American researchers have developed a new drug, that when administered along with chemotherapy, shows promise in treating advanced melanoma, delaying the progression of cancer and prolonging the lives of patients.
The new drug, STA-4783, is the first in a new class called oxidative stress inducers.
It works by increasing the amount of reactive oxygen species (ROS), such as hydrogen peroxide and superoxide, in cells. When the level exceeds the antioxidant capacity of cells, the cells are in a state of oxidative stress. All cells have some low level of ROS, but cancer cells naturally operate with a higher level of ROS and oxidative stress relative to normal cells.
The drug was developed by Synta, and the study on it was carried out by a team of researchers led by Dr Anthony Williams, vice president of clinical research at Synta Pharmaceuticals Corp. in Lexington, Massachusetts, USA.
The study was presented on Sept 26, 2007, at the European Cancer Conference (ECCO 14) in Barcelona. Williams conducted a study, which included 81 patients with metastatic melanoma. Out of those patients, 28 received treatment with the chemotherapy drug paclitaxel alone and 53 received paclitaxel plus the new drug, STA-4783.
"The median progression free survival was 1.8 months in the group who got chemotherapy alone, but 3.7 months in the group who got the combination. This doubling in progression free survival is impressive for this cancer, and the result was achieved without substantial additional toxicity," Williams said.
"Progression-free survival was linked to improvements in overall survival. Patients on the experimental combination survived on average for 12 months after being diagnosed, while those getting only paclitaxel survived on average 7.8 months. This is the first time an improvement in survival has been seen in a randomised, double-blind, multi-centre controlled trial for metastatic melanoma," he added.
Metastatic melanoma, where the skin cancer has spread to other parts of the body, is difficult to treat. Current therapies either have limited power or are highly toxic. The average survival of patients diagnosed with advanced melanoma is about six months.
Williams said that the study also indicated that STA-4783 might boost the efficiency of chemotherapy drugs that induce cell death, or apoptosis, because it appears to lower the hurdle for activating that process.
"These results are encouraging not only because of the findings in themselves but also because there are so few treatment options for patients. We believe STA-4783 has the potential to improve survival with a manageable side effect profile," he said.
"We also believe there is nothing unique about metastatic melanoma and that oxidative stress has the potential to be an entirely new class of cancer treatment that could have applications in other types of cancer," he added.
A further study of STA-4783 in melanoma patients across Europe is now in process to investigate the drug's potential.