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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.
Biran, Noa; Rowley, Scott D; Vesole, David H; Zhang, Shijia; Donato, Michele L; Richter, Joshua; Skarbnik, Alan P; Pecora, Andrew; Siegel, David S.
Afiliação
  • Biran N; John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
  • Rowley SD; John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey. Electronic address: srowley@hackensackumc.org.
  • Vesole DH; John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
  • Zhang S; Department of Medicine, Rutgers New Jersey Medical School, Newark, New Jersey.
  • Donato ML; John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
  • Richter J; John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
  • Skarbnik AP; John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
  • Pecora A; John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
  • Siegel DS; John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, New Jersey.
Biol Blood Marrow Transplant ; 22(12): 2165-2171, 2016 12.
Article em En | MEDLINE | ID: mdl-27590107
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Terapia de Salvação / Condicionamento Pré-Transplante / Bortezomib / Melfalan / Mieloma Múltiplo Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Terapia de Salvação / Condicionamento Pré-Transplante / Bortezomib / Melfalan / Mieloma Múltiplo Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article