American journal of hematology
October 4, 2026 · via Europe PMC
Chromosomal Abnormalities, Drug Sensitivity and Resistance in Hematological Malignancies: A Comprehensive Overview by the Francophone Group of Hematological Cytogenetics (GFCH).
Nguyen-Khac F, Bidet A, Chapiro E, +13 more, Véronèse L.
AI summary — for doctors, generated from the abstract only
This review links chromosomal abnormalities in hematological malignancies to drug sensitivity and resistance, and notes the rise of alteration-driven therapy.
What was studied
A comprehensive review by the Francophone Group of Hematological Cytogenetics of chromosomal abnormalities associated with drug response.
Key findings
- Some agents such as TKIs, menin inhibitors and venetoclax are used across entities sharing common molecular lesions
- Others remain disease-specific, such as in Helicobacter pylori-associated lymphomas
- Chromosomal abnormalities have a major clinical impact on treatment strategies
Clinical relevance
It is a reference for matching cytogenetic findings to targeted therapy.
Who should care
Limitations
A narrative review, with the available abstract lacking specifics.
Use cytogenetic results to guide targeted therapy choices; consult the full review for details.
This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.
Abstract
Chromosomal abnormalities have a major clinical impact on hematological malignancies, particularly with regard to treatment strategies. To preserve and consolidate fundamental knowledge in this rapidly evolving field, the Francophone Group of Hematological Cytogenetics (Groupe Francophone de Cytogénétique Hématologique, GFCH) conducted a comprehensive review of chromosomal abnormalities associated with drug sensitivity and resistance in hematological disorders. This work highlights the emergence of alteration-driven therapy, with certain agents (e.g., tyrosine kinase inhibitors, menin inhibitors, venetoclax) used across entities sharing common molecular lesions, while others remain disease-specific, such as in Helicobacter pylori-associated lymphomas.
DOI
10.1002/ajh.70499
PMID
42830228
Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.
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