PMID- 10673522 OWN - NLM STAT- MEDLINE DCOM- 20000713 LR - 20221109 IS - 0732-183X (Print) IS - 0732-183X (Linking) VI - 18 IP - 4 DP - 2000 Feb TI - Predictive role of interphase cytogenetics for survival of patients with multiple myeloma. PG - 804-12 AB - PURPOSE: Recent metaphase cytogenetic studies suggested that specific chromosomal abnormalities are of prognostic significance in patients with multiple myeloma (MM). Because the true incidence of chromosomal abnormalities in MM is much higher than that detected by metaphase analysis, we used interphase fluorescence in situ hybridization (FISH) to determine the prognostic value of specific chromosomal aberrations. PATIENTS AND METHODS: Bone marrow plasma cells from 89 previously untreated patients with MM were studied consecutively by FISH to detect the deletions of 13q14, 17p13, and 11q and the presence of t(11;14)(q13;q32). FISH results were analyzed in the context of clinical parameters (response to treatment and survival after conventional-dose chemotherapy), and a multivariate analysis of prognostic factors was performed. RESULTS: By FISH, the deletion of 13q14 occurred in 40 patients (44.9%), deletion of 17p13 in 22 (24.7%), and 11q abnormalities in 14 (15.7%; seven with t(11;14)). Deletions of 13q14 and 17p13 were associated with poor response to induction treatment (46.9% v 77.3% in those without deletions, P =.006 and 40.0% v 73.2%, P =.008, respectively) and short median overall survival (OS) time (24.2 v 88.1 months, P =. 008 and 16.2 v 51.3 months, P =.008, respectively). Short median OS time was also observed for patients with 11q abnormalities (13.1 v 41.6 months, P =.02). According to the number of unfavorable cytogenetic features (deletion of 13q14, deletion of 17p13, and aberrations of 11q) that were present in each patient (0 v 1 v 2 or 3), patients with significantly different OS times could be discriminated from one another (102.4 v 29.6 v 13.9 months, P <.001, respectively). CONCLUSION: For patients with MM who were treated with conventional-dose chemotherapy, interphase FISH for 13q14, 17p13, and 11q provides prognostically relevant information in addition to that provided by standard prognostic factors. This observation may be considered for risk-adapted stratifications of MM patients in future clinical trials. FAU - Konigsberg, R AU - Konigsberg R AD - First Department of Internal Medicine, Divisions of Clinical Oncology, University of Vienna, Vienna, Austria. FAU - Zojer, N AU - Zojer N FAU - Ackermann, J AU - Ackermann J FAU - Kromer, E AU - Kromer E FAU - Kittler, H AU - Kittler H FAU - Fritz, E AU - Fritz E FAU - Kaufmann, H AU - Kaufmann H FAU - Nosslinger, T AU - Nosslinger T FAU - Riedl, L AU - Riedl L FAU - Gisslinger, H AU - Gisslinger H FAU - Jager, U AU - Jager U FAU - Simonitsch, I AU - Simonitsch I FAU - Heinz, R AU - Heinz R FAU - Ludwig, H AU - Ludwig H FAU - Huber, H AU - Huber H FAU - Drach, J AU - Drach J LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Clin Oncol JT - Journal of clinical oncology : official journal of the American Society of Clinical Oncology JID - 8309333 SB - IM MH - Antineoplastic Combined Chemotherapy Protocols/therapeutic use MH - Bone Marrow Cells/pathology MH - Chromosome Aberrations/*genetics MH - Chromosome Deletion MH - Chromosome Disorders MH - Chromosomes, Human, Pair 11/genetics MH - Chromosomes, Human, Pair 13/genetics MH - Chromosomes, Human, Pair 17/genetics MH - Cytogenetics MH - Female MH - Forecasting MH - Humans MH - In Situ Hybridization, Fluorescence MH - Incidence MH - Interphase/*genetics MH - Male MH - Metaphase/genetics MH - Middle Aged MH - Multiple Myeloma/drug therapy/*genetics/pathology MH - Multivariate Analysis MH - Plasma Cells/pathology MH - Prognosis MH - Regression Analysis MH - Remission Induction MH - Survival Rate MH - Trisomy/genetics EDAT- 2000/02/16 09:00 MHDA- 2000/07/15 11:00 CRDT- 2000/02/16 09:00 PHST- 2000/02/16 09:00 [pubmed] PHST- 2000/07/15 11:00 [medline] PHST- 2000/02/16 09:00 [entrez] AID - 10.1200/JCO.2000.18.4.804 [doi] PST - ppublish SO - J Clin Oncol. 2000 Feb;18(4):804-12. doi: 10.1200/JCO.2000.18.4.804.