Anyone had radiation of the lung? What were the side effects? Results?
I am an 80 yo female just diagnosed, for the 2nd time, with lung cancer. My first was in the RUL surgically removed in 2016. This one is in the LUL and is still very small, barely 1cm.
This time my Oncologist wants to use radiation therapy. Has anyone had this tx and what were the side affects? Any and all answers will be greatly appreciated.
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I have Stage 3BN2Mo . She did say that normally Stage 4 gets Immunotherapy. I am planning to get on my portal and ask her about the immunotherapy. Thank you ! And God Bless you!!
Wow, I don't know what the N2Mo corresponds to. I've just heard stage 3b for me.
You are educating me.
Vlpr
Yes, I have had rad therapy for cancerous lung nodule found in another lobe. The first nodule was removed in a lobectomy in 2022. This second nodule was found in another lobe. I had 3 radiation treatments and I'm cancer free 3 months later.
The treatments were painless and quick without any side effects.
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4 ReactionsI’m looking into possibly getting radiation if the nodule has grown, I had surgery the first and second time but I can’t have anymore.
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1 ReactionI had a right nodule. 4 treatments total 1 daily on a Tuesday to Friday about 30 minutes each. Very easy. Painless. Mild fatigue for a week after. No big deal.
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1 Reaction@espiritu56 I agree that the actual radiation treatment is easy. Lie down on the table, then get up and walk away. However, complication can arise many months after the radiation, so it is important to pay attention. I developed pneumonitis 10 weeks after my first treatment. 2.5 years later I had new radiation treatment and have developed neuropathic pain which fortunately has much improved with medication.
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1 Reaction@vic83 Great advice. I am 4 weeks out. The radiologist says watch for pneumonitis for 12 weeks. Had it before as a result of immunotherapy. Not fun. Predisone was very effective in eliminating it.
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1 Reaction@vic83 For the neuropathic pain I’d highly recommend accupuncture in addition to what you’re doing. It is very accepted as an integrative support in cancer treatments. My insurance pays for it but even out of pocket it’s not very expensive.
@espiritu56 Thanks for the suggestion. I will see what my pulmonologist thinks...he is watching attentively
@espiritu56 Did you lose pulmonary capacity? When I had pneumonitis, I was prescribed Prednisone starting at 40mg and decreasing by 10mg every two weeks. It solved the pneumonitis issue right away. I tested again(near the end of prednisone), and my pulmonary function test values were a little bit better. Three months later I went back for follow up and pulmonary function test values had dropped significantly, and I was prescribed permanent oxygen