similar to worldwide reports with some exceptions. To the best of our knowledge, this is the first study to evaluate the molecular marker combinations in CRC in India.

Indexed as

clinicalcolorectal cancercorrelationIndiamolecular subtypespathologicalprofile

Identifiers

PMID41426155
PMCPMC12714463

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