Literature DB >> 28355112

Final Results of the IELSG-19 Randomized Trial of Mucosa-Associated Lymphoid Tissue Lymphoma: Improved Event-Free and Progression-Free Survival With Rituximab Plus Chlorambucil Versus Either Chlorambucil or Rituximab Monotherapy.

Emanuele Zucca1, Annarita Conconi1, Giovanni Martinelli1, Reda Bouabdallah1, Alessandra Tucci1, Umberto Vitolo1, Maurizio Martelli1, Ruth Pettengell1, Gilles Salles1, Catherine Sebban1, Armando Lopez Guillermo1, Graziella Pinotti1, Liliana Devizzi1, Franck Morschhauser1, Hervé Tilly1, Valter Torri1, Stefan Hohaus1, Andrés J M Ferreri1, Pierre Zachée1, André Bosly1, Corinne Haioun1, Caterina Stelitano1, Monica Bellei1, Maurilio Ponzoni1, Anne Moreau1, Andrew Jack1, Elias Campo1, Luca Mazzucchelli1, Franco Cavalli1, Peter Johnson1, Catherine Thieblemont1.   

Abstract

Purpose There is no consensus on the optimal systemic treatment of patients with extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue. The IELSG-19 phase III study, to our knowledge, was the first such study to address the question of first-line treatment in a randomized trial. Patients and Methods Eligible patients were initially randomly assigned (1:1 ratio) to receive either chlorambucil monotherapy (6 mg/m2/d orally on weeks 1 to 6, 9 to 10, 13 to 14, 17 to 18, and 21 to 22) or a combination of chlorambucil (same schedule as above) and rituximab (375 mg/m2 intravenously on day 1 of weeks 1, 2, 3, 4, 9, 13, 17, and 21). After the planned enrollment of 252 patients, the protocol was amended to continue with a three-arm design (1:1:6 ratio), with a new arm that included rituximab alone (same schedule as the combination arm) and with a final sample size of 454 patients. The main end point was event-free survival (EFS). Analysis of chlorambucil versus the combination arm was performed and reported separately before any analysis of the third arm. Results At a median follow-up of 7.4 years, addition of rituximab to chlorambucil led to significantly better EFS (hazard ratio, 0.54; 95% CI, 0.38 to 0.77). EFS at 5 years was 51% (95% CI, 42 to 60) with chlorambucil alone, 50% (95% CI, 42 to 59) with rituximab alone, and 68% (95% CI, 60 to 76) with the combination ( P = .0009). Progression-free survival was also significantly better with the combination ( P = .0119). Five-year overall survival was approximately 90% in each arm. All treatments were well tolerated. No unexpected toxicities were recorded. Conclusion Rituximab in combination with chlorambucil demonstrated superior efficacy in mucosa-associated lymphoid tissue lymphoma; however, improvements in EFS and progression-free survival did not translate into longer overall survival.

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Year:  2017        PMID: 28355112     DOI: 10.1200/JCO.2016.70.6994

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  35 in total

1.  Pre-Therapeutic Total Lesion Glycolysis on [18F]FDG-PET Enables Prognostication of 2-Year Progression-Free Survival in MALT Lymphoma Patients Treated with CD20-Antibody-Based Immunotherapy.

Authors:  Marius E Mayerhoefer; Anton Staudenherz; Barbara Kiesewetter; Michael Weber; Ingrid Simonitsch-Klupp; Peter Gibbs; Werner Dolak; Julius Lukas; Markus Raderer
Journal:  Mol Imaging Biol       Date:  2019-12       Impact factor: 3.488

Review 2.  Marginal Zone Lymphoma: Clinicopathologic Variations and Approaches to Therapy.

Authors:  Sabarish Ayyappan; Basem M William
Journal:  Curr Oncol Rep       Date:  2018-03-23       Impact factor: 5.075

Review 3.  Mature lymphoid malignancies: origin, stem cells, and chronicity.

Authors:  Simon Husby; Kirsten Grønbæk
Journal:  Blood Adv       Date:  2017-11-28

4.  Early progression of disease predicts shorter survival in MALT lymphoma patients receiving systemic treatment.

Authors:  Annarita Conconi; Catherine Thieblemont; Luciano Cascione; Valter Torri; Barbara Kiesewetter; Gloria Margiotta Casaluci; Gianluca Gaidano; Markus Raderer; Franco Cavalli; Armando Lopez Guillermo; Peter W Johnson; Emanuele Zucca
Journal:  Haematologica       Date:  2020-01-02       Impact factor: 9.941

5.  The underreporting of phase III chemo-therapeutic clinical trial data of older patients with cancer: A systematic review.

Authors:  Karlynn BrintzenhofeSzoc; Jessica L Krok-Schoen; Beverly Canin; Ira Parker; Amy R MacKenzie; Thuy Koll; Ritika Vankina; Christine D Hsu; Brian Jang; Kathy Pan; Jennifer L Lund; Edith Starbuck; Armin Shahrokni
Journal:  J Geriatr Oncol       Date:  2020-01-10       Impact factor: 3.599

Review 6.  Nodular pulmonary amyloidosis: a complex disease with malignancy association.

Authors:  Jacob M Core; Ali A Alsaad; Liuyan Jiang; Neal M Patel
Journal:  BMJ Case Rep       Date:  2017-10-15

Review 7.  Marginal Zone Lymphoma: State-of-the-Art Treatment.

Authors:  Ariel Sindel; Taha Al-Juhaishi; Victor Yazbeck
Journal:  Curr Treat Options Oncol       Date:  2019-12-05

Review 8.  How do we sequence therapy for marginal zone lymphomas?

Authors:  Alessandro Broccoli; Pier Luigi Zinzani
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2020-12-04

9.  Prolonged complete remission in a primary MALT lymphoma of the lung after rituximab monotherapy.

Authors:  M D Diamantidis; S Chatzileontiadou; D Pantelidou; M Papaioannou
Journal:  Hippokratia       Date:  2017 Apr-Jun       Impact factor: 0.471

10.  The use of whole-body fluorine-18-fluorodeoxyglucose positron emission tomography integrated with computed tomography for accurate staging and surveillance in the case of mucosa-associated lymphoid tissue.

Authors:  Shunqing Zhang; Allen Rossetti-Chung; Sumit Sood; Stephanie Terezakis
Journal:  J Radiol Case Rep       Date:  2021-03-31
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