Hi,
My name is Troy and I was hoping to get some opinions of fellow tc patients.
On the 22nd of may 2017, i had raised hcg, other markers were normal. Ct scan was clear. i was diagnosed with tc and had r/o on the 23rd May 2017. My pathology from stanford is mixed germ cell with (60%seminoma, 25%embryonal carcinoma, 10%teratoma and 5%yolk sac, rete testis and lvi invasion). One week after orchiectomy my hcg and all markers were back to normal. This puts me in the 1B stage and both the oncologists and urologists i've seen are suggesting surveillance opposed to 1x bep. I have seen a lot of people say at 1B they have had 1 x bep but i would love to know if there are any people out there to share their story on choosing surveillance with a 1B diagnosis and reaching the all clear? The doctors are saying i have a 30%chance of relapse but other articles suggest 50% given rete and lvi. Surveillance seems to be being pushed more than anything these days regardless of 1a or 1b
My name is Troy and I was hoping to get some opinions of fellow tc patients.
On the 22nd of may 2017, i had raised hcg, other markers were normal. Ct scan was clear. i was diagnosed with tc and had r/o on the 23rd May 2017. My pathology from stanford is mixed germ cell with (60%seminoma, 25%embryonal carcinoma, 10%teratoma and 5%yolk sac, rete testis and lvi invasion). One week after orchiectomy my hcg and all markers were back to normal. This puts me in the 1B stage and both the oncologists and urologists i've seen are suggesting surveillance opposed to 1x bep. I have seen a lot of people say at 1B they have had 1 x bep but i would love to know if there are any people out there to share their story on choosing surveillance with a 1B diagnosis and reaching the all clear? The doctors are saying i have a 30%chance of relapse but other articles suggest 50% given rete and lvi. Surveillance seems to be being pushed more than anything these days regardless of 1a or 1b
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