Early treatment intensification with R-ICE and 90Y-ibritumomab tiuxetan (Zevalin)-BEAM stem cell transplantation in patients with high-risk diffuse large B-cell lymphoma patients and positive interim PET after 4 cycles of R-CHOP-14
Mark Hertzberg,
Maher K. Gandhi,
Judith Trotman,
Belinda Butcher,
John Taper,
Amanda Johnston,
Devinder Gill,
Shir-Jing Ho,
Gavin Cull,
Keith Fay,
Geoff Chong,
Andrew Grigg,
Ian D. Lewis,
Sam Milliken,
William Renwick,
Uwe Hahn,
Robin Filshie,
George Kannourakis,
Anne-Marie Watson,
Pauline Warburton,
Andrew Wirth,
John F. Seymour,
Michael S. Hofman,
Rodney J. Hicks
Affiliations
Mark Hertzberg
Department of Haematology, Prince of Wales Hospital and University of NSW, Randwick, NSW, Australia
Maher K. Gandhi
The University of Queensland Diamantina Institute Woolloongabba, Brisbane, QLD, Australia;Department of Haematology, Princess Alexandra Hospital Brisbane, QLD, Australia
Judith Trotman
Department of Haematology, Repatriation General Hospital Concord and University of Sydney, NSW, Australia
Belinda Butcher
WriteSource Medical Pty Ltd., Lane Cove, NSW, Australia
John Taper
Nepean Cancer Care Centre, Nepean Hospital Nepean, NSW, Australia
Amanda Johnston
Department of Haematology, Westmead Hospital, NSW, Australia
Devinder Gill
Department of Haematology, Princess Alexandra Hospital Brisbane, QLD, Australia
Shir-Jing Ho
Department of Haematology, St George Hospital Kogarah, NSW, Australia
Gavin Cull
Department of Haematology, Sir Charles Gairdner Hospital Perth, WA, Australia
Keith Fay
Department of Haematology, Royal North Shore Hospital, St Leonard’s, NSW, Australia
Geoff Chong
Olivia Newton John Cancer & Wellness Centre, Austin Hospital, Heidelberg, VIC, Australia
Andrew Grigg
Department of Haematology, Austin Hospital, Heidelberg, VIC, Australia
Ian D. Lewis
Department of Haematology, Royal Adelaide Hospital Adelaide, SA, Australia
Sam Milliken
Department of Haematology, St Vincent’s Hospital Darlinghurst, NSW, Australia
William Renwick
Department of Haematology, Royal Melbourne Hospital Parkville, VIC, Australia
Uwe Hahn
Department of Haematology, The Queen Elizabeth Hospital, SA, Australia
Robin Filshie
Department of Haematology, St Vincent’s Hospital Melbourne, VIC, Australia
George Kannourakis
Ballarat Oncology and Haematology Service and Fiona Elsey Cancer Research Institute, Ballarat, VIC, Australia
Anne-Marie Watson
Department of Haematology, Liverpool Hospital, Liverpool, NSW, Australia
Pauline Warburton
Department of Haematology, Wollongong Hospital, Wollongong, NSW, Australia
Andrew Wirth
Department of Radiation Oncology, Peter MacCallum Cancer Centre East Melbourne, VIC, Australia
John F. Seymour
Department of Haematology, Peter MacCallum Cancer Centre East Melbourne and University of Melbourne, Parkville, VIC, Australia
Michael S. Hofman
Department of Cancer Imaging, Peter MacCallum Cancer Centre East Melbourne, VIC, Australia
Rodney J. Hicks
Department of Cancer Imaging, Peter MacCallum Cancer Centre East Melbourne, VIC, Australia
In the treatment of diffuse large B-cell lymphoma, a persistently positive [18F]fluorodeoxyglucose positron emission tomography (PET) scan typically carries a poor prognosis. In this prospective multi-center phase II study, we sought to establish whether treatment intensification with R-ICE (rituximab, ifosfamide, carboplatin, and etoposide) chemotherapy followed by 90Y-ibritumomab tiuxetan–BEAM (BCNU, etoposide, cytarabine, and melphalan) for high-risk diffuse large B-cell lymphoma patients who are positive on interim PET scan after 4 cycles of R-CHOP-14 (rituximab, cyclophosphamide, doxorubicin, and prednisone) can improve 2-year progression-free survival from a historically unfavorable rate of 40% to a rate of 65%. Patients received 4 cycles of R-CHOP-14, followed by a centrally-reviewed PET performed at day 17–20 of cycle 4 and assessed according to International Harmonisation Project criteria. Median age of the 151 evaluable patients was 57 years, with 79% stages 3–4, 54% bulk, and 54% International Prognostic Index 3–5. Among the 143 patients undergoing interim PET, 101 (71%) were PET-negative (96 of whom completed R-CHOP), 42 (29%) were PET-positive (32 of whom completed R-ICE and 90Y-ibritumomab tiuxetan-BEAM). At a median follow up of 35 months, the 2-year progression-free survival for PET-positive patients was 67%, a rate similar to that for PET-negative patients treated with R-CHOP-14 (74%, P=0.11); overall survival was 78% and 88% (P=0.11), respectively. In an exploratory analysis, progression-free and overall survival were markedly superior for PET-positive Deauville score 4 versus score 5 (P=0.0002 and P=0.001, respectively). Therefore, diffuse large B-cell lymphoma patients who are PET-positive after 4 cycles of R-CHOP-14 and who switched to R-ICE and 90Y-ibritumomab tiuxetan-BEAM achieved favorable survival outcomes similar to those for PET-negative R-CHOP-14-treated patients. Further studies are warranted to confirm these promising results. (Registered at: ACTRN12609001077257).