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The phase 2 LYSA study of prednisone, vinblastine, doxorubicin, and bendamustine for untreated Hodgkin lymphoma in older patients.
Ghesquières, Hervé; Krzisch, Daphné; Nicolas-Virelizier, Emmanuelle; Kanoun, Salim; Gac, Anne Claire; Guidez, Stéphanie; Touati, Mohamed; Laribi, Kamel; Morschhauser, Franck; Bonnet, Christophe; Waultier-Rascalou, Agathe; Orsini-Piocelle, Frédérique; André, Marc; Fournier, Marguerite; Morand, Fabienne; Berriolo-Riedinger, Alina; Burroni, Barbara; Damotte, Diane; Traverse-Glehen, Alexandra; Quittet, Philippe; Casasnovas, Olivier.
Afiliação
  • Ghesquières H; Department of Hematology, Hopital Lyon Sud, Claude Bernard Lyon 1 University, Pierre Benite, France.
  • Krzisch D; Department of Hematology, Assistance Publique Hopitaux de Paris, Hopital Saint Louis, Paris, France.
  • Nicolas-Virelizier E; Department of Hematology, Centre Leon Berard, Claude Bernard Lyon 1 University, Lyon, France.
  • Kanoun S; Department of Hematology, Cancer Research Center of Toulouse, Team 9, INSERM Unité Mixte de Recherche 1037, Toulouse, France.
  • Gac AC; Department of Hematology, Institut d'Hematologie de Basse Normandie, Caen, France.
  • Guidez S; Hematology Department, Centre Hospitalier Universitaire, Poitiers, France.
  • Touati M; Department of Hematology, Hôpital Dupuytren, Centre Hospitalier Universitaire, Limoges, France.
  • Laribi K; Hematology Department, Centre Hospitalier, Le Mans, France.
  • Morschhauser F; Department of Hematology, Centre Hospitalier Universitaire Lille, Universite de Lille, ULR 7365 Groupe de Recherche sur les formes Injectables et les Technologies Associées, Lille, France.
  • Bonnet C; Department of Hematology, University Hospital Liege, Liege, Belgium.
  • Waultier-Rascalou A; Hematology of Department, Centre Hospitalier Universitaire, Nimes, France.
  • Orsini-Piocelle F; Department of Hematology, Centre Hospitalier Annecy Genevois, Epagny Metz-Tessy, France.
  • André M; Department of Hematology, Centre Hospitalier Universitaire, Université Catholique de Louvain Namur, Université Catholique de Louvain, Yvoir, Belgium.
  • Fournier M; Department of Statistics, Lymphoma Study Association Clinical Research, Hopital Lyon Sud, Pierre Benite, France.
  • Morand F; Department of Statistics, Lymphoma Study Association Clinical Research, Hopital Lyon Sud, Pierre Benite, France.
  • Berriolo-Riedinger A; Department of Nuclear Medicine, Centre GF Leclerc, Dijon, France.
  • Burroni B; Department of Pathology, Université de Paris Cité, Centre de Recherche des Cordeliers UMRS U1138 et GH Paris Centre APHP, Paris, France.
  • Damotte D; Department of Pathology, Université de Paris Cité, Centre de Recherche des Cordeliers UMRS U1138 et GH Paris Centre APHP, Paris, France.
  • Traverse-Glehen A; Department of Pathology, Hopital Lyon Sud, Claude Bernard Lyon 1 University, Pierre Benite, France.
  • Quittet P; Department of Hematology, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.
  • Casasnovas O; Department of Hematology, University Hospital F. Mitterrand and INSERM Unité Mixte de Recherche 1231, Dijon, France.
Blood ; 143(11): 983-995, 2024 Mar 14.
Article em En | MEDLINE | ID: mdl-37979133
ABSTRACT: Older patients with classical Hodgkin lymphoma (cHL) require more effective and less toxic therapies than younger patients. In this multicenter, prospective, phase 2 study, we investigated a new firstline therapy regimen comprising 6 cycles of prednisone (40 mg/m2, days 1-5), vinblastine (6 mg/m2, day 1), doxorubicin (40 mg/m2, day 1), and bendamustine (120 mg/m2, day 1) (PVAB regimen) every 21 days for patients with newly diagnosed cHL aged ≥61 years with an advanced Ann Arbor stage. A Mini Nutritional Assessment score ≥17 was the cutoff value for patients aged ≥70 years. The primary end point was the complete metabolic response (CMR) rate after 6 cycles. The median age of the 89 included patients was 68 years (range, 61-88 years), with 35 patients (39%) aged ≥70 years. Seventy-eight patients (88%) completed the 6 cycles. The toxicity rate was acceptable, with a 20% rate of related serious adverse events. CMR was achieved by 69 patients (77.5%; 95% confidence interval [CI], 67-86). After a median follow-up of 42 months, 31 patients progressed or relapsed (35%), and 24 died (27%) from HL (n = 11), toxicity during treatment (n = 4), secondary cancers (n = 6), or other causes (n = 3). The 4-year progression-free survival (PFS) and overall survival rates were 50% and 69%, respectively. Multivariate analysis showed that liver involvement (P = .001), lymphopenia (P = .001), CRP (P = .0005), and comedications (P = .003) were independently associated with PFS. The PVAB regimen yielded a high CMR rate with acceptable toxicity. Over long-term follow-up, survival end points were influenced by unrelated lymphoma events. This trial was registered at www.clinicaltrials.gov as #NCT02414568 and at EudraCT as 2014-001002-17.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Hodgkin Limite: Aged / Aged80 / Humans / Middle aged Idioma: En Revista: Blood Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Hodgkin Limite: Aged / Aged80 / Humans / Middle aged Idioma: En Revista: Blood Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França