Lessons From Pediatric MDS: Approaches to Germline Predisposition to Hematologic Malignancies
Serine Avagyan,Akiko Shimamura +1 more
TL;DR: A framework for the evaluation of germline predisposition to MDS across all ages is presented, and characteristics of personal and family history, clinical exam and laboratory findings, and integration of genetic sequencing results are discussed to assist in the diagnostic evaluation.
read more
Abstract: Pediatric myelodysplastic syndromes (MDS) often raise concern for an underlying germline predisposition to hematologic malignancies, referred to as germline predisposition herein. With the availability of genetic testing, it is now clear that syndromic features may be lacking in patients with germline predisposition. Many genetic lesions underlying germline predisposition may also be mutated somatically in de novo MDS and leukemias, making it critical to distinguish their germline origin. The verification of a suspected germline predisposition informs therapeutic considerations, guides monitoring pre- and post-treatment, and allows for family counseling. Presentation of MDS due to germline predisposition is not limited to children and spans a wide age range. In fact, the risk of MDS may increase with age in many germline predisposition conditions and can present in adults who lack classical stigmata in their childhood. Furthermore, germline predisposition associated with DDX41 mutations presents with older adult-onset MDS. Although a higher proportion of pediatric patients with MDS will have a germline predisposition, the greater number of MDS diagnoses in adult patients may result in a larger overall number of those with an underlying germline predisposition. In this review, we present a framework for the evaluation of germline predisposition to MDS across all ages. We discuss characteristics of personal and family history, clinical exam and laboratory findings, and integration of genetic sequencing results to assist in the diagnostic evaluation. We address the implications of a diagnosis of germline predisposition for the individual, for their care after MDS therapy, and for family members. Studies on MDS with germline predisposition have provided unique insights into the pathogenesis of hematologic malignancies and mechanisms of somatic genetic rescue vs. disease progression. Increasing recognition in adult patients will inform medical management and may provide potential opportunities for the prevention or interception of malignancy.
read more
Chat with Paper
AI Agents for this Paper
Find similar papers on Google Scholar, PubMed and Arxiv
Write a critical review of this paper
Analyze citations of this paper to find unaddressed research gaps
Citations
Myelodysplastic syndromes.
TL;DR: Therapeutic goals in people with higher-risk MDS include decreasing the risk of AML transformation and prolonging survival, and how, when and in which patients with HCT for MDS should be performed remains controversial.
38
Myelodysplastic neoplasms: An overview on diagnosis, risk-stratification, molecular pathogenesis, and treatment.
TL;DR: In this paper , the Revised International Prognostic Scoring System (RIPS) was used to assess the risk of myelodysplastic neoplasms (MDS).
7
Optimizing diagnostic methods and stem cell transplantation outcomes in pediatric bone marrow failure: a 50-year single center experience.
TL;DR: Management guidelines and HSCT outcomes of pediatric BMF patients to pinpoint improvements and future challenges and comprehensive approach to identify the cause of BMF can prevent treatment delay and be useful to tailor treatment and follow-up protocols are reported on.
4
Germline Predisposition to Myeloid Neoplasms: Diagnostic Concepts and Classifications.
Ifeyinwa E. Obiorah,Kalpana Upadhyaya,Katherine R. Calvo +2 more
TL;DR: Recognition of myeloid malignancy associated with germline mutations is essential for proper therapy, disease surveillance, informing related donor selection for hematopoietic stem cell transplantation, and genetic counseling of the patient and affected family members.
3
The Times, They Are A-Changing: The Impact of Next-Generation Sequencing on Diagnosis, Classification, and Prognostication of Myeloid Malignancies With Focus on Myelodysplastic Syndrome, AML, and Germline Predisposition
TL;DR: A review of changes in the recently published classifications of AML and myelodysplastic syndrome, emerging prognostic scoring, and the role of germline deleterious variants in predisposing to MDS and AML can be found in this paper .
3
References
How I diagnose and manage individuals at risk for inherited myeloid malignancies.
Jane E. Churpek,Lucy A. Godley +1 more
TL;DR: The methods to identify, test, and manage individuals and families suspected of having a hereditary myeloid malignancy syndrome are presented and the areas of ongoing research in the field are addressed.
Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders
Véronique Latger-Cannard,Christophe Philippe,Alexandre Bouquet,Véronique Baccini,Marie-Christine Alessi,Annick Ankri,Anne Bauters,Sophie Bayart,Pascale Cornillet-Lefebvre,Sylvie Daliphard,Marie-Joelle Mozziconacci,Aline Renneville,Paola Ballerini,Guy Leverger,Hagay Sobol,Philippe Jonveaux,Claude Preudhomme,Paquita Nurden,Thomas Lecompte,Rémi Favier +19 more
TL;DR: Platelet dysfunction suggestive of defective δ-granule release could be of values for the diagnosis of FPD/AML particularly when the clinical presentation is an autosomal dominant thrombocytopenia with normal platelet size in the absence of familial malignancies.
Valves Are a Conserved Feature of the Zebrafish Lymphatic System.
Masahiro Shin,Takayuki Nozaki,Feston Idrizi,Sumio Isogai,Katsutoshi Ogasawara,Kinji Ishida,Shinya Yuge,Benjamin P. Roscoe,Scot A. Wolfe,Shigetomo Fukuhara,Naoki Mochizuki,Tomonori Deguchi,Nathan D. Lawson +12 more
TL;DR: In this article, functional and morphological evidence of valves in the zebrafish lymphatic system was provided, while live imaging using transgenic lines identified the developmental origins of lymphatic valve progenitors.
ERCC6L2 defines a novel entity within inherited acute myeloid leukemia.
Suvi P. M. Douglas,Pihla Siipola,Panu E. Kovanen,Marja Pyörälä,Sakari Kakko,Eeva-Riitta Savolainen,Urpu Salmenniemi,Katri Orte,Soili Kytölä,Esa Pitkänen,Kimmo Porkka,Outi Kilpivaara,Ulla Wartiovaara-Kautto +12 more
TL;DR: There is a Blood Commentary on this article in this issue of the British Medical Journal that discusses the use of blood transfusions in the treatment of certain types of cancer.