Prognostic utility of serum free light chain ratios and heavy-light chain ratios in multiple myeloma in three PETHEMA/GEM phase III clinical trials

Autor: Lopez-Anglada, Lucia, Cueto-Felgueroso, Cecilia, Rosinol, Laura, Oriol, Albert, Isabel Teruel, Ana, Lopez de la Guia, Ana, Bengoechea, Enrique, Palomera, Luis, de Arriba, Felipe, Mariano Hernandez, Jose, Granell, Miquel, Javier Penalver, Francisco, Garcia-Sanz, Ramon, Besalduch, Juan, Gonzalez, Yolanda, Benigno Martinez, Rafael, Teodoro Hernandez, Miguel, Gutierrez, Norma C., Puerta, Paloma, Valeri, Antonio, Paiva, Bruno, Blade, Joan, Mateos, Maria-Victoria, San Miguel, Jesus, Jose Lahuerta, Juan, Martinez-Lopez, Joaquin, GEM Grp Espanol MM, PETHEMA Programa El Estudio
Přispěvatelé: Red Temática de Investigación Cooperativa en Cáncer (España), Instituto de Salud Carlos III, Ministerio de Industria y Competitividad (España), European Commission, Asociación Española Contra el Cáncer, Fundación CRIS contra el Cáncer
Rok vydání: 2018
Předmět:
0301 basic medicine
Serum Proteins
Physiology
humanos
Complement System
lcsh:Medicine
Phases of clinical research
Drug research and development
Kaplan-Meier Estimate
Pathology and Laboratory Medicine
Biochemistry
Gastroenterology
Plasma Cell Disorders
cadenas ligeras de las inmunoglobulinas
Hematologic Cancers and Related Disorders
Binding Analysis
Clinical trials
0302 clinical medicine
Immune Physiology
Antineoplastic Combined Chemotherapy Protocols
Medicine and Health Sciences
Medicine
lcsh:Science
Multiple myeloma
Immune System Proteins
Multidisciplinary
medicine.diagnostic_test
protocolos de quimioterapia antineoplásica combinada
Hematology
Induction Chemotherapy
Prognosis
Blood proteins
Phase III clinical investigation
pronóstico
Myelomas
Oncology
030220 oncology & carcinogenesis
Serum protein electrophoresis
Multiple Myeloma
Immunoglobulin Heavy Chains
Research Article
estimación de Kaplan-Meier
medicine.medical_specialty
Immunology
mieloma múltiple
Immunoglobulin light chain
Immune Suppression
Transplantation
Autologous

Antibodies
trasplante de células madre
03 medical and health sciences
Signs and Symptoms
Diagnostic Medicine
Internal medicine
Humans
Autologous transplantation
Myelomas and Lymphoproliferative Diseases
quimioterapia de inducción
Chemical Characterization
Retrospective Studies
Pharmacology
Transplantation
business.industry
lcsh:R
estudios retrospectivos
Cancers and Neoplasms
Biology and Life Sciences
Proteins
Induction chemotherapy
trasplante
medicine.disease
Research and analysis methods
030104 developmental biology
Clinical Trials
Phase III as Topic

cadenas pesadas de las inmunoglobulinas
Clinical medicine
Immune System
lcsh:Q
Immunoglobulin Light Chains
business
Stem Cell Transplantation
Zdroj: Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
PLoS One
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
BASE-Bielefeld Academic Search Engine
Digital.CSIC. Repositorio Institucional del CSIC
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
PLoS ONE
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Zaguán. Repositorio Digital de la Universidad de Zaragoza
PLoS ONE, Vol 13, Iss 9, p e0203392 (2018)
ISSN: 1932-6203
Popis: © 2018 Lopez-Anglada et al.
We investigated the prognostic impact and clinical utility of serum free light chains (sFLC) and serum heavy-light chains (sHLC) in patients with multiple myeloma treated according to the GEM2005MENOS65, GEM2005MAS65, and GEM2010MAS65 PETHEMA/GEM phase III clinical trials. Serum samples collected at diagnosis were retrospectively analyzed for sFLC (n = 623) and sHLC (n = 183). After induction or autologous transplantation, 309 and 89 samples respectively were available for sFLC and sHLC assays. At diagnosis, a highly abnormal (HA) sFLC ratio (sFLCr) (32) was not associated with higher risk of progression. After therapy, persistence of involved-sFLC levels >100 mg/L implied worse survival (overall survival [OS], P = 0.03; progression-free survival [PFS], P = 0.007). Among patients that achieved a complete response, sFLCr normalization did not necessarily indicate a higher quality response. We conducted sHLC investigations for IgG and IgA MM. Absolute sHLC values were correlated with monoclonal protein levels measured with serum protein electrophoresis. At diagnosis, HA-sHLCrs (73) showed a higher risk of progression (P = 0.006). Additionally, involved-sHLC levels >5 g/L after treatment were associated with shorter survival (OS, P = 0.001; PFS, P = 0.018). The HA-sHLCr could have prognostic value at diagnosis; absolute values of involved-sFLC >100 mg/L and involved-sHLC >5 g/L could have prognostic value after treatment.
This research project was supported by grants PI06339, PS09/01370, and PI12/01761 awarded to Sara Borrell (CD13/00340) and Juan Rodes (JR14/00016) from the Fondo de Investigación Sanitaria (FIS), the Red Temática de Investigación Cooperativa en Cáncer (RTICC) of the Instituto de Salud Carlos III (Ministry of Economy, Industry, and Competitiveness, Madrid, Spain), FEDER (RD12/0036/0061, RD12/0036/0048m and RD12/0036/0058) from FIS, the Asociación Española Contra el Cáncer (AECC; GCB120981SAN), and the CRIS Foundation.
Databáze: OpenAIRE