Atacicept in relapsed/refractory multiple myeloma or active Waldenström's macroglobulinemia: a phase I study

J-F Rossi, J Moreaux, D Hose, G Requirand, M Rose, V Rouillé, I Nestorov, G Mordenti, H Goldschmidt, A Ythier, B Klein

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75 Citations (Scopus)

Abstract

BACKGROUND: Advanced multiple myeloma (MM) and Waldenström's macroglobulinemia (WM) are incurable B-cell malignancies. This is the first full clinical report of atacicept, a fusion protein that binds to and neutralises the B-cell survival factors, B-lymphocyte stimulator (BLyS) and A proliferation-inducing ligand (APRIL), in MM and WM.

METHODS: In this open-label phase-I study, 16 patients with advanced disease (12 MM, 4 WM) received one cycle of five once-weekly subcutaneous injections of atacicept (2, 4, 7 or 10 mg kg(-1)). Patients with stable disease after cycle 1 entered an extension study (either two additional cycles (2, 4 and 7 mg kg(-1) cohorts) or 15 consecutive weekly injections of atacicept 10 mg kg(-1)).

RESULTS: Atacicept was well tolerated, systemically and locally; the maximum tolerated dose was not identified. Of 11 patients with MM who completed initial treatment, five patients were progression-free after cycle 1 and four patients were progression-free after extended therapy. Of four patients with WM, three patients were progression-free after cycle 1. Consistent with atacicept's mechanism of action, polyclonal immunoglobulin isotypes and total B cells were reduced. Bone-marrow density, myeloma cell numbers and plasma concentrations of soluble CD138 also decreased.

CONCLUSION: Atacicept is well tolerated in patients with MM and WM, and shows clinical and biological activity consistent with its mechanism of action.

Original languageEnglish
Pages (from-to)1051-1058
Number of pages8
JournalBritish Journal of Cancer
Volume101
Issue number7
DOIs
Publication statusPublished - Sept 2009
Externally publishedYes

Keywords

  • Aged
  • Female
  • Humans
  • Immunoglobulin G/analysis
  • Immunoglobulin M/analysis
  • Male
  • Middle Aged
  • Multiple Myeloma/drug therapy
  • Recombinant Fusion Proteins/adverse effects
  • Syndecan-1/blood
  • Waldenstrom Macroglobulinemia/drug therapy

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