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
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.