In this episode of The Onco'Zine Brief, Peter Hofland talks with two experts about their research and the impact the outcomes from these studies may have on the treatment of patients diagnosed with cancer.

First, Hofland talks with Christopher Heery, MD.

Dr Heery is a board-certified medical oncologist with primary expertise in the translational and clinical development of immunotherapies, including, but not limited to PD-L1 inhibitors, therapeutic cancer vaccines, immune suppressor modulator, adoptive NK cells, and other therapeutics.

As the chief medical officer at Arcellx, he is responsible for medical oversight, clinical strategy, medical affairs, and regulatory strategy for the company’s pipeline of novel – investigational drug.

In the second half of the program, Hofland talks with Srdan Verstovsek, Dr Srdan Verstovsek, MD, PhD., a Medical Oncologist and Professor in the Department of Leukemia at The University of Texas MD Anderson Cancer Center, about some of the developments in the treatment of myeloproliferative neoplasm, which are types of blood cancer that begin with an abnormal mutation or change, in a stem cell in the bone marrow. These change leads to an overproduction of any combination of white cells, red blood cells and platelets – and results in a number of diseases, including:

• Essential Thrombocythemia (ET) Is a rare blood disease in which the bone marrow produces too many platelets;
• Myelofibrosis, a rare disorder in which abnormal blood cells and fibers build up in the bone marrow;
• Polycythemia Vera (PV) – a disease in which too many red blood cells are made in the bone marrow and, in many cases, the numbers of white blood cells and platelets are also elevated.

 In a new episode of The Onco'Zine Brief, Peter Hofland talks with David M. Cognetti, MD, a Professor and Chair in the Department Head and Neck Surgery at Thomas Jefferson University Hospital in Philadelphia.

Hofland and Cognetti talk about head and neck cancer and a novel treatment approach called Photoimmunotherapy.

Head and Neck Cancer
According to the American Cancer Society, Head and neck cancer accounts for about 4% of all cancers in the United States. In the United States in 2023, an estimated 67,000 people will be diagnosed with head and neck cancer and about 15,000 patients are expected to die of the disease.

Today, many cancers of the head and neck can be cured, especially if they are found early. And while eliminating the cancer is the primary goal of treatment, preserving the function of the nearby nerves, organs, and tissues is also very important.

Beyond Current Treatment
Photoimmunotherapy is a recently developed hybrid cancer therapy to treat diseases by linking specific antibodies with photosensitizers to form photoimmunoconjugates.

But let’s go back to the beginning.

Surgery, radiation, and chemotherapy have dominated the treatment of oncologic. These therapies aim to eradicate cancer cells but, unfortunately, do that at the expense of normal, or healthy cells/ In turn, this can lead to severe and sometimes lethal side-effects.

Overall, the success of surgery, radiation and chemotherapy is measured by what we call a ‘therapeutic index.’

This ‘therapeutic index’ compares the potential benefits of treatment to the potential risks associated with treatment.

Unfortunately, the unintended, off-target side effects of these therapies can have profound effects on the health-related quality of life of patients.

For example, both radiation and chemotherapy sometimes preferentially kill lymphocytes much earlier than cancer cells because of the increased radiation sensitivity and high proliferation rate of lymphocytes, potentially leading to dose-limiting toxicity for some chemotherapy regimens.
To find a solution, researchers have developed new therapeutic strategies. And while these therapies have created an exciting new direction for the treatment of cancer therapy, there remain limitation to these novel approaches.

Now, in theory, the perfect cancer therapy would both directly destroy cancer cells to minimize residual cancer cells as well as activate the local host immune response to wipe out remaining cancer cells.

And while such a therapy would be highly selective for cancer cells but have minimal or no off-target effects in the tumor microenvironment.

Photoimmunotherapy
And that’s where photoimmunotherapy comes in. Photoimmunotherapy, designed to selectively destroy target cells.

The therapy that induces direct cancer killing via immunogenic cell death, thus activating the anti-cancer immune system locally in the tumor microenvironment.

The specificity of this approach comes from the antibody that is designed to target an expressed antigen on the tumor surface and is conjugated to the photo-activating chemical.

The safety of Photoimmunotherapy is based on the fact that the antibody–photo-absorber conjugate predominantly binds to specifically targeted cancer cells and that it is only activated in areas exposed to Near-infrared light at a specific activating wavelength.

By choosing tumor-specific antigens, this therapy specifically destroys cancer cells while not or only minimally harming any adjacent normal or healthy cells, particularly tumor-infiltrating immune T cells or blood vessels. Furthermore, the photo-activating chemical is a water-soluble photo-absorbing dye without cytotoxic properties of its own.

Clinical studies have shown that this combination can enhance the immune response, and, as a result, have a good effect on the treatment of residual tumor and metastatic cancer.

The first human study of a Photoimmunotherapy was with ASP-1929 – which is being developed by Rakuten Medical to treat inoperable head and neck cancer.

ASP-1929 is a conjugate of cetuximab, an anti-EGFR antibody plus the photo-absorber called IR700.

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