A phase II trial to evaluate the combination of pixantrone and obinutuzumab for patients with relapsed aggressive lymphoma : final results of the prospective, multicentre GOAL trial

dc.contributor.authorHess, Georg
dc.contributor.authorHüttmann, Andreas
dc.contributor.authorWitzens-Harig, Mathias
dc.contributor.authorDreyling, Martin H.
dc.contributor.authorKeller, Ulrich
dc.contributor.authorMarks, Reinhard
dc.contributor.authorErnst, Thomas
dc.contributor.authorPott, Christiane
dc.contributor.authorViardot, Andreas
dc.contributor.authorFrontzek, Fabian
dc.contributor.authorTrautmann, Marcel
dc.contributor.authorRuckes, Christian
dc.contributor.authorDeuster, Oliver
dc.contributor.authorRosenwald, Andreas
dc.contributor.authorTheobald, Matthias
dc.contributor.authorLenz, Goerg
dc.date.accessioned2023-01-19T10:14:00Z
dc.date.available2023-01-19T10:14:00Z
dc.date.issued2022
dc.description.abstractThe prognosis of patients with relapsed diffuse large B-cell lymphoma (DLBCL) remains poor with current options. Here we prospectively evaluated the combination of pixantrone with obinutuzumab for up to six cycles for patients with relapsed or refractory DLBCL. Overall response rate (ORR) was the primary end-point. Sixty-eight patients were evaluated, median age was 75 years, median number of prior lines was three (range 1–10), 52 patients (76.5%) were diagnosed with DLBCL and 16 (23.5%) patients had transformed indolent lymphoma or follicular lymphoma (FL) IIIB. ORR was 35.3% for all and 40% for evaluable patients (16.6% complete response), median progression-free survival (PFS) and overall survival (OS) were 2.8 months and 8 months, respectively. Analysis of the cell of origin revealed a superior course for patients with non-GCB (germinal centre B-cell-like) phenotype [median OS not reached (n.r.) vs 5.2 months]. Patients with one prior line had an improved outcome over patients treated in later lines (PFS n.r. vs 2.5 months). Disease progression was the main reason for premature termination. Adverse events were mainly haematologic. The combination treatment revealed no unexpected adverse events. Most relevant non-haematologic toxicity was infection in 28% of patients. In summary, pixantrone–obinutuzumab showed clinical activity with sometimes long-term remission; however, the trial failed to meet its primary end-point.en_GB
dc.description.sponsorshipGefördert durch die Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 491381577de
dc.identifier.doihttp://doi.org/10.25358/openscience-8604
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/8620
dc.language.isoengde
dc.rightsCC-BY-NC-ND-4.0*
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleA phase II trial to evaluate the combination of pixantrone and obinutuzumab for patients with relapsed aggressive lymphoma : final results of the prospective, multicentre GOAL trialen_GB
dc.typeZeitschriftenaufsatzde
jgu.journal.issue3de
jgu.journal.titleEuropean journal of heart failurede
jgu.journal.volume198de
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.end491de
jgu.pages.start482de
jgu.publisher.doi10.1111/bjh.18161de
jgu.publisher.issn1365-2141de
jgu.publisher.nameWileyde
jgu.publisher.placeOxfordde
jgu.publisher.year2022
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode610de
jgu.subject.dfgLebenswissenschaftende
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTextde
jgu.type.versionPublished versionde

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