Positron emission tomography-guided therapy of Aggressive Non-Hodgkin Lymphomas (PETAL): A multicenter, randomized phase III trial

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Ulrich Dührsen - , University of Duisburg-Essen (Author)
  • Stefan Müller - , University of Duisburg-Essen (Author)
  • Bernd Hertenstein - , Zentrum für Moderne Diagnostik (Author)
  • Henrike Thomssen - , Zentrum für Moderne Diagnostik (Author)
  • Jörg Kotzerke - , Department of Nuclear Medicine (Author)
  • Rolf Mesters - , University of Münster (Author)
  • Wolfgang E. Berdel - , University of Münster (Author)
  • Christiane Franzius - , TUD Dresden University of Technology (Author)
  • Frank Kroschinsky - , Department of Internal Medicine I, Augusta Hospitals Bochum Hattingen (Author)
  • Matthias Weckesser - , University of Münster (Author)
  • Dorothea Kofahl-Krause - , Hannover Medical School (MHH) (Author)
  • Frank M. Bengel - , TUD Dresden University of Technology, Hannover Medical School (MHH) (Author)
  • Jan Dürig - , University of Duisburg-Essen (Author)
  • Johannes Matschke - , University of Duisburg-Essen (Author)
  • Christine Schmitz - , University of Duisburg-Essen (Author)
  • Thorsten Pöppel - , University of Duisburg-Essen (Author)
  • Claudia Ose - , University of Duisburg-Essen (Author)
  • Marcus Brinkmann - , University of Duisburg-Essen (Author)
  • Paul La Rosée - , Friedrich Schiller University Jena (Author)
  • Martin Freesmeyer - , Friedrich Schiller University Jena (Author)
  • Andreas Hertel - , Klinikum Fulda gAG (Author)
  • Heinz Gert Höffkes - , University of Duisburg-Essen (Author)
  • Dirk Behringer - , RWTH Aachen University (Author)
  • Gabriele Prange-Krex - , Pediatric Center Dresden-Friedrichstadt (Kid) (Author)
  • Stefan Wilop - , RWTH Aachen University (Author)
  • Thomas Krohn - , RWTH Aachen University (Author)
  • Jens Holzinger - , Ruhr University Bochum (Author)
  • Martin Griesshammer - , Ruhr University Bochum (Author)
  • Aristoteles Giagounidis - , Helios Clinics Duisburg (Author)
  • Aruna Raghavachar - , Helios University Hospital Wuppertal (Author)
  • Georg Maschmeyer - , Klinikum Ernst von Bergmann gGmbH (Author)
  • Ingo Brink - , Klinikum Ernst von Bergmann gGmbH (Author)
  • Helga Bernhard - , Heidelberg University  (Author)
  • Uwe Haberkorn - , Heidelberg University  (Author)
  • Tobias Gaska - , Brüderkrankenhaus St. Josef (Author)
  • Lars Kurch - , Leipzig University (Author)
  • Daniëlle M.E. Van Assema - , Vrije Universiteit Amsterdam (VU) (Author)
  • Wolfram Klapper - , Kiel University (Author)
  • Dieter Hoelzer - , ONKOLOGIKUM Frankfurt a.M. (Author)
  • Lilli Geworski - , Hannover Medical School (MHH) (Author)
  • Karl Heinz Jöckel - , University of Duisburg-Essen, Klinikum Fulda gAG (Author)
  • André Scherag - , University of Duisburg-Essen, Friedrich Schiller University Jena (Author)
  • Andreas Bockisch - , University of Duisburg-Essen (Author)
  • Jan Rekowski - , University of Duisburg-Essen (Author)
  • Andreas Hüttmann - , University of Duisburg-Essen (Author)

Abstract

Purpose: Interim positron emission tomography (PET) using the tracer, [18F]fluorodeoxyglucose, may predict outcomes in patients with aggressive non-Hodgkin lymphomas. We assessed whether PET can guide therapy in patients who are treated with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP). Patients and Methods: Newly diagnosed patients received two cycles of CHOP - plus rituximab (R-CHOP) in CD20-positive lymphomas - followed by a PET scan that was evaluated using the DSUVmax method. PET-positive patients were randomly assigned to receive six additional cycles of R-CHOP or six blocks of an intensive Burkitt's lymphoma protocol. PET-negative patients with CD20-positive lymphomas were randomly assigned or allocated to receive four additional cycles of R-CHOP or the same treatment with two additional doses rituximab. The primary end point was event-free survival time as assessed by log-rank test. Results: Interim PET was positive in 108 (12.5%) and negative in 754 (87.5%) of 862 patients treated, with statistically significant differences in event-free survival and overall survival. Among PET-positive patients, 52 were randomly assigned to R-CHOP and 56 to the Burkitt protocol, with 2-year event-free survival rates of 42.0% (95% CI, 28.2% to 55.2%) and 31.6% (95% CI, 19.3% to 44.6%), respectively (hazard ratio, 1.501 [95% CI, 0.896 to 2.514]; P = .1229). The Burkitt protocol produced significantly more toxicity. Of 754 PET-negative patients, 255 underwent random assignment (129 to R-CHOP and 126 to R-CHOP with additional rituximab). Event-free survival rates were 76.4% (95% CI, 68.0% to 82.8%) and 73.5% (95% CI, 64.8% to 80.4%), respectively (hazard ratio, 1.048 [95% CI, 0.684 to 1.606]; P = .8305). Outcome prediction by PET was independent of the International Prognostic Index. Results in diffuse large B-cell lymphoma were similar to those in the total group. Conclusion: Interim PET predicted survival in patients with aggressive lymphomas treated with R-CHOP. PET-based treatment intensification did not improve outcome.

Details

Original languageEnglish
Pages (from-to)2024-2034
Number of pages11
JournalJournal of clinical oncology
Volume36
Issue number20
Publication statusPublished - 10 Jul 2018
Peer-reviewedYes

External IDs

PubMed 29750632

Keywords

Sustainable Development Goals

ASJC Scopus subject areas

Library keywords