Front-line management of non-Hodgkin lymphoma in Australia. Part 1: follicular lymphoma.


Journal

Internal medicine journal
ISSN: 1445-5994
Titre abrégé: Intern Med J
Pays: Australia
ID NLM: 101092952

Informations de publication

Date de publication:
04 2019
Historique:
received: 22 02 2018
revised: 29 08 2018
accepted: 02 09 2018
pubmed: 20 9 2018
medline: 9 1 2020
entrez: 20 9 2018
Statut: ppublish

Résumé

Outcomes with follicular lymphoma (FL) have improved in the modern era and median survival is now beyond 15 years. Therapeutic decisions need to consider this increased survival as well as recent clinical trial data and emerging treatments. In this context, we present here current approaches to front-line management of FL in Australia. Treatment choices depend on the disease stage, tumour burden, the patient's age, symptoms, comorbidities and preferences. Only about 10-15% of patients with FL are diagnosed with early stage disease. For patients with low-grade, early stage disease, radiotherapy (RT) is recommended. The addition of chemotherapy has been shown to increase progression-free survival (PFS) but without demonstrated overall survival advantage. For patients with low-tumour-burden, advanced-stage FL, immediate treatment may not be required and we recommend considering active monitoring. For stage III/IV disease that is symptomatic and/or with high tumour burden, established first-line treatment is chemotherapy in combination with rituximab, often followed by rituximab maintenance. The listing of bendamustine and now obinutuzumab on the Pharmaceutical Benefits Scheme has expanded the first-line treatment options in Australia to include bendamustine in combination with rituximab (without rituximab maintenance permitted) or with obinutuzumab plus 2 years obintuzumab maintenance. In the FL subgroup of the Study group indolent Lymphomas (StiL) trial, therapy with bendamustine plus rituximab significantly increased PFS compared with rituximab in combination with cyclophosphamide, doxorubicin, vincristine and prednisolone, without rituximab maintenance. Initial tolerability may be more favourable with bendamustine in combination with anti-CD20 antibody therapy than other therapies overall, but clinical vigilance is still required because of concerns of late infectious toxicities associated with prolonged T-cell depletion.

Identifiants

pubmed: 30230156
doi: 10.1111/imj.14113
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Rituximab 4F4X42SYQ6
Vincristine 5J49Q6B70F
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
Bendamustine Hydrochloride 981Y8SX18M
obinutuzumab O43472U9X8

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

422-433

Subventions

Organisme : JANSSEN-CILAG Australia
Pays : International

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2018 Royal Australasian College of Physicians.

Auteurs

Judith Trotman (J)

Department of Haematology, Concord Hospital, Sydney, New South Wales, Australia.
Department of Medicine, University of Sydney, Sydney, New South Wales, Australia.

Chan Y Cheah (CY)

Department of Haematology, Sir Charles Gairdner Hospital, Western Australia, Australia.
Department of Haematology, Pathwest Laboratory Medicine, Western Australia, Australia.
School of Medicine, University of Western Australia, Perth, Western Australia, Australia.

Paula Marlton (P)

Division of Cancer Services, Clinical Haematology, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
University of Queensland School of Medicine, Brisbane, Queensland, Australia.

Stephen Opat (S)

Clinical Haematology and School of Clinical Sciences, Monash Health, Victoria, Australia.
Department of Medicine, Monash University, Melbourne, Victoria, Australia.

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Classifications MeSH