newly diagnosed lung cancer
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Lung cancer treatments today are worlds apart from those available in your mom’s or grandfather’s time. In the last 20 years, more progress has been made in lung cancer treatment than in all of modern medicine before. That’s no exaggeration. If I had been diagnosed just 20 years ago, I likely wouldn’t have survived. Hospice would have been a more common path than effective treatment. Yet here I am, in full remission, four and a half years on.
While you’re still unsure if it is cancer, radon-induced lung cancer often presents with a high tumor mutational burden (TMB), which can make it more susceptible to immunotherapy. Treatments like immunotherapy weren’t an option in your mom’s or grandparents’ time but are now game-changers. When you've learned more I'll be here to help answer questions or share more about what I’ve learned.
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hey dive buddy. Had my biopsy yesterday. 3.5-3.7 cm tumor with hilar node involvement 1.4 cm and the others a little smaller. The doctor didn’t have the rose. Tech but he said it was cancer and asked me if I had a preference of oncologists. We don’t have too. Many of them up here in podunk maine so I’m doing a little research this weekend as I said befor grandfather, mother and I all diagnosed with lung cancer at 59. I definitely don’t want to tell my 35 year old daughter as she will think she is going to get it at 59, nor my dad who will be 88 in April and already lost my sister at 44 to breast/ lung cancer. Not sure if I’ll be a candidate for surgery as I have several underlying conditions, so we will see. I hope I can get chemo pills instead of having to go in but again I have to wait. My immune system is compromised so maybe that immunotherapy will work too. Radiation too why not Lol. There is a tv show can’t remember the name but after this guy goes through some terrible stuff he is yelling at GOD, is that all you got, well bring it on. That will be my attitude, Bring it on…… Thanks for the knowledge and support Batman
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While absolutely everything points to malignancy, without putting the tissue under a microscope, they can't definitively say it's cancer. I don't care if you're the chief thoracic surgeon at MD Anderson.
Being in the boondocks may mean getting results back for genetic profiling takes longer, but it shouldn't take more than 4 to 6 weeks tops.
While it's not possible to confirm radon exposure as the cause, many cancers suspected of being linked to radon display high tumor mutation burdens (TMB). This makes immunotherapy a potentially good treatment option. Additionally, mutations in EGFR and KRAS G12C are often seen in these cases, both of which have targeted treatments available.
Given your family history and the fact that you're a never-smoker, this likely points to a combination of environmental and genetic factors. Living in Maine—where radon exposure is a known risk—further supports the case for environmental contributions.
They don’t normally run tests that specifically point to radon exposure because it wouldn’t change the course of treatment. These tests are specialized and expensive. However, research facilities near you may offer access. On the other hand, mutations in TP53 or BRCA2 are routinely tested for, as these inherited mutations can increase susceptibility to cancer, even though they don’t directly cause it. Hopefully, these tests will be part of your genetic workup.
I recommend testing your home for radon and monitoring levels over time. It's equally, if not more, important to test your daughter's home. Radon detectors are relatively inexpensive for what they do, and if high levels are found, the houses can undergo radon mitigation. Here's a link to a guide on radon detectors:
Genetic testing for cancer susceptibility is also available. With your family history, it may be possible for your daughter to have insurance cover this cost. If your cancer is found to have mutations in TP53 or BRCA2, this would provide further evidence to support insurance coverage for her testing.
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hey dive buddy thanks for the advice on radon detectors, I already have one as well carbon monoxide. My daughter tried getting the genetic testing a few years ago but insurance would not cover it. Maybe they will now, who knows. I’m trying to get my mothers 20 year old hospital records in Mass, I still have some friends down there, but I don’t know if they will have them , but doesn’t hurt to look. I am really curious as to what type she had and any other applicable information. I have lived in Maine since 2001 but Mass before that. At some point I found out that the neighborhood where I grew up was built over a giant dump. Many younger people in my neighborhood ended up with all sorts of weird cancers, with a lot of them dying young. I would say a lot of genetics but my mom, dad, grandparents, sister and friends smoked back in the day, and prior to the late 80s or 90s nobody was worried about second hand smoke. I remember flying on planes when they still smoked, like flying in an ashtray. Also my childhood doctor always was smoking right in his office. Times have changed for the better in that regard. I also have a bunch of calcifications on my 2.4 cm thyroid nodule, I thought that was why I have been having trouble with swallowing. Always feels like it going down the wrong pipe. I’ll know all soon, and thanks for all the advice I truly appreciate it. Have a great Sunday. I’m going for a little walk before it turns below zero next week. Batman
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