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Minimal Residual Disease Status Predicts Outcome in Patients With Previously Untreated Follicular Lymphoma: A Prospective Analysis of the Phase III GALLIUM Study.
Pott, Christiane; Jurinovic, Vindi; Trotman, Judith; Kehden, Britta; Unterhalt, Michael; Herold, Michael; Jagt, Richard van der; Janssens, Ann; Kneba, Michael; Mayer, Jiri; Young, Moya; Schmidt, Christian; Knapp, Andrea; Nielsen, Tina; Brown, Helen; Spielewoy, Nathalie; Harbron, Chris; Bottos, Alessia; Mundt, Kirsten; Marcus, Robert; Hiddemann, Wolfgang; Hoster, Eva.
Affiliation
  • Pott C; University Hospital Schleswig-Holstein, Kiel, Germany.
  • Jurinovic V; Department of Internal Medicine III, University Hospital of the Ludwig-Maximilians-University Munich, Munich, Germany.
  • Trotman J; Institute for Medical Information Processing, Biometry, and Epidemiology, Faculty of Medicine, Ludwig-Maximilians-University Munich, Munich, Germany.
  • Kehden B; Concord Repatriation General Hospital, University of Sydney, Sydney, NSW, Australia.
  • Unterhalt M; University Hospital Schleswig-Holstein, Kiel, Germany.
  • Herold M; Department of Internal Medicine III, University Hospital of the Ludwig-Maximilians-University Munich, Munich, Germany.
  • Jagt RV; HELIOS Klinikum, Erfurt, Germany.
  • Janssens A; University of Ottawa, Ottawa Hospital, Ottawa, ON, Canada.
  • Kneba M; University Hospitals Leuven, Leuven, Belgium.
  • Mayer J; University Hospital Schleswig-Holstein, Kiel, Germany.
  • Young M; University Hospital and Masaryk University, Brno, Czech Republic.
  • Schmidt C; East Kent Hospital, Canterbury, United Kingdom.
  • Knapp A; Department of Internal Medicine III, University Hospital of the Ludwig-Maximilians-University Munich, Munich, Germany.
  • Nielsen T; F. Hoffmann-La Roche Ltd, Basel, Switzerland.
  • Brown H; F. Hoffmann-La Roche Ltd, Basel, Switzerland.
  • Spielewoy N; Roche Products Ltd, Welwyn Garden City, United Kingdom.
  • Harbron C; F. Hoffmann-La Roche Ltd, Basel, Switzerland.
  • Bottos A; Roche Products Ltd, Welwyn Garden City, United Kingdom.
  • Mundt K; F. Hoffmann-La Roche Ltd, Basel, Switzerland.
  • Marcus R; F. Hoffmann-La Roche Ltd, Basel, Switzerland.
  • Hiddemann W; Kings College Hospital, London, United Kingdom.
  • Hoster E; Department of Internal Medicine III, University Hospital of the Ludwig-Maximilians-University Munich, Munich, Germany.
J Clin Oncol ; 42(5): 550-561, 2024 Feb 10.
Article de En | MEDLINE | ID: mdl-38096461
ABSTRACT

PURPOSE:

We report an analysis of minimal residual/detectable disease (MRD) as a predictor of outcome in previously untreated patients with follicular lymphoma (FL) from the randomized, multicenter GALLIUM (ClinicalTrials.gov identifier NCT01332968) trial. PATIENTS AND

METHODS:

Patients received induction with obinutuzumab (G) or rituximab (R) plus bendamustine, or cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP) or cyclophosphamide, vincristine, prednisone (CVP) chemotherapy, followed by maintenance with the same antibody in responders. MRD status was assessed at predefined time points (mid-induction [MI], end of induction [EOI], and at 4-6 monthly intervals during maintenance and follow-up). Patients with evaluable biomarker data at diagnosis were included in the survival analysis.

RESULTS:

MRD positivity was associated with inferior progression-free survival (PFS) at MI (hazard ratio [HR], 3.03 [95% CI, 2.07 to 4.45]; P < .0001) and EOI (HR, 2.25 [95% CI, 1.53 to 3.32]; P < .0001). MRD response was higher after G- versus R-chemotherapy at MI (94.2% v 88.9%; P = .013) and at EOI (93.1% v 86.7%; P = .0077). Late responders (MI-positive/EOI-negative) had a significantly poorer PFS than early responders (MI-negative/EOI-negative; HR, 3.11 [95% CI, 1.75 to 5.52]; P = .00011). The smallest proportion of MRD positivity was observed in patients receiving bendamustine at MI (4.8% v 16.0% in those receiving CHOP; P < .0001). G appeared to compensate for less effective chemotherapy regimens, with similar MRD response rates observed across the G-chemo groups. During the maintenance period, more patients treated with R than with G were MRD-positive (R-CHOP, 20.7% v G-CHOP, 7.0%; R-CVP, 21.7% v G-CVP, 9.4%). Throughout maintenance, MRD positivity was associated with clinical relapse.

CONCLUSION:

MRD status can determine outcome after induction and during maintenance, and MRD negativity is a prerequisite for long-term disease control in FL. The higher MRD responses after G- versus R-based treatment confirm more effective tumor cell clearance.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Lymphome folliculaire / Gallium Limites: Humans Langue: En Journal: J Clin Oncol Année: 2024 Type de document: Article Pays d'affiliation: Allemagne

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Lymphome folliculaire / Gallium Limites: Humans Langue: En Journal: J Clin Oncol Année: 2024 Type de document: Article Pays d'affiliation: Allemagne
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