During a Targeted Oncology™ Case-Based Roundtable™ event, Hussein A. Tawbi, MD, PhD, asked several participants to share their experiences treating patients with metastatic melanoma with nivolumab plus relatlimab. This is the second of 2 articles based on this event.
DISCUSSION QUESTION
What is your experience with nivolumab plus relatlimab-rmbw (Opdualag)? Have you used it in a clinical trial or in a real-world practice setting?
HUSSEIN TAWBI, MD, PHD: Nivolumab and relatlimab is now a fixed-dose combination that's FDA approved, based on RELATIVITY-047 [NCT03470922]. Half of you have used it as a standard of care, and the other half hasn't. Dr Ramadoss, tell us more about your experience.
UMASANKAR RAMADOSS, MD: I have a patient who had multiple lung metastases, and no brain metastases, and he still works full time. I thought he would be a perfect candidate. He has gotten 2 cycles so far, with no [significant] adverse events [AEs] so far. He's been happy. He did have some coughing, which has improved 2 or 3 weeks after the second cycle. He's due to come next week again for his treatment.
TAWBI: Has anyone else used nivolumab/relatlimab? What are your experiences so far?
HANI ALKHATIB, MD: I have 4 patients already on it. I like it more than ipilimumab/nivolumab and the 4 of them have done well, including a young woman aged 35 years with brain and liver metastases and lymph node disease who I have been treating for 3 or 4 years. The brain lesions [received] stereotactic body radiation therapy or whole brain radiation. She was BRAF positive so I treated her before with encorafenib [Braftovi] and binimetinib [Mektovi] and treated the brain metastases…. Also, she's been on nivolumab/relatlimab for close to 6 months now and her disease is in complete remission, cranial and extracranial.
TAWBI: Wonderful, that's fascinating. That's a great experience, thank you for sharing, because the data [for nivolumab/relatlimab] in the second line is a bit less impressive than the first line.1 Did that patient have any AEs with the combination?
ALKHATIB: No, she has done well with the oral treatments and the intravenous treatments. She's in complete remission…with no significant AEs, and the other 3 patients have not had any AEs from immunotherapy. They have done well with this combination compared with ipilimumab…. I used to use ipilimumab/nivolumab; there was a large amount of toxicity from ipilimumab so I have been trying to avoid it, although it's category 1, but once they approved [nivolumab plus] relatlimab I switched to this protocol as first-line treatment.
TAWBI: That's interesting. That's even better than my experiences. I do see some toxicity. For the half who haven't used nivolumab/relatlimab, is it an issue of access? Or is it not having the right patients?
MAGDALENA FLEJSIEROWICZ, MD: I think it's just not the right patient, in my case.
KURT DEMEL, MD: I tend not to see much melanoma, so I haven't used it yet. I haven't had the right patient.
TAWBI: Would anyone else like to share their experiences?
YAN JI, MD: I have treated probably 5 or 6 patients with this regimen. My experience is mixed. For the first 2, it was bad. One patient developed hypophysitis and hypotension, [plus] itching and fatigue, and we had to hospitalize him and start the hormone supplement. The second patient was worse; they got myasthenia gravis, so we had to immediately admit the patient. Luckily, that plateaued, and then for the next 4, the experience has been good, and I have not seen any grade 3 toxicity. [I have seen] grade 2 AEs; some patients had some gastrointestinal AEs. Fatigue is another common complaint. But so far, I have seen a partial response in all of the patients—that's one of the good things. There was even [a response in] a patient we only treated with a couple cycles and stopped because of grade 3 toxicity.
TAWBI: Thank you for sharing. Myasthenia gravis is always tough and completely unpredictable. Those are rough cases, but it’s great to hear.
Reference:
1. Ascierto PA, Lipson EJ, Dummer R, et al. Nivolumab and relatlimab in patients with advanced melanoma that had progressed on anti-programmed death-1/programmed death ligand 1 therapy: results from the phase I/IIa RELATIVITY-020 trial. J Clin Oncol. 2023;41(15):2724-2735. doi:10.1200/JCO.22.02072
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