Minimal Residual Disease Status Predicts Outcome in Patients With Previously Untreated Follicular Lymphoma: A Prospective Analysis of the Phase III GALLIUM Study

Author:

Pott Christiane1ORCID,Jurinovic Vindi23,Trotman Judith4ORCID,Kehden Britta1,Unterhalt Michael2,Herold Michael5ORCID,Jagt Richard van der6ORCID,Janssens Ann7,Kneba Michael1,Mayer Jiri8ORCID,Young Moya9,Schmidt Christian2,Knapp Andrea10,Nielsen Tina10,Brown Helen11ORCID,Spielewoy Nathalie10,Harbron Chris11,Bottos Alessia10,Mundt Kirsten10,Marcus Robert12,Hiddemann Wolfgang2,Hoster Eva23ORCID

Affiliation:

1. University Hospital Schleswig-Holstein, Kiel, Germany

2. Department of Internal Medicine III, University Hospital of the Ludwig-Maximilians-University Munich, Munich, Germany

3. Institute for Medical Information Processing, Biometry, and Epidemiology, Faculty of Medicine, Ludwig-Maximilians-University Munich, Munich, Germany

4. Concord Repatriation General Hospital, University of Sydney, Sydney, NSW, Australia

5. HELIOS Klinikum, Erfurt, Germany

6. University of Ottawa, Ottawa Hospital, Ottawa, ON, Canada

7. University Hospitals Leuven, Leuven, Belgium

8. University Hospital and Masaryk University, Brno, Czech Republic

9. East Kent Hospital, Canterbury, United Kingdom

10. F. Hoffmann-La Roche Ltd, Basel, Switzerland

11. Roche Products Ltd, Welwyn Garden City, United Kingdom

12. Kings College Hospital, London, United Kingdom

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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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