All patients achieved immediate/rapid or slow complete regression as demonstrated by normalization of previously elevated LDH and B-HCG levels and by CT scans. In five (19%) patients, in whom the tumoral mass shrinkage was very slow, follow-up consisted of CT scans, and six patients also had PET scans (Table 2). In two patients, para-aortic lymph node

packets could be followed Inhibitors,research,lifescience,medical on CT scans during 1 year of follow-up until disappearance. No evidence of persistent or regrowing masses was demonstrated. The three patients with pathologically and radiologically confirmed IIIA disease also responded completely to BEP. After a median follow-up of 120 months (range 24–268 months) all patients are alive with no evidence of disease. Table 2. Treatment Modalities, Side Effects, and Results. One patient (Table 3, #22) developed lung metastases 4 years after his first CR. He responded to vinblastine/ifosfamide/cisplatinum (VeIP) salvage chemotherapy for 4 years, but eventually

his disease recurred in the Inhibitors,research,lifescience,medical lungs and pelvis. This patient entered Inhibitors,research,lifescience,medical a third CR following high-dose chemotherapy (HDCT) with autologous peripheral stem cell transplantation (APSCT) and local radiation therapy, resulting in long-term (third) CR. Currently, 16 years following his last treatment, he is alive with no evidence of testicular tumor. Another patient (#19) preferred surveillance initially, but relapsed after 9 months with a IIC abdominal mass and achieved prompt and durable complete remission with three BEP cycles. Table 3. Staging, Chemotherapy Regimens, Fostamatinib purchase Response, and Latest Status. Side effects were manageable (Table 2). In three patients, cisplatinum was replaced by carboplatin due to the development Inhibitors,research,lifescience,medical of tinnitus and mild hearing loss, respectively. In seven patients, bleomycin was omitted for the fourth

cycle, and the fourth cycle was modified in two patients due to neutropenic fever. Within a range of 2–4 months, three patients Inhibitors,research,lifescience,medical developed clinical and radiological signs of bleomycin lung toxicity through after reaching a cumulative dose in the range of 180–240 units of bleomycin. Clinically, they presented with non-productive cough, exertional dyspnea, and low-grade fever. The chest X-ray showed bilateral, bibasilar infiltrates, with later consolidation (Figure 1, panels A and B) which was totally reabsorbed with no progression (Figure 1, Panel C) into irreversible diffuse fibrosis. The three patients responded well to high-dose steroids and broad-spectrum antibiotics. Figure 1. A CT Scan Following Completion of BEP Regimen (cumulative bleomycin dose 240 units) at 2 Months (A), 5 Months (B), 10 Months (C). Following a thorough search on the website of the Ministry of Interior Affairs, we found that all the treated patients are alive and well with no evidence of their previous testicular tumor.