New Treatment Trains Immune System To Kill Cancer
Al writes "A vaccine in clinical trials at the University of Pittsburgh School of Medicine triggers the human immune system to attack a faulty protein that's often abundant in colorectal cancer tissue and precancerous tissue. If it works as hoped, it could remove the need for repeated colonoscopies in patients at high risk for developing colorectal cancer. The vaccine has already proven safe in patients with advanced pancreatic cancer. It works by spurring the body to manufacture antibodies against the abnormal version of a mucous protein called MUC1. While moderate amounts of the protein are found in the lining of normal intestines, high levels of a defective form of MUC1 are present in about half of advanced adenomas and the majority of colorectal cancers."
While I laud this development - we have had multiple form of immune therapy for cancer - including tumor vaccines, cancer antigen vaccines, immunostimulatory drugs, and anti-tolerance drugs for years now. There are some responders, but this field has generally been a disappointment. here's to hoping we eventually figure out how to harness this approach.
I can't believe people have actually claimed that the quality of Slashdot comments has gone down in recent years.
How could you possibly claim that with gems like these?
You go here: http://clinicaltrials.gov/
And find the trial you are interested in, and see if you meet the requirements.
In the case of this one:
http://clinicaltrials.gov/ct2/show/NCT00773097?term=colorectal+vaccine&rank=2
Inclusion Criteria:
Age 40 - 70 years of age.
History of any of the following conditions (operative notes, endoscopy reports, and/or pathology reports must be reviewed locally to confirm that the candidate meets at least one of the following entry criteria).
1. Colorectal adenoma(s) 1 cm in maximal diameter
2. Colorectal adenoma(s) with villous or tubulovillous histology
3. Colorectal adenoma(s) with high-grade dysplasia
o Willingness to avoid pregnancy or impregnate (see below) for the period of active study (1 year).
o ECOG performance status 0 or 1
o Hemoglobin greater than 95% of the lower limit of institutional normal. Platelets 100,000/L.
o AST (SGOT), ALT (SGPT), alkaline phosphatase, total bilirubin, BUN, creatinine 1.5x upper limit of institutional normal.
o ANA 1:160
Exclusion Criteria:
* Receiving any other investigational agents.
* Presence of an active acute or chronic infection
* History of allergic reactions attributed to compounds of similar chemical or biologic composition to the study agents.
* History of heritable cancer syndrome (FAP, HNPCC)
* Patients with a history of auto-immune disease such as, but not restricted to, inflammatory bowel disease, systemic lupus erythematosus, rheumatoid arthritis, ankylosing spondylitis, scleroderma, or multiple sclerosis.
* History of malignancy 5 years prior to the Registration/Randomization evaluation, excluding non-melanoma skin cancer.
* Any use of oral corticosteroids 12 weeks prior to Registration/Randomization.
* Current or planned use of immunomodulators including: Remicade, 6-MP (Mercaptopurine), Methotrexate, cyclosporine, or other immunomodulatory drugs.
* Pregnant women, because the teratogenic or abortifacient effects of the study agents remain incompletely defined. Breastfeeding women, because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with the study agents.