Skip to content

A single administration of a specific treatment might eradicate cancer cells.

A single shot could potentially eradicate cancer.

Direct injection of a single dosage into a solid tumor potentially signifies a breakthrough in...
Direct injection of a single dosage into a solid tumor potentially signifies a breakthrough in cancer treatment.

A Groundbreaking One-time Treatment for Multiple Types of Cancer

A single administration of a specific treatment might eradicate cancer cells.

In the ever-evolving landscape of cancer research, a novel approach to combat this devastating disease is gaining traction. Scientists at Stanford University School of Medicine have devised an innovative treatment that involves a targeted injection, showing significant success in eliminating tumors in mice.

The latest research, spearheaded by Dr. Ronald Levy, explores the potential of stimulating the body's immune response directly into a cancerous solid tumor. This approach sidesteps the need for identifying tumor-specific immune targets and avoids the need for a comprehensive activation of the immune system.

The study, published in the journal Science Translational Medicine, details the successful use of the treatment on mice, leading to the elimination of tumors across the body. The researchers have every reason to believe a speedier trajectory toward clinical trials for this method, as one of the agents involved has already been approved for human therapy, and the other is currently under clinical trial for lymphoma treatment.

Dr. Levy, a lymphoma specialist, explains that their approach employs a one-time application of minuscule amounts of two agents, designed to stimulate immune cells specifically within the tumor. This allows the immune cells to learn how to fight against that specific type of cancer, subsequently migrating and destroying all existing tumors.

Cancer cells often outwit the body's immune system, aiding their growth and spread through complex mechanisms. A type of white blood cell called T cells plays a crucial role in regulating the immune response. However, cancer cells frequently find ways to deceive these T cells and evade the immune response.

In the new study, Dr. Levy and his team delivered micrograms of two specific agents into one tumor site in each of the affected mice. The agents reinforced the immune cells' ability to express a receptor called OX40, found on the surface of T cells, while activating the T cells. The activated T cells migrated to other parts of the body and "hunted down" and destroyed other tumors.

Significantly, this method could potentially be used to target various kinds of cancer, as the T cells would adapt to combat the specific type of cancer they had been exposed to. Initial experiments in the mouse model of lymphoma yielded impressive results, with 87 out of 90 mice becoming cancer-free. Similarly successful outcomes were witnessed in the mouse models of breast, colon, and skin cancer. Even mice engineered genetically to develop breast cancer responded well to this treatment method.

However, the technique's targeted nature was evident when transplanting two distinct cancer tumors—lymphoma and colon cancer—in the same animal, calling for injection only at the lymphoma site. Though the lymphoma tumors receded, the same did not hold true for the colon cancer tumor, demonstrating that the T cells learned to deal only with the cancer cells in their immediate vicinity before the injection.

The researchers anticipate preparing a clinical trial to assess the effectiveness of this treatment in individuals with low-grade lymphoma. If the clinical trial proves successful, they anticipate extending this therapy to a broad spectrum of cancer tumors in humans.

"I don't think there's a limit to the type of tumor we could potentially treat, as long as it has been infiltrated by the immune system," Dr. Levy concludes.

While a "one-time targeted injection" isn't a current standard treatment, advancements in targeted therapies and immunotherapies are rapidly progressing, aiming to improve treatment effectiveness and reduce the need for multiple treatments.

  1. Targeted Therapies Using Protein Degraders: Researchers are developing BRD4 PROTAC protein degrader drugs, which target the BRD4 protein in tumor cells to reduce cancer growth and spread. The RNK05047 trial, launched in 2022, is the first in-human trial examining this drug for advanced solid tumors, including diffuse large B-cell lymphoma, and is expected to conclude in late 2025.
  2. Immunotherapies and Combinations: Clinical trials are exploring the use of cancer vaccines, including mRNA and peptide vaccines, along with innovative treatment methods such as pembrolizumab injections combined with intralesional IL-2 and radiotherapy for patients who have failed checkpoint blockade therapy.
  3. Cancer Vaccines: Cancer vaccines are being developed to educate the immune system to recognize and attack cancer cells. Ongoing clinical trials include a phase I/II trial comparing a peptide vaccine with standard care for KRAS-mutated colorectal and pancreatic cancers.

As these approaches show promise, more research is necessary to determine their long-term efficacy and safety in diverse human populations. With continued advancements in targeted therapies and cancer vaccines, the dream of a one-time targeted treatment for multiple types of cancer may soon become a reality.

  • The new treatment, utilizing a one-time application of two agents to stimulate immune cells within tumors, is designed to combat various types of cancer. This approach, if successful in clinical trials, could extend beyond low-grade lymphoma to a broad spectrum of other cancers.
  • In the realm of scientific advancements, immunotherapies like cancer vaccines are being developed to educate the immune system, which could potentially recognize and attack other medical-conditions like cancer cells. Ongoing trials include those comparing peptide vaccines with standard care for KRAS-mutated colorectal and pancreatic cancers.
  • The BRD4 PROTAC protein degrader drugs, under development as targeted therapies, aim to reduce cancer growth and spread by targeting the BRD4 protein in tumor cells. The RNK05047 trial, launched in 2022, is investigating this drug for advanced solid tumors, including diffuse large B-cell lymphoma, and expected to complete in late 2025.
  • As the study spearheaded by Dr. Levy at Stanford University School of Medicine demonstrates, scientists are employing immune-system-based approaches, such as their one-time targeted injection, to tackle otherlymphomas and potentially other cancer types. It's crucial that we continue to explore these new therapies and treatments to improve health-and-wellness outcomes for individuals with cancer.

Read also:

    Latest