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A multicenter retrospective comparison of induction chemoimmunotherapy regimens on outcomes in transplant-eligible patients with previously untreated mantle cell lymphoma.
Ng, Zi Yun; Bishton, Mark; Ritchie, David; Campbell, Robert; Gilbertson, Michael; Hill, Kate; Ratnasingam, Sumita; Schwarer, Anthony; Manos, Kate; Shorten, Sophie; Ng, Melissa; Nelson, Niles; Xin, Liu; De Mel Widanalage, Sanjay; Sunny, Tenny; Purtill, Duncan; Poon, Michelle; Johnston, Anna; Cochrane, Tara; Lee, Hui-Peng; Hapgood, Greg; Tam, Constantine; Opat, Stephen; Hawkes, Eliza; Seymour, John; Cheah, Chan Yoon.
Afiliação
  • Ng ZY; Department of Haematology, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
  • Bishton M; Department of Haematology, Nottingham University Hospitals NHS Trust, Nottingham, UK.
  • Ritchie D; Department of Haematology, Royal Melbourne Hospital & Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, Victoria, Australia.
  • Campbell R; Department of Medical Oncology and Clinical Haematology, Olivia Newton John Cancer Research and Wellness Centre, Austin Health, Heidelberg, Victoria, Australia.
  • Gilbertson M; Clinical Haematology, Monash Health and Monash University, Clayton, Victoria, Australia.
  • Hill K; Cancer Care Services, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
  • Ratnasingam S; Clinical Haematology, Monash Health and Monash University, Clayton, Victoria, Australia.
  • Schwarer A; Department of Medical Oncology, Eastern Health, Box Hill, Victoria, Australia.
  • Manos K; Department of Haematology, Flinders Medical Centre, Bedford Park, South Australia, Australia.
  • Shorten S; Department of Haematology, St. Vincent's Hospital, Fitzroy, Victoria, Australia.
  • Ng M; Department of Haematology, Gold Coast University Hospital, Southport, Queensland, Australia.
  • Nelson N; Department of Haematology, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Xin L; Department of Haematology-Oncology, National University Cancer Institute Singapore, National University Health System, Singapore.
  • De Mel Widanalage S; Department of Haematology-Oncology, National University Cancer Institute Singapore, National University Health System, Singapore.
  • Sunny T; Department of Haematology, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.
  • Purtill D; Department of Haematology, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.
  • Poon M; Department of Haematology-Oncology, National University Cancer Institute Singapore, National University Health System, Singapore.
  • Johnston A; Department of Haematology, Royal Hobart Hospital, Hobart, Tasmania, Australia.
  • Cochrane T; Department of Haematology, Gold Coast University Hospital, Southport, Queensland, Australia.
  • Lee HP; Department of Haematology, Flinders Medical Centre, Bedford Park, South Australia, Australia.
  • Hapgood G; Cancer Care Services, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
  • Tam C; Department of Haematology, Royal Melbourne Hospital & Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, Victoria, Australia.
  • Opat S; Department of Haematology, St. Vincent's Hospital, Fitzroy, Victoria, Australia.
  • Hawkes E; Clinical Haematology, Monash Health and Monash University, Clayton, Victoria, Australia.
  • Seymour J; Department of Medical Oncology and Clinical Haematology, Olivia Newton John Cancer Research and Wellness Centre, Austin Health, Heidelberg, Victoria, Australia.
  • Cheah CY; Department of Medical Oncology, Eastern Health, Box Hill, Victoria, Australia.
Hematol Oncol ; 37(3): 253-260, 2019 Aug.
Article em En | MEDLINE | ID: mdl-30983008
Mantle cell lymphoma (MCL) is an uncommon and typically aggressive form of lymphoma. Although often initially chemosensitive, relapse is common. Several induction and conditioning regimens are used in transplant-eligible patients, and the optimal approach remains unknown. We performed an international, retrospective study of transplant-eligible patients to assess impact of induction chemoimmunotherapy and conditioning regimens on clinical outcomes. We identified 228 patients meeting inclusion criteria. Baseline characteristics were similar among the induction groups except for some variation in age. The type of induction chemoimmunotherapy received did not influence overall response rates (ORRs) (0.43), progression-free survival (PFS) (P > .67), or overall survival (OS) (P > .35) on multivariate analysis (PFS and OS). Delivery of autologous stem cell transplant (ASCT) was associated with favorable PFS and OS (0.01) on univariate analysis only; this benefit was not seen on multivariate analysis-PFS (0.36) and OS (0.21). Compared with busulfan and melphalan (BuMel), the use of the carmustine, etoposide, cytarabine, melphalan (BEAM)-conditioning regimen was associated with inferior PFS (HR = 2.0 [95% CI 1.1-3.6], 0.02) but not OS (HR = 1.1 [95% CI 0.5-2.3], 0.81) on univariate analysis only. Within the limits of a retrospective study and modest power for some comparisons, type of induction therapy did not influence ORR, PFS, or OS for transplant-eligible patients with MCL. International efforts are required to perform randomized clinical trials evaluating chemoimmunotherapy induction regimens.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Linfoma de Célula do Manto / Quimioterapia de Indução / Imunoterapia Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Linfoma de Célula do Manto / Quimioterapia de Indução / Imunoterapia Idioma: En Ano de publicação: 2019 Tipo de documento: Article