| Literature DB >> 30423479 |
Hiroyuki Takamatsu1, Takeshi Yamashita2, Shingo Kurahashi3, Takayuki Saitoh4, Tadakazu Kondo5, Takeshi Maeda6, Hideyuki Nakazawa7, Makoto Murata8, Tomoko Narita9, Junya Kuroda10, Hisako Hashimoto11, Koji Kawamura12, Toshihiro Miyamoto13, Sumihisa Honda14, Tatsuo Ichinohe15, Yoshiko Atsuta16, Kazutaka Sunami17.
Abstract
Conventional cytogenetic analyses and fluorescent in situ hybridization (FISH) are helpful for stratifying patients with multiple myeloma (MM) into high-risk [t(4;14), t(14;16), and/or del 17p] and standard-risk [t(11;14)] categories. However, the prognosis of patients with MM treated with autologous stem cell transplantation (ASCT) stratified according to these categories remains unclear. This retrospective observational study analyzed 97 patients with MM who received a single, planned ASCT after treatment with 200 mg/m2 melphalan between 2001 and 2011. The patients were grouped according to chromosomal abnormality, including t(11;14) (n = 45), t(4;14) (n = 31), del 17p (n = 10), t(11;14) with del 17p (n = 7), and t(4;14) with del 17p (n = 4). Median overall survival (OS) of the t(11;14) group (64.1 months) was not significantly different from that of the t(4;14) group (not reached), but it was significantly longer than that of the del 17p group (23.0 months; P = .002). G-banding revealed that the median OS of the t(11;14) group with additional chromosomal abnormalities (ACAs) (46.2 months) was significantly shorter than that of the t(11;14) group without ACAs (not reached; P = .005) and the t(4;14) group (not reached; P = .010). These findings highlight the importance of G-banding in patients with t(11;14) MM.Entities:
Keywords: Autologous stem cell transplantation; Multiple myeloma; t(11;14)
Mesh:
Year: 2018 PMID: 30423479 DOI: 10.1016/j.bbmt.2018.11.003
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742