Intravenous administration of the radiopharmaceutical imaging agent technetium-99m (99mTc) tilmanocept promises in first-in-human Phase 1/Phase II study demonstrates to be a safe, well-tolerated, noninvasive means of monitoring rheumatoid arthritis disease activity. At present, there is no reliable noninvasive way to directly monitor inflammation in joints of RA patients. But the study was present at the 2019 Annual Meeting of the Society of Nuclear Medicine and Molecular Imaging (SNMMI).
According to the Rheumatoid Arthritis Support Network, rheumatoid arthritis (RA)—a chronic, autoimmune; inflammatory joint disease—affects more than 1.3 million Americans. Activated macrophages release pro-inflammatory cytokines and chemokines; that significantly contribute to the initiation and propagation of RA. 99mTc tilmanocept (TCT) binds to the macrophage mannose receptor CD206; which is highly express on activate macrophages in RA. Previous clinical studies have shown subcutaneous administration of TCT to be safe and effective.
Immuno diagnostic information in rheumatoid arthritis
“Intravenous (IV) administration of TCT provides a novel noninvasive molecular imaging marker that demonstrates joint-specific; CD206-expressing synovial macrophage involvement,” explains Arash Kardan, associate professor of radiology at Case Western University in Cleveland; Ohio. “It reveals potentially significant qualitative and quantitative immuno diagnostic information regarding; the distribution and severity of active disease involvement in RA patients.”
For the study, 39 subjects (33 with active RA and six healthy controls) are divide into 11 groups; and received various combinations of intravenous 99mTc at 1, 5 and 10 mCi with 50, 200, or 400 μg of tilmanocept. However, they then have standard gamma camera whole-body planar imaging; as well as spot view of the hands and wrists from front to back at one hour and three hours post-injection. But twelve of the 39 subjects (six RA/six healthy controls) underwent whole-body planar scans for radiodosimetry assessment and pharmacokinetic analysis.
No adverse drug reactions
No adverse drug reactions or serious adverse events were observed in any dose group. Planar imaging reveal that TCT localizes specifically in the inflamed joints; of RA patients and not in the joints of healthy individuals. However, the qualitative and quantitative data analysis and modeling establish an optimal mass dose of 134 μg tilmanocept/10 mCi of 99m TC; stable over an imaging time frame of one to three hours post-injection. For the purposes of accuracy and streamlining practice; a mass dose of 150 μg and imaging time frame of one to three hours post-injection are recommended for future use.
Kardan says, “These results enable the initiation of further clinical studies to assess if intravenous 99mTc tilmanocept imaging can provide physicians with a noninvasive; receptor-specific molecular imaging marker of rheumatoid arthritis disease activity status to guide the most effective therapeutic strategy for their patients. This includes when to initiate therapy and evaluation of response to therapy, thereby improving outcomes for all patients with rheumatoid arthritis.”