SCIMITAR: Effects of Radioactive Iodine on the Immune System in Thyroid Cancer
Study Details
Study Description
Brief Summary
Blood will be drawn 1 month before and 2 month after regular radioactive iodine treatment. Monocytes will be isolated. The three main outcomes are whole blood counts, cytokine production upon in vitro stimulation of monocytes and in vitro ROS production by monocytes. These results are compared between patients treated in adjuvant setting and patients treated for persistent structural disease, and between pre- and post-treatment status.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed Description
Earlier studies have shown that, particularly advanced, thyroid carcinomas are highly immunogenic tumors. The immune system is involved in both pathogenesis and progression of thyroid carcinoma (TC), as in other malignancies. For example, it is known that increased tumor infiltration with tumor-associated macrophages is associated with decreased survival in TC patients. In a previous study from our group, changes in the programming of myeloid immune cells were identified in newly diagnoses TC patients. That study showed that upon stimulation, cytokine production was decreased in monocytes from TC patients when compared to monocytes from healthy volunteers or from patients with benign thyroid tumors. Also, reactive oxygen species (ROS) production (known to be tumorigenic) from monocytes was increased in TC patients when compared to healthy volunteers. In the mentioned study, several effects of radioactive iodine (RAI)-treatment, after surgery, on the systemic immune system were observed. For instance, lymphocyte counts were significantly reduced after treatment with RAI, an effect also observed in other studies. Moreover, after RAI-treatment, ROS levels produced by monocytes decreased to levels similar to those produced by monocytes of healthy controls. Although, the effect of RAI-treatment on ROS-production was less pronounced than that of surgery. There was no clear effect of RAI-treatment on the cytokine production capacity. However, it should be noted that in most patients in this study RAI was administered in a setting of remnant ablation, meaning that only a low dose of RAI was administered and that only a very low amount (or none) of cancer cells were present at the time of administration. Furthermore, the number of included patients was too low to perform subgroup analyses. The current study aims to assess the effect of RAI-treatment in patients with structural disease, as a higher dose of beta-radiation will be present in these patients, and compare these effects to that in patients treated with RAI in an adjuvant setting.
The investigators hypothesize that RAI-treatment will have a more pronounced effect on the systemic innate immune system in patients with structural disease when compared to patients treated in an adjuvant setting. This study will give us more insights in the interplay between RAI and the immune system in patients with TC.
The aim of the study is to assess the effect of RAI-treatment on the innate immune system in TC patients and to compare these effects between patients with and without structural disease in a prospective explorative study.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| I/adjuvant 15 patients with thyroid carcinoma that are treated with radioacitive iodine in an adjuvant setting |
Other: Blood drawing
Blood is drawn twice in all subjects. Once before treatment with radioacitve iodine and once after.
|
| II/structutral disease 15 patients with thyroid carcinoma that are treated with radioactive iodine with the indication of persistent structural disease |
Other: Blood drawing
Blood is drawn twice in all subjects. Once before treatment with radioacitve iodine and once after.
|
Outcome Measures
Primary Outcome Measures
- Whole blood counts [2 months]
Whole blood counts with leukocyte subtypes (neutrophils, lymphocytes and monocytes) are compared before and after radioactive iodine treatment
- Cytokine production upon monocyte stimulation [2 months]
Cytokine produciton (tumor necrosis factor, interleukin-6, interleukin-8) will be compared before and after treatment with radioactive iodine
- Reactive oxygen species (ROS) production by monocytes [2 months]
In vitro ROS production by monocytes will be compared before and after treatment with radioactive iodine
Secondary Outcome Measures
- Monocyte transcriptome [2 months]
Possibly, transcriptome of monocytes will be compared before and after treatment with radioactive iodine
- Plasma proteome [2 months]
Possibly, plasma proteome (especially inflammatory markers) will be compared before and treatment with radioactive iodine.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Pathologically confirmed non-medullary thyroid cancer
-
Undergoing radioactive iodine treatment in an adjuvant setting or for persistent structural disease
-
Aged ≥ 18 years
Exclusion Criteria:
-
Inflammatory or infectious comorbidities
-
Using medication interfering with the immune system
-
Pregnancy
-
A self-reported alcohol consumption of >21 units per week
-
Other active malignancies, defined as malignancies not in complete remission for <2 years
-
Previous systemic anti-cancer treatment such as chemotherapy, targeted therapy, radiotherapy or immunotherapy within 3 years before study procedures
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Radboud University Medical Center | Nijmegen | Netherlands |
Sponsors and Collaborators
- Radboud University Medical Center
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2023-16623