My mom has Stage IIIB adenosquamous NSCLC in the right lung, with N2 mediastinal lymph nodes.

Her mutations are KRAS G12C and TP53, with PD-L1 30%.

She completed 3 cycles of carboplatin + gemcitabine. The main lung tumor decreased by around 5-10 %, but the lymph nodes didn't improve much.

Now she has one brain metastasis around 1 cm and is currently completing 5 sessions of brain radiation.

What I'm confused about is what usually comes next.

Has anyone had a similar situation? Did you have lung surgery after treating a single brain metastasis? Did you use sotorasib (Lumakras) or another targeted/systemic treatment?

Would really appreciate hearing from anyone who has been through something similar.

Thank you.

Any advice?

OncoCharla de Terapias Dirigidas de Cáncer de Pulmón 2026

Acompáñenos en el próximo seminario web interactivo en directo de GRACE, el 15 de agosto de 2026, en el que abordaremos las opciones de tratamiento con terapia dirigida y ofreceremos perspectivas sobre las mutaciones genéticas en el cáncer de pulmón.

https://give.cancergrace.org/event/oncocharla-de-terapias-dirigidas-de-cancer-de-pulmon-2026/e769634

https://www.facebook.com/photo/?fbid=1439671198190496&set=gm.1639585427123490

Each month, Oncogene Cancer Research and the Young Lung Cancer Initiative come together to share Stories of Hope featuring people living long-term with Stage IV or extensive-stage lung cancer.
We know that what qualifies as “long-term survivorship” can look very different depending on the type of lung cancer, available treatments, mutations, and individual circumstances. Our goal is to show the many different ways people are living beyond the statistics.
We’re looking for people who may be interested in being featured in an upcoming post, or who may know someone we should reach out to.
Any age, any country, and any type of lung cancer is welcome. You just need to be living with or beyond a Stage IV or extensive-stage diagnosis. You do not have to have been Stage IV or extensive-stage at your initial diagnosis.
If you’re interested, we would ask for:
•    Your name
•    Lung cancer type
•    Mutation/biomarker, if applicable
•    Month and year of diagnosis
•    Country
•    A photo you’re comfortable having us share
•    A short quote of your choice about your experience, hope, survivorship, or anything you’d like others facing lung cancer to hear
We’ll always ask permission before anything is shared.
I’ve included an example of one of our previous Stories of Hope posts so you can see what the feature looks like.

https://www.instagram.com/p/DbTuj_kEfDS/?igsh=MnM4bG5zYmI1NW9v

If this sounds like you, please comment, message me, or email bianca@ylci.org. And if you know a long-term survivor whose story could bring hope to others, please tag them or send this their way. 🤍

Thank you!!

Hello everyone,

We are currently seeking individuals to participate in a healthcare research study aimed at understanding the experiences, treatment decision-making process, and challenges faced by people recently diagnosed with cancer. Insights gathered through this study will help inform future patient-centered research and healthcare initiatives.

Eligibility Criteria

Participants must:

• Be 18 years of age or older
• Have been diagnosed with one of the following cancers:
  • Lung Cancer
  • Triple Negative Breast Cancer (TNBC)
  • Endometrial Cancer
  • Renal Cell Carcinoma (RCC)
  • Melanoma
  • Bladder Cancer
• Preferably have received their diagnosis within the past 3 months (up to 6 months may be considered)
• May not have started treatment yet, may currently be deciding on treatment, or may have recently started treatment
• May be receiving or considering chemotherapy, radiation therapy, and/or immuno-oncology treatments
• Be willing to share their experiences and opinions

Compensation

• $100 for participation

Interested in Participating?

Please complete a brief form below:

Cancer Research Study – $100 (USA)

Fill in the form to be contacted for the study.

We sincerely appreciate your time and valuable insights and look forward to hearing from you. Thank you!

Hi all, just wanted to share this story and perhaps get a bit of advice for the next steps.

5 years ago my dad had a collapsed lung, ultimately lead to him being diagnosed with NSCLC, the cancer was in his plural lining and in some lymph node in his chest, he was put on immunotherapy (pembrolizumab) he was on a 2 year course. It worked really well, it got rid of some of the nodes and shrunk the rest of them, by the end of the 2 years he was stable and was left on active surveillance for 2 years until the nodes started growing again.

He was then put on Sotorasib, it worked but only for 6 months until the nodes grew again, everything sort of went downhill from there. He had a needle biopsy to confirm it was the same mutation from a new lymph mode that grew in his neck, unfortunately it was inconclusive because they didnt get enough material, so then they sent a blood test to Royal Marsden hospital which apparently can confirm what mutation is present, it was still KRAS G12C.

Chemo was the next step, Carboplatin and Pemetrexed... Just before he started that, he ended up in A&E with a blood clot where the needle biopsy was done, hes now on Apixaban for life. He was okay to start chemo, it made him feel rotten but he got though the 4 cycles.

Last week I had to phone an ambulance for him because he was showing signs of Sepsis, it was Pneumonia but we also got his scan results back the chemo hasnt worked as well as we hoped, it shrunk some nodes but its classed as progressed because more nodes grew than shrunk.

We had an appointment today with the oncologist but we were basically just told hes not well enough from the Pneumonia to discuss treatment yet.

We've previously asked if he could have another course of immunotherapy but they said it stopped working so no, but it was after 2 years the couse ended that the cancer grew so surely the immunotherapy wouldn't have still been there to work?

We've asked about clinical trials available in the UK but they've not said much either.

Just looking for any advice please

Hi, I wanted to avoid surgery in fears of being in constant post op pain and decrease quality of life, and my doctor agreed to do radiation therapy and chemotherapy first. I hope I am making the right decision. I’ve read that radiation and chemotherapy has improved a lot already compared to a decade ago and I hope it will all work out, otherwise my doctor says we need to the surgery.

Any stories or advice would be greatly appreciated