Evidence map›Paper›PMID 40351324›Full record

ArticleTherapeutic advances in medical oncology2025

Next-generation sequencing in the management of cancer: an evaluation of the clinical effectiveness in Jordan.

Yousef Abbasi, Omar Altamimi, Majdi Al-Shehab, Hamza Nabulsi, Salah Abbasi

Abstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 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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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Yousef AbbasiSchool of Medicine, University of Jordan, Queen Rania Street, Amman 11942, Jordan.ORCID https://orcid.org/0009-0005-1546-7636
Omar AltamimiSchool of Medicine, University of Jordan, Amman, Jordan.ORCID https://orcid.org/0009-0007-3898-3152
Majdi Al-ShehabSchool of Medicine, University of Jordan, Amman, Jordan.ORCID https://orcid.org/0009-0002-1636-4944
Hamza NabulsiSchool of Medicine, University of Jordan, Amman, Jordan.ORCID https://orcid.org/0009-0004-8475-6442
Salah AbbasiOncology, Al Khalidi Hospital, Amman, Jordan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The widespread use of next-generation sequencing (NGS) panels to guide targeted therapies in advanced malignancies raises questions regarding their real-world impact on clinical outcomes and affordability. Objectives: The study aims to find trends in targetable genetic alterations among late-stage cancer patients in the Jordanian population and to assess the clinical effectiveness of NGS testing in Jordan. Design: This article is a retrospective observational analysis. Data extracted from patient files were used to determine genetic alteration trends and for a comparative assessment of progression-free survival (PFS) between patients receiving NGS-guided personalized treatment compared to those receiving conventional treatment. Methods: Two hundred thirteen nonselected late-stage cancer patients from three Jordanian hospitals (2019-2024) were included in this study. Key data points included demographics, genetic variations, and treatment details. Statistical analysis involved the use of the Cox proportional hazards model to evaluate PFS between the two groups of patients. Results: Clinically significant genetic alterations were found in 89 patients (42%), with the most common genes being KRAS (20%), PIK3CA (9%), ERBB2 (7%), EGFR (6%), and BRCA1 and 2 (1.5% each). Microsatellite instability-high status was seen in 8 patients (3.7%). Out of the 89 patients with targetable genetic variations, 80.9% received their recommended NGS-guided treatments, while 19.1% did not due to cost or drug unavailability. PFS was significantly improved for patients receiving NGS-guided targeted treatment compared to conventional treatment in the general population with a hazard ratio (HR) of 0.216, the colorectal cancer population (HR of 0.185), the breast cancer population (HR of 0.239), and the lung cancer population (HR of 0.089). Conclusion: NGS testing is a very beneficial tool for patients with advanced malignancies to select targeted therapies and potentially improve survival. However, the incorporation of NGS testing in Jordan faces challenges such as high testing and treatment costs and drug unavailability.

Indexed as

cancer genomicseconomic burden of cancergenomicslate-stage cancernext-generation sequencingtargeted therapy

Identifiers

PMID40351324
PMCPMC12062634

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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.