Malignant pheochromocytomas have exhibited partial responses to treatments
with 131-I metaiodobenzylguanidine (MIBG) and with chemotherapy. The author
s combined these two therapeutic methods to determine if beneficial effects
from each would be additive. Patients with documented malignant pheochromo
cytomas were recruited with the intent of administering 131-I MIBG in three
substantial amounts of radioactivity at 3-month intervals followed by a ye
ar of chemotherapy in which cyclophosphamide, dacarbazine, and vincristine
were to be given in 21-day cycles. Six patients entered the protocol. After
the 131-I MIBG treatments, three patients manifested declines in the prese
nce of tumor (smaller tumor volume or abnormalities on bone and 131-I MIBG
scans) and the function of tumor (decreased rate of normetanephrine excreti
on as the major index). Two patients completed at least 9 months of chemoth
erapy and showed further reductions in the presence and function of tumors
and were classified as having partial responses. Progressive disease afflic
ted three of the other four subjects. Even though toxicity was minimal from
131-I MIBG, it was sufficient to force reduction in the dosages or duratio
n of chemotherapy. A combination of 131-I MIBG treatments and chemotherapy
produced additive effects in reducing malignant pheochromocytomas. Toxicity
moderately curtailed the proposed chemotherapy protocol.