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Tumor Engraftment in a Xenograft Mouse Model of Human Mantle Cell Lymphoma
Published on: March 30, 2018
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Primary gastrointestinal mantle cell lymphoma: a retrospective study
Lokanatha Dasappa1, M C Suresh Babu, Nagesh T Sirsath
1Department of Medical Oncology, Kidwai Memorial Institute of Oncology, M.H. Mari Gowda Road, Banglore, Karnataka, 560029, India.
Journal of Gastrointestinal Cancer
|October 16, 2014
Summary
Primary gastrointestinal mantle cell lymphoma is a rare and aggressive cancer. Patients often have poor outcomes and respond inadequately to standard chemotherapy, suggesting a need for novel therapeutic approaches.
Area of Science:
- Oncology
- Hematology
- Gastroenterology
Background:
- Primary gastrointestinal tract mantle cell lymphoma (GI-MCL) is exceptionally rare.
- Limited data exists on the natural history and prognosis of this specific entity.
Purpose of the Study:
- To investigate the clinical characteristics, epidemiological factors, and treatment outcomes of primary GI-MCL patients.
- To analyze the response to standard chemotherapy regimens and identify prognostic indicators.
Main Methods:
- Retrospective observational study of seven primary GI-MCL patients diagnosed between 2001 and 2012.
- Analysis of patient demographics, disease sites, histological subtypes, and treatment protocols.
Main Results:
- All seven patients were male, with a median age of 67.7 years. Stomach, colon, and rectum were affected.
- Three patients had blastoid variant, three had diffuse variant, and one had nodular pattern.
- Only one patient achieved complete remission with CHOP chemotherapy; others showed poor response and short survival (median 6 months).
Conclusions:
- Primary GI-MCL is highly aggressive, with high-risk MIPI scores and poor survival compared to nodal MCL.
- Standard CHOP chemotherapy demonstrates limited efficacy in this patient group.
- Consideration of rituximab for remission induction and maintenance is recommended for elderly patients ineligible for transplant.

