› Forums › Cutaneous Melanoma Community › Late Post Treatment Strategy?
- This topic has 9 replies, 4 voices, and was last updated 7 years, 6 months ago by
cancersnewnormal.
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- December 17, 2017 at 2:37 am
I was diagnosed with Stage 1a Melanoma on December 6th, 2013. It was .30mm, no ulceration, 0 mitosis, and no other negative prognostic factors. My follow up treatment was WLE, skin checks every 3 months for two years, then every 6 months since. Now I’m confused. I went for my normal skin check last week, everything looked good, but my dermatologist ordered for a chest X-ray and blood work to check my Ldh1. Being a very anxious person anyway this freaked me out. I mean out of these 4 years, I was never told I needed any if this stuff and now all of a sudden it needs to be done? If it was something that was suppose to be done why not when I was first diagnosed? Now I’m waiting for the results freaking out, thinking the worst. Has anyone else had to do this for a 1a and did they wait 4 years out before requesting such tests? My dermatologist was diagnosed with breast cancer, she had surgery, and chemotherapy. She is cancer free now, but is she just being extra safe since her diagnosis? Any and all answers will help. Thanks in advance.
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- December 17, 2017 at 5:14 am
I'd say overkill relating to her diagnosis. Most stage I individuals don't have those tests – maybe a baseline chest x-ray or bloodwork, but not recurring ones. I think she's probably just being extra careful now but honestly, I wouldn't spend any time worrying about any of that. The vast majority of melanoma – when it does spread – hits the lymph nodes first, not directly to lungs or stage IV. So chest x-rays really have limited value especially for your stage. You're 4 years out from a very early melanoma and the longer you go, the better. Honestly, DO NOT STRESS!
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- December 17, 2017 at 3:00 pm
Hi Wendy, as always go with the advice that Janner gave you!!! That being said is sounds like a dermatologist playing Oncologist, did they give you a reason??? Maybe they had to hit there yearly quota of scans!!! I would rather look at your situation of something to celebrate and put the worry in the back window of life. As long as Derm is checking your nodes by physical exam and you are being sun smart and following advice that Janner always gives about keeping photographic records of your moles, I would really ask Derm what they are thinking ordering x-ray and blood work and why!!!! Best Wishes!!!Ed
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- December 17, 2017 at 5:30 pm
Thanks! She just said better to be safe than sorry. Not that she thinks its spread or anything. So, I was confused a little because I’ve never had them to order those tests in the 4 years since my diagnosis. I don’t go in the sun hardly ever and when I do I’m looking for shade and using sunscreen. My derm has pics of my moles and when she checked me last week she said everything looked great. So, go figure. I just hate having to wait on tests results thinking the worst. Ugh…
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- December 19, 2017 at 2:39 pm
It definitely sounds like an extra note of caution. It's an inexpensive option for them to order these things and typically is covered by a patient's insurance. I wouldn't worry too much about it, but I do applaud your doc for ordering it up. I fall into that oddball 2-4% for whom a chest x-ray at 4-5 years out would have detected a problem much sooner. If I could write a letter to the me from 8 years ago, I'd tell "her" to go for the xray and worry when/if there is something to worry about.
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- December 21, 2017 at 10:17 pm
At the risk of sending you into an unnecessary flurry of concern……… I was 1a. Nothing to indicate it might be in that "likely to spread" risk area. A few years ago, I was brought into a So Cal Derm Conference as a "learning tool" about the dangers of skin cancer, and how seriously derms should be taking proactive measures. I had my original pathology report with me. As the derms came into the room to speak with me about my current condition, and they read the report, there were several who got rather wide eyed and said "Wow. You're like a one in a million chance of spread. How did this happen?". Yeah… wish someone could explain that to me too. Just an oddball unlucky in the looooow odds zone. That said, I think at least a few of them left the conference with the idea that perhaps a chest xray and some follow up blood labs once per year miiiiight not be such a bad idea for their patients with a known melanoma diagnosis…. no matter what their risk level. ALLLLL of that aside… I never had a sentinal node biopsy. The depth wasn't enough for the standards to call for it. So, technically, I may have been an oddball that had a stage 3 diagnosis with early infiltration to the lymph nodes, that we were unaware of… because the diagnostic difference between 1 and 3, is nodal involvement. If we haven't checked any nodes… how do we really know? Or, it could have gone straight to the blood and made its way through the body that way.
There are statistics that show folks with minimal depth and early catch are very unlikely to spread. Your only concern, is whether you're in that pack of outlier oddballs who like to ruin doctor's clean statistical curves.
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- December 22, 2017 at 2:28 pm
I know with this new staging system coming in effect that a lot of 1a’s will become 1b’s. All based on Breslow depth. Now if you’re .80mm you are considered 1b with or without ulceration. My Breslow depth was .30mm at diagnosis. So, I’m still in the 1a category. What was your depth if you don’t mind me asking? And did they ever give you a Clarks level, because they didn’t with mine? They just said there was no mitosis or ulceration etc.. -
- December 22, 2017 at 10:44 pm
Let's see… I had an "atypical" punch biopsy from my family doctor's office. That was why he sent me off to a surgeon for removal. Looking at my surgical report (from the FIRST time the surgeon cut… June 2007), I was: superficial spreading type, clarks level III, .6mm breslow, growth phase radial, epitheliod cell type, mitotic count "low" (1 mitotic figure per 10 high power fields), tumor infiltrating lymphocytic response "absent", ulceration absent, vascular invasion absent, neurotropism absent, satellite metastasis absent.
The report then stated: "Additional surgery at this site should enhance the likelihood of local control" Sooooooo…. nearly a month to the day later (July 2007)… the surgeon went in and cut out larger margins, scooping out everything down to the muscle level. Sadly, at the time, I thought "No biggie. Doc and surgeon feel like this is all that is needed, so I'm good to go.". I never even bothered to get the path report following the second surgery. You can imagine my surprise when I woke up on the floor at work, after having a VERY unexpected grand mal seizure in April 2013. At the ER, I had brain CT, followed by brain MRI (for a better look at what they'd found), and a chest x-ray followed 2 days later. There were 5 brain lesions… the largest measuring 1.2 cm and loaded with edema (that caused the seizure). My chest xray showed 3 additional lesions. The largest being a 5 cm "golf ball sized" beast in my right lower lung lobe. THAT is the one we probably would have seen prior to the spread to the brain. FIVE cm… how long had it taken to grow to that size? Would it have FOR SURE been caught on a chest xray before any additional metastasis? We can't say for sure… buuuuuut… would it have been worth getting a chest xray or two each year along with my regular follow up skin checks? YES. Because if we had seen "something"… it would not likely have been the size of a golf ball when it was first spotted. If I could have had the lung surgery and gotten some treatments prior to brain metastasis, I may have been spared the two craniotomies and 10 rounds of gamma radiation. Maybe. Sooner is always better than later when it comes to melanoma. If your derm or doc want to take the occasional peek inside your chest walls…. why not?
My primary was on my right shoulder… direct center on top. Right lower lung lobe was the biggest blob of metastasis. The left frontal lobe of the brain had the biggest bit found in my head. Right shoulder to right lung makes sense…… settling into the left region on the brain… that had to have followed the closer proximity of the lung invasion. THANKFULLY, it's all becoming a rapid blur behind me these days, as I've been clear for almost 2 years (brain) and 3 years for the body.
Funny thing….. I did go back in 2014, and ask the pathology lab for my report from the second surgical removal from July 2007. They somehow "lost" the one from July. Uh huh. Whaaaatever. I'm thinking someone was doing some "I don't want to get sued" save your a** thing. OR… the surgeon never bothered to send the removed skin in on the second go round…. hmmmmmmm. ALWAYS ALWAYS ALWAYS get copies of your reports.
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Tagged: cutaneous melanoma
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