Literature DB >> 31347731

Gastric MALT lymphoma in a population-based study in France: clinical features, treatments and survival.

Tamara Matysiak-Budnik1, Philippe Jamet1, Agnès Ruskoné-Fourmestraux1,2, Antoine de Mascarel1,3, Michel Velten4,5, Marc Maynadié4,6, Anne-Sophie Woronoff4,7, Brigitte Trétarre4,8, Emilie Marrer4,9, Patricia Delafosse4,10, Karine Ligier4,11, Bénédicte Lapôtre Ledoux4,12, Laetitia Daubisse4,13, Laïla Bouzid4,14, Sébastien Orazio4,14, Anne Cowppli-Bony4,15, Alain Monnereau5,15.   

Abstract

BACKGROUND: Gastric mucosa-associated lymphoid tissue (MALT) lymphoma is a rare disease, and most available data on gastric MALT lymphoma (GML) come from clinical studies of selected patients treated in centres of excellence. AIMS: To analyse the clinical features, management and survival of GML patients in a population-based study in France
METHODS: All new cases of GML diagnosed between 2002 and 2010 in 11 French areas covered by cancer registries were included. Pathology reports were verified and, if necessary, reviewed by an expert pathologist. All clinical data were retrospectively collected from medical files and analysed using stata V. 14 software.
RESULTS: Four hundred and sixteen patients with confirmed GML (50% male, median age 67 years) were identified. Among them, 44 showed an early transformation into diffuse large B cell lymphoma and were considered to have had an initially missed high-grade lymphoma. At diagnosis, 76% of patients were at stage IE/II, and 24% at stage III/IV of the disease. Helicobacter pylori infection was found in 57% of the patients. Eradication treatment was administered to 76% of patients and complete remission (CR) was obtained in 39%. One hundred and ninety patients received at least one other treatment, including 10 already in CR after eradication. Altogether, CR was obtained in 70% of patients and the 5-year overall survival was 79% (95% CI [75-83]).
CONCLUSIONS: In comparison to clinical series, in the general population, GMLs are more frequently diagnosed at an advanced stage, their clinical management is heterogeneous, and there is a risk of misdiagnosis and overtreatment. These results highlight the necessity of following currently available guidelines in this field.
© 2019 John Wiley & Sons Ltd.

Entities:  

Year:  2019        PMID: 31347731     DOI: 10.1111/apt.15409

Source DB:  PubMed          Journal:  Aliment Pharmacol Ther        ISSN: 0269-2813            Impact factor:   8.171


  5 in total

1.  Long-Term Clinical Outcomes of Gastric MALT Lymphoma: A Nationwide Multicenter Study in Korea.

Authors:  Joon Sung Kim; Jun Chul Park; Jong Yeul Lee; Ji Yong Ahn; Sun Hyung Kang; Hyo-Joon Yang; Su Jin Kim; Moon Kyung Joo; Jae Myung Park
Journal:  Front Oncol       Date:  2021-10-14       Impact factor: 6.244

2.  Dieulafoy disease with gastric MALT lymphoma: A case report.

Authors:  Qin Zeng; Jin Feng Dai; Haijun Cao; Shuo Zhang
Journal:  Medicine (Baltimore)       Date:  2020-10-09       Impact factor: 1.817

Review 3.  Mucosa-Associated Lymphoid Tissue (MALT) Lymphoma in the Gastrointestinal Tract in the Modern Era.

Authors:  Eri Ishikawa; Masanao Nakamura; Akira Satou; Kazuyuki Shimada; Shotaro Nakamura
Journal:  Cancers (Basel)       Date:  2022-01-17       Impact factor: 6.639

4.  Second Primary Cancers After Gastric Cancer, and Gastric Cancer as Second Primary Cancer.

Authors:  Guoqiao Zheng; Kristina Sundquist; Jan Sundquist; Tianhui Chen; Asta Försti; Akseli Hemminki; Kari Hemminki
Journal:  Clin Epidemiol       Date:  2021-07-02       Impact factor: 4.790

5.  Long Spinal Cord Lesions Caused by Venous Congestive Myelopathy Associated with Intravascular Large B-cell Lymphoma.

Authors:  Takeshi Miura; Shoji Saito; Rie Saito; Tomohiro Iwasaki; Naomi Mezaki; Tomoe Sato; Yoichi Ajioka; Akiyoshi Kakita; Takuya Mashima
Journal:  Intern Med       Date:  2021-06-19       Impact factor: 1.271

  5 in total

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