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Impact and utility of follicular lymphoma GELF criteria in routine care: an Australasian Lymphoma Alliance study.
Barraclough, Allison; Agrawal, Shivam; Talaulikar, Dipti; Chong, Geoffrey; Yoo, Edward; Cheah, Chan Y; Franco, Nunzio; Nguyen, Bianca; Mutsando, Howard; Tahir, Fatima; Trotman, Judith; Huang, Jing; Keane, Colm; Lincoln, Mitchel; Cochrane, Tara; Johnston, Anna M; Dickinson, Michael; Opat, Stephen; McQuilten, Zoe K; Wood, Erica M; St George, Gayathri; Hawkes, Eliza A.
Afiliação
  • Barraclough A; Olivia Newton John Cancer Research and Wellness Centre, Austin Health, Victoria, Australia; Fiona Stanley Hospital, Western Australia.
  • Agrawal S; Olivia Newton John Cancer Research and Wellness Centre, Austin Health, Victoria, Australia; Prince of Wales Hospital, New South Wales.
  • Talaulikar D; Canberra Health Services, Australian Capital Territory, Australia; College of Health and Medicine, Australian National University, Australian Capital Territory.
  • Chong G; Olivia Newton John Cancer Research and Wellness Centre, Austin Health, Victoria, Australia; Ballarat Regional Integrated Cancer Centre, Ballarat Health Services, Victoria.
  • Yoo E; Fiona Stanley Hospital, Western Australia, Australia; Sir Charles Gairdner Hospital, Western Australia.
  • Cheah CY; Sir Charles Gairdner Hospital, Western Australia, Australia; Medical School, University of Western Australia, Western Australia.
  • Franco N; Canberra Health Services, Australian Capital Territory, Australia; College of Health and Medicine, Australian National University, Australian Capital Territory.
  • Nguyen B; Fiona Stanley Hospital, Western Australia.
  • Mutsando H; Toowoomba Hospital, Queensland, Australia; University of Queensland Rural Clinical School, Queensland.
  • Tahir F; Concord Repatriation General Hospital, University of Sydney, New South Wales.
  • Trotman J; Concord Repatriation General Hospital, University of Sydney, New South Wales.
  • Huang J; School of Clinical Sciences at Monash Health, Monash University, Victoria.
  • Keane C; Princess Alexandra Hospital, Queensland.
  • Lincoln M; Alfred Hospital, Victoria.
  • Cochrane T; Gold Coast University Hospital, Queensland, Australia; School of Medicine, Griffith University, Queensland.
  • Johnston AM; Royal Hobart Hospital, Tasmania.
  • Dickinson M; Peter MacCallum Cancer Centre and The Royal Melbourne Hospital, Victoria.
  • Opat S; School of Clinical Sciences at Monash Health, Monash University, Victoria, Australia; School of Public Health and Preventive Medicine, Monash University, Victoria.
  • McQuilten ZK; School of Clinical Sciences at Monash Health, Monash University, Victoria, Australia; School of Public Health and Preventive Medicine, Monash University, Victoria.
  • Wood EM; School of Clinical Sciences at Monash Health, Monash University, Victoria, Australia; School of Public Health and Preventive Medicine, Monash University, Victoria.
  • St George G; School of Public Health and Preventive Medicine, Monash University, Victoria.
  • Hawkes EA; Olivia Newton John Cancer Research and Wellness Centre, Austin Health, Victoria, Australia; School of Public Health and Preventive Medicine, Monash University, Victoria. eliza.hawkes@onjcri.org.au.
Haematologica ; 2024 Mar 07.
Article em En | MEDLINE | ID: mdl-38450504
ABSTRACT
Follicular Lymphoma (FL) treatment initiation is largely determined by tumor burden and symptoms. In the pre-rituximab era, the Group d'Etude des Lymphomes Folliculaires (GELF) developed widely adopted criteria to identify high tumor burden FL patients to harmonize clinical trial populations. The utilization of GELF criteria (GELFc) in routine therapeutic decision-making is poorly described. This multicenter retrospective study evaluated patterns of GELFc at presentation and GELFc utilization in therapeutic decision-making in newly diagnosed, advanced stage rituximab-era FL. Associations between GELFc, treatment given, and patient survival were analyzed in 300 eligible cases identified between 2002-2019. 163 (54%) had ≥1 GELFc at diagnosis. The presence or cumulative number of GELFc did not predict PFS in patients undergoing watch-and-wait (WW) or those receiving systemic treatment. Of interest, in patients with ≥1 GELFc, 16/163 (10%) underwent initial watch-and-wait (comprising 22% of the watchand- wait cohort). In those receiving systemic therapy +/- radiotherapy, 74/215 (34%) met no GELFc. Our data suggest clinicians are using adjunctive measures to make decisions regarding treatment initiation in a significant proportion of patients. By restricting FL clinical trial eligibility only to those meeting GELFc, reported outcomes may not be applicable to a significant proportion of patients treated in routine care settings.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article