Sustained bone marrow and imaging MRD negativity for 3 years drives discontinuation of maintenance post-ASCT in myeloma

E Evangelos Terpos P Panagiotis Malandrakis (1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece) I Ioannis Ntanasis-Stathopoulos (1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece) I Ioannis V. Kostopoulos (2Department of Biology, National and Kapodistrian University of Athens, Athens, Greece) E Evangelos Eleutherakis-Papaiakovou (1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece) N Nikolaos Kanellias (1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece) V Vasiliki Spiliopoulou (1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece) M Magdalini Migkou (1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece) D Despina Fotiou (1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece) F Foteini Theodorakakou (Department of Clinical Therapeutics, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece) E Efstathios Kastritis M Maria Gavriatopoulou (National and Kapodistrian University of Athens) O Ourania E. Tsitsilonis (2Department of Biology, School of Science, National and Kapodistrian University of Athens, Athens, Greece) M Meletios-Athanasios Dimopoulos (1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece)

Abstract

Abstract Discontinuation of lenalidomide maintenance after autologous stem cell transplantation is a burning question within the multiple myeloma (MM) community, especially after the inclusion of minimal residual disease (MRD) in the disease response criteria. In this prospective study, we evaluated the conversion to MRD positivity, the treatment-free survival (TFS), and the progression-free survival (PFS) in 52 patients with MM who discontinued lenalidomide maintenance after achieving sustained bone marrow and imaging MRD negativity for 3 years. Patients who developed MRD positivity after lenalidomide discontinuation restarted lenalidomide maintenance at the same dose. The median follow-up from lenalidomide discontinuation was 3 years. Overall, 12 (23%) patients obtained MRD positivity and restarted lenalidomide maintenance. Only 4 (7.6%) patients progressed; 3 had a biochemical progression and 1 had a clinical progression. The overall median PFS was not reached, whereas the 7-year PFS from diagnosis was 90.2%. The 1-, 2-, and 3-year TFS rates were 93.9%, 91.6%, and 75.8%, respectively, whereas the 1-, 2-, and 3-year landmark PFS rates from maintenance discontinuation (study entrance) were 96.0%, 96.0%, and 92.9%, respectively. There were no statistically significant associations among age, sex, Second Revision International Staging System, type of induction therapy, and use of consolidation therapy and the effect outcomes of PFS and TFS. We conclude that maintenance discontinuation after 3 years of sustained marrow and imaging MRD negativity is associated with low rates of MRD conversion and progressive disease. Thus, in the era of modern antimyeloma treatments, a subgroup of patients may remain treatment free while in complete remission without jeopardizing disease response.

Article Details

Journal Blood
Volume / Issue Vol. 145, Issue 20
Published May 15, 2025
Pages 2353-2360
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (14)

E

Evangelos Terpos

P

Panagiotis Malandrakis

1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece

I

Ioannis Ntanasis-Stathopoulos

1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece

I

Ioannis V. Kostopoulos

2Department of Biology, National and Kapodistrian University of Athens, Athens, Greece

E

Evangelos Eleutherakis-Papaiakovou

1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece

N

Nikolaos Kanellias

1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece

V

Vasiliki Spiliopoulou

1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece

M

Magdalini Migkou

1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece

D

Despina Fotiou

1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece

F

Foteini Theodorakakou

Department of Clinical Therapeutics, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece

E

Efstathios Kastritis

M

Maria Gavriatopoulou

National and Kapodistrian University of Athens

O

Ourania E. Tsitsilonis

2Department of Biology, School of Science, National and Kapodistrian University of Athens, Athens, Greece

M

Meletios-Athanasios Dimopoulos

1Department of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece