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   <dc:title>High-risk cytogenetic abnormalities in multiple myeloma: PETHEMA-GEM experience</dc:title>
   <dc:creator>González-Calle, Verónica</dc:creator>
   <dc:creator>Calasanz, Maria J.</dc:creator>
   <dc:creator>Guijarro, Manuela</dc:creator>
   <dc:creator>Martinez-Lopez, Joaquin</dc:creator>
   <dc:creator>Rodriguez-Otero, Paula</dc:creator>
   <dc:creator>Rosiñol, Laura</dc:creator>
   <dc:contributor>Institut Català de la Salut</dc:contributor>
   <dc:contributor>[González‐Calle V] Department of Hematology, Hospital Universitario de Salamanca, Instituto de Investigacion Biomedica de Salamanca (IBSAL), Centro de Investigación del Cancer (IBMCC‐USAL, CSIC), CIBERONC, Salamanca, Spain. [Rodriguez‐Otero P, Calasanz MJ] Department of Hematology, Cancer Center Clinica Universidad de Navarra, CCUN, Centro de Investigacion Medica Aplicadas (Cima); Instituto de Investigación Sanitaria de Navarra (IDISNA), CIBERONC, Pamplona, Spain. [Guijarro M, Martínez‐López J] Department of Hematology, Hospital Universitario 12 de Octubre, I + 12, CNIO, Complutense University, CIBERONC, Madrid, Spain. [Rosiñol L] Department of Hematology, Hospital Clínic, IDIBAPS, Barcelona, Spain. [Gironella M] Servei d’Hematologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain</dc:contributor>
   <dc:contributor>Vall d'Hebron Barcelona Hospital Campus</dc:contributor>
   <dc:subject>Mieloma múltiple - Prognosi</dc:subject>
   <dc:subject>Anomalies cromosòmiques</dc:subject>
   <dc:subject>Mieloma múltiple - Aspectes genètics</dc:subject>
   <dc:subject>DISEASES::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Chromosome Aberrations</dc:subject>
   <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Diagnosis::Prognosis</dc:subject>
   <dc:subject>DISEASES::Cardiovascular Diseases::Vascular Diseases::Hemostatic Disorders::Multiple Myeloma</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::/genetics</dc:subject>
   <dc:subject>ENFERMEDADES::afecciones patológicas, signos y síntomas::procesos patológicos::aberraciones cromosómicas</dc:subject>
   <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::diagnóstico::pronóstico</dc:subject>
   <dc:subject>ENFERMEDADES::enfermedades cardiovasculares::enfermedades vasculares::trastornos hemostáticos::mieloma múltiple</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/genética</dc:subject>
   <dc:description>Cytogenetic abnormalities; Multiple myeloma</dc:description>
   <dc:description>Anomalías citogenéticas; Mieloma múltiple</dc:description>
   <dc:description>Anomalies citogenètiques; Mieloma múltiple</dc:description>
   <dc:description>This study examines the impact of cytogenetic abnormalities and their co-segregation on the prognosis of newly diagnosed multiple myeloma patients. The analysis included 1304 patients from four different GEM-PETHEMA clinical trials. Genetic alterations, such as t(4;14), t(14;16), del(17p), +1q, and del(1p), were investigated using FISH on CD38 purified plasma cells. The frequency of genetic alterations detected were as follows: del(17p) in 8%, t(4;14) in 12%, t(14;16) in 3%, +1q in 43%, and del(1p) in 8%. The median follow-up was 61 months, and the median progression-free survival (PFS) and overall survival (OS) were 44 months and not reached, respectively. Consistent with previous reports, the presence of t(4;14) was associated with shorter PFS and OS. In our series, the presence of t(14;16) did not impact survival, maybe due to limitations in sample size. Del(17p) was linked to poor prognosis using a cut-off level of ≥20% positive cells, without any impact of higher cut-off in prognosis, except for patients with clonal fraction ≥80% who had a dismal outcome. Cosegregation of cytogenetic abnormalities patients worsened the prognosis in t(4;14) patients but not in patients with del(17p), which retained its adverse prognosis even as a solitary abnormality. Gain(1q) was associated with significantly shorter PFS and OS, while del(1p) affected PFS but not OS. Nevertheless, when co-segregation was eliminated, the detrimental effect of +1q or del(1p) was no longer observed. In conclusion, this study confirms the prognostic significance of high-risk cytogenetic abnormalities in MM and highlights the importance of considering co-occurrence for accurate prognosis assessment.</dc:description>
   <dc:date>2025-01-29T07:42:09Z</dc:date>
   <dc:date>2025-01-29T07:42:09Z</dc:date>
   <dc:date>2024-12-10</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>González-Calle V, Rodriguez-Otero P, Calasanz MJ, Guijarro M, Martínez-López J, Rosiñol L, et al. High-risk cytogenetic abnormalities in multiple myeloma: PETHEMA-GEM experience. HemaSphere. 2024 Dec 10;8(12):e70031.</dc:identifier>
   <dc:identifier>2572-9241</dc:identifier>
   <dc:identifier>https://hdl.handle.net/11351/12503</dc:identifier>
   <dc:identifier>10.1002/hem3.70031</dc:identifier>
   <dc:identifier>39665068</dc:identifier>
   <dc:identifier>001373893200001</dc:identifier>
   <dc:identifier>http://hdl.handle.net/11351/12503</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>HemaSphere;8(12)</dc:relation>
   <dc:relation>https://doi.org/10.1002/hem3.70031</dc:relation>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Wiley</dc:publisher>
   <dc:source>Scientia</dc:source>
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