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For further information, see CMDT Part 39-11: Gastric Lymphoma

Key Features

  • Second most common gastric malignancy, 3–5% of gastric cancers

  • Distinguish between primary gastric lymphoma with adjacent nodal spread and advanced systemic lymphoma with secondary gastric involvement

  • More than 95% are non-Hodgkin B-cell lymphomas consisting of

    • Mucosa-associated lymphoid tissue (MALT) lymphoma, or

    • Diffuse large B-cell lymphoma, or

    • Gastric T-cell lymphoma (rare)

  • Gastric T-cell lymphoma, associated with human T-lymphotropic virus (HTLV) type 1 infection, is rare and makes up 7% of primary gastric lymphomas

  • Infection with Helicobacter pylori is an important risk factor for primary gastric lymphoma; > 90% of low-grade primary gastric lymphomas are associated with H pylori

Clinical Findings

  • Dyspepsia

  • Abdominal pain

  • Weight loss

  • Upper gastrointestinal bleeding

  • Anemia

  • Patients with diffuse large B-cell lymphoma are more likely to have systemic symptoms and to present at an advanced stage

Diagnosis

  • Upper gastrointestinal series or endoscopy show thickened folds, ulcer, mass, or diffusely infiltrating lesion; diagnosis established with endoscopic biopsy

  • Biopsies of both suspicious and normal-appearing areas are recommended

  • Biopsy specimens should be tested for H pylori and, if positive, for gene translocations that might be harbored by the tumor (eg, t[11;18])

  • Endoscopic ultrasonography is the most sensitive test for determining the depth of invasion and presence of perigastric lymphadenopathy

  • CT scanning of chest, abdomen, and pelvis useful in staging

  • For patients with gastric MALT lymphomas, the Lugano staging system is most frequently used

  • For patients with diffuse large B-cell lymphomas involving the stomach, the following may be required for staging and management:

    • Combination PET-CT imaging

    • Bone marrow aspirate with biopsy

    • Tumor lysis laboratory tests

    • Hepatitis B and HIV serologies

Treatment

  • Depends on tumor histology, grade, and stage

  • MALT-type lymphomas

    • Regression after successful H pylori eradication occurs in ~ 75% of cases of stage I and ~ 55% of stage IIE low-grade lymphomas

    • Remission may take as long as a year, and relapse occurs in ~ 2% of cases per year

    • Many patients with minimal disease after successful H pylori eradication may be observed closely without further therapy

    • Failure of antibiotic treatment to achieve lymphoma regression may be due to gene translocations harbored by the tumor

      • Of cancers positive for t(11;18), 95% do not respond to antibiotics

    • Patients with localized marginal zone (MALT-type) lymphomas who are not infected with H pylori may be treated with radiation therapy

    • Endoscopic surveillance is recommended every 3–6 months for 5 years

    • Surgical resection is not recommended

    • Long-term survival for stage I is > 90% and for stage II, 35–65%

  • Diffuse large B-cell lymphoma

    • Usually presents at an advanced stage with widely disseminated disease and is treated according to stage and subtype of lymphoma

    • Surgery has been associated with a better prognosis than conservative treatment

    • Chemoimmunotherapy or radiation therapy is used for gastrointestinal bleeding, threatened end-organ function, bulky disease, or progression

      • Two chemotherapeutic ...

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