Limitations of Primary Retroperitoneal Lymphadenectomy in Clinical Stage II Non-Seminomatous Testicular Cancer

1987 ◽  
Vol 137 (6) ◽  
Author(s):  
G. Pizzocaro
1998 ◽  
Vol 12 (6) ◽  
pp. 561-566 ◽  
Author(s):  
G. GIUSTI ◽  
P. BELTRAMI ◽  
C. TALLARIGO ◽  
G. BIANCHI ◽  
G. MOBILIO

1986 ◽  
Vol 4 (1) ◽  
pp. 35-40 ◽  
Author(s):  
G Pizzocaro ◽  
F Zanoni ◽  
A Milani ◽  
R Salvioni ◽  
L Piva ◽  
...  

Sixty-two consecutive patients with clinical stage I nonseminomatous testicular cancer were entered into a prospective study to receive no treatment after orchiectomy until clinical evidence of recurrent disease. Of 59 evaluable cases, 41 (69.5%) remained continuously disease free for a median duration of 30 months (range, 18 to 46 months), and evidence of metastatic disease developed in 18 patients (30.5%) from 2 to 36 months after orchiectomy. The median disease-free interval for relapsing patients was 6 months. Retroperitoneal metastases developed in ten patients; seven patients had pulmonary metastases, and one patient had progressive elevation of the serum alpha-fetoprotein level. Relapses were significantly more frequent in patients with either embryonal carcinoma, infiltrating testicular cancer (pT greater than 1), peritumoral vascular invasion, or in those who underwent transscrotal biopsy. One patient with relapse refused salvage therapy and died. The remaining 17 patients have been rendered disease free with cisplatin combination chemotherapy and/or surgery. However, two patients showed further recurrence, with one in the lung and the other one also in the retroperitoneal nodes. In our opinion, surveillance following orchiectomy will provide useful information in clinical stage I nonseminomatous testicular cancer, but it is a difficult study. For the time being, it should be restricted to specialized centers only. In the meanwhile, retroperitoneal lymphadenectomy remains the standard treatment.


1992 ◽  
Vol 59 (1_suppl) ◽  
pp. 166-169
Author(s):  
N. Nicolai ◽  
G. Pizzocaro ◽  
R. Salvioni

Between January 1985 and December 1990, 208 consecutive patients underwent retroperitoneal lymphadenectomy (RPLND) for low-stage (negative imaging or retroperitoneal disease up to 3 cm) non-seminomatous germ cell testicular tumors. Before RPLND, patients were staged with computed tomography (CT) or magnetic resonance imaging (MRI) of abdomen and pelvis, alpha-fetoprotein (AFP) and beta submit of human chorionic gonadotropin (b-HCG) assay. Lymphangiography (LAG) was performed in 139 cases. Out of 208, 173 (83%) patients belonged to clinical stage I, 21 (10%) to clinical stage II-A (retroperitoneal disease up to 2 cm) and 14 (7%) to clinical stage ll-B (retroperitoneal disease from 2 to 3 cm). Before RPLND, serum markers AFP and b-HCG were pathological in 16 (9%) of 173 patients in clinical stage I, in 7 (33%) of 21 in clinical stage ll-A and in 6 (43%) of 14 in clinical stage ll-B < 3 cm. Retroperitoneal metastases were pathologically found in 46 (27%) of 173 patients in clinical stage I, in 15 (71%) of 21 in clinical stage ll-A and in all 14 clinical stage ll-B < 3 cm. As many as 31 (20%) of 157 in clinical stage I with negative markers and only 8 (57%) of 14 clinical stage II-A with negative markers had retroperitoneal metastases. The low reliability of clinical staging enforces RPLND as the most accurate staging procedure for marker negative clinical stage I and II-A patients.


1990 ◽  
Vol 8 (3) ◽  
pp. 509-518 ◽  
Author(s):  
O Klepp ◽  
A M Olsson ◽  
H Henrikson ◽  
N Aass ◽  
O Dahl ◽  
...  

Between 1981 and 1986, 279 consecutive patients with clinical stage I (CS1) nonseminomatous germ cell tumors (NSGCT) of the testis underwent pathological staging (PS) with retroperitoneal lymphadenectomy (RPLND). Patients with retroperitoneal metastases (PS2) received adjuvant chemotherapy. The median follow-up time after RPLND was 50 months (range, 30 to 90). Clinical and histopathologic features were registered prospectively and analyzed for association with risk of having PS2, relapse despite pathological stage 1 (PS1) or the combined risk of either event, metastatic disease (MET). Seventy-five (26.9%) of the patients had PS2 disease, and 30 (14.7%) of the 204 PS1 patients relapsed, indicating that at least 105 (37.6%) of this CS1 population had subclinical MET at the time of orchiectomy. Four (1.4%) of the 279 CS1 patients died of testicular cancer. Multivariate analyses showed several variables to be significantly associated with outcome for the CS1 patients; vascular invasion in primary tumor and normal preorchiectomy serum alpha-fetoprotein (Pre-AFP) level indicated PS2 disease. If Pre-AFP was excluded from the model, the absence of teratoma or yolk sac elements in the primary tumor became significant predictors of PS2. Vascular invasion, absence of teratoma, and a short interval between orchiectomy and RPLND indicated increased risk of relapse in PS1 patients. Vascular invasion, normal Pre-AFP, absence of teratoma elements, and a short orchiectomy to RPLND interval were predictive of MET. Our results indicate that prognostic factors useful for stratification of CS1 patients with NSGCT to different treatment options may be established.


Cancer ◽  
1984 ◽  
Vol 53 (6) ◽  
pp. 1363-1368 ◽  
Author(s):  
Giorgio Pizzocaro ◽  
Fulvio Zanoni ◽  
Angelo Milani ◽  
Luigi Piva ◽  
Roberto Salvioni ◽  
...  

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