In the study, 13 patients with metastatic melanoma (a deadly form of skin cancer) who had not responded to standard treatments were treated with immune cells produced in the laboratory specifically to destroy their tumors. The treatment resulted in at least 50 percent tumor shrinkage in six of the patients, with no growth or appearance of new tumors. Four additional patients had some cancer growths disappear.
Researchers have tried previously to treat cancer with immune cells but the cells did not survive well in the body. "In the past, only a fraction of a percent of the cells we injected were able to survive, and they would persist for only a few days," said Steven A. Rosenberg, M.D., Ph.D., of the National Cancer Institute, the lead researcher on the study.
Improvements in the way immune cells are generated in the laboratory and the way patients' bodies are prepared to receive them, however, have led to dramatically different results. "We have been able to generate a very large number of immune cells that appear in the blood and constitute a majority of the immune system of the patient. These persist for over four months and are able to attack the tumor," Rosenberg said.
The adoptive transfer technique fights cancer with T cells, immune cells that recognize and kill foreign cells that have invaded the body. Researchers used a small fragment of each patient's melanoma tumor to grow T cells in the laboratory, using T cells originally taken from the patients. Exposure to the tumor activated the immune cells so that they would recognize and attack cells from each specific cancer.
Once the T cells had multiplied to a sufficient number to be used for treatment, they were administered to patients. Patients were also given a high dose of a protein called interleukin-2 (IL-2), which stimulates continued T cell growth in the body. Prior to the immunotherapy, chemotherapy had been used to deplete patients' own immune cells, which had proven ineffective at fighting the cancer. Diminishing the old cells provided an opportunity for the new T cells to repopulate patients' immune systems.
Analysis of blood and tumor samples from many of the patients who responded favorably to the treatment revealed that the administered immune cells were thriving, multiplying rapidly, and attacking tumor tissue. T cells activated against melanoma became the major component in patients' immune systems. They persisted for several months and were able to destroy metastases throughout the body.
Over time, patients' old immune systems recovered, restoring their ability to fight infections. Researchers report that among the patients in the study, only occasional opportunistic infections developed during treatment.
Other side effects were mild autoimmune disorders. T cells act by recognizing a protein fragment called an antigen on the outside of the tumor cells. Antigens found on tumor cells may also be found on certain normal cells in the body, making them vulnerable to attack. Autoimmune effects among the patients in the study were mild and easily controlled.
Although the treatment is highly experimental, researchers are optimistic that it may, in the future, extend beyond the treatment of patients with melanoma. It should be possible, they say, to raise immune cells that will recognize and attack many tumor types.
Similarly, the same technique could potentially be used to treat some infectious diseases, such as AIDS.
For more information about this study and other clinical studies at the NCI taking place at the NIH in Bethesda, Md., call 1-888-624-1937. Phone operators are available Monday through Friday, 9:00 a.m. to 5:30 p.m. EDT.
For information on clinical studies taking place elsewhere, please visit the NCI Web site at www.cancer.gov or contact the NCI Cancer Information Service at 1-800-4-CANCER. Phone operators are available Monday through Friday, 9:00 a.m. to 4:30 p.m. local time.
For more information about melanoma, visit the NCI's Melanoma Home Page at http://cancer.gov/cancer_information/cancer_type/melanoma/