Literature DB >> 33256131

First Line Systemic Treatment for MALT Lymphoma-Do We Still Need Chemotherapy? Real World Data from the Medical University Vienna.

Barbara Kiesewetter1, Ingrid Simonitsch-Klupp2, Marius E Mayerhoefer3,4, Werner Dolak5, Julius Lukas6, Markus Raderer1.   

Abstract

There is no clear therapeutic algorithm for mucosa-associated lymphoid tissue (MALT) lymphoma beyond Helicobacter pylori eradication and while chemotherapy-based regimens are standard for MALT lymphoma patients in need of systemic treatment, it appears of interest to also investigate chemotherapy-free strategies. We have retrospectively assessed MALT lymphoma patients undergoing upfront systemic treatment, classified either as chemotherapy (=classical cytostatic agents +/- rituximab) or immunotherapy (=immunomodulatory agents or single anti-CD20 antibodies) at the Medical University Vienna 1999-2019. The primary endpoint was progression-free survival (PFS). In total, 159 patients were identified with a median follow-up of 67 months. The majority of patients had extragastric disease (80%), but we also identified 32 patients (20%) with Helicobacter pylori negative or disseminated gastric lymphoma. Regarding the type of first line treatment and outcome, 46% (74/159) received a chemotherapy-based regimen and 54% (85/159) immunotherapy including IMiDs lenalidomide/thalidomide (37%), anti-CD20-anitbodies rituximab/ofatumumab (27%), macrolides clarithromycin/azithromycin (27%) and proteasome inhibitor bortezomib (9%). Median PFS was 76 months (95%CI 50-102), and while the overall response (90% vs. 68%, p < 0.01) and the complete remission rate (75% vs. 43%, p < 0.01) was significantly higher for chemotherapy, there was no difference in PFS between chemotherapy (median 81 months, 95%CI 47-116) and immunotherapy (76 months, 95%CI 50-103, p = 0.57), suggesting comparable long-term outcomes. To conclude, our data show higher response rates with chemo- compared to immunotherapy, but this did not translate into a superior PFS. Given the biological background of MALT lymphoma, and the favorable toxicity profile of novel immunomodulatory treatments, this should be further investigated.

Entities:  

Keywords:  MALT lymphoma; chemotherapy; extranodal lymphoma; immunomodulatory treatment

Year:  2020        PMID: 33256131      PMCID: PMC7761357          DOI: 10.3390/cancers12123533

Source DB:  PubMed          Journal:  Cancers (Basel)        ISSN: 2072-6694            Impact factor:   6.639


  37 in total

1.  Six-month oral clarithromycin regimen is safe and active in extranodal marginal zone B-cell lymphomas: final results of a single-centre phase II trial.

Authors:  Silvia Govi; Giuseppina P Dognini; Giada Licata; Roberto Crocchiolo; Antonio Giordano Resti; Maurilio Ponzoni; Andrés J M Ferreri
Journal:  Br J Haematol       Date:  2010-04-28       Impact factor: 6.998

2.  EGILS consensus report. Gastric extranodal marginal zone B-cell lymphoma of MALT.

Authors:  A Ruskoné-Fourmestraux; W Fischbach; B M P Aleman; H Boot; M Q Du; F Megraud; C Montalban; M Raderer; A Savio; A Wotherspoon
Journal:  Gut       Date:  2011-02-11       Impact factor: 23.059

3.  Bendamustine plus rituximab versus CHOP plus rituximab as first-line treatment for patients with indolent and mantle-cell lymphomas: an open-label, multicentre, randomised, phase 3 non-inferiority trial.

Authors:  Mathias J Rummel; Norbert Niederle; Georg Maschmeyer; G Andre Banat; Ulrich von Grünhagen; Christoph Losem; Dorothea Kofahl-Krause; Gerhard Heil; Manfred Welslau; Christina Balser; Ulrich Kaiser; Eckhart Weidmann; Heinz Dürk; Harald Ballo; Martina Stauch; Fritz Roller; Juergen Barth; Dieter Hoelzer; Axel Hinke; Wolfram Brugger
Journal:  Lancet       Date:  2013-02-20       Impact factor: 79.321

4.  Long-term results of a phase 2 study of rituximab and bendamustine for mucosa-associated lymphoid tissue lymphoma.

Authors:  Antonio Salar; Eva Domingo-Domenech; Carlos Panizo; Concepción Nicolás; Joan Bargay; Ana Muntañola; Miguel Canales; José Luis Bello; Juan Manuel Sancho; José Francisco Tomás; María José Rodríguez; Javier Peñalver; Carlos Grande; José Javier Sánchez-Blanco; Luis Palomera; Reyes Arranz; Eulogio Conde; Mar García; Juan Fernando García; Dolores Caballero; Carlos Montalbán
Journal:  Blood       Date:  2017-08-11       Impact factor: 22.113

5.  A phase 2 study of rituximab plus lenalidomide for mucosa-associated lymphoid tissue lymphoma.

Authors:  Barbara Kiesewetter; Ella Willenbacher; Wolfgang Willenbacher; Alexander Egle; Peter Neumeister; Daniela Voskova; Marius Erik Mayerhoefer; Ingrid Simonitsch-Klupp; Thomas Melchardt; Richard Greil; Markus Raderer
Journal:  Blood       Date:  2016-11-22       Impact factor: 22.113

6.  Revised response criteria for malignant lymphoma.

Authors:  Bruce D Cheson; Beate Pfistner; Malik E Juweid; Randy D Gascoyne; Lena Specht; Sandra J Horning; Bertrand Coiffier; Richard I Fisher; Anton Hagenbeek; Emanuele Zucca; Steven T Rosen; Sigrid Stroobants; T Andrew Lister; Richard T Hoppe; Martin Dreyling; Kensei Tobinai; Julie M Vose; Joseph M Connors; Massimo Federico; Volker Diehl
Journal:  J Clin Oncol       Date:  2007-01-22       Impact factor: 44.544

7.  Clinical activity of bortezomib in relapsed/refractory MALT lymphomas: results of a phase II study of the International Extranodal Lymphoma Study Group (IELSG).

Authors:  A Conconi; G Martinelli; A Lopez-Guillermo; P L Zinzani; A J M Ferreri; L Rigacci; L Devizzi; U Vitolo; S Luminari; F Cavalli; E Zucca
Journal:  Ann Oncol       Date:  2010-09-01       Impact factor: 32.976

8.  Randomized trial of bendamustine-rituximab or R-CHOP/R-CVP in first-line treatment of indolent NHL or MCL: the BRIGHT study.

Authors:  Ian W Flinn; Richard van der Jagt; Brad S Kahl; Peter Wood; Tim E Hawkins; David Macdonald; Mark Hertzberg; Yiu-Lam Kwan; David Simpson; Michael Craig; Kathryn Kolibaba; Samar Issa; Regina Clementi; Doreen M Hallman; Mihaela Munteanu; Ling Chen; John M Burke
Journal:  Blood       Date:  2014-03-03       Impact factor: 22.113

9.  Marginal zone lymphomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.

Authors:  E Zucca; L Arcaini; C Buske; P W Johnson; M Ponzoni; M Raderer; U Ricardi; A Salar; K Stamatopoulos; C Thieblemont; A Wotherspoon; M Ladetto
Journal:  Ann Oncol       Date:  2019-12-04       Impact factor: 32.976

10.  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:  2020-11-01       Impact factor: 9.941

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  3 in total

1.  Role in staging and prognostic value of pretherapeutic F-18 FDG PET/CT in patients with gastric MALT lymphoma without high-grade transformation.

Authors:  Yong-Jin Park; Seung Hyup Hyun; Seung Hwan Moon; Kyung-Han Lee; Byung Hoon Min; Jun Haeng Lee; Won Seog Kim; Seok Jin Kim; Joon Young Choi
Journal:  Sci Rep       Date:  2021-04-29       Impact factor: 4.379

Review 2.  Current Status of the Spectrum and Therapeutics of Helicobacter pylori-Negative Mucosa-Associated Lymphoid Tissue Lymphoma.

Authors:  Sung-Hsin Kuo; Kun-Huei Yeh; Chung-Wu Lin; Jyh-Ming Liou; Ming-Shiang Wu; Li-Tzong Chen; Ann-Lii Cheng
Journal:  Cancers (Basel)       Date:  2022-02-16       Impact factor: 6.639

3.  Rare primary rectal mucosa-associated lymphoid tissue lymphoma with curative resection by endoscopic submucosal dissection: A case report and review of literature.

Authors:  Yan Tao; Qiong Nan; Zi Lei; Ying-Lei Miao; Jun-Kun Niu
Journal:  World J Clin Cases       Date:  2022-07-26       Impact factor: 1.534

  3 in total

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