July 25: Cancer Report
After 6 hours at the Seattle Cancer Care Alliance today, here's what I know:
1. My MRI was boring. This is excellent. By "boring" I mean that nothing unexpected was found. The tumor size is 2.0 cm at its widest. It's only 2 mm from my skin, but not "involved" in the skin, which is good.
2. My biopsy (the one that really hurt) was worth it. They ran a bunch more tests than I thought they would. My "prognostics" are:
.....very strong findings for estrogen and progesterone receptors. These are the garden variety, super-well-understood markers for tumor cells that respond to super-well-figured-out chemo, like Tamoxifen.
.....no HER2/neu found. This is a truly nasty bugger to have; I'm delighted to not have it. They will do more tests to be more sure later.
.....15% Ki-67. The presence of Ki-67 means the tumor is growing. When they read this again after surgery, the comparison of the two numbers will help determine what chemo I get.
3. My surgeon is from South Africa and I totally dig him. He gave me every shred of info I wanted. Lumpectomy should be scheduled within a month. The details on this, and on the way he'll pick a lymph node to pull out, are fascinating. Best case: done in one day, one lymph node comes out with the tumor, 2-3 days recovery. Worst case: bunches of lymph nodes have to come out, overnight stay, I'll wear a drain in the incision, and much systemic badness follows.
4. My medical oncologist is a woman older than me and I totally dig her too. After surgery, she'll run the diagnostics to figure out what, if any, chemo I need. There's no real way to predict what kind or how long, and she said not to assume that I'd lose my hair or start menopause. Best case: no chemo. Worst case: up to a year on cell-killing, baldifying, nasty stuff with a port in my chest, and THEN I'd start radiation while I have hot flashes.
5. Radiation! Not sure how I had myself convinced that this wasn't part of the story. When they do a lumpectomy instead of a mastectomy, after chemo, they do radiation to clean up any cookie crumbs still lying around. Radiation is a for sure, then, and it's a 15 minute deal every day for some 6-8 weeks. After chemo, if any.
So, big day at the SCCA. Kinda serious, kinda fun, and now back to waiting for the next thing to happen. Surgery. Sometime in August.
1. My MRI was boring. This is excellent. By "boring" I mean that nothing unexpected was found. The tumor size is 2.0 cm at its widest. It's only 2 mm from my skin, but not "involved" in the skin, which is good.
2. My biopsy (the one that really hurt) was worth it. They ran a bunch more tests than I thought they would. My "prognostics" are:
.....very strong findings for estrogen and progesterone receptors. These are the garden variety, super-well-understood markers for tumor cells that respond to super-well-figured-out chemo, like Tamoxifen.
.....no HER2/neu found. This is a truly nasty bugger to have; I'm delighted to not have it. They will do more tests to be more sure later.
.....15% Ki-67. The presence of Ki-67 means the tumor is growing. When they read this again after surgery, the comparison of the two numbers will help determine what chemo I get.
3. My surgeon is from South Africa and I totally dig him. He gave me every shred of info I wanted. Lumpectomy should be scheduled within a month. The details on this, and on the way he'll pick a lymph node to pull out, are fascinating. Best case: done in one day, one lymph node comes out with the tumor, 2-3 days recovery. Worst case: bunches of lymph nodes have to come out, overnight stay, I'll wear a drain in the incision, and much systemic badness follows.
4. My medical oncologist is a woman older than me and I totally dig her too. After surgery, she'll run the diagnostics to figure out what, if any, chemo I need. There's no real way to predict what kind or how long, and she said not to assume that I'd lose my hair or start menopause. Best case: no chemo. Worst case: up to a year on cell-killing, baldifying, nasty stuff with a port in my chest, and THEN I'd start radiation while I have hot flashes.
5. Radiation! Not sure how I had myself convinced that this wasn't part of the story. When they do a lumpectomy instead of a mastectomy, after chemo, they do radiation to clean up any cookie crumbs still lying around. Radiation is a for sure, then, and it's a 15 minute deal every day for some 6-8 weeks. After chemo, if any.
So, big day at the SCCA. Kinda serious, kinda fun, and now back to waiting for the next thing to happen. Surgery. Sometime in August.
1 Comments:
Sounds like you have way cool doctors. Keep updating when you know dates. Either way, we're crashing you sometime around 9/4, no matter what your state is :)
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