The study of multiple primary neoplasms may provide more insight into
the pathogenesis of specific cancers and, secondly, it addresses the i
ssue of treatment-related induction of second tumors. 584 consecutive
patients with testicular germ cell tumors treated during 1969-1992 in
Berlin were retrospectively analyzed for the prevalence of multiple pr
imary neoplasms. 23 patients (16 pure seminoma, 7 nonseminoma) develop
ing nontesticular malignancies in addition to testis cancer were ident
ified (3.9%, 95 confidence intervals +/- 1.6%). The mean age at the ti
me of the testis cancer was 42.8 years, and mean age at the time of no
ntesticular malignancy was 50.2 years. In 4 cases, the nontesticular m
alignancy preceded testis cancer, in 3 patients both neoplasms occurre
d simultaneously, and in 16, nontesticular malignancies developed subs
equently to testis cancer. In 4 patients, triple malignancies were obs
erved. Bladder carcinoma and bronchogenic cancer with each 3 cases wer
e the most frequent second neoplasms seen in these patients. 9 consecu
tive cancers developed within radiation fields, the median latency per
iod in these cases was 12 years. None of the subsequent cancers develo
ped after chemotherapy. It is concluded that genetic predisposition an
d radiation effects are the most important factors contributing to the
occurrence of multiple primary neoplasms in patients with testicular
germ cell cancer. The high rate of multiple primary neoplasms in these
patients lends further evidence to the theory of genetic anticipation
of germ cell cancer.