Quick Update

September 7, 2010 at 10:40 PM (Research, Treatment) (, , , , , )

So. Multiple conversations at The Cancer Factory today elucidated the rationale behind the slightly ambiguous bi-directional recommendations of my multi-partite team of oncological specialists.

If the previous sentence took you three or four tries to make sense, you now know how I felt.

My CA-125 finally came back at about 10:30, reading 137, a five-point increase over the previous test two weeks ago. That might sound like a statistically significant increase, but it’s not. Dr. B finally came to see me in the clinic and we hashed back and forth for a few minutes. I told him that the steady increase in my CA-125 since mid-July gave me the impression that the trial wasn’t working, and shouldn’t we oughta switch to chemo? He said that despite the CA-125, which may not be a good indicator for this trial (and certainly hasn’t been a good indicator for me very often), my CT scans showed good stabilization in my disease up to the scan two weeks ago. Even as my CA-125 was rising, my scans showed stability in the disease.

Dr. B did apologize for his earlier discussion with me, and his email to Dr. A, that gave the impression that he wanted me to quit the trial and switch to conventional chemo this week. He wanted me to meet with Dr. A to discuss the next steps in the event that I go off the trial in the future, not to actually plan my switch, which is what she and I talked about last week.

We talked together about getting another data point next week with a CT on Friday to see how my lungs look, as apparently Drs. A and B discussed (after my appointment with Dr. A) that my lungs didn’t look all that definitively worse on the scan after all. Once we get that scan, THEN we will decide what to do. I’ll need a Vitamin B12 and a folate shot a week before I start Carbo and Alimta, so I would do that next Friday and then start chemo after my trip.

Or, the CA-125 and CT will both show relative stability, and we’ll keep on with the trial, because there aren’t that many good PI3K Phase I trials available right now, and to jump off this one at the first sign of trouble would be foolhardy, as I probably wouldn’t be able to get back on it again. And if nausea and fatigue keep being a problem on the trial, I could go to the reduced dosage (330 mg vs. my 450 mg) that’s being used as maximum for the Phase II trial now going on, to see if that reduces my side effects.

Short story long: keep on the trial this week. Next week is my week off the drug. Friday’s chest CT will decide if I continue the study or switch to chemo, which I’d start late in the month.

Clear as mud, right?

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5 Comments

  1. Mr. Wonderful said,

    Well that clears that up. 😉

  2. patricia said,

    That IS a mouthful…a brainful…and then some!! Enjoy your trip and put it all on the back burner [and get a spa treatment]!! My prayers continue for incredible things in your treatment…your spirit is obviously still NOT taking this laying down [or standing up for that matter].. Goooo girl! xx’s & oo’x

  3. Adrienne St.Clair said,

    You have AMAZING strength ,Honey, hang in there! You are in our hearts and our prayers every day!
    Ada

  4. Catherine Jacobs said,

    Whew, I’m confused! But sounds like you have been keeping those silly doctors on the straight and narrow – keep it up

  5. Kim ostien said,

    Somehow I missed this and am just reading it now…..sounds like a good plan and we’re just going to keep throwing every ounce of strength we have up to you.

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