Not eligible for Immunotherapy. Now what?
I have stage 3/4 adenocarcinoma non small cell . I have tumors in upper and lower right lobes as well as several affected lymph nodes is the neck area. Diagnosed about a year ago. Went through 5 rounds of chemo and 30 radiation treatments. I was told early on that I’m not eligible for immunotherapy due to not having the markers (?) and a past history of Colitis. I just got my first 3 month post treatment scan. Not good news. One tumor in upper lobe shrank but tumor in lower lobe increased. All of the lymph nodes in neck area increased in size with notes in my portal saying probable metastasis. Obviously very discouraged at this point. Just numb. I don’t see oncologist until Friday so don’t know what will happen next. Knowing that I’m not eligible for immunotherapy my guess is more chemo. Has anyone else gone through “round two” of chemo because you couldn’t get immunotherapy? We’re other treatments offered to you?
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He gives does talks on an array of cancers. Lots of different adenocarcinoma mutations in addition to small cell. He's an advisor at CancerGRACE.org and regularly presents at ASCO.
He is my second opinion doctor and if need be I'll try back. I see Dr Winegarden at StJoes Trinity in Ann Arbor. If someone in my region can't get to Mayo, I recommend him next.
I've seen Dr. Gadgeel give talks specific to ALK lung cancer, he seems amazing! I'm glad he's your doc. Exciting.
Hi @detroitmom23, It's great to hear from you, but we all wish you were feeling better. Possibly you are still experiencing side effects from the treatments. Your body has been through so much. I know this isn't easy, but until I actually have the scan reports, I try to focus on the current day, and not speculate too much. Without knowing what's happening, it's hard to know what treatments may be available. I do hope you have access to the Grand Rounds again or a second opinion. Additional feedback for your case is a good idea.
The presence or absence of PD-L1 tells whether or not immunotherapy will work. I have PD-L1 with strong expression, but I'm still not a candidate for immunotherapy because I have the EGFR Exon 19 mutation. If an Oncologist tells someone they are not a candidate for immunotherapy, it means it won't work. 85% of lung cancer cases are non-small cell, so that's no help. She needs to ask her doctor what else he knows besides non-small cell adenocarcinoma. Nowadays, they're able to identify a lot of different subtypes, each with their own treatment recommendations.
We still have an awful lot to learn about lung cancer and cancer in general, but we are past the point of "try it and see if it works." At least for the most part. There are always exceptions.
It's my understanding that Keytruda has been approved for all levels of pd 1 or pdl 1 including negative. Please check with your oncologist.
Not me but others I've met through Lungevity and Go2 Foundation.
You mentioned earlier that your oncologist participated in a Grand Rounds program that sounds a bit like a tumor board. Please still consult a second opinion doctor. I saw Dr Shireesh Gadgeel at Henry Ford. They hired him away from UM to be new head of Thoracic Oncology. My 20 minute new patient consult lasted an hour and he told me more about my cancer than I had heard from my oncologist in 8 years.
I was diagnosed with stage 3c adenocarcinoma Non small cell in December 2022, I was not eligible for surgery because the cancer had spread to lymph nodes in my clavicle area. I underwent 5 rounds of chemo and 30 radiation treatments. About 6 months later I went through it all again. 5 more rounds of chemo and 15 radiation treatments. I just finished those second rounds 3 months ago and have another scan scheduled in about 10 days. I’m terrified because I haven’t been feeling well; increase in pain as well as coughing, I’m wondering how many times they would advise additional chemo and radiation when I’ve already been through it twice? Will they continue trying or tell me there’s nothing more they can do? I’m not eligible for immunotherapy. I don’t have the markers for it. Has anyone been through chemo and radiation more than twice?
I just saw your post on here and I had just sent you a message. I'm hoping you're getting those messages on this site, I just don't know sometimes. It almost looks like I'm sending it to myself. Anyway, I just read this post and I'm not happy to hear about this news. I Don't really understand why they wouldn't try immunotherapy if it could possibly help. How do they know it's not going to help? I mean I would want them to try everything. So I understand that. Have you seen the doctor at all since you posted this? Or talk to anyone? I sent you a private message so just respond there. I'm thinking about you.
Angela
Hi @hlolson, I'm glad you are doing well on your targeted therapy. I was also fortunate enough to have a gene mutation with a targeted therapy option (ALK+, 3.5 years).
Unfortunately, we need more research to improve treatments for those lung cancers that aren't driven by gene mutations. There are way too many people suffering with this disease, it's disheartening.
A second opinion can be very useful. I recently added another lung cancer specific oncologist and their fellow to my team. More eyes on my case can only help as we move forward. Best of luck to you, I'm glad that you found a good fit with your care team!
Thank you for the feedback. My oncologist has recommended another round of chemo. The same combo of drugs I had 7-8 months ago.
I am in the process of getting a second opinion. I have an option through my insurance called Grand Rounds where a team of specialists will review my medical records and provide an opinion. I’m still at a loss about the immunotherapy and hoping this second opinion will enlighten me.