Evidence map›Paper›PMID 41970411›Full record

ArticleHealth science reports2026

Advancing the Diagnosis of Non-Hodgkin Lymphoma Through Next-Generation Sequencing in Developing Countries: An Evaluation of Progress-A Narrative Review.

Mohammadreza Saeidnia, Mehdi Shokri, Hassan Nourmohammadi, Safa Radmehr, Mashallah Babashahi, Mohamad Moradi, Maryam Karimian, Mohammad Panji, Elahe Motevaseli

Abstract read
In one paragraph

Article in Health science reports, 2026. 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. 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

9 authors.

Mohammadreza SaeidniaDepartment of Hematology, School of Paramedical Shiraz University of Medical Sciences Shiraz Iran.ORCID https://orcid.org/0000-0002-9632-4493
Mehdi ShokriDepartment of Pediatrics, School of Medicine, Imam Khomeini Hospital Ilam University of Medical Sciences Ilam Iran.
Hassan NourmohammadiDepartment of Internal Medicine, Razi Hospital Ilam University of Medical Sciences Ilam Iran.
Safa RadmehrThalassemia & Hemoglobinopathy Research Center, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences Ahvaz Iran.
Mashallah BabashahiDepartment of Pathobiology, School of Medicine Ilam University of Medical Sciences Ilam Iran.
Mohamad MoradiDepartment of Pediatrics, School of Medicine, Imam Khomeini Hospital Ilam University of Medical Sciences Ilam Iran.
Maryam KarimianBrigham and Women's Hospital Harvard Medical School Brigham and Women's Hospital. Boston Boston Massachusetts USA.
Mohammad PanjiDepartment of Molecular Medicine School of Advance Technologies in Medical Tehran University of Medical Sciences Tehran Iran.
Elahe MotevaseliDepartment of Molecular Medicine School of Advance Technologies in Medical Tehran University of Medical Sciences Tehran Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Non-Hodgkin lymphoma (NHL) is the most prevalent hematological malignancy worldwide and accounts for approximately 3% of all cancer cases and fatalities. Next-generation sequencing (NGS) has advanced molecular diagnosis and targeted treatment in developed countries. However, developing countries face barriers like limited infrastructure, funding, and expertise, hindering wide NGS adoption. This narrative review evaluates the progress, challenges, and feasibility of using NGS for NHL diagnosis in developing countries. Methods: A comprehensive narrative literature review was conducted. We searched the PubMed, Scopus, and Google Scholar databases for relevant English-language articles published between January 2008 and December 2025. The focus was on synthesizing evidence from studies applying NGS for NHL diagnosis, with particular emphasis on data from developing countries and comparisons with advancements in developed regions. Results: NGS has improved NHL subclassification accuracy and identified clinically relevant mutations, enabling personalized therapies. Studies from China, India, and South Africa demonstrate successful implementation of panel-based NGS strategies. Despite this, challenges persist, including high costs, lack of standardized protocols, infrastructural deficits, and workforce shortages, limiting broader utilization in resource-limited settings. Collaborative efforts and investments have begun to address these issues in some developing countries. Conclusion: NGS promises significant benefits in NHL diagnosis and management in developing countries. Overcoming financial, technical, and training barriers through targeted policies, funding, and international cooperation is crucial to harnessing its full potential. With ongoing advancements, NGS is poised to become a crucial tool for diagnosis and guiding therapy worldwide, including in resource-limited settings.

Indexed as

developing countriesdiagnosisnext‐generation sequencingNHL

Identifiers

PMID41970411
PMCPMC13069596

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Registered trials

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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.