Your browser doesn't support javascript.
loading
Primary gastric diffuse large B-cell lymphoma: A multicentre retrospective study.
Lewis, Cameron S; Joy, Greta; Jensen, Paw; Barraclough, Allison; Franco, Nunzio; Talaulikar, Dipti; Hawkes, Eliza A; El-Galaly, Tarec Christoffer; Villa, Diego; Dickinson, Michael; Seymour, John F; Cheah, Chan Y.
Affiliation
  • Lewis CS; Department of Haematology, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
  • Joy G; Department of Haematology, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, Victoria, Australia.
  • Jensen P; Centre for Lymphoid Cancer, British Columbia Cancer, Vancouver, British Columbia, Canada.
  • Barraclough A; University of British Columbia, Vancouver, British Columbia, Canada.
  • Franco N; Department of Hematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
  • Talaulikar D; Department of Haematology, Austin Health, Melbourne, Victoria, Australia.
  • Hawkes EA; Department of Haematology, Fiona Stanley Hospital, Perth, Western Australia, Australia.
  • El-Galaly TC; Department of Haematology, ACT Pathology, Canberra Health Services, Canberra, Australian Capital Territory, Australia.
  • Villa D; Department of Haematology, ACT Pathology, Canberra Health Services, Canberra, Australian Capital Territory, Australia.
  • Dickinson M; College of Health and Medicine, Australian National University, Canberra, Australian Capital Territory, Australia.
  • Seymour JF; Department of Haematology, Austin Health, Melbourne, Victoria, Australia.
  • Cheah CY; School of Public Health and Preventative Medicine, Monash University, Melbourne, Victoria, Australia.
Br J Haematol ; 205(2): 534-541, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38632873
ABSTRACT
Primary gastric diffuse large B-cell lymphoma (PG-DLBCL) accounts for the majority of extra-nodal DLBCL. Even so, literature is lacking on early, localised presentations. We studied a cohort of patients with stage I disease, diagnosed between 2006 and 2018, from six centres between Australia, Canada and Denmark. Our goal was to characterise outcomes, review treatment and investigate the role of interim positron emission tomography (iPET). Thirty-seven eligible patients were identified. The median duration of follow-up was 42.2 months. All received chemoimmunotherapy with 91.9% (n = 34) given rituximab, cyclophosphamide, doxorubicin, vincristine and prednisolone (R-CHOP). 35.1% (n = 13) underwent consolidative radiotherapy. Eighteen patients were H. pylori positive and 11 had the documentation of H. pylori eradication therapy. The 4-year progression-free survival and overall survival of R-CHOP was 88% (95% CI 71-95) and 91% (95% CI 75-97) respectively. All patients who achieved a partial metabolic response or complete metabolic response on iPET went on to achieve complete response at the end of treatment. R-CHOP-based therapy with iPET assessment appears to offer favourable outcomes, with radiotherapy and H. pylori eradication therapy implemented on a case-by-case basis.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stomach Neoplasms / Antineoplastic Combined Chemotherapy Protocols / Lymphoma, Large B-Cell, Diffuse Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Br J Haematol / Br. j. haematol / British journal of haematology Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stomach Neoplasms / Antineoplastic Combined Chemotherapy Protocols / Lymphoma, Large B-Cell, Diffuse Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Br J Haematol / Br. j. haematol / British journal of haematology Year: 2024 Document type: Article Affiliation country: Country of publication: