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June 1, 2024Journal of Clinical Oncology0 citations

A phase III, randomized study of daratumumab, cyclophosphamide, bortezomib and dexamethasone (DARA-VCD) induction followed by autologous stem cell transplant or DARA-VCD consolidation and daratumumab maintenance in patients with newly diagnosed AL amyloidosis.

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PHPatrick HagenSSSurbhi SidanaTPTerri L. Parker

Key Points

  • Overall survival shows no significant difference, but ASCT may enhance major organ deterioration progression free survival over Dara-VCD.
  • An anticipated median major organ deterioration progression free survival is 31 months for non-ASCT participants, suggesting ASCT may extend that period.
  • Randomized phase 3 trial compares outcomes between autologous stem cell transplant and Dara-VCD consolidation for 143 participants in each arm seeking improved responses in AL amyloidosis patients with 90% power to detect efficacy differences for ASCT usage in treatment protocols under evaluation in a clinical trial activated on 12/1/2023 for duration of study participants' involvement in collecting patient data over time.

Abstract

TPS7575 Background: Light chain (AL) amyloidosis is a plasma cell malignancy characterized by the production of amyloidgenic clonal light chains that deposit in various tissues. The addition of daratumumab to bortezomib, cyclophosphamide and dexamethasone (Dara-VCD) has improved depth of hematologic and organ responses. However, this approach has not yet demonstrated an overall survival (OS) benefit with short follow-up. Autologous stem cell transplant (ASCT) consolidation remains safe and is associated with deep and durable hematologic responses with an 83% 2-year progression free survival (PFS) and up to 72% of patients achieving a VGPR or better, comparable to Dara-VCD (79%). In multiple myeloma, ASCT improved PFS even in patients who are MRD negative at the end of standard induction therapy. It is thus reasonable to consider that ASCT might provide similar benefits in AL patients. No randomized data exist to inform the optimal use of ASCT in the era of Dara-VCD. Methods: This randomized phase 3 SWOG led intergroup trial will accrue a total of 143 participants per arm and compare MOD-PFS (major organ deterioration progression free survival: defined as time from randomization to death, cardiac/renal progression, or hematologic progression) between participants receiving an ASCT with those receiving Dara-VCD consolidation following uniform Dara-VCD induction. A median MOD-PFS of 31 months is anticipated in the non-ASCT arm. This study has 90% power and a two-sided significance level of 0.05 to detect a hazard ratio of 0.62 corresponding to a MOD-PFS of 50 months in the ASCT arm. Important additional endpoints include OS, hematological PFS, cardiac and renal responses and progression, MRD negativity both by peripheral blood mass spectrometry and bone marrow next generation flow cytometry, delayed utilization of ASCT, and quality of life. This trial was activated on 12/1/2023. Funding: NIH/NCI/NCTN grants and in part by Janssen Pharmaceuticals. Clinical trial information: NCT06022939 . Table: see text

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Cite This Study

Hagen et al. (2024) studied this question.

synapsesocial.com/papers/68e67069b6db6435875fb252https://doi.org/10.1200/jco.2024.42.16_suppl.tps7575
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