| Joined: Mar 2021 Posts: 3 Member | OP Member Joined: Mar 2021 Posts: 3 | My diagnosis is stage 4A invasive squamous cell carcinoma, intermediate differentiation. I've had two partial glossectomies and 10 lymph nodes removed and examined. Three of the latter showed some cancer, the largest example was less 2mm. The treatment recommended by the Tumor Board is six weeks of radiation with three 4-6 hour IV cisplatin sessions. This will begin on 3/29. I had a clean CT scan in between glossectomies, and a clean PET scan after the second one. My team's original plan was radiation alone, but the board discussion them pushed them into favoring chemo as well.
I hope you will permit me this indulgence: Let's say you believe there is a good chance that there is a serial murderer in Paris. You're not absolutely sure that he's there and you're not sure that you can hit him. Still, your first tactic is to carpet bomb the city and trust that the French people are resilient enough to survive and rebuild the city. This is a parallel scenario to my team's cancer strategy.
Most of my working life has involved me being required to make quick decisions based upon limited information. There's a pretty straightforward strategy in these cases. You determine an approach which seems likely to succeed which offers limited ancillary consequences. If that doesn't solve it, you move to something which might have more potential for collateral damage. And so on. What you never do is to opt for the most extreme of options immediately. That would be considered a panic response. I think this points out how limited our understanding is of this disease.
With that out of the way, I have read with appreciation ChristineB's observations regarding the importance of hydration and caloric intake and am developing strategies around that. I'm interested in other observations and experience you folks might think useful as well.
Thanks in advance.
DW Wheeler
| | | | Joined: Feb 2015 Posts: 134 Likes: 7 Senior Member (100+ posts) | Senior Member (100+ posts) Joined: Feb 2015 Posts: 134 Likes: 7 | I have just gone through six weeks of radiation w Erbutux (monoclonal antibody) for squamous cell cancer in my lower lip. It started in December and ended in January. I don't know that my experience will be that close to yours, but I will tell you that I managed to get through the process and of course there was a good deal of lip and mouth pain that has now almost finished. I can't say anything about chemo. although I appreciate your analogy. Hang in there. you'll get through this.
SCC stage 1 Nov. '03, SCC stage 2 (clear mrg, no rad, no chemo) RND, Feb. '15 SCC stage 1, lower gum Mar '23, all lower gums and teeth removed
TLC356
| 1 member likes this:
DonVila | | | | Joined: Oct 2012 Posts: 1,275 Likes: 7 Assistant Admin Patient Advocate (1000+ posts) | Assistant Admin Patient Advocate (1000+ posts) Joined: Oct 2012 Posts: 1,275 Likes: 7 | My understanding is cisplatin is a radio-sensitizer. It helps the radiation work better. Of course, it also wipes out any possible stray cancer cell in the body which the radiation doesn’t get to. I know it’s disappointing for you but it may be for the better in the minds of the Tumour Board members.
Gloria She stood in the storm, and when the wind did not blow her way, she adjusted her sails... Elizabeth Edwards
Wife to John,dx 10/2012, BOT, HPV+, T3N2MO, RAD 70 gy,Cisplatinx2 , PEG in Dec 6, 2012, dx dvt in both legs after second chemo session, Apr 03/13 NED, July 2013 met to lungs, Phase 1 immunotherapy trial Jan 18/14 to July/14. Taxol/carboplatin July/14. Esophagus re-opened Oct 14. PEG out April 8, 2015. Phase 2 trial of Selinexor April to July 2015. At peace Jan 15, 2016. | 1 member likes this:
DonVila | | |
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