Primary failure of bortezomib in newly diagnosed multiple myeloma--understanding the magnitude, predictors, and significance

Leuk Lymphoma. 2016;57(6):1382-8. doi: 10.3109/10428194.2015.1121258. Epub 2016 Jan 4.

Abstract

Botezomib-based induction is highly effective for the treatment of newly diagnosed multiple myeloma (NDMM). We investigated the outcomes of NDMM patients who failed to respond to bortezomib-based induction in a 'real-life' clinical setting. In a cohort of 295 consecutive NDMM patients in 3 medical centers, 74 (25%) failed to achieve at least partial response after 4 induction cycles, and were classified as non-responsive. Compared to induction responders, they were older, more frequently anemic, had a higher incidence of del17p and ISS-3, and a worse performance status. In multivariable analysis, bortezomib-based induction failure occurred in 25% of patients and was the strongest independent factor predicting mortality with a 5-fold hazard ratio (95% CI 1.44-8.68). Three-year overall survival in responsive vs. non-responsive patients were 76% vs. 53%, respectively (p < 0.0001). Survival from time of salvage second-line treatment was significantly shorter among induction non-responders vs. responders (25 months vs. not-reached, p = 0.024).

Keywords: Bortezomib; induction; myeloma; resistance; survival.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / therapeutic use*
  • Bortezomib / administration & dosage
  • Bortezomib / therapeutic use*
  • Combined Modality Therapy
  • Drug Resistance, Neoplasm
  • Female
  • Hematopoietic Stem Cell Transplantation
  • Humans
  • Male
  • Middle Aged
  • Multiple Myeloma / diagnosis
  • Multiple Myeloma / drug therapy*
  • Multiple Myeloma / mortality
  • Neoplasm Recurrence, Local
  • Neoplasm Staging
  • Paraproteins
  • Prognosis
  • Proportional Hazards Models
  • Remission Induction
  • Treatment Failure
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • Paraproteins
  • Bortezomib