Myelodysplastic syndromes with del(5q): indications and strategies for cytogenetic testing.

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Myelodysplastic syndromes with del(5q): indications and strategies for cytogenetic testing. / Haferlach, Claudia; Bacher, Ulrike; Tiu, Ramon; Maciejewski, Jaroslaw P; List, Alan.

in: CANCER GENET-NY, Jahrgang 187, Nr. 2, 2, 2008, S. 101-111.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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Haferlach C, Bacher U, Tiu R, Maciejewski JP, List A. Myelodysplastic syndromes with del(5q): indications and strategies for cytogenetic testing. CANCER GENET-NY. 2008;187(2):101-111. 2.

Bibtex

@article{33851280404b44a2af21c98a3d403e24,
title = "Myelodysplastic syndromes with del(5q): indications and strategies for cytogenetic testing.",
abstract = "Cytogenetics is a major predictor of disease behavior and treatment outcome in myelodysplastic syndromes (MDS). Deletion of the long arm of chromosome 5, del(5q), is the most common chromosomal abnormality found in patients with MDS. The development of lenalidomide (Revlimid; Celgene, Summit, NJ) as an effective targeted therapy for low/intermediate-risk MDS with a del(5q) has increased the importance of karyotyping in disease management. In the present review, the importance of an accurate cytogenetic diagnosis in del(5q) MDS, its impact on prognosis, and the effect it can have on the choice of treatment was discussed. In addition, the strengths and limitations of conventional and novel cytogenetic testing techniques currently available for patients with del(5q) MDS were evaluated. A practical diagnostic algorithm was provided to help facilitate the early detection and optimal treatment of MDS patients with a del(5q) abnormality. While the gold standard for genetic testing remains metaphase karyotyping, emerging novel molecular techniques such as fluorescence in situ hybridization may provide clinically valuable complementary and supplemental data.",
author = "Claudia Haferlach and Ulrike Bacher and Ramon Tiu and Maciejewski, {Jaroslaw P} and Alan List",
year = "2008",
language = "Deutsch",
volume = "187",
pages = "101--111",
journal = "CANCER GENET-NY",
issn = "2210-7762",
publisher = "Elsevier BV",
number = "2",

}

RIS

TY - JOUR

T1 - Myelodysplastic syndromes with del(5q): indications and strategies for cytogenetic testing.

AU - Haferlach, Claudia

AU - Bacher, Ulrike

AU - Tiu, Ramon

AU - Maciejewski, Jaroslaw P

AU - List, Alan

PY - 2008

Y1 - 2008

N2 - Cytogenetics is a major predictor of disease behavior and treatment outcome in myelodysplastic syndromes (MDS). Deletion of the long arm of chromosome 5, del(5q), is the most common chromosomal abnormality found in patients with MDS. The development of lenalidomide (Revlimid; Celgene, Summit, NJ) as an effective targeted therapy for low/intermediate-risk MDS with a del(5q) has increased the importance of karyotyping in disease management. In the present review, the importance of an accurate cytogenetic diagnosis in del(5q) MDS, its impact on prognosis, and the effect it can have on the choice of treatment was discussed. In addition, the strengths and limitations of conventional and novel cytogenetic testing techniques currently available for patients with del(5q) MDS were evaluated. A practical diagnostic algorithm was provided to help facilitate the early detection and optimal treatment of MDS patients with a del(5q) abnormality. While the gold standard for genetic testing remains metaphase karyotyping, emerging novel molecular techniques such as fluorescence in situ hybridization may provide clinically valuable complementary and supplemental data.

AB - Cytogenetics is a major predictor of disease behavior and treatment outcome in myelodysplastic syndromes (MDS). Deletion of the long arm of chromosome 5, del(5q), is the most common chromosomal abnormality found in patients with MDS. The development of lenalidomide (Revlimid; Celgene, Summit, NJ) as an effective targeted therapy for low/intermediate-risk MDS with a del(5q) has increased the importance of karyotyping in disease management. In the present review, the importance of an accurate cytogenetic diagnosis in del(5q) MDS, its impact on prognosis, and the effect it can have on the choice of treatment was discussed. In addition, the strengths and limitations of conventional and novel cytogenetic testing techniques currently available for patients with del(5q) MDS were evaluated. A practical diagnostic algorithm was provided to help facilitate the early detection and optimal treatment of MDS patients with a del(5q) abnormality. While the gold standard for genetic testing remains metaphase karyotyping, emerging novel molecular techniques such as fluorescence in situ hybridization may provide clinically valuable complementary and supplemental data.

M3 - SCORING: Zeitschriftenaufsatz

VL - 187

SP - 101

EP - 111

JO - CANCER GENET-NY

JF - CANCER GENET-NY

SN - 2210-7762

IS - 2

M1 - 2

ER -