

Episode 032: Lung Cancer Series, Pt. 9: Metastatic NSCLC without driver mutations
Lung cancer is one of the most commonly diagnosed type of cancer and so it is fitting that we start the first of our disease-specific oncology series with this diagnosis. This week, we start our discussion on metastatic non-small cell lung cancer, focusing on NSCLC without driver mutations.
* The approach to treatment of a patient with widespread metastatic NSCLC (mNSCLC) is very different than a patient without distant disease, which highlights why we do what we do:
- Important to complete staging (discussed in prior episodes) to determine the extent of disease
- Important to check molecular testing (looking for mutations in the cancer cells) and IHC for tumor proportion score (TPS) helps determine treatment options
* Choosing a treatment is based on:
- Histology - cannot use pemetrexed or bevacizumab in squamous cell
- Platinum - Carboplatin is usually used (as opposed to our prior discussions about using Cisplatin because of LACE pooled analysis data)
-- Why is Cisplatin not a great idea? Cisplatin should not be used if patients have (***high yield to know cisplatin eligibility criteria!!***):
--- Poor performance status
--- Patients with eGFR <60
--- If a patient has baseline hearing loss
--- If a patient has baseline neuropathy
--- Patients with NYHF class III+
--If patient is getting “palliative” / non-curative setting, you want to spare patients these terrible potential side effects
-Immunotherapy - All patients with mNSCLC should have IO considered for treatment, unless they have contraindications. Considerations include:
-- Patients with EGFR and ALK mutations - patients with these mutations do NOT respond well to IO so should not use
-- TPS score:
--- Patients with score >50% can get IO monotherapy (spared chemotherapy)
---- KEYNOTE 024: approval for pembrolizumab monotherapy in patient with PDL1>50%
----- Study compared pembro to platinum doublet
----- OS 70% vs. 50% at one year
---- IMPOWER110: approval for atezolizumab monotherapy
----- Study compared atezo to chemotherapy
----- OS 64.9% vs 50% at 12 months
--- Patients with score <50% can get IO + chemotherapy
---- KEYNOTE 189: Showed that the addition of Pembrolizumab to carboplatin/pemetrexed followed by pembro/pemetrexed maintenance in mNSCLC with adenocarcinoma histology had impressive benefits
---- Carbo/taxol/pembro for squamous histology
--- Lots of other trials, check out NCCN for a comprehensive list
* Putting this all together:
- In PDL1 >50% WITHOUT SYMPTOMS: IO alone
- In PDL1 >50% WITH SYMPTOMS: Chemo + IO
- In PDL1 <50%:
-- Lots of options, but usually some combination of chemotherapy + IO
-- Many people use Pembro, as it was first to market
* Management of mNSCLC to the brain:
- Recommend discussion with radiation oncology about role of SRS
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