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Intensive salvage chemotherapy with VDTPACE or mCBAD followed by hematopoietic stem-cell support for refractory/relapsed multiple myeloma.
Marques, Carolina Perrone; Ovigli, Danielle; Kerbauy, Mariana Nassif; Silveira, Ana Carolina de Almeida; Helman, Ricardo; da Silva, Cinthya Correa; Ribeiro, Andreza Alice Feitosa; Hamerschlak, Nelson; Arcuri, Leonardo Javier.
Afiliação
  • Marques CP; Bone Marrow Transplant Department, Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Ovigli D; Bone Marrow Transplant Department, Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Kerbauy MN; Bone Marrow Transplant Department, Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Silveira ACA; Bone Marrow Transplant Department, Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Helman R; Bone Marrow Transplant Department, Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • da Silva CC; Bone Marrow Transplant Department, Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Ribeiro AAF; Bone Marrow Transplant Department, Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Hamerschlak N; Bone Marrow Transplant Department, Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Arcuri LJ; Bone Marrow Transplant Department, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Eur J Haematol ; 113(4): 460-464, 2024 Oct.
Article em En | MEDLINE | ID: mdl-38890814
ABSTRACT

INTRODUCTION:

Triple- and quad-refractory multiple myeloma patients usually have an aggressive course and a poor prognosis. Available therapeutic options are scarce.

METHODS:

The objective of the current study was to evaluate responses and toxicities of VDTPACE or mCBAD with hematopoietic stem-cell support as a bridge to subsequent therapies in patients with refractory/relapsed multiple myeloma.

RESULTS:

Thirteen patients were included (11 mCBAD, 2 VDTPACE), and 21 cycles of chemotherapy with hematopoietic stem-cell support were delivered. Mean number of previous therapies was 4.8. Stem cells were infused on a median day 9.9 after chemotherapy. Mean time to neutrophil recovery was 18.2 days in patients receiving the first cycle and 15.9 following subsequent cycles. Before therapy, most patients were in PD (77%), PR (15%), or VGPR (8%). Following treatment, the best responses achieved were PR (46%), VGPR (46%), and CR (8%). Median overall and progression-free survivals were 17 and 9 months. There has been no case of non-relapse mortality. In the 21 cycles, the main complications were infectious.

CONCLUSION:

Intensive chemotherapy can decrease disease burden in patients with relapsed/refractory MM, and stem-cell support can successfully decrease toxicities and treatment-related mortality associated with these regimens and may be a good bridging option.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Terapia de Salvação / Transplante de Células-Tronco Hematopoéticas / Mieloma Múltiplo Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Terapia de Salvação / Transplante de Células-Tronco Hematopoéticas / Mieloma Múltiplo Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article