Showing posts with label anti-PD-1. Show all posts
Showing posts with label anti-PD-1. Show all posts

Monday, October 1, 2018

The 2018 Noble prize for medicine awarded for pioneering research in cancer immunotherapy

James Allison and Tasuku Honjo

American James Allison and Japan's Tasuku Honjo have won the 2018 Nobel Prize in Medicine for a pioneering approach to cancer treatment. The pair received the prize for their work in harnessing the body’s immune response to attack cancer cells.

Dr. James Allison studied a protein that acts as a brake on the immune system to mount a response against the cancer cells. He developed a way to “release the brake” so as the immune system could attack cancer cells.

Dr. Tasuku Honjo also discovered a similar protein that prevents the cells to attack cancer cells, but the mechanism is different. Therapies based on this joint discovery led to the development of an entirely new class of drugs called ‘checkpoint inhibitors’ have revolutionized the cancer immunotherapy.

Several scientists have observed that T-cell protein CTLA-4 blocks the T-cell from attacking the cancer cells. Working at his laboratory in University of California, Berkeley, James P. Allison developed an antibody that could bind to CTLA-4 and block its function. After performing animal studies, in 2010, a human study showed promising results in patients with advanced melanoma.

Figure: Upper left: Activation of T cells requires that the T-cell receptor binds to structures on other immune cells recognized as ”non-self”. A protein functioning as a T-cell accelerator is also required for T cell activation. CTLA- 4 functions as a brake on T cells that inhibits the function of the accelerator. Lower left: Antibodies (green) against CTLA-4 block the function of the brake leading to activation of T cells and attack on cancer cells.Upper right: PD-1 is another T-cell brake that inhibits T-cell activation. Lower right: Antibodies against PD-1 inhibit the function of the brake leading to activation of T cells and highly efficient attack on cancer cells.

In 1992, few years before Allison discovered T-cell protein CTLA-4, Tasuku Honjo discovered PD-1, another protein expressed on the surface of T-cells. Further research showed that PD-1 also functions as a T-cell brake like CTLA-4 but via a different pathway. After animal studies were successful, clinical study in humans showed promising results leading to long-term remission and a possible cure in several patients with metastatic cancer, a condition that had previously been considered virtually untreatable.

We now know that the drugs called “immune checkpoint therapy” have fundamentally changed the way certain cancers are treated.

Example of CTLA-4 inhibitor includes Ipilimumab (Yervoy), used to treat melanoma of the skin and some other cancers. PD-1 Inhibitors include Pembrolizumab (Keytruda), Nivolumab (Opdivo), and Cemiplimab (Libtayo).

These drugs have been shown to be helpful in treating several types of cancer, including melanoma of the skin, non-small cell lung cancer, kidney cancer, bladder cancer, head and neck cancers, and Hodgkin lymphoma. They are also being studied for use against many other types of cancer.

New clinical studies indicate that combination therapy, targeting both CTLA-4 and PD-1, can be even more effective, as demonstrated in patients with melanoma.

Checkpoint therapy has now revolutionized the way we view how cancer can be managed. It has already prolonged life of millions of people with cancer worldwide.


Here is a short video about Dr. Jim Allison of MD Anderson Cancer Center:


Also, here is an earlier video of Dr. Tasuku Honjo discussing some of his work







Wednesday, June 13, 2018

KEYTRUDA gains FDA approval for treatment of recurrent or metastatic cervical cancer

The U.S. Food and Drug Administration (FDA) has approved Merck’s pembrolizumab (KEYTRUDA®), for the treatment of patients with recurrent or metastatic cervical cancer whose disease had worsened on or after chemotherapy and whose tumors express programmed cell death ligand 1 (PD-L1), as determined by an FDA approved test.

The US FDA has approved the Dako PD-L1 IHC 22C3 pharmDx assay for expanded use as a companion diagnostic test for Keytruda for cervical cancer.

The approval comes in way ahead of the previously decided date of June 28. Furthermore, the drug is approved under the FDA’s accelerated approval regulations based on tumor response rate and durability of response.

Continued approval in future will be based upon verification and description of clinical benefit in the ongoing trials ahead.

The accelerated approval was based on results of ongoing KEYNOTE-158, a multi-center, non-randomized, open-label, multi-cohort trial (NCT02628067). The trial enrolled patients with multiple types of advanced solid tumor, who have not responded to usual chemotherapy or are intolerant to it.

Patients with autoimmune diseases or requiring immunosuppression were excluded from the trial.

The patients received KEYTRUDA intravenously at a dose of 200 mg every three weeks until unacceptable toxicity or documented disease progression or for 24 months in patients without disease progression.

Among the 98 patients with advanced cervical cancer, 77 (79%) had tumors that expressed PD-L1 with a Combined Positive Score (CPS) ≥1 and have received at least one line of chemotherapy in the metastatic setting.

The objective response rate in these 77 patients was 14.3 percent, with a complete response in 2 patients (2.6%) and partial response in 9 patients (11.7%).

Ninety-one percent of patients experienced duration of response exceeding 6 months or longer. Eight patients discontinued the drug because of serious side effects like anemia, fistula, hemorrhage, and infection.

The other common side effects of KEYTRUDA are fatigue, musculoskeletal pain, diarrhea, pain and abdominal pain and decreased appetite (21%).

 No responses were observed in patients whose tumors did not have the PD-L1 expression (CPS<1).

KEYTRUDA is a humanized monoclonal antibody that blocks the interaction between PD-1 and its ligands, PD-L1 and PD-L2, thereby activating T lymphocytes which may affect both tumor cells and healthy cells. This increases the ability of the body's immune system to help detect and fight tumor cells.

Dr. Roy Baynes, senior vice president and head of global clinical development, chief medical officer, Merck Research Laboratories said, “KEYTRUDA is now the first anti-PD-1 therapy approved for the treatment of advanced cervical cancer, providing an important new second-line option for certain patients with this disease. This approval also marks the first indication for KEYTRUDA in gynecologic cancer and reflects our ongoing commitment to bring forward innovative treatment options across a broad range of cancers, including cancers that disproportionately affect women,” in a news release.

KEYTRUDA has already been approved by FDA for treatment of melanoma, head and neck cancer, lung cancer, urothelial cancer, and gastric cancer.