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  • Time for a decision

    I went to see the oncologist today and found out my desicion may not be so easy. He is leaning away from surviellance due to the fact that my tumor makers where negative pre surgery. So now I can either go with rplnd or chemo. I am still trying to take it all in. I thought i had my desicion made before seeing the doc today. I am going to take a few days and process it and then try to decide what best suits me. Any advice would be great. I am also waiting on the 2nd pathology report. The first didnt specify vascular invasion or not. So I really cant make a desicion until I get that piece of the puzzle.

  • #2
    what is the pathology? What was/is your tumor markers before and after surgery? FYI i was 24 when Diagnosed (25 now). Chose survelliance (95% embryonal 5% seminoma). AFP fell from 210 before surgery to 4.2 after. Well a month or so later, it started to climb. Had to do 4 x EP. AFP went to 4.6. . .hmmmmm i was thinking. Well sure enough 6 weeks later after 4 x EP, AFP started to climb again to over 600 with the tumor showing up around my spinal cord. Time for a week of VIP, plus 17 radiation treatments. Tumor gone, and off to cincinnati for HDC of 1500 mg/ daily x 3 and 750 mg Carboplatin x 3. This was one transplant, always tandem is done.

    Now 9 months later I am still at 3.1-3.2 AFP since the first transplant. Hopefully, the second transplant was "overkill." Now we know this number is my natural level of AFP, not 4.2 or 4.6. I'm lucky though AFP is the only tumor marker i've had trouble with. If BHCG played a role in my whole fiasco, I'd probably would have died a long time ago.

    My point, I should have done chemo FIRST instead of survelliance while my AFP was low (post surgery for a short time). Its a hard decision, but chemo isn't all that bad. . .sure it was rough espeically towards the end of EP, but you may want to consider it. I would also favor 3 x BEP to 4 x EP (one less cycle, and some doctors i have saw say they feel that bleomycin is a "must")
    Diagnosed August 2005
    R/O August 2005 AFP 210

    4xEP beginning December 2005
    End Feb/March 2006 AFP 4.6
    April 2006 AFP 22 and rising

    Tandem Stem Cell Transplant 7/06 - 9/06
    December 07 AFP = 3.3
    December 07 CT = Clear!

    15+ months remission

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    • #3
      I don't know your patology report, but i wanna tell you my experience...
      I was very scared by rplnd, i take a month to take the same decision...with 95% embryonal and vascoular invasion...
      I did rplnd and it's no so bad...in the first 2/3 days you have morphine and you don't fell nothing...you sleep a lot, then you can have some more pain drugs for a week...after a week you can go home...
      now i'm 3 1/2 weeks after rplnd, i can drive, i did a concert few days ago, i can work...i'm tired, with a little diffuse pain but every day is really better.
      And the best is that now i have some chanche to avoid chemo...i'm hoping it!
      Even if you don't chose to have surgery remind chemo works very very well...
      I can assume from your words that you are stage 1 and cure rate for this is 98%...with surveillance or with rplnd...

      the difference is that with rplnd you have more chanche to avoid chemo and all the side effects and long period risks...
      rplnd take only 1 months of your life, chemo seems to be longer and worst...

      good luck for all! everything you will chose will be the right chose...at the end you will be cured!
      davide
      left I/O 1/9/07 - 95% embrional carcinoma 5% seminoma with vascular invasion afp 27 bhcg 80- 2/10/07 ct and markers clean, left rplnd 4/23/07 3 microscopic lynph node found with ec - 3/30/09 all clean

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      • #4
        I chose surveillance...same pathology as you...no markers pre surgery...during surveillance, 2 months out...bhcg went up and I showed an enlarged node....did 3xBEP....

        but if no markers and no vasc. invasion, clear chest xray and clear CT scan....chances are approx 70% you are cured with the surgery....that's why I chose surveillance....most important, einhorn & benedetto said as long as I kept to the surveillance schedule, if I did have a recurrence, having the 3xbep my "cure" rate would be the same, as if I had 2xBEP immediately post orchiectomy....

        einhorn said either surveillance, rplnd or 2xbep were all good options for me....

        one thing to consider with rplnd, is that with embryonal, sometimes it skips the lymph nodes and goes to the lungs via the vascular system....so there is a risk of doing an rplnd, and still needing chemo....

        but most important, your cure rate is 98% no matter what.

        pete
        - lump first noticed 11/20/2005
        - I/O right Dec 8, 2005
        - 95% embryonal / 5% seminoma
        - normal markers PRE surgery
        - no vascular invasion, tunica free of cancer, epididymis free of cancer, lungs free, lymph free
        - Stage I diagnosis
        - surveillance
        - mid feb '06, beta hcg slightly elevated = 4.6...small enlarged lower node seen on CT scan...
        - 3BEP began feb 20, 2006
        - finished 3 BEP, last bleo, april 17, 2006
        - CT scan, blood markers, chest..all clear
        - back on surveillance

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        • #5
          Was your oncologist leaning more toward chemo or RPLND? Did he give you a recommendation for which option he thinks is best for your situation?

          Comment


          • #6
            Original path 95% seminoma 5% embryonal didnt specify vascular invasion.

            The doc said he was going to consult with the other doctors on the team but I kept pressing him to tell which way he would go. He said if he had to make the decision by himself he would go with the rplnd.

            Comment


            • #7
              Hi Ski,
              My doctor told me that surveillance was a good fit for people who's markers were elevated before surgery because if your markers went up once, it's very likely they will go up again in case of a recurrence. I'm extrapolating, but it sounds like your doctor has the same opinion and because your markers never elevated they're concerned that they might not elevate again in case of a recurrence, which would let the cancer go undetected. I was a nonseminoma Stage 1 Pt2, by the way. It turned out chemo was the prefered option for me.

              I think you're right that the vascular invasion is a key question to answer, along with understanding what type of cancer you're dealing with and how it spreads so that you'll know whether removing the lymph nodes is an effective treatment. I'd also ask them what are the time limitations for starting these treatments because you wouldn't want to lose out on an option simply because the decision making process took too long.

              If you haven't seen it already, one of my favorite resources is the NCCN guidelines for treatment. It really helped me understand the processes I was going through. It's been posted in the cancer resources room at:

              http://www.tc-cancer.com/forum/showthread.php?t=4589

              That provides a nice decision tree that shows how the different stages are treated in general terms. After looking at that, I was able to go to the resource center's website and get a little more detail about each specific type of tumor and the treatment recommendations. It's at:

              http://tcrc.acor.org/

              Take care,
              Dan

              Comment


              • #8
                Ski,
                The proportion of embryonal is very small compared to that of seminoma, which is probably why you haven't shown markers to begin with. Embryonal doesn't always show markers, so it seems that in your case, the bloodwork won't help much in the decision making.

                Although I did not have any of the more aggressive embryonal component, the point that tipped the balance toward surveillance rather than other courses of action (after much consultation with multiple docs) was that 1) there was no evidence of lymphovascular invasion based on the pathology; 2) the viable tumor was < 1 cm; and 3) I have ready access to a medical facility that would aid in keeping close tabs on monitoring my surveillance.

                The RPLND is a viable treatment option; however, as many have said before, embryonal has the ability to travel through the bloodstream and plant itself in the lungs, at which point, removing the lymph nodes would not be curative.

                It will be a tough call, but you should consider all of your options and try to trace a logical path for your further treatment.
                "Life moves pretty fast; if you don't stop and look around once in a while, you could miss it." -Ferris Bueller
                11.22.06 -Dx the day before Thanksgiving
                12.09.06 -Rt I/O; 100% seminoma, multifocal; Stage I-A; Surveillance; Six years out! I consider myself cured.

                Comment


                • #9
                  Originally posted by Ski11181
                  Original path 95% seminoma 5% embryonal didnt specify vascular invasion.

                  The doc said he was going to consult with the other doctors on the team but I kept pressing him to tell which way he would go. He said if he had to make the decision by himself he would go with the rplnd.
                  Ski,
                  You only have 5% EC- that is good news! EC can skip the nodes and go into the vascular system- which is what happened to me. And my RPLND was negative...
                  I recommend you have your path read again, maybe twice to answer the vascular invasion question. Then you can make a more informed decision on RPLND vs chemo.
                  In my case, RPLND was much easier to recover from, with less long term side effects- chemo is a much bigger animal, I hope you can avoid it.
                  Best,
                  Stage III. Embryonal Carcinoma, Mature Teratoma, Choriocarcinoma.
                  Diagnosed 4/19/06, Right I/O 4/21/06, RPLND 6/21/06, 4xEP, All Clear 1/29/07, RPLND Incisional Hernia Surgery 11/24/08, Hydrocelectomy and Vasectomy 11/23/09.

                  Please see a physician for medical advice!

                  My 2013 LiveSTRONG Site
                  The 2013 Already Balders

                  Comment


                  • #10
                    .

                    Maybe you'll consider strange but I'm glad I had embryonal Carcinoma because it has skiped my lymph nodes directly to the lungs. So the RPLND was not needed[in EC case is very ineffective]. I think that RPLND is a major surgery with posible major psichological side effects and 3xBEP [4xEP] can be censidered as an alternative
                    2005-03
                    Stage III EC 85% + Sem 15%
                    AFP=2.6; HCG=10, 20,28 and rising
                    FULL CAT scan:
                    -abdominal lymph clear
                    -subpleural lungs metastasis [bipulmonary lesions with diam <= 1cm]
                    4 x BEP changed to 3 x BEP at my request
                    from 2005-05....Surveillance

                    Comment


                    • #11
                      Robert is right. My son had 4x EP and there is a residual mass. He will be having RPLND soon.

                      Tammy

                      Son Anthony DX 12/11/06
                      L/O 12/20/06 Stage IIIA, 95% EC, 5% Yolk Sac
                      4XEP 1/29-4/6/ 07
                      AFP started increasing3 wks later
                      Residual abdominal mass found on CT
                      RPLND 6/8/07
                      Cancer in pathology-
                      80% mature teratoma, 20% Yolk Sac. --
                      No adjuvent chemo and
                      AFP normalised

                      July 22, 2010 ---- 3 years all clear!

                      Comment


                      • #12
                        Thank you all for your advice. I have decided that I am going to go with rplnd. I comes down to the fact that I want to know now where I stand and this is the best way for accurate staging. Without the markers I am afraid of the cancer implanting itself deeper before we detect it on a ct scan.

                        I also think the doc is going to send me for a brain mri. I have been having some dizzy spells and he wants to check it just in case. I dont think its anything but better to safe then sorry.

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                        • #13
                          SKI

                          I think you made a good decision. Check the private message I sent you, there is a doctor in Denver that has done a lot of rplnd's and is very good (he did mine). I would be more than happy to talk to you about it over the phone if you are interested.
                          May 2000 I/O 100% Emb. Carc./June 2000 RPLND, 1 Node with Micro Involvement/ July 2000 1xBEP, 1xEP

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                          • #14
                            RPLND isn't so bad...the whole thing goes by pretty fast. I barely remember it, with all the pain meds they gave me.

                            Comment


                            • #15
                              Embryonal doesn't always show markers, so it seems that in your case, the bloodwork won't help much in the decision making.
                              Are you sure of this or is it that Seminoma doesn't always show in bloodwork??? I had 95% Embryonal so how do you know if it doesn't always show up in blood work (AFP)??????????????????????????????
                              Diagnosed August 2005
                              R/O August 2005 AFP 210

                              4xEP beginning December 2005
                              End Feb/March 2006 AFP 4.6
                              April 2006 AFP 22 and rising

                              Tandem Stem Cell Transplant 7/06 - 9/06
                              December 07 AFP = 3.3
                              December 07 CT = Clear!

                              15+ months remission

                              Comment

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