Aims: CD30 has been shown to be consistently strongly expressed in embryona
l carcinomas. Our aim was to examine changes in CD30 expression in embryona
l carcinomas before and after treatment with chemotherapy.
Methods and results: One hundred and eighteen retroperitoneal lymph node di
ssections from patients with metastatic germ cell tumours were reviewed. Se
venteen contained embryonal carcinoma deposits. In nine cases. the matching
pre-chemotherapy orchidectomy specimens were available. The cases were imm
unohistochemically stained for CD30. All nine pre-chemotherapy orchidectomy
specimens showed embryonal carcinoma and stained strongly positively for C
D30. However. only tour out of nine of the matched post-chemotherapy retrop
eritoneal lymph node dissection specimens and a total of SIX Out of 17 (35%
) with embryonal carcinoma deposits stained for CD30. Ten seminomas were ne
gative for CD30. Loss of CD30 did not appear to influence the relapse rate
of the patients.
Conclusions: Loss of CD30 expression occurs frequently in metastatic embryo
nal carcinomas after chemotherapy. This finding has implications in the use
of CD30 in the diagnosis of metastatic non-seminomatous germ cell tumours
and suggests that chemotherapy may alter the immunophenotype of embryonal c
arcinoma while retaining its characteristic histological appearances.