CHEMOTHERAPY FOR PATIENTS WITH PULMONARY KAPOSIS-SARCOMA - BENEFIT OFFILGRASTIM (G-CSF) IN SUPPORTING DOSE ADMINISTRATION

Citation
E. Sloand et al., CHEMOTHERAPY FOR PATIENTS WITH PULMONARY KAPOSIS-SARCOMA - BENEFIT OFFILGRASTIM (G-CSF) IN SUPPORTING DOSE ADMINISTRATION, Southern medical journal, 86(11), 1993, pp. 1219-1224
Citations number
25
Categorie Soggetti
Medicine, General & Internal
Journal title
ISSN journal
00384348
Volume
86
Issue
11
Year of publication
1993
Pages
1219 - 1224
Database
ISI
SICI code
0038-4348(1993)86:11<1219:CFPWPK>2.0.ZU;2-B
Abstract
Kaposi's sarcoma (KS) is common in individuals infected with the human immunodeficiency virus (HIV-1). Although KS is frequently indolent, i t can also be aggressive and life-threatening, especially in patients with pulmonary involvement (PKS), who have poor survival rates when un treated. In an effort to develop treatment regimens for PKS that would prolong life or reduce clinical symptoms, we used combination chemoth erapy to treat 18 patients who had AIDS and PKS; 13 (72%) of them had a history of previous opportunistic infections. Doxorubicin, bleomycin , vinblastine, vincristine, actinomycin D, and dacarbazine were used i n 3-week cycles with concomitant zidovudine, zalcitabine (dideoxycytid ine), or didanocine (dideoxyinosine). Antiviral therapy was continued with chemotherapy. A partial or complete response to chemotherapy was obtained in 15 of the 18 patients (83%), as characterized by clearing of infiltrates on chest films and resolution of dyspnea and cough. Onl y 2 patients had opportunistic infections during treatment. Median sur vival was 9 months; patients who received dose reductions in less than three cycles of chemotherapy survived more than 1 year. Most deaths w ere related to unresponsive PKS. These results indicate that patients with symptomatic PKS can be safely and effectively treated with combin ation chemotherapy while receiving myelosuppressive drugs such as zido vudine. Such patients receive substantial relief from dyspnea and coug h. Survival for treated patients exceeds survival for untreated histor ical controls.