Evidence map›Paper›PMID 42620816›Full record

ReviewTherapeutic advances in hematology2026

Isolated del(5q) with myeloproliferative driver mutations: A systematic review of published cases and clinical implications.

Mohammed Abdulgayoom, Abdulrahman F Al-Mashdali, Awni Alshurafa, Mohammad S Afana, Anas M Babiker, Mohammad Bakheet, Shehab F Mohamed, Mohamed A Yassin

Abstract readReview
In one paragraph

Review in Therapeutic advances in hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

8 authors.

Mohammed AbdulgayoomDepartment of Hematology, Hamad Medical Corporation, National Center for Cancer Care and Research, Doha, Qatar.ORCID https://orcid.org/0000-0003-0622-8455
Abdulrahman F Al-MashdaliDepartment of Hematology, Hamad Medical Corporation, National Center for Cancer Care and Research, Doha, Qatar.ORCID https://orcid.org/0000-0002-1393-5302
Awni AlshurafaDepartment of Hematology, Hamad Medical Corporation, National Center for Cancer Care and Research, Doha, Qatar.ORCID https://orcid.org/0000-0002-4454-5307
Mohammad S AfanaDepartment of Hematology, Hamad Medical Corporation, National Center for Cancer Care and Research, Doha, Qatar.
Anas M BabikerDepartment of Hematology, Hamad Medical Corporation, National Center for Cancer Care and Research, Doha, Qatar.
Mohammad BakheetCollege of Medicine, Omdurman Islamic University, Khartoum, Sudan.
Shehab F MohamedDepartment of Hematology, Hamad Medical Corporation, National Center for Cancer Care and Research, Doha, Qatar.
Mohamed A YassinDepartment of Hematology, Hamad Medical Corporation, National Center for Cancer Care and Research, Doha, Qatar.ORCID https://orcid.org/0000-0002-1144-8076

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Myeloid neoplasms harboring both an isolated deletion of chromosome 5q (del(5q)) and myeloproliferative neoplasm (MPN) driver mutations ( Methods: We systematically reviewed published case reports and case series of adult patients with myeloid neoplasms and concomitant isolated del(5q) and MPN driver mutations. A comprehensive search of PubMed and Google Scholar from inception through 31 December 2024 was performed using terms related to "del(5q)", " Results: Twenty publications reporting 24 patients (diagnosed between 2006 and 2021) met the inclusion criteria. The median age was 70.5 years with a female predominance. Most patients presented with macrocytic anemia, thrombocytosis, and megakaryocytic dysplasia, frequently accompanied by marrow fibrosis. Conclusion: Reported cases with isolated del(5q) and an MPN driver mutation suggest a rare overlap presentation with mixed dysplastic and proliferative features. Lenalidomide appears to provide hematologic and cytogenetic benefit in some patients, although molecular persistence and progression to AML have been observed. Given the limited number and heterogeneity of published cases, these observations should be interpreted with caution. Larger, systematically collected datasets are needed to better understand the clinical significance and optimal management of this combination.

Indexed as

CALRdel(5q)JAK2 V617FMDS/MPN overlapMPLmyeloid neoplasms

Identifiers

PMID42620816
PMCPMC13487117

What OpenQuestion holds

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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.