Baseline and interim PET-based outcome prediction in peripheral T-cell lymphoma: A subgroup analysis of the PETAL trial.


Journal

Hematological oncology
ISSN: 1099-1069
Titre abrégé: Hematol Oncol
Pays: England
ID NLM: 8307268

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 03 10 2019
revised: 18 11 2019
accepted: 19 11 2019
pubmed: 19 2 2020
medline: 1 9 2020
entrez: 19 2 2020
Statut: ppublish

Résumé

The prospective randomized Positron Emission Tomography (PET)-Guided Therapy of Aggressive Non-Hodgkin Lymphomas (PETAL) trial was designed to test the ability of interim PET (iPET) to direct therapy. As reported previously, outcome remained unaffected by iPET-based treatment changes. In this subgroup analysis, we studied the prognostic value of baseline total metabolic tumor volume (TMTV) and iPET response in 76 patients with T-cell lymphoma. TMTV was measured using the 41% maximum standardized uptake value (SUV

Identifiants

pubmed: 32067259
doi: 10.1002/hon.2697
doi:

Substances chimiques

Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

244-256

Subventions

Organisme : Amgen Germany
Organisme : Deutsche Krebshilfe
ID : 107592
Organisme : Deutsche Krebshilfe
ID : 110515
Organisme : Roche Pharma

Informations de copyright

© 2019 John Wiley & Sons, Ltd.

Références

Swerdlow SH, Campo E, Harris NL, et al., eds. WHO Classification of Tumours of the Haematopoetic and Lymphoid Tissues. Lyon, France: IARC Press; 2008.
Ellin F, Landström J, Jerkeman M, Relander T. Real-world data on prognostic factors and treatment in peripheral T-cell lymphomas: a study from the Swedish lymphoma registry. Blood. 2014;124(10):1570-1577.
Schmitz N, de Leval L. How I manage peripheral T-cell lymphoma, not otherwise specified and angioimmunoblastic T-cell lymphoma: current practice and a glimpse into the future. Br J Haematol. 2017;176(6):851-866.
Broccoli A, Zinzani PL. Peripheral T-cell lymphoma, not otherwise specified. Blood. 2017;129(9):1103-1112.
Gleeson M, Peckitt C, To YM, et al. CHOP versus GEM-P in previously untreated patients with peripheral T-cell lymphoma (CHEMO-T): a phase 2, multicentre, randomised, open-label trial. Lancet Haematol. 2018;5(5):e190-e200.
Li L, Duan W, Zhang L, et al. The efficacy and safety of gemcitabine, cisplatin, prednisone, thalidomide versus CHOP in patients with newly diagnosed peripheral T-cell lymphoma with analysis of biomarkers. Br J Haematol. 2017;178(5):772-780.
Fossard G, Broussais F, Coelho I, et al. Role of up-front autologous stem-cell transplantation in peripheral T-cell lymphoma for patients in response after induction: an analysis of patients from LYSA centers. Ann Oncol. 2018;29(3):715-723.
Le Gouill S, Milpied N, Buzyn A, et al. Graft-versus-lymphoma effect for aggressive T-cell lymphomas in adults: a study by the Societé Francaise de Greffe de Moelle et de Thérapie Cellulaire. J Clin Oncol. 2008;26(14):2264-2271.
Schmitz N, Lenz G, Stelljes M. Allogeneic hematopoietic stem cell transplantation for T-cell lymphomas. Blood. 2018;132(3):245-253.
Cheson BD, Fisher RI, Barrington SF, et al. Recommendations for initial evaluation, staging, and response assessment of Hodgkin and non-Hodgkin lymphoma: the Lugano classification. J Clin Oncol. 2014;32(27):3059-3068.
Kanoun S, Rossi C, Berriolo-Riedinger A, et al. Baseline metabolic tumour volume is an independent prognostic factor in Hodgkin lymphoma. Eur J Nucl Med Mol Imaging. 2014;41(9):1735-1743.
Sasanelli M, Meignan M, Haioun C, et al. Pretherapy metabolic tumour volume is an independent predictor of outcome in patients with diffuse large B-cell lymphoma. Eur J Nucl Med Mol Imaging. 2014;41(11):2017-2022.
Meignan M, Cottereau AS, Versari A, et al. Baseline metabolic tumor volume predicts outcome in high-tumor-burden follicular lymphoma: a pooled analysis of three multicenter studies. J Clin Oncol. 2016;34(30):3618-3626.
Cottereau AS, Becker S, Broussais F, et al. Prognostic value of baseline total metabolic tumor volume (TMTV0) measured on FDG-PET/CT in patients with peripheral T-cell lymphoma (PTCL). Ann Oncol. 2016;27(4):719-724.
Barrington SF, Mikhaeel NG, Kostakoglu L, et al. Role of imaging in the staging and response assessment of lymphoma: consensus of the international conference on malignant lymphomas imaging working group. J Clin Oncol. 2014;32(27):3048-3058.
Dührsen U, Müller S, Hertenstein B, et al. Positron-emission tomography-guided therapy of aggressive non-Hodgkin lymphomas (PETAL): a multicenter, randomized phase 3 trial. J Clin Oncol. 2018;36(20):2024-2034.
Hoelzer D, Walewski J, Döhner H, et al. German Multicenter Study Group for Adult Acute Lymphoblastic Leukemia. Improved outcome of adult Burkitt lymphoma/leukemia with rituximab and chemotherapy: report of a large prospective multicenter trial. Blood. 2014;124(26):3870-3879.
Pfreundschuh M, Schubert J, Ziepert M, et al. German high-grade non-Hodgkin lymphoma study group (DSHNHL). Six versus eight cycles of bi-weekly CHOP-14 with or without rituximab in elderly patients with aggressive CD20+ B-cell lymphomas: a randomised controlled trial (RICOVER-60). Lancet Oncol. 2008;9(2):105-116.
Spaepen K, Stroobants S, Dupont P, et al. [(18)F]FDG PET monitoring of tumour response to chemotherapy: does [(18)F]FDG uptake correlate with the viable tumour cell fraction? Eur J Nucl Med Mol Imaging. 2003;30(5):682-688.
Boellaard R. Quantitative oncology molecular analysis suite: ACCURATE. J Nucl Med. 2018;59(suppl 1):1753.
Boellaard R, Delgado-Bolton R, Oyen WJ, et al. FDG PET/CT: EANM procedure guidelines for tumour imaging: version 2.0. Eur J Nucl Med Mol Imaging. 2015;42(2):328-354.
Lin C, Itti E, Haioun C, et al. Early 18F-FDG PET for prediction of prognosis in patients with diffuse large B-cell lymphoma: SUV-based assessment versus visual analysis. J Nucl Med. 2007;48(10):1626-1632.
Cheson BD, Pfistner B, Juweid ME, et al. International Harmonization Project on Lymphoma. Revised response criteria for malignant lymphoma. J Clin Oncol. 2007;25(5):579-586.
National Cancer Institute. Common Terminology Criteria for Adverse Events v3.0 (CTCAE). 2006; https://ctep.cancer.gov/protocoldevelopment/electronic_applications/docs/ctcaev3.pdf. Accessed 1 Oct 2007
International Non-Hodgkin's Lymphoma Prognostic Factors Project. A predictive model for aggressive non-Hodgkin's lymphoma. N Engl J Med. 1993;329(14):987-994.
Heagerty PJ, Lumley T, Pepe MS. Time-dependent ROC curves for censored survival data and a diagnostic marker. Biometrics. 2000;56(2):337-344.
Cottereau AS, El-Galaly TC, Becker S, et al. Predictive value of PET response combined with baseline metabolic tumor volume in peripheral T-cell lymphoma patients. J Nucl Med. 2018;59(4):589-595.
Li YJ, Li ZM, Xia XY, et al. Prognostic value of interim and posttherapy 18F-FDG PET/CT in patients with mature T-cell and natural killer cell lymphomas. J Nucl Med. 2013;54(4):507-515.
El-Galaly TC, Pedersen MB, Hutchings M, et al. Utility of interim and end-of-treatment PET/CT in peripheral T-cell lymphomas: a review of 124 patients. Am J Hematol. 2015;90(11):975-980.
Mehta-Shah N, Ito K, Bantilan K, et al. Baseline and interim functional imaging with PET effectively risk stratifies patients with peripheral T-cell lymphoma. Blood Adv. 2019;3(2):187-197.
Schmitz C, Hüttmann A, Müller SP, et al. Dynamic risk assessment based on positron emission tomography scanning in diffuse large B-cell lymphoma: post-hoc analysis from the PETAL trial. Eur J Cancer. 2020;124:25-36.
Cottereau AS, Hapdey S, Chartier L, et al. Baseline total metabolic tumor volume measured with fixed or different adaptive thresholding methods equally predicts outcome in peripheral T cell lymphoma. J Nucl Med. 2017;58(2):276-281.
Barrington SF, Meignan MA. Time to prepare for risk adaptation in lymphoma by standardizing measurement of metabolic tumor burden. J Nucl Med. 2019;60(8):1096-1102.
Hüttmann A, Rekowski J, Müller SP, et al. Six versus eight doses of rituximab in patients with aggressive B cell lymphoma receiving six cycles of CHOP: results from the “Positron Emission Tomography-Guided Therapy of Aggressive Non-Hodgkin Lymphomas” (PETAL) trial. Ann Hematol. 2019;98(4):897-907.
Cahu X, Bodet-Milin C, Brissot E, et al. 18F-fluorodeoxyglucose-positron emission tomography before, during and after treatment in mature T/NK lymphomas: a study from the GOELAMS group. Ann Oncol. 2011;22(3):705-711.
Casulo C, Schöder H, Feeney J, et al. 18F-fluorodeoxyglucose positron emission tomography in the staging and prognosis of T cell lymphoma. Leuk Lymphoma. 2013;54(10):2163-2167.
Pellegrini C, Argnani L, Broccoli A, et al. Prognostic value of interim positron emission tomography in patients with peripheral T-cell lymphoma. Oncologist. 2014;19(7):746-750.
Moon SH, Lee AY, Kim WS, et al. Value of interim FDG PET/CT for predicting outcome of patients with angioimmunoblastic T-cell lymphoma. Leuk Lymphoma. 2017;58(6):1341-1348.
Eslick R, Dunlop L, Lin M, Hsu D, Ling S. The prognostic value of 18-FDG positron emission tomography in T cell non-Hodgkin lymphoma. Blood Cancer J. 2017;7(4):e556.
Jung SH, Ahn JS, Kim YK, et al. Prognostic significance of interim PET/CT based on visual, SUV-based, and MTV-based assessment in the treatment of peripheral T-cell lymphoma. BMC Cancer. 2015;15:198.
Ham JS, Kim SJ, Choi JY, et al. The prognostic value of interim and end-of-treatment PET/CT in patients with newly diagnosed peripheral T-cell lymphoma. Blood Cancer J. 2016;6:e395.
Juweid ME, Stroobants S, Hoekstra OS, et al. Use of positron emission tomography for response assessment of lymphoma: consensus of the Imaging Subcommittee of International Harmonization Project in Lymphoma. J Clin Oncol. 2007;25(5):571-578.
Horwitz S, O'Connor OA, Pro B, et al. Brentuximab vedotin with chemotherapy for CD30-positive peripheral T-cell lymphoma (ECHELON-2): a global, double-blind, randomised, phase 3 trial. Lancet. 2019;393(10168):229-240.
Scherer LD, Brenner MK, Mamonkin M. Chimeric antigen receptors for T-cell malignancies. Front Oncol. 2019;9:126.

Auteurs

Christine Schmitz (C)

Klinik für Hämatologie, Universitätsklinikum Essen, Essen, Germany.

Jan Rekowski (J)

Institut für Medizinische Informatik, Biometrie und Epidemiologie, Universität Duisburg-Essen, Essen, Germany.

Stefan P Müller (SP)

Klinik für Nuklearmedizin, Universitätsklinikum Essen, Essen, Germany.

Bernd Hertenstein (B)

Medizinische Klinik I, Klinikum Bremen-Mitte, Bremen, Germany.

Christiane Franzius (C)

Zentrum für moderne Diagnostik (Zemodi), Zentrum für Nuklearmedizin und PET/CT, Bremen, Germany.

Arnold Ganser (A)

Klinik für Hämatologie, Hämostaseologie, Onkologie und Stammzelltransplantation, Medizinische Hochschule Hannover, Hannover, Germany.

Frank M Bengel (FM)

Klinik für Nuklearmedizin, Medizinische Hochschule Hannover, Hannover, Germany.

Frank Kroschinsky (F)

Medizinische Klinik I, Universitätsklinikum Carl Gustav Carus, Dresden, Germany.

Jörg Kotzerke (J)

Klinik für Nuklearmedizin, Universitätsklinikum Carl Gustav Carus, Dresden, Germany.

Paul La Rosée (P)

Klinik für Innere Medizin II, Universitätsklinikum Jena, Jena, Germany.

Martin Freesmeyer (M)

Klinik für Nuklearmedizin, Universitätsklinikum Jena, Jena, Germany.

Heinz-Gert Hoeffkes (HG)

Tumorklinik, Klinikum Fulda, Fulda, Germany.

Andreas Hertel (A)

Klinik für Diagnostische und Therapeutische Nuklearmedizin, Klinikum Fulda, Fulda, Germany.

Dirk Behringer (D)

Klinik für Hämatologie, Onkologie und Palliativmedizin, Augusta-Kranken-Anstalt, Bochum, Germany.

Rolf Mesters (R)

Medizinische Klinik A, Universitätsklinikum Münster, Münster, Germany.

Matthias Weckesser (M)

Klinik für Nuklearmedizin, Universitätsklinikum Münster, Münster, Germany.

Stefan Mahlmann (S)

Klinik für Innere Medizin 1, Westpfalz-Klinikum, Kaiserslautern, Germany.

Uwe Haberkorn (U)

Radiologische Klinik und Poliklinik, Universitätsklinikum Heidelberg, Heidelberg, Germany.

Uwe Martens (U)

Klinik für Innere Medizin III: Hämatologie, Onkologie, Palliativmedizin, Klinikum am Gesundbrunnen, Heilbronn, Germany.

Gabriele Prange-Krex (G)

Onkologische Gemeinschaftspraxis, Dresden, Germany.

Winfried Brenner (W)

Klinik für Nuklearmedizin, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Aristoteles Giagounidis (A)

Klinik für Onkologie, Hämatologie und Palliativmedizin, Marien Hospital, Düsseldorf, Germany.

Regina Moeller (R)

Hämatologisch-onkologische Gemeinschaftspraxis, Halle, Germany.

Volker Runde (V)

Klinik für Innere Medizin mit den Schwerpunkten Hämatologie, Onkologie und Palliativmedizin, Wilhelm-Anton-Hospital, Goch, Germany.

Matthias Sandmann (M)

Klinik für Innere Medizin III - Hämatologie und Onkologie, Palliativmedizin, Petrus-Krankenhaus, Wuppertal, Germany.

Hubertus Hautzel (H)

Klinik für Nuklearmedizin, Universitätsklinikum Düsseldorf, Düsseldorf, Germany.

Stefan Wilop (S)

Klinik für Hämatologie, Onkologie, Hämostaseologie und Stammzelltransplantation, Universitätsklinikum Aachen, Aachen, Germany.

Thomas Krohn (T)

Klinik für Nuklearmedizin, Universitätsklinikum Aachen, Aachen, Germany.

Heinz Dürk (H)

Klinik für Hämatologie, Onkologie und Palliativmedizin, Evangelisches Krankenhaus, Hamm, Germany.

Michael Heike (M)

Klinik für Gastroenterologie, Hämatologie und internistische Onkologie und Endokrinologie, Klinikum Dortmund, Germany.

Ferras Alashkar (F)

Klinik für Hämatologie, Universitätsklinikum Essen, Essen, Germany.

Marcus Brinkmann (M)

Zentrum für Klinische Studien Essen (ZKSE), Universität Duisburg-Essen, Essen, Germany.

Guido Trenn (G)

Klinik für Innere Medizin I, Knappschaftskrankenhaus, Bottrop, Germany.

Dietmar Wacker (D)

Medizinische Klinik III, Hämatologie, Onkologie und Palliativmedizin, Klinikum Vest, Recklinghausen, Germany.

Christiane Kreisel-Büstgens (C)

Zentrum für Hämatologie und Onkologie, Porta Westfalica, Germany.

Helga Bernhard (H)

Medizinische Klinik V, Klinikum Darmstadt, Darmstadt, Germany.

Gerhard Heil (G)

Klinik für Hämatologie und Onkologie, Klinikum Lüdenscheid, Lüdenscheid, Germany.

Rolf Larisch (R)

Klinik für Nuklearmedizin, Klinikum Lüdenscheid, Lüdenscheid, Germany.

Lars Kurch (L)

Klinik und Poliklinik für Nuklearmedizin, Universitätsklinikum Leipzig, Leipzig, Germany.

Karl-Heinz Jöckel (KH)

Institut für Medizinische Informatik, Biometrie und Epidemiologie, Universität Duisburg-Essen, Essen, Germany.

Dieter Hoelzer (D)

Onkologikum, Frankfurt/Main, Germany.

Wolfram Klapper (W)

Institut für Pathologie, Sektion für Hämatopathologie, Universitätsklinikum Schleswig-Holstein, Kiel, Germany.

Ronald Boellaard (R)

Department of Radiology and Nuclear Medicine, Amsterdam University Medical Centers, Location VUMC, Amsterdam, the Netherlands.

Ulrich Dührsen (U)

Klinik für Hämatologie, Universitätsklinikum Essen, Essen, Germany.

Andreas Hüttmann (A)

Klinik für Hämatologie, Universitätsklinikum Essen, Essen, Germany.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH