Helicobacter pylori eradication therapy in gastric high grade Non Hodgkin's lymphoma (NHL)

Citation
B. Alpen et al., Helicobacter pylori eradication therapy in gastric high grade Non Hodgkin's lymphoma (NHL), ANN HEMATOL, 80, 2001, pp. B106-B107
Citations number
9
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
ANNALS OF HEMATOLOGY
ISSN journal
09395555 → ACNP
Volume
80
Year of publication
2001
Supplement
3
Pages
B106 - B107
Database
ISI
SICI code
0939-5555(200111)80:<B106:HPETIG>2.0.ZU;2-4
Abstract
Background: Primary gastric low-grade lymphoma of the mucosa associated lym phoid tissue (MALT) develops on the background of a chronic Helicobacter py lori (H. pylori) infection. Stable remissions can be induced by H. pylori e radication therapy as shown in clinical trials. In 8 cases of high-grade ga stric lymphomas remissions after H. pylori eradication were observed retros pectively. Aim: We started a pilot-trial to investigate the value of H. pylori eradica tion therapy in early gastric high-grade B-cell lymphoma prospectively. Patients and Methods: So far, two H. pylori positive patients with high-gra de B-cell lymphoma of the stomach stage Ann Arbor I E are included. They re ceived a triple eradication-therapy (Clarithromycin 500 mg/d, Metronidazol 800 mg/d and Omeprazol 40 mg/d) for 7 days. Endoscopic controls are preform ed every 4 weeks. Results: Both patients became H. pylori negative after eradication therapy. One patient achieved complete remission (CR) 38 days after eradication. Th e continuous complete remission lasts now for 170 days. The second patient received only a partial remission (PR) 4 weeks after eradication and showed a slight progress 4 weeks later. He presently receives chemotherapy (CHOP) . Conclusions: Patients with early high-grade gastric B-cell lymphomas should receive H. pylori eradication only within clinical trials. It seems to be possible to induce remissions of early high-grade gastric B-cell lymphomas with exclusive H. pylori eradication therapy. The stability of remission re mains to be unclear and should be evaluated by following up the patients cl osely.