PMID- 31171473 OWN - NLM STAT- MEDLINE DCOM- 20200806 LR - 20200806 IS - 2152-2669 (Electronic) IS - 2152-2669 (Linking) VI - 19 IP - 8 DP - 2019 Aug TI - Role of Conventional Karyotyping in Multiple Myeloma in the Era of Modern Treatment and FISH Analysis. PG - e470-e477 LID - S2152-2650(19)30143-0 [pii] LID - 10.1016/j.clml.2019.04.011 [doi] AB - BACKGROUND: The Revised International Staging System (R-ISS) has been widely adopted to prognosticate multiple myeloma. As a result, the continued utility of conventional metaphase karyotyping has been called into question. PATIENTS AND METHODS: A multi-center study for newly diagnosed patients with multiple myeloma who received novel agent(s) at induction was conducted. Conventional metaphase karyotype information was categorized based on ploidy. We evaluated the impact of ploidy on overall survival (OS) including multivariate analysis, taking into account the R-ISS stages, transplant status, age, and novel agent(s) used at induction. We also evaluated if it is possible to identify high-risk (HR) patients with conventional karyotyping when a fluorescence in situ hybridization analysis is not available. Results were validated in an independent cohort. RESULTS: There were 308 patients evaluable. Ploidy significantly affected the OS of patients with R-ISS stage II, with non-hyperdiploid patients doing the worst. In the multivariate analysis, ploidy was significantly associated with OS. R-ISS stage II patients with or without non-hyperdiploid karyotype had significantly different survival. We replaced HR fluorescence in situ hybridization abnormalities with HR metaphase karyotypic abnormalities (non-hyperdiploid karyotype). When compared with R-ISS, there was a high level of concordance in HR patients identified using HR karyotypic abnormalities. These results were validated with an independent cohort of 375 patients. CONCLUSION: Conventional metaphase karyotyping is an independent prognostic factor even in the setting of R-ISS. CI - Copyright (c) 2019 Elsevier Inc. All rights reserved. FAU - Soekojo, Cinnie Yentia AU - Soekojo CY AD - National University Cancer Institute, National University Health System, Singapore, Singapore. FAU - Wang, Guo-Miao AU - Wang GM AD - Peking University Institute of Hematology, Beijing, China. FAU - Chen, Yunxin AU - Chen Y AD - Department of Hematology, Singapore General Hospital, Singapore, Singapore. FAU - Casan, Joshua AU - Casan J AD - Alfred Hospital, Melbourne, Victoria, Australia. FAU - Wolyncewicz, Grace AU - Wolyncewicz G AD - Alfred Hospital, Melbourne, Victoria, Australia. FAU - Lin, Adeline AU - Lin A AD - National University Cancer Institute, National University Health System, Singapore, Singapore. FAU - Poon, Li Mei AU - Poon LM AD - National University Cancer Institute, National University Health System, Singapore, Singapore. FAU - de Mel, Sanjay AU - de Mel S AD - National University Cancer Institute, National University Health System, Singapore, Singapore. FAU - Koh, Liang Piu AU - Koh LP AD - National University Cancer Institute, National University Health System, Singapore, Singapore. FAU - Tan, Lip Kun AU - Tan LK AD - National University Cancer Institute, National University Health System, Singapore, Singapore. FAU - Ooi, Melissa G AU - Ooi MG AD - National University Cancer Institute, National University Health System, Singapore, Singapore. FAU - Nagarajan, Chandramouli AU - Nagarajan C AD - Department of Hematology, Singapore General Hospital, Singapore, Singapore. FAU - Liu, Yang AU - Liu Y AD - Peking University Institute of Hematology, Beijing, China. FAU - Lai, Yue-Yun AU - Lai YY AD - Peking University Institute of Hematology, Beijing, China. FAU - Huang, Xiao-Jun AU - Huang XJ AD - Peking University Institute of Hematology, Beijing, China. FAU - Spencer, Andrew AU - Spencer A AD - Alfred Hospital, Melbourne, Victoria, Australia. FAU - Gopalakrishnan, Sathish Kumar AU - Gopalakrishnan SK AD - Department of Hematology, Singapore General Hospital, Singapore, Singapore. FAU - Lu, Jin AU - Lu J AD - Peking University Institute of Hematology, Beijing, China. Electronic address: jin1lu@sina.com. FAU - Chng, Wee Joo AU - Chng WJ AD - National University Cancer Institute, National University Health System, Singapore, Singapore; Cancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore. Electronic address: mdccwj@nus.edu.sg. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20190428 PL - United States TA - Clin Lymphoma Myeloma Leuk JT - Clinical lymphoma, myeloma & leukemia JID - 101525386 SB - IM MH - Aged MH - *Chromosome Aberrations MH - Disease Progression MH - Female MH - Follow-Up Studies MH - Hematopoietic Stem Cell Transplantation/*mortality MH - Humans MH - In Situ Hybridization, Fluorescence/*methods MH - Karyotyping/*methods MH - Male MH - Multiple Myeloma/genetics/*pathology/therapy MH - Neoplasm Staging MH - Retrospective Studies MH - Survival Rate MH - Transplantation, Autologous OTO - NOTNLM OT - Chromosomal abnormalities OT - Cytogenetics OT - Myeloma OT - Prognosis OT - Survival EDAT- 2019/06/07 06:00 MHDA- 2020/08/07 06:00 CRDT- 2019/06/08 06:00 PHST- 2019/02/02 00:00 [received] PHST- 2019/04/09 00:00 [revised] PHST- 2019/04/19 00:00 [accepted] PHST- 2019/06/07 06:00 [pubmed] PHST- 2020/08/07 06:00 [medline] PHST- 2019/06/08 06:00 [entrez] AID - S2152-2650(19)30143-0 [pii] AID - 10.1016/j.clml.2019.04.011 [doi] PST - ppublish SO - Clin Lymphoma Myeloma Leuk. 2019 Aug;19(8):e470-e477. doi: 10.1016/j.clml.2019.04.011. Epub 2019 Apr 28.