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Kristie L. Kahl is vice president of content at MJH Life Sciences, overseeing CURE®, CancerNetwork®, the journal ONCOLOGY, Targeted Oncology, and Urology Times®. She has been with the company since November 2017.
Following a CURE® Educated Patient® Lung Cancer Summit, the City of Hope expert answered 10 commonly asked questions from patients with lung cancer.
Following a lung cancer diagnosis, many patients wonder what the next steps are — from treatment options, next-generation sequencing, surveillance and more.
To ensure patients can always best advocate for themselves in their treatment journey and beyond, CURE® spoke with Dr. Jyoti Malhotra, director of thoracic medical oncology at City of Hope and a presenter at the Educated Patient® Lung Cancer Summit held on June 15, to answer the 10 most commonly asked patient questions in the lung cancer space. Malhotra focused on post-treatment monitoring, emerging treatment options and managing potential side effects.
Malhotra: After five years, guidelines recommend continuing with annual surveillance scans. This may be more frequent if there are radiological findings that are being monitored on the scan.
RNA sequencing is preferred and recommended in addition to DNA sequencing for next-generation sequencing for lung cancer. This is because some of the genomic changes, such as fusions, are more effectively detected by RNA sequencing.
Currently, the recommended treatment for interstitial nephritis is steroids as well as consultation and regular follow-up with a nephrologist for additional work-up and treatment. The most commonly used steroid in the outpatient setting is prednisone.
We know that some targeted therapies such as new-generation EGFR and ALK inhibitors (Tagrisso [osimertinib], Lorbrena [lorlatinib] and Alecensa [alectinib], for example) have good penetration across the blood-brain barrier. We do not have a good understanding of the degree to which other therapies are able to get into the brain. We do not have clear data to support that radiation opens the blood-brain barrier to other therapies.
Pneumonitis is treated by holding the drug treatment and starting high-dose steroids. It is important to treat with steroids for more than four weeks followed by a gradual taper of dose. Patients who don’t respond to steroids or have severe pneumonitis are admitted to the hospital for additional supportive care and management.
For advanced/metastatic EGFR-mutated NSCLC, both chemotherapy combined with Tagrisso and Tagrisso alone, are approved regimens. As the approval for chemotherapy plus Tagrisso is recent, so we are still trying to understand when to use the combination therapy rather than monotherapy with Tagrisso. We still do not have survival data for chemotherapy plus Tagrisso from the trial (the phase 3 FLAURA2 trial), but we should have it in the next few years and this will also help answer this question.
LEARN MORE: Combining Drugs, Radiation Is ‘Practice-Changing’ for Some Lung Cancer Subsets
This is variable and depends on multiple factors. There is significant variability between patients.
The recommended dose of Tagrisso is 80 mg. A lower dose of 40 mg is only used if the 80 mg dose is associated with significant side effects and is not tolerable. We do not know if the 40-mg dose will work as well as the 80-mg dose.
This depends on the presentation and extent of the cancer. So it is important to form an individualized treatment plan for each patient with input from a multidisciplinary clinical team. This would include surgery, radiation oncology as well as medical oncology.
The treatment for oligometastatic lung cancer is similar to the treatment for metastatic lung cancer in general. Many physicians do consider more definitive therapies such as radiation for oligometastatic cancer in addition to systemic therapy. But this approach is still under investigation in ongoing clinical trials.
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