Daratumumab + bortezomib, thalidomide, and dexamethasone (D-VTd) in transplant-eligible newly diagnosed multiple myeloma (TE NDMM): Baseline SLiM-CRAB based subgroup analysis of CASSIOPEIA.

Authors

null

Cyrille Touzeau

Centre Hospitalier Universitaire, Nantes, France

Cyrille Touzeau , Philippe Moreau , Aurore Perrot , Cyrille Hulin , Mamoun Dib , Mourad Tiab , Denis Caillot , Thierry Facon , Xavier Leleu , Niels W.C.J. van de Donk , Annemiek Broijl , Sonja Zweegman , Mark-David Levin , Michel Delforge , Lixia Pei , Veronique Vanquickelberghe , Carla De Boer , Tobias Kampfenkel , Jessica Vermeulen , Pieter Sonneveld

Organizations

Centre Hospitalier Universitaire, Nantes, France, Hematology, University Hospital Hôtel-Dieu, Nantes, France, Hematology Department, University Cancer Institute IUCT, Toulouse, France, Department of Hematology, Hôpital Haut Lévêque, University Hospital Bordeaux, Pessac, France, CHRU-Hôpital du Bocage, Angers, France, CHD Vendée, La Roche-sur-Yon, France, CHU Dijon, Hôpital Du Bocage, Dijon, France, University of Lille, CHU Lille, Service des Maladies du Sang, Lille, France, CHU Poitiers-Hôpital la Milétrie, Poitiers, France, Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Hematology, Amsterdam, Netherlands, Erasmus MC Cancer Institute, Rotterdam, Netherlands, Albert Schweitzer Hospital, Dordrecht, Netherlands, Universitaire Ziekenhuizen Leuven, Leuven, Belgium, Janssen Research & Development, LLC, Raritan, NJ, Janssen Research & Development, Beerse, Belgium, Janssen Research & Development, LLC, Leiden, Netherlands

Research Funding

Pharmaceutical/Biotech Company
Janssen Research & Development, LLC

Background: In the phase 3 CASSIOPEIA study, D-VTd significantly improved outcomes vs VTd in TE NDMM pts at an 18.8-mo median follow-up. To allow earlier diagnosis and treatment of MM, the IMWG added 3 validated biomarkers (≥60% clonal bone marrow plasma cells, serum free light chain ratio ≥100, and > 1 focal bone lesion by MRI; “slim”) to the conventional “CRAB” diagnostic criteria. We present a subgroup analysis of CASSIOPEIA based on baseline slimCRAB criteria. Methods: TE NDMM pts were randomized 1:1 to 4 pre-ASCT induction and 2 post-ASCT consolidation cycles of D-VTd or VTd. The “slim-only” subgroup excludes pts with ≥1 conventional CRAB criterion based on data collected at baseline; the remaining pts were included in the “CRAB” subgroup. Results: Of 1085 randomized pts (543 D-VTd; 542 VTd), 81 were included in the slim-only subgroup (36 D-VTd; 45 VTd) and 1004 were included in the CRAB subgroup. In slim-only vs CRAB pts, 22% vs 54% had an ECOG score of ≥1, 4% vs 16% had ISS Stage III disease, and 11% vs 16% had high-risk cytogenetics. For D-VTd vs VTd pts in the slim-only group, these rates were 22% vs 22%, 8% vs 0%, and 6% vs 16%, respectively. Overall response rates (ORR) and rates of sCR, ≥CR, and MRD negativity were similar between slim-only and CRAB pts; for slim-only pts, rates were significantly higher for D-VTd vs VTd (Table). After an 18.8-mo median follow-up, progression-free survival (PFS) was not significantly different in slim-only vs CRAB pts, or in D-VTd vs VTd slim-only pts (Table). For D-VTd vs VTd CRAB pts, 18-mo PFS rates were 92% vs 84%, and 24-mo PFS rates were 89% vs 76%. Conclusions: Baseline characteristics indicate that slim-only pts were slightly fitter and of lower risk status vs CRAB pts; however, response rates, MRD-negativity rates, and PFS did not differ significantly between these groups. Among slim-only pts, significantly higher response and MRD-negativity rates were achieved with D-VTd vs VTd. Among CRAB pts, PFS rates were higher with D-VTd vs VTd. Clinical trial information: NCT02541383.

Slim-only
CRAB
PvalueSlim-only
(n = 81)(n = 1004)D-Vth
(n = 36)
Vth
(n = 45)
Pvalue
ORR, %90910.405397840.0377
sCR25250.977636160.0083
≥CR32330.969050180.0003
MRD neg(MFC, 10−5), %46540.12616729< 0.0001
Median PFS, moNRNR-NRNR-
PFS HR (95% CI)0.73 (0.36-1.50)0.38881.19 (0.30-4.78)0.8023

MFC, multiparametric flow cytometry; NR, not reached.

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Abstract Details

Meeting

2020 ASCO Virtual Scientific Program

Session Type

Poster Session

Session Title

Hematologic Malignancies—Plasma Cell Dyscrasia

Track

Hematologic Malignancies

Sub Track

Multiple Myeloma

Clinical Trial Registration Number

NCT02541383

Citation

J Clin Oncol 38: 2020 (suppl; abstr 8538)

DOI

10.1200/JCO.2020.38.15_suppl.8538

Abstract #

8538

Poster Bd #

438

Abstract Disclosures