| Literature DB >> 16737912 |
Yuko Ishii1, Hui-Hua Hsiao, Goro Sashida, Yoshikazu Ito, Keisuke Miyazawa, Atsushi Kodama, Junko H Ohyashiki, Kazuma Ohyashiki.
Abstract
Therapy-related myelodysplastic syndrome (MDS) is a major problem in long-term cancer survivors, therefore early detection and prevention of therapy-related secondary neoplasia is an important issue. We searched for therapy-related MDS and analyzed cytogenetic changes in 155 patients with multiple myeloma (MM) from a single institution. Of the total 155 MM patients with cytogenetic results, 7 patients showed de novo appearance of myeloid-related cytogenetic changes, and 5/7 had -7/7q-, including 3 with der(1;7)(q10;p10): 3 patients developed MDS (i.e. 2 patients with der(1;7)(q10;p10) and 1 with a complex abnormality including -5 and 7q-). Among five patients receiving more than 2 g of melphalan, three developed MDS, and two of them showed der(1;7)(q10;p10) before or at the time of MDS diagnosis. Although morphologic identification of MDS was difficult in some cases, we concluded that the presence of 7q-, specifically der(1;7)(q10;p10), during chemotherapy involving melphalan for MM patients might indicate hidden MDS status and appropriate therapeutic options should be considered for such patients.Entities:
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Year: 2006 PMID: 16737912 DOI: 10.1016/j.cancergencyto.2006.01.002
Source DB: PubMed Journal: Cancer Genet Cytogenet ISSN: 0165-4608