A multicenter retrospective comparison of induction chemoimmunotherapy regimens on outcomes in transplant-eligible patients with previously untreated mantle cell lymphoma.


Journal

Hematological oncology
ISSN: 1099-1069
Titre abrégé: Hematol Oncol
Pays: England
ID NLM: 8307268

Informations de publication

Date de publication:
Aug 2019
Historique:
received: 18 03 2019
accepted: 11 04 2019
pubmed: 16 4 2019
medline: 10 9 2019
entrez: 16 4 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 30983008
doi: 10.1002/hon.2618
doi:

Substances chimiques

Cytarabine 04079A1RDZ
Etoposide 6PLQ3CP4P3
Melphalan Q41OR9510P
Carmustine U68WG3173Y

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

253-260

Informations de copyright

© 2019 John Wiley & Sons, Ltd.

Références

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Auteurs

Zi Yun Ng (ZY)

Department of Haematology, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.

Mark Bishton (M)

Department of Haematology, Nottingham University Hospitals NHS Trust, Nottingham, UK.

David Ritchie (D)

Department of Haematology, Royal Melbourne Hospital & Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, Victoria, Australia.

Robert Campbell (R)

Department of Medical Oncology and Clinical Haematology, Olivia Newton John Cancer Research and Wellness Centre, Austin Health, Heidelberg, Victoria, Australia.

Michael Gilbertson (M)

Clinical Haematology, Monash Health and Monash University, Clayton, Victoria, Australia.

Kate Hill (K)

Cancer Care Services, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Sumita Ratnasingam (S)

Clinical Haematology, Monash Health and Monash University, Clayton, Victoria, Australia.

Anthony Schwarer (A)

Department of Medical Oncology, Eastern Health, Box Hill, Victoria, Australia.

Kate Manos (K)

Department of Haematology, Flinders Medical Centre, Bedford Park, South Australia, Australia.

Sophie Shorten (S)

Department of Haematology, St. Vincent's Hospital, Fitzroy, Victoria, Australia.

Melissa Ng (M)

Department of Haematology, Gold Coast University Hospital, Southport, Queensland, Australia.

Niles Nelson (N)

Department of Haematology, Royal Hobart Hospital, Hobart, Tasmania, Australia.

Liu Xin (L)

Department of Haematology-Oncology, National University Cancer Institute Singapore, National University Health System, Singapore.

Sanjay De Mel Widanalage (S)

Department of Haematology-Oncology, National University Cancer Institute Singapore, National University Health System, Singapore.

Tenny Sunny (T)

Department of Haematology, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.

Duncan Purtill (D)

Department of Haematology, Fiona Stanley Hospital, Murdoch, Western Australia, Australia.

Michelle Poon (M)

Department of Haematology-Oncology, National University Cancer Institute Singapore, National University Health System, Singapore.

Anna Johnston (A)

Department of Haematology, Royal Hobart Hospital, Hobart, Tasmania, Australia.

Tara Cochrane (T)

Department of Haematology, Gold Coast University Hospital, Southport, Queensland, Australia.

Hui-Peng Lee (HP)

Department of Haematology, Flinders Medical Centre, Bedford Park, South Australia, Australia.

Greg Hapgood (G)

Cancer Care Services, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Constantine Tam (C)

Department of Haematology, Royal Melbourne Hospital & Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, Victoria, Australia.
Department of Haematology, St. Vincent's Hospital, Fitzroy, Victoria, Australia.

Stephen Opat (S)

Clinical Haematology, Monash Health and Monash University, Clayton, Victoria, Australia.

Eliza Hawkes (E)

Department of Medical Oncology and Clinical Haematology, Olivia Newton John Cancer Research and Wellness Centre, Austin Health, Heidelberg, Victoria, Australia.
Department of Medical Oncology, Eastern Health, Box Hill, Victoria, Australia.

John Seymour (J)

Department of Haematology, Royal Melbourne Hospital & Peter MacCallum Cancer Centre, University of Melbourne, Melbourne, Victoria, Australia.

Chan Yoon Cheah (CY)

Department of Haematology, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
Medical School, University of Western Australia, Crawley, Western Australia, Australia.

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