8 mm lung nodule possible malignancy: What should I do?
I had a CT scan and they found a nodule which has grown to 8 mm from 6 mm 12 months ago. The report says "slowly growing malignancy cannot be excluded". My doctor (GP) recommends another CT in 3 months but I am concerned that this approach is not aggressive enough. It has clearly changed from 6 mm to 8 mm.
What do I do?
Should I be seeing an oncologist now?
Should something more aggressive me done?
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Best wishes with your surgery. Seems you are in good hands. I had robotic segmentectomy left lower area of lung 1.5 cm nodule. Surgery went very well. Pathology was clear for lymph nodes no spread. I am 63 and my Recovery was smooth. My biggest struggle was getting comfortable to sleep. I began walking as soon as I could. I did have numbness in the left abdominal and still have some. Not very noticeable. At 8 weeks I was quite active. Now At 12 weeks I have not noticed much reduction in my lung function.
I’m scheduled for segmentectomy at Mayo on Oct. 10. 9mm nodule grew by 1 mm at ct scan last week.
My cat scans and even a negative bronchoscope with lymph tests have revealed no lymphadenopathy. I’m hoping this holds true at pathology exam following surgery.
How was recovery for segmentectomy? Does your case resemble mine in any way? Thanks.
I was blessed due to early stage 1A that my situation only required Segmentectomy removal. All tests showed no other cancer. No other treatments at this time.
No new information yet. I am having another Chest CT at 3 months that is scheduled for mid-November. It's on my mind all the time, but I'm trying to focus on other things. I did read about the possible tests of a PET scan or possibly a biopsy. Some sources say they would do those things after finding the 11 mm nodule, but others say to do the Chest CT first. Does anyone on this thread have any information about the order of what happens?
Thanks for the inquiry, sorry I don't have anything new to tell yet. I will have more info in November.
Take care everybody.
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1 ReactionWelcome @dwcar. I saw in another post that you were 12 weeks from surgery at that time. Are you having any other treatments, beside surgery?
Hi @ready2talk2000, Have you learned any more about the nodules seen on the last CT scan? Has your doctor outlined the next steps?
@hatterasj10202, Oh, you don't need to send the actual report, it's probably best if you don't (for privacy reasons). I was just curious how things are going. It sounds like you have come to a plan along with your oncologist. Enjoy your medication vacation. I hope some of the side effects resolve for you over the next six weeks.
Will try to send PET SCAN
results.
No therapy for now, but may restart target drug in 6 weeks accepting side effect profile once again, since target drug is still being productive, by keeping cancer in check with no progression.
Hi @hatterasj10202 , These drugs can be powerful, and sometimes they are too much for the other systems in our bodies to handle. I'm sorry that you had to discontinue the targeted therapies. Are you on any treatment at this time? Would you like to share the results of your recent PET scan?
I see an oncologist at Dana Farber quarterly. I get a CT with contrast during each visit. The surveillance is comforting. After each visit he compares the growth of nodules with prior CTs. He occasionally consults with the radiation oncologist and we discuss options if there is continued growth. My metastatic disease remains a major concern and I am on hormonal therapy. In my opinion, getting care from a specialized oncologist is getting the best possible care.