Blood Advances (Oct 2019)
Outcomes of stage I/II follicular lymphoma in the PET era: an international study from the Australian Lymphoma Alliance
- Joshua W.D. Tobin,
- Gabrielle Rule,
- Katherine Colvin,
- Lourdes Calvente,
- David Hodgson,
- Stephen Bell,
- Chengetai Dunduru,
- James Gallo,
- Erica S. Tsang,
- Xuan Tan,
- Jonathan Wong,
- Jessica Pearce,
- Robert Campbell,
- Shao Tneh,
- Sophie Shorten,
- Melissa Ng,
- Tara Cochrane,
- Constantine S. Tam,
- Emad Abro,
- Eliza Hawkes,
- Georgina Hodges,
- Roopesh Kansara,
- Dipti Talaulikar,
- Michael Gilbertson,
- Anna M. Johnston,
- Kerry J. Savage,
- Diego Villa,
- Kirk Morris,
- Sumi Ratnasingam,
- Wojt Janowski,
- Robert Kridel,
- Chan Y. Cheah,
- Michael MacManus,
- Nicholas Matigian,
- Peter Mollee,
- Maher K. Gandhi,
- Greg Hapgood
Affiliations
- Joshua W.D. Tobin
- Department of Haematology, Princess Alexandra Hospital, Brisbane, QLD, Australia;
- Gabrielle Rule
- Department of Haematology, Sir Charles Gairdner Hospital, Perth, WA, Australia;
- Katherine Colvin
- Department of Haematology, Sir Charles Gairdner Hospital, Perth, WA, Australia;
- Lourdes Calvente
- Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, Canada;
- David Hodgson
- Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, Canada;
- Stephen Bell
- Department of Haematology, Calvary Mater Health, Newcastle, NSW, Australia;
- Chengetai Dunduru
- Department of Haematology, Andrew Love Cancer Centre, University Hospital Geelong, Geelong, VIC, Australia;
- James Gallo
- Department of Haematology, Royal Brisbane Hospital, Brisbane, QLD, Australia;
- Erica S. Tsang
- Division of Medical Oncology, BC Cancer, Vancouver, BC, Canada;
- Xuan Tan
- Department of Haematology, Royal Hobart Hospital, Hobart, TAS, Australia;
- Jonathan Wong
- Department of Clinical Haematology, Monash Health, Melbourne, Victoria, Australia
- Jessica Pearce
- Department of Haematology, Townsville Hospital, Townsville, QLD, Australia;
- Robert Campbell
- Department of Oncology and Clinical Haematology, Austin Hospital, Melbourne, VIC, Australia;
- Shao Tneh
- Department of Haematology, Mater Hospital Brisbane, Brisbane, QLD, Australia;
- Sophie Shorten
- Department of Haematology, St Vincent's Hospital, Melbourne, VIC, Australia;
- Melissa Ng
- Department of Haematology, Gold Coast University Hospital, Gold Coast, QLD, Australia;
- Tara Cochrane
- Department of Haematology, Gold Coast University Hospital, Gold Coast, QLD, Australia;
- Constantine S. Tam
- Department of Haematology, St Vincent's Hospital, Melbourne, VIC, Australia;
- Emad Abro
- Department of Haematology, Mater Hospital Brisbane, Brisbane, QLD, Australia;
- Eliza Hawkes
- Department of Oncology and Clinical Haematology, Austin Hospital, Melbourne, VIC, Australia;
- Georgina Hodges
- Department of Haematology, Townsville Hospital, Townsville, QLD, Australia;
- Roopesh Kansara
- Section of Medical Oncology and Haematology, University of Manitoba, Winnipeg, MB, Canada;
- Dipti Talaulikar
- Department of Haematology, Canberra Hospital, Canberra, ACT, Australia;
- Michael Gilbertson
- Department of Clinical Haematology, Monash Health, Melbourne, Victoria, Australia
- Anna M. Johnston
- Department of Haematology, Royal Hobart Hospital, Hobart, TAS, Australia;
- Kerry J. Savage
- Division of Medical Oncology, BC Cancer, Vancouver, BC, Canada;
- Diego Villa
- Division of Medical Oncology, BC Cancer, Vancouver, BC, Canada;
- Kirk Morris
- Department of Haematology, Royal Brisbane Hospital, Brisbane, QLD, Australia;
- Sumi Ratnasingam
- Department of Haematology, Andrew Love Cancer Centre, University Hospital Geelong, Geelong, VIC, Australia;
- Wojt Janowski
- Department of Haematology, Calvary Mater Health, Newcastle, NSW, Australia;
- Robert Kridel
- Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, Canada;
- Chan Y. Cheah
- Department of Haematology, Sir Charles Gairdner Hospital, Perth, WA, Australia;
- Michael MacManus
- Peter MacCallum Cancer Centre, Melbourne, VIC, Australia
- Nicholas Matigian
- QFAB Bioinformatics, Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia
- Peter Mollee
- Department of Haematology, Princess Alexandra Hospital, Brisbane, QLD, Australia;
- Maher K. Gandhi
- Department of Haematology, Princess Alexandra Hospital, Brisbane, QLD, Australia;
- Greg Hapgood
- Department of Haematology, Princess Alexandra Hospital, Brisbane, QLD, Australia;; Greg Hapgood, Princess Alexandra Hospital, 199 Ipswich Rd, Woolloongabba, Brisbane, QLD 4102, Australia;
- Journal volume & issue
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Vol. 3,
no. 19
pp. 2804 – 2811
Abstract
Abstract: Management practices in early-stage (I/II) follicular lymphoma (FL) are variable and include radiation (RT), systemic therapy, or combined modality therapy (CMT). There is a paucity of data regarding maintenance rituximab in this cohort. We conducted an international retrospective study of patients with newly diagnosed early-stage FL staged with positron emission tomography (PET)–computed tomography and bone marrow biopsy. Three hundred sixty-five patients (stage I, n = 221), median age 63 years, treated from 2005-2017 were included, with a median follow-up of 45 months. Management included watchful waiting (WW; n = 85) and active treatment (n = 280). The latter consisted of RT alone (n = 171) or systemic therapy (immunochemotherapy [n = 63] or CMT [n = 46]). Forty-nine systemically treated patients received maintenance rituximab; 72.7% of stage I patients received RT alone, compared to 42.6% with stage II (P < .001). Active therapies yielded comparable overall response rates (P = .87). RT alone and systemic therapy without maintenance rituximab yielded similar progression-free survival (PFS) (hazard ratio [HR], 1.32; 95% confidence interval [CI], 0.77-2.34; P = .96). Maintenance rituximab improved PFS (HR, 0.24; 95% CI, 0.095-0.64; P = .017). The incidence of transformation was lower with systemic therapy compared to RT or WW (HR, 0.20; 95% CI, 0.070-0.61; P = .034). Overall survival was similar among all practices, including WW (P = .40). In the largest comparative assessment of management practices in the modern era, variable practices each resulted in similar excellent outcomes. Randomized studies are required to determine the optimal treatment in early-stage FL.