PMID- 11238092 OWN - NLM STAT- MEDLINE DCOM- 20010426 LR - 20210216 IS - 0006-4971 (Print) IS - 0006-4971 (Linking) VI - 97 IP - 6 DP - 2001 Mar 15 TI - Chromosome 13 abnormalities identified by FISH analysis and serum beta2-microglobulin produce a powerful myeloma staging system for patients receiving high-dose therapy. PG - 1566-71 AB - A careful prognostic evaluation of patients referred for high-dose therapy (HDT) is warranted to identify those who maximally benefit from HDT as well as those who clearly fail current HDT and are candidates for more innovative treatments. In a series of 110 patients with myeloma who received HDT as first-line therapy, times to event (disease progression and death) were studied through proportional hazard models, in relation to different prognostic factors, including a chromosome 13 fluorescence in situ hybridization (FISH) analysis using a D13S319 probe. Delta13 was detected in 42 patients (38%). Follow-up time among surviving patients and survival time were 48 +/- 3 and 51 +/- 7 months, respectively (median +/- SE). In the univariate analysis, Delta13 was the most powerful adverse prognostic factor for all times to event, especially for the survival time (P <.0001) and was followed by beta2-microglobulin (beta2m) levels 2.5 mg/L or higher (P =.0001). The comparison of survival prognostic models including beta2m 2.5 mg/L or greater and another factor favored the Delta13/beta2m combination. In 22 patients (20%) with no unfavorable factor, the median survival time was not reached at 111 months. In contrast, among 55 patients (50%) with one unfavorable factor and 33 patients (30%) with 2 unfavorable factors, median survival times were 47.3 +/- 4.6 months and 25.3 +/- 3.2 months, respectively (P <.0001). We conclude that delta13, adequately detected by FISH analysis, is a very strong factor related to poor survival, especially when associated with a beta2m level of 2.5 mg/L or higher. Routine FISH Delta13 assessment is strongly recommended for patients considered for HDT. FAU - Facon, T AU - Facon T AD - Service d'Hematologie and Laboratoire de Genetique Medicale, Lille, France. t-facon@chru-lille.fr FAU - Avet-Loiseau, H AU - Avet-Loiseau H FAU - Guillerm, G AU - Guillerm G FAU - Moreau, P AU - Moreau P FAU - Genevieve, F AU - Genevieve F FAU - Zandecki, M AU - Zandecki M FAU - Lai, J L AU - Lai JL FAU - Leleu, X AU - Leleu X FAU - Jouet, J P AU - Jouet JP FAU - Bauters, F AU - Bauters F FAU - Harousseau, J L AU - Harousseau JL FAU - Bataille, R AU - Bataille R FAU - Mary, J Y AU - Mary JY CN - Intergroupe Francophone du Myelome LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Blood JT - Blood JID - 7603509 RN - 0 (beta 2-Microglobulin) SB - IM MH - Actuarial Analysis MH - Adult MH - Aged MH - Antineoplastic Combined Chemotherapy Protocols/administration & dosage/therapeutic use MH - Chromosome Aberrations/*genetics MH - Chromosome Disorders MH - Chromosomes, Human, Pair 13/*genetics MH - Dose-Response Relationship, Drug MH - Drug Monitoring/methods MH - Follow-Up Studies MH - Humans MH - In Situ Hybridization, Fluorescence MH - Middle Aged MH - Multiple Myeloma/blood/*genetics/*pathology MH - Neoplasm Staging/*methods MH - Prognosis MH - Risk Factors MH - Severity of Illness Index MH - Treatment Outcome MH - beta 2-Microglobulin/*blood EDAT- 2001/03/10 10:00 MHDA- 2001/05/01 10:01 CRDT- 2001/03/10 10:00 PHST- 2001/03/10 10:00 [pubmed] PHST- 2001/05/01 10:01 [medline] PHST- 2001/03/10 10:00 [entrez] AID - S0006-4971(20)56169-7 [pii] AID - 10.1182/blood.v97.6.1566 [doi] PST - ppublish SO - Blood. 2001 Mar 15;97(6):1566-71. doi: 10.1182/blood.v97.6.1566.