Background. This study relates our experience in the diagnosis and tre
atment of a rare clinical entity, non-Hodgkin's primary lymphoma of bo
ne. Methods. Seventeen cases of patients with primary lymphoma of bone
diagnosed and treated at a single institution between 1975 and 1992 a
re reviewed. Ten patients received combined-modality therapy, consisti
ng of an anthracycline-containing combination chemotherapy (CT) regime
n, followed by adjuvant radiotherapy (RT) to the primary site of disea
se. Five patients were treated with CT alone; one patient received RT
alone; and one patient was treated with CT after emergency RT for spin
al cord compression. Results. Thirteen patients presented with Stage I
disease, two with Stage II; and two with Stage IV disease (multiple b
ony sites only). Thirteen patients had an intermediate-grade diffuse l
arge cell lymphoma; two had an intermediate-grade mixed small and larg
e cell lymphoma; and two had a high-grade lymphoma (one immunoblastic
and one small non-cleaved cell lymphoma). The overall response rate wa
s 94% (18% complete response, 58% partial response 1, and 18% partial
response 2). Thirteen patients are alive and disease-free at a median
of 29 months; 10 of these received CT + RT, and 3 received CT alone. T
hree patients have died; one of these received CT + RT and one CT alon
e, and one relapsed immediately after CT. One patient, who was initial
ly treated with RT and then with CT + RT after relapse, was lost to fo
llow-up 40 months from the start of treatment. Conclusions. Because ex
perience in the literature suggests a 50% distant relapse rate in prim
ary lymphoma of bone treated with RT alone, our policy is to treat all
patients with combined-modality therapy (CT + RT). However, only a Ph
ase III randomized, controlled clinical trial will determine whether C
T + RT is superior to either modality alone.