Metastatic Differentiated Thyroid Cancer
Conditions
Keywords
Thyroid cancer, dosimetry, 124-I, therapy optimization
Brief summary
Failure of conventional radioiodine therapy of metastatic differentiated thyroid cancer could be explained by: * a suboptimal therapeutic approach, based on the administration of empirically fixed amount of radioactivity * the presence of lesions with impaired iodine uptake, due to the expression of specific mutations The study aims to: * optimize therapy with pre-treatment 124-I blood and lesion dosimetry * collect genetic data to check if specific mutations and/or miRNA over-expression could be related to low iodine uptake or to radioresistance
Detailed description
TRIAL DESIGN This is a one-stage, phase II, single-arm, bi-centric study. Enrollment centres are the Istituto Nazionale Tumori in Milan, and the Sacro Cuore Don Calabria Hospital in Negrar, close to Verona. Both centres are located in North Italy. 124-I is produced by cyclotron in Negrar Radiopharmacy unit, while high-activity 131-I therapy will be delivered in Milan. Patients with ascertained metastatic differentiated thyroid cancer are studied with FDG PET and CT. 124-I blood and lesion PET dosimetry is used to optimize the 131-I therapeutic activity. The same 124-I PET scans are repeated 6 months after therapy as response assessment. 124-I and 131-I administration are performed after hormon withdrawal. Primary tumour tissue and circulating miRNA will be analyzed to check the genetical features. According to 124-I dosimetric PET data published by Jentzen et al, good efficacy (Tumour Control Probability \> 80%) is obtained with absorbed dose \> 80 Gy to soft tissue metastases, and \> 650 Gy to bone metastases. Seen this difference, only soft tissue lesions are considered as target for the calculation of the complete response rate. However, for ethical reasons, therapeutic activity will be chosen in order to be effective both on soft tissue and bone lesions. Patients with too low predicted lesion absorbed dose even administering the Maximum Tolerable Activity (2 Gy to blood) will exit the protocol to receive the standard of care. PRIMARY END-POINT Evaluation of complete response (CR) rate on soft tissue metastases 6 months after treatment, or later. The best response will be considered. SECONDARY END-POINTS Assessment of: * acute toxicity rate and severity * the association among pre-treatment glucose metabolism, 124-I uptake and therapy response * the association among genetic mutations (BRAF V600E, TERT promoter, others) on thyroid cancer tissue, pre- and post-treatment miRNA expression, pre- and post-treatment glucose metabolism, iodine uptake, and 131-I therapy response SAMPLE SIZE AND POPULATION By considering a complete response (CR) rate in patients of soft tissue metastases after fixed activity approach as published by Klubo-Gwiezdzinska et al and by assuming an increment of 15% in CR rate after dosimetry-based administration, 46 evaluable patients will be required to test the above hypotheses.
Interventions
DRUGRadioiodine optimized therapy
124-I blood and lesion dosimetry will be used to optimize the 131-I therapeutic activity. Both 124-I and 131-I administration will be performed after hormon withdrawal. Primary tumour tissue and circulating miRNA will be analyzed to check the genetic status.
Sponsors
Associazione Italiana per la Ricerca sul Cancro
Carlo Chiesa
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Histo-pathological diagnosis of DTC * At least one documented non surgically-curable soft-tissue metastasis previously untreated * ECOG performance status = 0 - 1 * Life expectancy \> 6 months * Females of childbearing age must have negative serum pregnancy test prior to registration and agree to use birth control throughout the study and for 6 months after completion of therapy * Preserved hematologic and renal function (hemoglobin \> 10 g/dL; WBC \> 3500/uL; neutrophils \> 50%; PLT \> 100000/uL; albumin ≥ 2.5 g/dL; creatinine ≤ 2 mg/dL) * Signed informed consent
Exclusion criteria
* All lesions surgically resectable * Minimal lymph nodal disease (diameter \< 1 cm, up to 2 nodes) * Patient with skeletal metastases only * Lung diffuse miliary micro-metastases * Ongoing pregnancy * Breast-feeding (enrollment could be considered after suspension) * Refusal of male and female patients to use an effective contraception method during the study and for 6 months after completion of protocol therapy * Impossibility to undergo follow-up procedures * Presence of medical, psychiatric or surgical condition, not adequately controlled by treatment, which would likely affect subjects' ability to complete the protocol * Assumption of any anti-tumor therapy including chemotherapy, biological or investigational drug treatments * Assumption of any myelotoxic drugs * Previous or concomitant assumption of Amiodarone * Any other oncologic disease that required treatment in the last 5 years. * Participation in a clinical trial in which an investigational drug was administered within 30 days or 5 half-lives prior to the study drug.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Response | 6 months, repeated through study completion, an average of 2 year | Evaluation of complete response (CR) rate on soft tissue metastases 6 months after treatment, or later. The best response will be considered. RECIST 1.1 Evaluation of the best response rate on soft tissue metastases |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Association between presence/absence of metastatic pre-treatment FDG uptake and response | 6 months, repeated through study completion, for an average of 2 year | Statistical tests will be applied to test the significance of the association. |
| Association between the presence/absence of specific mutations in neoplastic thyroid tissue and response | 6 months, repeated through study completion, for an average of 2 year | Statistical tests will be applied to test the significance of the association. |
| Progression Free Survival interval (PFS) [months] from the first iodine treatment. | every 6 months or more frequently, through study completion, for an average of 2 years | PFS will be assessed according to the standard clinical practice |
| Overall Survival [months] from the first iodine treatment. | At the end of the study, an average of 2 years | Survival status will be collected |
| Association between circulating miRNA deregulation and response | 6 months, repeated through study completion, for an average of 2 years | Statistical tests will be applied to test the significance of the association. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 | Through study completion, an average of 2 years | The frequece and the grade of sialoadenitis as well as the occurrence of xerostomia will be reported as adverse event, as well as hematological toxicity nadir. |
Countries
Italy
Contacts
Primary ContactEttore Seregni, MD
Backup ContactDaria Scienza, MD
Outcome results
None listed