AI Article Synopsis

  • The study aimed to evaluate an intensive chemotherapy regimen for patients suffering from HIV-associated non-Hodgkin lymphoma (NHL) to find an effective treatment method without worsening their immunodeficiency.
  • Thirty-eight patients underwent a series of chemotherapy treatments along with antiretroviral therapy, showing a 60.5% complete response rate and 79% overall response rate, with significant improvement in viral load and survival rates.
  • The findings suggest that intensive chemotherapy can be both effective and tolerable for treating HIV-associated NHL, although the levels of CD4-positive T lymphocytes decreased slightly post-treatment.

Article Abstract

Background: Optimal treatment of human immunodeficiency virus (HIV)-associated non-Hodgkin lymphoma (NHL) has yet to be defined, because chemotherapy could exacerbate immunodeficiency, with subsequent adverse effects for patients.

Methods: The authors investigated the feasibility of an intensive chemotherapy regimen for HIV-associated NHL. Thirty-eight patients were treated with a first course of cyclophosphamide (Cy), vincristine, and prednisone; followed by 3 courses of high-dose Cy (2000 mg/m2), doxorubicin (Doxo; 50 mg/m2), vincristine, and prednisone (modified high-dose CHOP); 1 course of high-dose methotrexate (MTX; 8000 mg/m2); and 1 course of high-dose cytarabine (8000 mg/m2). Radiotherapy was added to the treatment regimen for patients with bulky disease or residual tumor. Chemotherapy was administered in conjunction with granulocyte-colony-stimulating factor and antiretroviral therapy.

Results: Patients received 91.5%, 93%, 66%, and 63% of the scheduled doses of Cy, Doxo, MTX, and cytarabine, respectively. The complete response rate was 60.5%, with a total response rate of 79%. The 40-month overall survival rate was 43%, the disease-free survival rate was 65%, and the recurrence-free survival rate was 39%. Both an International Prognostic Index score of 0 or 1 and Burkitt-type histology had positive effects on survival, whereas CD4-positive lymphocyte counts, viral burden, and previous highly active antiretroviral therapy did not. CD4-positive T lymphocyte levels decreased from 0.197 +/- 0.156 x10(9)/L before treatment to 0.152 +/- 0.1 x10(9)/L at 6 months after the end of treatment. A decrease in viral load, from 380,000 +/- 785,000 copies/mL before treatment to 25,000 +/- 43,000 copies/mL at 6 months after the end of treatment, also was observed.

Conclusions: The results of the current study indicate that intensive chemotherapy is effective and tolerable for patients with HIV-associated NHL.

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Source
http://dx.doi.org/10.1002/cncr.20019DOI Listing

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