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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.
Hertzberg, Mark; Gandhi, Maher K; Trotman, Judith; Butcher, Belinda; Taper, John; Johnston, Amanda; Gill, Devinder; Ho, Shir-Jing; Cull, Gavin; Fay, Keith; Chong, Geoff; Grigg, Andrew; Lewis, Ian D; Milliken, Sam; Renwick, William; Hahn, Uwe; Filshie, Robin; Kannourakis, George; Watson, Anne-Marie; Warburton, Pauline; Wirth, Andrew; Seymour, John F; Hofman, Michael S; Hicks, Rodney J.
Afiliação
  • Hertzberg M; Department of Haematology, Prince of Wales Hospital and University of NSW, Randwick, NSW, Australia mhertzberg10@gmail.com.
  • Gandhi MK; The University of Queensland Diamantina Institute Woolloongabba, Brisbane, QLD, Australia.
  • Trotman J; Department of Haematology, Princess Alexandra Hospital Brisbane, QLD, Australia.
  • Butcher B; Department of Haematology, Repatriation General Hospital Concord and University of Sydney, NSW, Australia.
  • Taper J; WriteSource Medical Pty Ltd., Lane Cove, NSW, Australia.
  • Johnston A; Nepean Cancer Care Centre, Nepean Hospital Nepean, NSW, Australia.
  • Gill D; Department of Haematology, Westmead Hospital, NSW, Australia.
  • Ho SJ; Department of Haematology, Princess Alexandra Hospital Brisbane, QLD, Australia.
  • Cull G; Department of Haematology, St George Hospital Kogarah, NSW, Australia.
  • Fay K; Department of Haematology, Sir Charles Gairdner Hospital Perth, WA, Australia.
  • Chong G; Department of Haematology, Royal North Shore Hospital, St Leonard's, NSW, Australia.
  • Grigg A; Olivia Newton John Cancer & Wellness Centre, Austin Hospital, Heidelberg, VIC, Australia.
  • Lewis ID; Department of Haematology, Austin Hospital, Heidelberg, VIC, Australia.
  • Milliken S; Department of Haematology, Royal Adelaide Hospital Adelaide, SA, Australia.
  • Renwick W; Department of Haematology, St Vincent's Hospital Darlinghurst, NSW, Australia.
  • Hahn U; Department of Haematology, Royal Melbourne Hospital Parkville, VIC, Australia.
  • Filshie R; Department of Haematology, The Queen Elizabeth Hospital, SA, Australia.
  • Kannourakis G; Department of Haematology, St Vincent's Hospital Melbourne, VIC, Australia.
  • Watson AM; Ballarat Oncology and Haematology Service and Fiona Elsey Cancer Research Institute, Ballarat, VIC, Australia.
  • Warburton P; Department of Haematology, Liverpool Hospital, Liverpool, NSW, Australia.
  • Wirth A; Department of Haematology, Wollongong Hospital, Wollongong, NSW, Australia.
  • Seymour JF; Department of Radiation Oncology, Peter MacCallum Cancer Centre East Melbourne, VIC, Australia.
  • Hofman MS; Department of Haematology, Peter MacCallum Cancer Centre East Melbourne and University of Melbourne, Parkville, VIC, Australia.
  • Hicks RJ; Department of Cancer Imaging, Peter MacCallum Cancer Centre East Melbourne, VIC, Australia.
Haematologica ; 102(2): 356-363, 2017 02.
Article em En | MEDLINE | ID: mdl-28143954
ABSTRACT
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).
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma Difuso de Grandes Células B / Tomografia por Emissão de Pósitrons Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Haematologica Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma Difuso de Grandes Células B / Tomografia por Emissão de Pósitrons Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Haematologica Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Austrália