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Abstract

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Purpose : We reviewed clinical characteristics and prognostic factors in testicular germ
cell tumor in adults.
Materials and Methods : We reviewed the records of 42 patients with testicular germ
cell tumors managed at Seoul National University Hospital between January 1985 and
May 1997. Patients were followed regularly to determine clinical outcome with tumor
markers, chest X-ray and abdominal CT. Mean follow-up was 5.75 years ranging from
3 months to 238 months.
Results : Painless testiscular enlargement(86%) was the most common presenting
symptom and history of cryptorchidism was noted in 6 patients. Among 21 seminoma
patients, 11 were stage ¥°, 9 were stage ¥±, and 1 was unknown and among 21
nonseminomatous germ cell tumor(NSGCT) patients, 14 were stage ¥°, 1 was stage ¥±,
5 were stage ¥², and 1 was unknown. Of the 11 patients with stage ¥° seminoma, there
was no recurrence in 7 patients who received retroperitoneal low-dose radiation therapy
after orchiectomy, but 2(50%) of 4 patients who had surveillance after orchiectomy,
showed relapse at retroperitoneal lymph nodes. One of 3 patients who had elevated level
of serum ¥â-HCG at initial presentation showed tumor relapse at retroperitoneal lymph
node. Among 11 patients with stage ¥° NSGCT under surveillance after radical
orchiectomy, 7 patients(63.6%) had relapse. Vascular invasion of tumor was noted in
orchiectomy specimens in 3 cases of the 7 relapsed cases compared to no vascular
invasion in 4 non-relapsed cases. Also, 4 of 7 patients with elevation of tumor marker
resulted in relapse. Although primary pathologic stage T2 was noted in 2 patients with
clinical stage ¥° NSGCT, no recurrence occurred after adjuvant combined chemotherapy.
Fifteen patients with stage ¥± or stage ¥² were treated with systemic combination
chemotherapy after radical orchiectomy and 7 of these patients had residual
retroperitoneal mass. Of these patients, salvage chemotherpy was done in 2 patients,
salvage RPLND and salvage chemotherapy with RPLND was performed in 1 patient
respectively. Of the patients with stage ¥± or ¥². One patient with stage ¥±B seminoma
died despite of salvage chemotherapy with RPLND. The remaining 3 patients with
residual mass were followed regulary without further treatment. They had no evidence
of recurrence which was evaluated by tumor marker, chest X-ray and abdominal CT.
The marked reduction of residual mass after adjuvant therapy were found in this group.
The overall survival rate in total patients was 98% at 5.75 years from initial diagnosis.
Conclusions : Adjuvant low-dose radiation therapy after radical orchiectomy was
recommended to reduce recurrence rates in stage ¥° seminoma. The vascular invasion,
pre-orchiectomy elevation of tumor markers, or pathologic T2 or more stage were risk
factors for relapse in stage ¥° NSGCT. In advanced staged germ cell tumor, high
survival rate was achieved by cis-platin based combination chemotherapy. Especially, in
the patients with marked reduction of tumor mass after chemotherapy, close surveillance
might be adequate in stead of second look operation for the retroperitoneal mass.
Irrelevant of its histopathologic finding and stage, the testicular germ cell tumor showed
excellent therapeutic end-results. Further studies should be directed at developing
therapeutic modalities that could achieve better therapeutic results with least therapeutic
complication and sequelae.

Å°¿öµå

Testis; Germ cell tumor; Clinical characteristics; Prognostic factors;

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