Publication details
Gain of 1q21 Is an Unfavorable Genetic Prognostic Factor for Multiple Myeloma Patients Treated with High
-Dose Chemotherapy
| Basic information | |
|---|---|
| Original title: | Gain of 1q21 Is an Unfavorable Genetic Prognostic Factor for Multiple Myeloma Patients Treated with High -Dose Chemotherapy |
| Authors: | Pavel Němec, Zuzana Zemanová, Henrieta Grešliková, Kyra Michalová, Hana Filková, Jana Tajtlová, Dana Králová, Renata Kupská, Jan Smetana, Marta Krejčí, Luděk Pour, Lenka Zahradová, Viera Sandecká, Zdeněk Adam, Tomáš Büchler, Ivan Špička, Evžen Gregora, Petr Kuglík, Roman Hájek |
| Further information | |
|---|---|
| Citation: | NĚMEC, Pavel, Zuzana ZEMANOVÁ, Henrieta GREŠLIKOVÁ, Kyra
MICHALOVÁ, Hana FILKOVÁ, Jana TAJTLOVÁ, Dana KRÁLOVÁ, Renata
KUPSKÁ, Jan SMETANA, Marta KREJČÍ, Luděk POUR, Lenka ZAHRADOVÁ,
Viera SANDECKÁ, Zdeněk ADAM, Tomáš BÜCHLER, Ivan ŠPIČKA, Evžen
GREGORA, Petr KUGLÍK and Roman HÁJEK. Gain of 1q21 Is an
Unfavorable Genetic Prognostic Factor for Multiple Myeloma
Patients Treated with High -Dose Chemotherapy. Biology of Blood
and Marrow Transplantation, USA: Carden Jennings Publishing,
2010, vol. 16, No 4, p. 548 -554. ISSN 1083 -8791.Export BibTeX |
| Original language: | English |
| Field: | Oncology and hematology |
| Type: | Article in Periodical |
| Keywords: | Multiple myeloma; 1q21 Gain; Survival; Chromosomal aberrations; Fluorescein in situ hybridization |
The prognostic significance of 1q21 gain, del(13)(q14), del(17)(p13), t(4;14)(p16.3;q32), and t(11;14)(q13;q32) detected by interphase fluorescein in situ hybridization (FISH) was studied in a cohort of 91 patients with newly diagnosed multiple myeloma (MM). 1q21 gain was detected in 37 of 91 patients (40.7%). In comparison with patients lacking 1q21 gain, patients with 1q21 gain had significantly shorter progression-free survival (PFS) (14.9 versus 27.4 months; P = .044) and worse 4-year overall survival (OS) (40.1% versus 76.2% of patients; P = <.001). PFS or OS were not influenced by the presence or absence of the other studied chromosomal abnormalities. Although the occurrence of 1q21 gain correlated with deletion of 13q14, the presence of 1q21 gain can be considered an independent prognostic factor, as no impact of del(13)(q14) as an isolated chromosomal abnormality on either PFS or OS has been observed. We conclude that 1q21 gain defines a prognostically unfavorable group of MM patients.
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