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January 24, 2017

PD-1s show early promise in melanoma brain metastases

One of the most frequent and terminal complications of advanced melanoma is melanoma brain metastases (MBM), which occurs in approximately 40%-50% of Stage IV melanoma patients.

One of the most frequent and terminal complications of advanced melanoma is melanoma brain metastases (MBM), which occurs in approximately 40%-50% of Stage IV melanoma patients.

MBM is a major cause of treatment failure and is linked to poor prognosis and significant morbidity. However, it has been appreciably under-investigated. Despite being an admittedly ominous diagnosis, MBM is not necessarily a death sentence.

The use of systemic therapies could provide much needed solutions in MBM. Fortunately, clinical trials investigating such therapies have started demonstrating noteworthy results. In particular, immune checkpoint inhibitors that target programmed cell death protein 1 (PD-1) are emerging as potential therapeutic strategies in MBM.

Bristol-Myers Squibb’s (BMS) PD-1 immunotherapy drug Opdivo (nivolumab) is used by physicians in many countries in the first-line setting of unresectable or metastatic melanoma, either alone or in combination with BMS’s other immune-based treatment Yervoy (ipilimumab).

However, Opdivo has not yet demonstrated survival benefits in a MBM patient cohort. To address this, an ongoing Phase II clinical trial named CheckMate 204 evaluated the safety and efficacy of Opdivo + Yervoy followed by Opdivo monotherapy in patients with MBM. In an update of the CheckMate 204 trial at the 2016 Society for Melanoma Research Congress, BMS revealed that the safety profile of Opdivo + Yervoy was similar to that of previously documented melanoma patients without MBM, with no elevated neurologic adverse events.

Merck and Co.’s immuno-oncology agent PD-1 Keytruda (pembrolizumab) has also been established as a treatment option in first-line advanced melanoma. Similarly to Opdivo, Keytruda is being investigated in patients with MBM. In an ongoing Phase II study, Keytruda has had notable responses in patients with MBM, demonstrating the potential role that systemic therapy could have for this complication.

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There is light on the treatment horizon for patients with MBM, with compelling data from clinical trials involving PD-1s. The number of MBM trials that involve immunotherapies is steadily rising. These trials might be favourable signs marking the potential for more therapeutic options for MBM to be developed, which could offer renewed hope for this patient population.

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