NIH Study: New Immunotherapy Method Could Be Effective Against Wide Range of Cancers
Treatment targets mutant proteins in epithelial cells
A new method for using immunotherapy to specifically attack tumor cells that have mutations unique to a patient’s cancer has been developed by scientists at the National Cancer Institute, part of the National Institutes of Health (NIH).
The researchers demonstrated that the human immune system can mount a response against mutant proteins expressed by cancers that arise in epithelial cells, which can line the internal and external surfaces of the body (such as the skin). These cells give rise to many types of common cancers, such as those that develop in the digestive tract, lung, pancreas, and bladder.
The new research provides evidence that this immune response can be harnessed for therapeutic benefit in patients, according to the scientists. The study appeared in the May 9 edition of Science.
“Our study deals with the central problem in human cancer immunotherapy, which is how to effectively attack common epithelial cancers,” said lead investigator Steven A. Rosenberg, MD, PhD. “The method we have developed provides a blueprint for using immunotherapy to specifically attack sporadic or driver mutations, unique to a patient’s individual cancer.”
All malignant tumors have genetic alterations, some of which may lead to the production of mutant proteins that are capable of triggering an antitumor immune response. Prior research by Rosenberg and his colleagues had shown that human melanoma tumors often contain mutation-reactive immune cells called tumor-infiltrating lymphocytes (TILs). The presence of these cells may help explain the effectiveness of adoptive cell therapy (ACT) and other forms of immunotherapy in the treatment of melanoma.
In ACT, a patient’s own TILs are collected, and those with the best antitumor activity are grown in the laboratory to produce large populations, which are infused into the patient. However, prior to the new research it had not been clear whether the human immune system could mount an effective response against mutant proteins produced by epithelial-cell cancers. These cells comprise more than 80% of all cancers. It was also not known whether such a response could be used to develop personalized immunotherapies for these cancers.
In the new study, Rosenberg and his colleagues set out to determine whether TILs from patients with metastatic gastrointestinal (GI) cancers could recognize patient-specific mutations. They analyzed TILs from a patient with bile-duct cancer that had metastasized to the lung and liver and that had not been responsive to standard chemotherapy. The patient, a 43-year-old woman, was enrolled in an NIH trial of ACT for patients with GI cancers.
The researchers first conducted whole-exome sequencing, in which the protein-coding regions of DNA were analyzed to identify mutations that the patient’s immune cells might recognize. Further testing showed that some of the patient’s TILs recognized a mutation in the ERBB2-interacting protein (ERBB2IP). The patient then underwent adoptive cell transfer of 42.4 billion TILs, approximately 25% of which were ERBB2IP mutation-reactive T lymphocytes, which are primarily responsible for activating other cells to aid cellular immunity, followed by treatment with four doses of the anticancer drug interleukin-2 to enhance T-cell proliferation and function.
After the transfer of the TILs, the patient’s metastatic lung and liver tumors stabilized. When the patient’s disease eventually progressed, after about 13 months, she was re-treated with ACT in which 95% of the transferred cells were mutation-reactive T cells, and she experienced tumor regression that was ongoing as of the last follow-up (6 months after the second T-cell infusion). According to the authors, these results provide evidence that a T-cell response against a mutant protein can be harnessed to mediate the regression of metastatic epithelial-cell cancer.
“Given that a major hurdle for the success of immunotherapies for gastrointestinal and other cancers is the apparent low frequency of tumor-reactive T cells, the strategies reported here could be used to generate a T-cell adoptive cell therapy for patients with common cancers,” Rosenberg said.
Source: NIH; May 8, 2014.