Literature DB >> 27590107

A Phase I/II Study of Escalating Doses of Bortezomib in Conjunction with High-Dose Melphalan as a Conditioning Regimen for Salvage Autologous Peripheral Blood Stem Cell Transplantation in Patients with Multiple Myeloma.

Noa Biran1, Scott D Rowley2, David H Vesole1, Shijia Zhang3, Michele L Donato1, Joshua Richter1, Alan P Skarbnik1, Andrew Pecora1, David S Siegel1.   

Abstract

Escalating doses of bortezomib with high-dose melphalan was evaluated as as a conditioning regimen for autologous stem cell transplantation (ASCT) in patients with relapsed or refractory multiple myeloma (MM). MM patients with less than a partial remission (PR) (or 50% reduction) compared to their pretransplantation paraprotein parameters after a prior ASCT with melphalan conditioning, or who were in relapse after a prior autologous transplantation, were eligible for study. Bortezomib was dose escalated in steps of 1, 1.3, and 1.6 mg/m2 (3 × 3 design) on days -4 and -1 before transplantation with melphalan 200 mg/m2 given on day -2. Thirty-two patients were enrolled: 12 in the phase I dose escalation phase and an additional 20 in phase II to gain additional experience with the regimen. Twenty-four (75%) patients were Durie Salmon stage III, and 12 (37.5%) had >2 prior lines of therapy. The overall response rate (≥PR) was 44% with 22% complete remission. Two-year overall survival and progression-free survival were 76% and 39%, respectively, with a median follow-up of 31.7 months. The most common grade 3 and 4 nonhematologic adverse events were neutropenic fever (25%), nausea (18.8%), and mucositis (9.4%). Serious adverse events included intensive care unit admission (9.4%), seizure (3.1%), prolonged diarrhea (3.1%), and Guillain-Barre syndrome (3.1%). Two patients (6%) died of sepsis. There was no emergent peripheral neuropathy nor increase in any pre-existing peripheral neuropathy. The addition of bortezomib to melphalan as conditioning for salvage ASCT was well tolerated. More importantly, it can provide durable remission for patients who have a suboptimal response to prior single-agent melphalan conditioning for ASCT, without requiring a reduction in the dose of melphalan. Larger randomized prospective studies to determine the effect of combination conditioning are being conducted.
Copyright © 2016 The American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Bortezomib; Melphalan; Multiple myeloma; Peripheral blood autologous stem cell transplantation

Mesh:

Substances:

Year:  2016        PMID: 27590107     DOI: 10.1016/j.bbmt.2016.08.017

Source DB:  PubMed          Journal:  Biol Blood Marrow Transplant        ISSN: 1083-8791            Impact factor:   5.742


  3 in total

Review 1.  The evolution of stem-cell transplantation in multiple myeloma.

Authors:  Sarakshi Mahajan; Nidhi Tandon; Shaji Kumar
Journal:  Ther Adv Hematol       Date:  2018-03-05

2.  Guillain-Barré syndrome in a patient with multiple myeloma after bortezomib therapy: A case report.

Authors:  Yu-Ling Xu; Wei-Hua Zhao; Zhong-Yuan Tang; Zhong-Qing Li; Yuan Long; Peng Cheng; Jun Luo
Journal:  World J Clin Cases       Date:  2019-09-26       Impact factor: 1.337

3.  Outcomes after delayed and second autologous stem cell transplant in patients with relapsed multiple myeloma.

Authors:  Christopher Lemieux; Lori S Muffly; David J Iberri; Juliana K Craig; Laura J Johnston; Robert Lowsky; Parveen Shiraz; Andrew R Rezvani; Matthew J Frank; Wen-Kai Weng; Everett Meyer; Judith A Shizuru; Sally Arai; Michaela Liedtke; Robert S Negrin; David B Miklos; Surbhi Sidana
Journal:  Bone Marrow Transplant       Date:  2021-06-23       Impact factor: 5.174

  3 in total

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