Haematologica (Nov 2016)

Autotransplant with and without induction chemotherapy in older multiple myeloma patients: long-term outcome of a randomized trial

  • Christian Straka,
  • Peter Liebisch,
  • Hans Salwender,
  • Burkhard Hennemann,
  • Bernd Metzner,
  • Stefan Knop,
  • Sigrid Adler-Reichel,
  • Christian Gerecke,
  • Hannes Wandt,
  • Martin Bentz,
  • Tim Hendrik Bruemmendorf,
  • Marcus Hentrich,
  • Michael Pfreundschuh,
  • Hans-Heinrich Wolf,
  • Orhan Sezer,
  • Ralf Bargou,
  • Wolfram Jung,
  • Lorenz Trümper,
  • Bernd Hertenstein,
  • Else Heidemann,
  • Helga Bernhard,
  • Nicola Lang,
  • Norbert Frickhofen,
  • Holger Hebart,
  • Ralf Schmidmaier,
  • Andreas Sandermann,
  • Tobias Dechow,
  • Albrecht Reichle,
  • Brigitte Schnabel,
  • Kerstin Schäfer-Eckart,
  • Christian Langer,
  • Martin Gramatzki,
  • Axel Hinke,
  • Bertold Emmerich,
  • Hermann Einsele

DOI
https://doi.org/10.3324/haematol.2016.151860
Journal volume & issue
Vol. 101, no. 11

Abstract

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Autologous transplantation is controversial for older patients with multiple myeloma. The role of age-adjusted high-dose melphalan and the impact of induction chemotherapy cycles is still unclear. A total of 434 patients aged 60–70 years were randomly assigned to 4 cycles of standard anthracycline-based induction chemotherapy or no induction. For all patients, double autologous transplantation after melphalan 140 mg/m2 (MEL140) was planned. The primary end point was progression-free survival. Of 420 eligible patients, 85% received a first transplant and 69% completed double transplantation. Treatment duration was short with a median of 7.7 months with induction chemotherapy cycles and 4.6 months without induction. On an intention-to-treat basis, median progression-free survival with induction chemotherapy cycles (207 patients) was 21.4 months versus 20.0 months with no induction cycles (213 patients) (hazard ratio 1.04, 95% confidence interval 0.84–1.28; P=0.36). Per protocol, progression-free survival was 23.7 months versus 23.0 months (P=0.28). Patients aged 65 years or over (55%) did not have an inferior outcome. Patients with low-risk cytogenetics [absence of del17p13, t(4;14) and 1q21 gains] showed a favorable overall survival and included the patients with sustained first remission. MEL140 was associated with a low rate of severe mucositis (10%) and treatment-related deaths (1%). Based on hazard ratio, the short treatment arm consisting of mobilization chemotherapy and tandem MEL140 achieved 96% of the progression-free survival, demonstrating its value as an independent component of therapy in older patients with multiple myeloma who are considered fit for autologous transplantation. (clinicaltrials.gov identifier: 02288741)