`Solitary plasmacytoma of bone (SPB) and extramedullary plasmacytoma (
EMP) are rare. High local control rates are reported with radiotherapy
, although the optimal dose and extent of radiotherapy portals remains
controversial. Between 1983 and 1993, 30 patients with solitary plasm
acytoma were seen at the Regional Cancer Centre, Trivandrum, India. 23
patients had SPB and seven EMP. The mean age was 52 years and the mal
e to female ratio 3.2:1. Diagnosis of SPB was confirmed by biopsy in 1
6 patients and tumour excision in seven. 20 patients received megavolt
age radiotherapy to the bone lesion with limited margins, and one rece
ived chemotherapy. Two patients who underwent complete tumour excision
received no further treatment. All seven patients with EMP received m
egavoltage radiotherapy, four following biopsy and three after tumour
excision. Local control was achieved in all patients with SPB. Nine pr
ogressed to multiple myeloma and one developed a solitary plasmacytoma
in another bone. Six patients with EMP achieved local control. Three
later progressed to multiple myeloma and one had local relapse. Median
time to relapse was 28 months in SPB and 30 months in EMP. 5-year ove
rall survival rates were 82% and 57% for patients with SPB and EMP; re
spectively. The corresponding progression free survival rates were 55%
and 50%, respectively. Age, sex, site of tumour, serum M protein and
haemoglobin levels did not significantly influence progression free su
rvival. The extent of surgery, radiotherapy dose or time to relapse we
re not significant prognostic factors. Radiotherapy appears to be an e
ffective modality of treatment of solitary plasmacytoma. No dose-respo
nse relationship is observed, and high local control rates are achieve
d with limited portals. Progression to multiple myeloma is the commone
st pattern of failure, although no prognostic factors for progression
are identified. The role of chemotherapy in preventing disease progres
sion needs further evaluation.