Abstract
Over the past decade, therapeutic options in multiple myeloma (MM) have changed dramatically. Given the unprecedented efficacy of novel agents, the role of hematopoietic cell transplantation (HCT) in MM remains under scrutiny. Rapid advances in myeloma immunotherapy including the recent approval of chimeric antigen receptor (CAR) T-cell therapy will impact the MM therapeutic landscape. The American Society for Transplantation and Cellular Therapy convened an expert panel to formulate clinical practice recommendations for role, timing, and sequencing of autologous (auto-HCT), allogeneic (allo-HCT) and CAR T-cell therapy for patients with newly diagnosed (NDMM) and relapsed/refractory MM (RRMM). The RAND-modified Delphi method was used to generate consensus statements. Twenty consensus statements were generated. The panel endorsed continued use of auto-HCT consolidation for patients with NDMM as a standard-of-care option, whereas in the front line allo-HCT and CAR-T were not recommended outside the setting of clinical trial. For patients not undergoing auto-HCT upfront, the panel recommended its use in first relapse. Lenalidomide as a single agent was recommended for maintenance especially for standard risk patients. In the RRMM setting, the panel recommended the use of CAR-T in patients with 4 or more prior lines of therapy. The panel encouraged allo-HCT in RRMM setting only in the context of clinical trial. The panel found RAND-modified Delphi methodology effective in providing a formal framework for developing consensus recommendations for the timing and sequence of cellular therapies for MM.
Original language | English (US) |
---|---|
Pages (from-to) | 284-293 |
Number of pages | 10 |
Journal | Transplantation and Cellular Therapy |
Volume | 28 |
Issue number | 6 |
DOIs | |
State | Published - Jun 2022 |
Keywords
- Allogeneic transplantation
- Autologous transplantation
- CAR T-cells
- Cellular therapy
- Consensus
- Multiple myeloma
ASJC Scopus subject areas
- Immunology and Allergy
- Molecular Medicine
- Hematology
- Cell Biology
- Transplantation
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In: Transplantation and Cellular Therapy, Vol. 28, No. 6, 06.2022, p. 284-293.
Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - ASTCT Clinical Practice Recommendations for Transplantation and Cellular Therapies in Multiple Myeloma
AU - Dhakal, Binod
AU - Shah, Nina
AU - Kansagra, Ankit
AU - Kumar, Ambuj
AU - Lonial, Sagar
AU - Garfall, Alfred
AU - Cowan, Andrew
AU - Poudyal, Bishesh Sharma
AU - Costello, Caitlin
AU - Gay, Francesca
AU - Cook, Gordon
AU - Quach, Hang
AU - Einsele, Herman
AU - Schriber, Jeff
AU - Hou, Jian
AU - Costa, Luciano
AU - Aljurf, Mahmoud
AU - Chaudhry, Maria
AU - Beksac, Meral
AU - Prince, Miles
AU - Mohty, Mohamad
AU - Janakiram, Murali
AU - Callander, Natalie
AU - Biran, Noa
AU - Malhotra, Pankaj
AU - Otero, Paula Rodriguez
AU - Moreau, Philippe
AU - Abonour, Rafat
AU - Iftikhar, Raheel
AU - Silberman, Rebecca
AU - Mailankody, Sham
AU - Gregory, Tara
AU - Lin, Yi
AU - Carpenter, Paul
AU - Hamadani, Mehdi
AU - Usmani, Saad
AU - Kumar, Shaji
N1 - Funding Information: Financial disclosure: None. Conflict of interest statement: B. Dhakal reports grant/research support from Amgen, Takeda, ACS, LLS, Janssen, Carsgen, Cartesian, Sanofi, Arcellx and Celgene/BMS; member speaker's bureau of Celgene/BMS, Sanofi, and Karyopharm; and advisory board of Amgen, Takeda, GSK, Janssen, Natera, Arcellx, and Sanofi. N. Shah reports research funding from Celgene/BMS, Janssen, Bluebird Bio, Sutro Biopharma, Teneobio, Poseida, Nektar, and Precision Biosciences; and advisory role for GSK, Amgen, Indapta Therapeutics, Sanofi, CareDx, Kite, Karyopharm, Oncopeptides, and CSL Behrin. S. Lonial reports consulting for Takeda, Janssen, Novartis, ABBVIE, GSK, BMS, and Celgene; research support for trials Takeda, Janssen, BMS, Novartis; and board of directors membership with stock for TG Therapeutics. A. Garfall reports consultant/advisory board membership for Janssen and Amgen Research; and funding from Novartis, Janssen, Tmunity, and CRISPR Therapeutics. A. Cowan reports research funding from Harpoon, Janssen, Adaptive, Abbvie, BMS, Sanofi, Celgene-Juno, and Nektar; and consultancy for Doximity, Janssen, Abbvie, Sanofi, Secura Bio, GSK, and Celgene. C. Costello reports research funding from BMS, Janssen, and Takeda; and an advisory role for BMS, Janssen, Pfizer, and Takeda. F. Gay reports honoraria and an advisory role for Janssen, Amgen, BMS, Sanofi, and Abbvie; and an advisory role for Roche, Oncopeptides, Adaptive, and Pfizer. G. Cook reports honoraria from lectures from BMS, Janssen, Sanofi, Amgen, and Takeda; consultancy for BMS, Janssen, Sanofi, Roche, Abbvie, Oncopeptides, Takeda, Pfizer, and GSK; and research funding from Takeda and BMS. H. Quach reports research funding from: Amgen, GSK, Sanofi, Karyopharm, Celgene, and BMS; and advisory board roles for Amgen, GSK, Sanofi, Karyopharm, Celgene, BMS, Takeda, and Jansen. H. Einsele reports consulting or advisory roles for BMS/Celgene, Janssen, Amgen, Takeda, Sanofi, GSK, and Novartis; research funding from BMS/Celgene, Janssen, Amgen, GSK, and Sanofi; honoraria from BMS/Celgene, Janssen, Amgen, Takeda, Sanofi, GSK, and Novartis; and travel/accommodation expenses from BMS/Celgene, Janssen, Amgen, Takeda, and Novartis. J. Hou reports honoraria from lectures from Xi'an-Janssen, Sanofi, Beigene, Pfizer, and Takeda; participation in Ad Board meetings for Novartis, Janssen, and Takeda; and is a consultant for Legend and FOSUNKite. L. Costa reports honoraria from Amgen, Celgene-Bristol Myers Squibb, AbbVie, Adaptive Biotechnologies, Janssen, Sanofi, and Takeda; and research funding from Amgen, Celgene-Bristol Myers Squibb, and Janssen. M. Chaudhry reports honoraria and an advisory role for Janssen, Amgen, BMS, Sanofi, and Abbvie; and an advisory role for Roche, Oncopeptides, Adaptive, and Pfizer. M. Beksac reports advisory board or speakers bureau role for Amgen, Janssen, Sanofi, Takeda and Oncopeptides. M. Prince reports consultant/advisory board roles for BMS, Janssen, Amgen, Sanofi; and research funding from BMS. N. Biran reports consultant/advisory board roles for BMS, Janssen, Pfizer, and Sanofi; research funding from Janssen, Merck, Karyopharm, Amgen, and BMS; and a speaker role for Janssen, BMS, and Sanofi. M. Janakiram reports honoraria from BMS and ADCT Therapeutics. P. Rodriguez Otero reports honoraria for lectures from BMS, Janssen, Sanofi, GSK, Amgen, Regeneron, and Takeda; participation in ad board meetings for BMS, Janssen, Sanofi, Kite Pharma, Abbvie, Oncopeptides, Takeda, Pfizer, and GSK; and a consultant role for BMS and Pfizer. R. Abonour reports consultation, honoraria, advisory board, and steering committees for BMS, Takeda, and GSK. R. Silberman reports consultant/ad board for Sanof-Aventis and Janssen. S. Mailankody reports research funding from NCI, Allogene Therapeutics, Janssen Oncology, BMS/Juno Therapeutics, Takeda Oncology, and Fate Therapeutics; honoraria from Physician Education Resource, Plexus Education, MJH Life Sciences, and OncLive; and an advisory role for Janssen, Legend Biotech, and Evicore. T. Gregory reports research funding from Sarah Cannon Research Institute, Abbvie, Amgen, Acetylon, Bluebird, Bristol-Myers Squibb, Celgene, Celularity, Constellation, CRISP Therapeutics, CURIS, EMD Sorono, Genentech, Glenmark, Janssen, Kesios, Lilly, Novartis, Poseida, Sanofi, Takeda, Teva, and Vivolux. Y. Lin reports no personal compensation, all funds paid to Mayo. Merck, Takeda, BMS, BlueBird Bio, Legend, Janssen, Novartis, Kite/Gilead, Gamida Cells, Pfizer, Sorrento. M. Hamadani reports consultancy for Incyte Corporation, ADC Therapeutics, Pharmacyclics, Omeros, Verastem, Genmab, Morphosys, Kite, Novartis, and Kadmon; and speaker's bureau for Sanofi Genzyme, AstraZeneca, BeiGene, and ADC Therapeutics. Authorship statement: B.D. A.K. N.S. P.C. M.H. designed the study. B.D. A.K. N.S. A.K. M.H. collected and assembled the data. A.K. analyzed the data. All authors interpreted the data. B.D. prepared the first draft. All authors helped revise the manuscript. All authors gave final approval of the manuscript. Financial disclosure: See Acknowledgments on page XXXX. Funding Information: Conflict of interest statement: B. Dhakal reports grant/research support from Amgen, Takeda, ACS, LLS, Janssen, Carsgen, Cartesian, Sanofi, Arcellx and Celgene/BMS; member speaker's bureau of Celgene/BMS, Sanofi, and Karyopharm; and advisory board of Amgen, Takeda, GSK, Janssen, Natera, Arcellx, and Sanofi. N. Shah reports research funding from Celgene/BMS, Janssen, Bluebird Bio, Sutro Biopharma, Teneobio, Poseida, Nektar, and Precision Biosciences; and advisory role for GSK, Amgen, Indapta Therapeutics, Sanofi, CareDx, Kite, Karyopharm, Oncopeptides, and CSL Behrin. S. Lonial reports consulting for Takeda, Janssen, Novartis, ABBVIE, GSK, BMS, and Celgene; research support for trials Takeda, Janssen, BMS, Novartis; and board of directors membership with stock for TG Therapeutics. A. Garfall reports consultant/advisory board membership for Janssen and Amgen Research; and funding from Novartis, Janssen, Tmunity, and CRISPR Therapeutics. A. Cowan reports research funding from Harpoon, Janssen, Adaptive, Abbvie, BMS, Sanofi, Celgene-Juno, and Nektar; and consultancy for Doximity, Janssen, Abbvie, Sanofi, Secura Bio, GSK, and Celgene. C. Costello reports research funding from BMS, Janssen, and Takeda; and an advisory role for BMS, Janssen, Pfizer, and Takeda. F. Gay reports honoraria and an advisory role for Janssen, Amgen, BMS, Sanofi, and Abbvie; and an advisory role for Roche, Oncopeptides, Adaptive, and Pfizer. G. Cook reports honoraria from lectures from BMS, Janssen, Sanofi, Amgen, and Takeda; consultancy for BMS, Janssen, Sanofi, Roche, Abbvie, Oncopeptides, Takeda, Pfizer, and GSK; and research funding from Takeda and BMS. H. Quach reports research funding from: Amgen, GSK, Sanofi, Karyopharm, Celgene, and BMS; and advisory board roles for Amgen, GSK, Sanofi, Karyopharm, Celgene, BMS, Takeda, and Jansen. H. Einsele reports consulting or advisory roles for BMS/Celgene, Janssen, Amgen, Takeda, Sanofi, GSK, and Novartis; research funding from BMS/Celgene, Janssen, Amgen, GSK, and Sanofi; honoraria from BMS/Celgene, Janssen, Amgen, Takeda, Sanofi, GSK, and Novartis; and travel/accommodation expenses from BMS/Celgene, Janssen, Amgen, Takeda, and Novartis. J. Hou reports honoraria from lectures from Xi'an-Janssen, Sanofi, Beigene, Pfizer, and Takeda; participation in Ad Board meetings for Novartis, Janssen, and Takeda; and is a consultant for Legend and FOSUNKite. L. Costa reports honoraria from Amgen, Celgene-Bristol Myers Squibb, AbbVie, Adaptive Biotechnologies, Janssen, Sanofi, and Takeda; and research funding from Amgen, Celgene-Bristol Myers Squibb, and Janssen. M. Chaudhry reports honoraria and an advisory role for Janssen, Amgen, BMS, Sanofi, and Abbvie; and an advisory role for Roche, Oncopeptides, Adaptive, and Pfizer. M. Beksac reports advisory board or speakers bureau role for Amgen, Janssen, Sanofi, Takeda and Oncopeptides. M. Prince reports consultant/advisory board roles for BMS, Janssen, Amgen, Sanofi; and research funding from BMS. N. Biran reports consultant/advisory board roles for BMS, Janssen, Pfizer, and Sanofi; research funding from Janssen, Merck, Karyopharm, Amgen, and BMS; and a speaker role for Janssen, BMS, and Sanofi. M. Janakiram reports honoraria from BMS and ADCT Therapeutics. P. Rodriguez Otero reports honoraria for lectures from BMS, Janssen, Sanofi, GSK, Amgen, Regeneron, and Takeda; participation in ad board meetings for BMS, Janssen, Sanofi, Kite Pharma, Abbvie, Oncopeptides, Takeda, Pfizer, and GSK; and a consultant role for BMS and Pfizer. R. Abonour reports consultation, honoraria, advisory board, and steering committees for BMS, Takeda, and GSK. R. Silberman reports consultant/ad board for Sanof-Aventis and Janssen. S. Mailankody reports research funding from NCI, Allogene Therapeutics, Janssen Oncology, BMS/Juno Therapeutics, Takeda Oncology, and Fate Therapeutics; honoraria from Physician Education Resource, Plexus Education, MJH Life Sciences, and OncLive; and an advisory role for Janssen, Legend Biotech, and Evicore. T. Gregory reports research funding from Sarah Cannon Research Institute, Abbvie, Amgen, Acetylon, Bluebird, Bristol-Myers Squibb, Celgene, Celularity, Constellation, CRISP Therapeutics, CURIS, EMD Sorono, Genentech, Glenmark, Janssen, Kesios, Lilly, Novartis, Poseida, Sanofi, Takeda, Teva, and Vivolux. Y. Lin reports no personal compensation, all funds paid to Mayo. Merck, Takeda, BMS, BlueBird Bio, Legend, Janssen, Novartis, Kite/Gilead, Gamida Cells, Pfizer, Sorrento. M. Hamadani reports consultancy for Incyte Corporation, ADC Therapeutics, Pharmacyclics, Omeros, Verastem, Genmab, Morphosys, Kite, Novartis, and Kadmon; and speaker's bureau for Sanofi Genzyme, AstraZeneca, BeiGene, and ADC Therapeutics. Publisher Copyright: © 2022 The American Society for Transplantation and Cellular Therapy
PY - 2022/6
Y1 - 2022/6
N2 - Over the past decade, therapeutic options in multiple myeloma (MM) have changed dramatically. Given the unprecedented efficacy of novel agents, the role of hematopoietic cell transplantation (HCT) in MM remains under scrutiny. Rapid advances in myeloma immunotherapy including the recent approval of chimeric antigen receptor (CAR) T-cell therapy will impact the MM therapeutic landscape. The American Society for Transplantation and Cellular Therapy convened an expert panel to formulate clinical practice recommendations for role, timing, and sequencing of autologous (auto-HCT), allogeneic (allo-HCT) and CAR T-cell therapy for patients with newly diagnosed (NDMM) and relapsed/refractory MM (RRMM). The RAND-modified Delphi method was used to generate consensus statements. Twenty consensus statements were generated. The panel endorsed continued use of auto-HCT consolidation for patients with NDMM as a standard-of-care option, whereas in the front line allo-HCT and CAR-T were not recommended outside the setting of clinical trial. For patients not undergoing auto-HCT upfront, the panel recommended its use in first relapse. Lenalidomide as a single agent was recommended for maintenance especially for standard risk patients. In the RRMM setting, the panel recommended the use of CAR-T in patients with 4 or more prior lines of therapy. The panel encouraged allo-HCT in RRMM setting only in the context of clinical trial. The panel found RAND-modified Delphi methodology effective in providing a formal framework for developing consensus recommendations for the timing and sequence of cellular therapies for MM.
AB - Over the past decade, therapeutic options in multiple myeloma (MM) have changed dramatically. Given the unprecedented efficacy of novel agents, the role of hematopoietic cell transplantation (HCT) in MM remains under scrutiny. Rapid advances in myeloma immunotherapy including the recent approval of chimeric antigen receptor (CAR) T-cell therapy will impact the MM therapeutic landscape. The American Society for Transplantation and Cellular Therapy convened an expert panel to formulate clinical practice recommendations for role, timing, and sequencing of autologous (auto-HCT), allogeneic (allo-HCT) and CAR T-cell therapy for patients with newly diagnosed (NDMM) and relapsed/refractory MM (RRMM). The RAND-modified Delphi method was used to generate consensus statements. Twenty consensus statements were generated. The panel endorsed continued use of auto-HCT consolidation for patients with NDMM as a standard-of-care option, whereas in the front line allo-HCT and CAR-T were not recommended outside the setting of clinical trial. For patients not undergoing auto-HCT upfront, the panel recommended its use in first relapse. Lenalidomide as a single agent was recommended for maintenance especially for standard risk patients. In the RRMM setting, the panel recommended the use of CAR-T in patients with 4 or more prior lines of therapy. The panel encouraged allo-HCT in RRMM setting only in the context of clinical trial. The panel found RAND-modified Delphi methodology effective in providing a formal framework for developing consensus recommendations for the timing and sequence of cellular therapies for MM.
KW - Allogeneic transplantation
KW - Autologous transplantation
KW - CAR T-cells
KW - Cellular therapy
KW - Consensus
KW - Multiple myeloma
UR - http://www.scopus.com/inward/record.url?scp=85128352615&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85128352615&partnerID=8YFLogxK
U2 - 10.1016/j.jtct.2022.03.019
DO - 10.1016/j.jtct.2022.03.019
M3 - Article
C2 - 35306217
AN - SCOPUS:85128352615
SN - 2666-6367
VL - 28
SP - 284
EP - 293
JO - Transplantation and Cellular Therapy
JF - Transplantation and Cellular Therapy
IS - 6
ER -