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News|Videos|April 8, 2026

Personalized Cancer Vaccines Show Promise for Select Melanoma Populations

Jamin C. Morrison, MD, discussed the shift toward personalized cancer vaccines in melanoma.

The landscape of melanoma treatment is shifting from generic, off-the-shelf options toward highly individualized therapies. According to Jamin C. Morrison, MD, the most effective cancer vaccines are those manufactured specifically for a single patient’s unique disease profile.

While these personalized vaccines hold significant promise, the specialized manufacturing process currently requires a window of 6 to 9 weeks. This delay necessitates careful patient selection; those with a heavy burden of disease often require immediate systemic immunotherapy, whereas patients with a lower disease burden or more indolent melanoma may be the most appropriate candidates for this evolving vaccine strategy.

Morrison is head of the Division of Hematology/Medical Oncology, a hematologist/medical oncologist, and medical director in the Division of Hematology/Medical Oncology at Cooper University Health Care; and associate professor of clinical medicine at Cooper Medical School of Rowan University.

Transcript:

Cancer vaccine therapy has a long history, and what is increasingly clear is that the most effective cancer vaccines are not off-the-shelf or generic. They’re not going to work for every single person. Instead, we’ve entered the world of a personalized vaccine therapy, by which we mean a vaccine against one individual patient’s melanoma [that] can be manufactured and administered. Now, the challenge we currently face is that manufacturing period, by its very nature—given the science we have available to us today—can take 6 weeks, 9 weeks, or longer. You’re talking about a couple months until a vaccine can be successfully manufactured and then given to the patient. There is a delay in there.

When we think about which patients are most appropriate for cancer vaccine therapy, we have to keep in mind a number of factors around the patient and their actual cancer. In particular, patients who have what I’d call a heavy burden of disease—a lot of areas of cancer involvement—are probably not best suited for this. Those patients probably need to move relatively quickly to our conventional systemic immunotherapy treatments. On the other hand, patients who have a relatively small burden of disease, or whose melanoma has proven itself to be relatively indolent or not particularly aggressive—which is always a soft call or a difficult determination to make—are probably best suited for these personalized vaccines that do hold a lot of promise.

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