Single-point and kinetics of peripheral residual disease by mass spectrometry to predict outcome in patients with high-risk smoldering multiple myeloma included in the GEM-CESAR trial

The value of quantitative immunoprecipitation mass spectrometry (QIP-MS) to identify the M-protein is being investigated in patients with monoclonal gammopathies but no data are yet available in high-risk smoldering myeloma (HRsMM). We have, therefore, investigated QIP-MS to monitor peripheral resid...

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Autores: Puig, Noemí|||0000-0001-7535-3861, Agulló, Cristina, Contreras, Teresa, Pérez, José Juan, Aires, Irene, Calasanz, M.J.|||0000-0002-0374-3008, García-Sanz, Ramón|||0000-0003-4120-2787, Castro, Sergio, Martínez-López, Joaquín|||0000-0001-7908-0063, Rodriguez-Otero, Paula|||0000-0001-5236-7785, González-Calle, Verónica|||0000-0002-5493-6707, González, Marta S., Oriol, Albert|||0000-0001-6804-2221, Gutierrez, Norma|||0000-0001-5834-9510, Ríos-Tamayo, Rafael|||0000-0001-8193-1402, Rosiñol, Laura|||0000-0002-2534-9239, Álvarez, Miguel Ángel, Bargay, Joan|||0000-0002-6739-3916, Gonzalez-Rodriguez, Ana P., Alegre, Adrian|||0000-0002-2423-822X, Escalante, Fernando|||0000-0003-4501-9066, Iñigo Rodríguez, María Belén, de la Rubia, Javier|||0000-0002-8354-768X, Teruel, Ana Isabel|||0000-0003-1559-7607, De Arriba, Felipe|||0000-0002-4451-1318, Palomera, Luis|||0000-0003-0359-7191, Hernández, Miguel Teodoro|||0000-0002-6576-7881, López-Jiménez, Javier, Reinoso, Marta, García-Mateo, Aránzazu, Ocio, Enrique M.|||0000-0002-5765-0085, Bladé Creixenti, Juan|||0000-0002-4563-3405, Lahuerta, J. J.|||0000-0002-3393-9570, Cedena, María Teresa|||0000-0001-5851-3720, Paiva, Bruno|||0000-0003-1977-3815, San Miguel, Jesús F., Mateos, M. V.|||0000-0003-2390-1218
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:311095
Acceso en línea:https://ddd.uab.cat/record/311095
https://dx.doi.org/urn:doi:10.3324/haematol.2024.285742
Access Level:acceso abierto
Palabra clave:Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols
Female
Humans
Male
Mass Spectrometry
Middle Aged
Multiple Myeloma
Myeloma Proteins
Neoplasm, Residual
Prognosis
Smoldering Multiple Myeloma
Treatment Outcome
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oai_identifier_str oai:ddd.uab.cat:311095
network_acronym_str ES
network_name_str España
repository_id_str
dc.title.none.fl_str_mv Single-point and kinetics of peripheral residual disease by mass spectrometry to predict outcome in patients with high-risk smoldering multiple myeloma included in the GEM-CESAR trial
title Single-point and kinetics of peripheral residual disease by mass spectrometry to predict outcome in patients with high-risk smoldering multiple myeloma included in the GEM-CESAR trial
spellingShingle Single-point and kinetics of peripheral residual disease by mass spectrometry to predict outcome in patients with high-risk smoldering multiple myeloma included in the GEM-CESAR trial
Puig, Noemí|||0000-0001-7535-3861
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols
Female
Humans
Male
Mass Spectrometry
Middle Aged
Multiple Myeloma
Myeloma Proteins
Neoplasm, Residual
Prognosis
Smoldering Multiple Myeloma
Treatment Outcome
title_short Single-point and kinetics of peripheral residual disease by mass spectrometry to predict outcome in patients with high-risk smoldering multiple myeloma included in the GEM-CESAR trial
title_full Single-point and kinetics of peripheral residual disease by mass spectrometry to predict outcome in patients with high-risk smoldering multiple myeloma included in the GEM-CESAR trial
title_fullStr Single-point and kinetics of peripheral residual disease by mass spectrometry to predict outcome in patients with high-risk smoldering multiple myeloma included in the GEM-CESAR trial
title_full_unstemmed Single-point and kinetics of peripheral residual disease by mass spectrometry to predict outcome in patients with high-risk smoldering multiple myeloma included in the GEM-CESAR trial
title_sort Single-point and kinetics of peripheral residual disease by mass spectrometry to predict outcome in patients with high-risk smoldering multiple myeloma included in the GEM-CESAR trial
dc.creator.none.fl_str_mv Puig, Noemí|||0000-0001-7535-3861
Agulló, Cristina
Contreras, Teresa
Pérez, José Juan
Aires, Irene
Calasanz, M.J.|||0000-0002-0374-3008
García-Sanz, Ramón|||0000-0003-4120-2787
Castro, Sergio
Martínez-López, Joaquín|||0000-0001-7908-0063
Rodriguez-Otero, Paula|||0000-0001-5236-7785
González-Calle, Verónica|||0000-0002-5493-6707
González, Marta S.
Oriol, Albert|||0000-0001-6804-2221
Gutierrez, Norma|||0000-0001-5834-9510
Ríos-Tamayo, Rafael|||0000-0001-8193-1402
Rosiñol, Laura|||0000-0002-2534-9239
Álvarez, Miguel Ángel
Bargay, Joan|||0000-0002-6739-3916
Gonzalez-Rodriguez, Ana P.
Alegre, Adrian|||0000-0002-2423-822X
Escalante, Fernando|||0000-0003-4501-9066
Iñigo Rodríguez, María Belén
de la Rubia, Javier|||0000-0002-8354-768X
Teruel, Ana Isabel|||0000-0003-1559-7607
De Arriba, Felipe|||0000-0002-4451-1318
Palomera, Luis|||0000-0003-0359-7191
Hernández, Miguel Teodoro|||0000-0002-6576-7881
López-Jiménez, Javier
Reinoso, Marta
García-Mateo, Aránzazu
Ocio, Enrique M.|||0000-0002-5765-0085
Bladé Creixenti, Juan|||0000-0002-4563-3405
Lahuerta, J. J.|||0000-0002-3393-9570
Cedena, María Teresa|||0000-0001-5851-3720
Paiva, Bruno|||0000-0003-1977-3815
San Miguel, Jesús F.
Mateos, M. V.|||0000-0003-2390-1218
author Puig, Noemí|||0000-0001-7535-3861
author_facet Puig, Noemí|||0000-0001-7535-3861
Agulló, Cristina
Contreras, Teresa
Pérez, José Juan
Aires, Irene
Calasanz, M.J.|||0000-0002-0374-3008
García-Sanz, Ramón|||0000-0003-4120-2787
Castro, Sergio
Martínez-López, Joaquín|||0000-0001-7908-0063
Rodriguez-Otero, Paula|||0000-0001-5236-7785
González-Calle, Verónica|||0000-0002-5493-6707
González, Marta S.
Oriol, Albert|||0000-0001-6804-2221
Gutierrez, Norma|||0000-0001-5834-9510
Ríos-Tamayo, Rafael|||0000-0001-8193-1402
Rosiñol, Laura|||0000-0002-2534-9239
Álvarez, Miguel Ángel
Bargay, Joan|||0000-0002-6739-3916
Gonzalez-Rodriguez, Ana P.
Alegre, Adrian|||0000-0002-2423-822X
Escalante, Fernando|||0000-0003-4501-9066
Iñigo Rodríguez, María Belén
de la Rubia, Javier|||0000-0002-8354-768X
Teruel, Ana Isabel|||0000-0003-1559-7607
De Arriba, Felipe|||0000-0002-4451-1318
Palomera, Luis|||0000-0003-0359-7191
Hernández, Miguel Teodoro|||0000-0002-6576-7881
López-Jiménez, Javier
Reinoso, Marta
García-Mateo, Aránzazu
Ocio, Enrique M.|||0000-0002-5765-0085
Bladé Creixenti, Juan|||0000-0002-4563-3405
Lahuerta, J. J.|||0000-0002-3393-9570
Cedena, María Teresa|||0000-0001-5851-3720
Paiva, Bruno|||0000-0003-1977-3815
San Miguel, Jesús F.
Mateos, M. V.|||0000-0003-2390-1218
author_role author
author2 Agulló, Cristina
Contreras, Teresa
Pérez, José Juan
Aires, Irene
Calasanz, M.J.|||0000-0002-0374-3008
García-Sanz, Ramón|||0000-0003-4120-2787
Castro, Sergio
Martínez-López, Joaquín|||0000-0001-7908-0063
Rodriguez-Otero, Paula|||0000-0001-5236-7785
González-Calle, Verónica|||0000-0002-5493-6707
González, Marta S.
Oriol, Albert|||0000-0001-6804-2221
Gutierrez, Norma|||0000-0001-5834-9510
Ríos-Tamayo, Rafael|||0000-0001-8193-1402
Rosiñol, Laura|||0000-0002-2534-9239
Álvarez, Miguel Ángel
Bargay, Joan|||0000-0002-6739-3916
Gonzalez-Rodriguez, Ana P.
Alegre, Adrian|||0000-0002-2423-822X
Escalante, Fernando|||0000-0003-4501-9066
Iñigo Rodríguez, María Belén
de la Rubia, Javier|||0000-0002-8354-768X
Teruel, Ana Isabel|||0000-0003-1559-7607
De Arriba, Felipe|||0000-0002-4451-1318
Palomera, Luis|||0000-0003-0359-7191
Hernández, Miguel Teodoro|||0000-0002-6576-7881
López-Jiménez, Javier
Reinoso, Marta
García-Mateo, Aránzazu
Ocio, Enrique M.|||0000-0002-5765-0085
Bladé Creixenti, Juan|||0000-0002-4563-3405
Lahuerta, J. J.|||0000-0002-3393-9570
Cedena, María Teresa|||0000-0001-5851-3720
Paiva, Bruno|||0000-0003-1977-3815
San Miguel, Jesús F.
Mateos, M. V.|||0000-0003-2390-1218
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universitat Autònoma de Barcelona
dc.subject.none.fl_str_mv Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols
Female
Humans
Male
Mass Spectrometry
Middle Aged
Multiple Myeloma
Myeloma Proteins
Neoplasm, Residual
Prognosis
Smoldering Multiple Myeloma
Treatment Outcome
topic Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols
Female
Humans
Male
Mass Spectrometry
Middle Aged
Multiple Myeloma
Myeloma Proteins
Neoplasm, Residual
Prognosis
Smoldering Multiple Myeloma
Treatment Outcome
description The value of quantitative immunoprecipitation mass spectrometry (QIP-MS) to identify the M-protein is being investigated in patients with monoclonal gammopathies but no data are yet available in high-risk smoldering myeloma (HRsMM). We have, therefore, investigated QIP-MS to monitor peripheral residual disease (PRD) in 62 HRsMM patients enrolled in the GEM-CESAR trial. After 24 cycles of maintenance, detecting the M-protein by MS or clonal plasma cells by next-generation flow cytometry (NGF) identified cases with a significantly shorter median progression-free survival (mPFS) (MS: not reached vs. 1.4 years, P=0.001; NGF: not reached vs. 2 years, P=0.0002) but reaching complete response (CR) + stringent CR (sCR) did not discriminate between patients with different outcome. With NGF as a reference, the combined results of NGF and MS showed a high negative predictive value (NPV) of MS: 81% overall and 73% at treatment completion. When sequential results were considered, sustained negativity by MS or NGF was associated with a very favorable outcome with an mPFS not yet reached versus 1.66 years and 2.18 years in cases never attaining PRD or minimal residual disease (MRD) negativity, respectively. We can, thus, conclude that: 1) the standard response categories of the International Myeloma Working Group do not seem to be useful for monitoring treatment in HRsMM patients; 2) MS could be used as a valuable, non-invasive, clinical tool with the capacity of guiding timely bone marrow evaluations (based on its high NPV with NGF as a reference); and 3) similarly to NGF, sequential results of MS are able to identify a subgroup of HRsMM patients with long-term disease control. This study was registered at www.clinicaltrials.gov (clinicaltrials.gov identifier: 02415413).
publishDate 2024
dc.date.none.fl_str_mv 2
2024-01-01
2024
2024-01-01
dc.type.none.fl_str_mv Article
http://purl.org/coar/resource_type/c_6501
VoR
http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv https://ddd.uab.cat/record/311095
https://dx.doi.org/urn:doi:10.3324/haematol.2024.285742
url https://ddd.uab.cat/record/311095
https://dx.doi.org/urn:doi:10.3324/haematol.2024.285742
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.relation.none.fl_str_mv Instituto de Salud Carlos III https://doi.org/10.13039/501100004587 PI21/01751
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2
https://creativecommons.org/licenses/by-nc/4.0/
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2
https://creativecommons.org/licenses/by-nc/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Dipòsit Digital de Documents de la UAB
instname:Universitat Autònoma de Barcelona
instname_str Universitat Autònoma de Barcelona
reponame_str Dipòsit Digital de Documents de la UAB
collection Dipòsit Digital de Documents de la UAB
repository.name.fl_str_mv
repository.mail.fl_str_mv
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spelling Single-point and kinetics of peripheral residual disease by mass spectrometry to predict outcome in patients with high-risk smoldering multiple myeloma included in the GEM-CESAR trialPuig, Noemí|||0000-0001-7535-3861Agulló, CristinaContreras, TeresaPérez, José JuanAires, IreneCalasanz, M.J.|||0000-0002-0374-3008García-Sanz, Ramón|||0000-0003-4120-2787Castro, SergioMartínez-López, Joaquín|||0000-0001-7908-0063Rodriguez-Otero, Paula|||0000-0001-5236-7785González-Calle, Verónica|||0000-0002-5493-6707González, Marta S.Oriol, Albert|||0000-0001-6804-2221Gutierrez, Norma|||0000-0001-5834-9510Ríos-Tamayo, Rafael|||0000-0001-8193-1402Rosiñol, Laura|||0000-0002-2534-9239Álvarez, Miguel ÁngelBargay, Joan|||0000-0002-6739-3916Gonzalez-Rodriguez, Ana P.Alegre, Adrian|||0000-0002-2423-822XEscalante, Fernando|||0000-0003-4501-9066Iñigo Rodríguez, María Belénde la Rubia, Javier|||0000-0002-8354-768XTeruel, Ana Isabel|||0000-0003-1559-7607De Arriba, Felipe|||0000-0002-4451-1318Palomera, Luis|||0000-0003-0359-7191Hernández, Miguel Teodoro|||0000-0002-6576-7881López-Jiménez, JavierReinoso, MartaGarcía-Mateo, AránzazuOcio, Enrique M.|||0000-0002-5765-0085Bladé Creixenti, Juan|||0000-0002-4563-3405Lahuerta, J. J.|||0000-0002-3393-9570Cedena, María Teresa|||0000-0001-5851-3720Paiva, Bruno|||0000-0003-1977-3815San Miguel, Jesús F.Mateos, M. V.|||0000-0003-2390-1218AgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansMaleMass SpectrometryMiddle AgedMultiple MyelomaMyeloma ProteinsNeoplasm, ResidualPrognosisSmoldering Multiple MyelomaTreatment OutcomeThe value of quantitative immunoprecipitation mass spectrometry (QIP-MS) to identify the M-protein is being investigated in patients with monoclonal gammopathies but no data are yet available in high-risk smoldering myeloma (HRsMM). We have, therefore, investigated QIP-MS to monitor peripheral residual disease (PRD) in 62 HRsMM patients enrolled in the GEM-CESAR trial. After 24 cycles of maintenance, detecting the M-protein by MS or clonal plasma cells by next-generation flow cytometry (NGF) identified cases with a significantly shorter median progression-free survival (mPFS) (MS: not reached vs. 1.4 years, P=0.001; NGF: not reached vs. 2 years, P=0.0002) but reaching complete response (CR) + stringent CR (sCR) did not discriminate between patients with different outcome. With NGF as a reference, the combined results of NGF and MS showed a high negative predictive value (NPV) of MS: 81% overall and 73% at treatment completion. When sequential results were considered, sustained negativity by MS or NGF was associated with a very favorable outcome with an mPFS not yet reached versus 1.66 years and 2.18 years in cases never attaining PRD or minimal residual disease (MRD) negativity, respectively. We can, thus, conclude that: 1) the standard response categories of the International Myeloma Working Group do not seem to be useful for monitoring treatment in HRsMM patients; 2) MS could be used as a valuable, non-invasive, clinical tool with the capacity of guiding timely bone marrow evaluations (based on its high NPV with NGF as a reference); and 3) similarly to NGF, sequential results of MS are able to identify a subgroup of HRsMM patients with long-term disease control. This study was registered at www.clinicaltrials.gov (clinicaltrials.gov identifier: 02415413).Universitat Autònoma de Barcelona 22024-01-0120242024-01-01Articlehttp://purl.org/coar/resource_type/c_6501VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttps://ddd.uab.cat/record/311095https://dx.doi.org/urn:doi:10.3324/haematol.2024.285742reponame:Dipòsit Digital de Documents de la UABinstname:Universitat Autònoma de BarcelonaInglésengInstituto de Salud Carlos III https://doi.org/10.13039/501100004587 PI21/01751open accesshttp://purl.org/coar/access_right/c_abf2Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original.https://creativecommons.org/licenses/by-nc/4.0/info:eu-repo/semantics/openAccessoai:ddd.uab.cat:3110952026-06-06T12:50:31Z
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