OncoMatch/Clinical Trials/NCT04892303
Combination Radiotherapy and Radiopharmaceutical Therapy Treatment Planning for Thyroid Cancer
Is NCT04892303 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies Combination treatment (CXRPT) of external beam radiation (XRT) plus radioactive iodine (RAI) for recurrent thyroid cancer.
Treatment: Combination treatment (CXRPT) of external beam radiation (XRT) plus radioactive iodine (RAI) — The goal of this study is to evaluate combined radioactive iodine (RAI, 131-I) and external beam radiotherapy (XRT) to optimize the radiation dose delivered to treat well differentiated thyroid cancers (DTC) with iodine-avid metastases. The investigators hypothesize that precise dosimetric planning will permit this combined RAI-XRT radiotherapeutic approach to be safe and permit higher tumor radiation doses than could otherwise be delivered. Patients with metastatic well-differentiated DTC) that is not completely resectable with macroscopic invasion of tumor into cervical soft tissues and/or non-resectable distant metastases, are the target study population. The primary objective is to evaluate safety as defined by the incidence of maximum grade 3 or greater NCI CTCAE toxicity observed during the treatment period and for the first 30 days following completion of radiotherapy. Secondary endpoints will evaluate efficacy at 6 months and feasibility of this combination to deliver a minimum cumulative dose of 80 Gy to the index tumors selected prior to treatment initiation. The investigators plan to enroll 48 subjects at an accrual rate of 1 subject per month over a study duration of 4 years.
Check if I qualifyExtracted eligibility criteria
Cancer type
Thyroid Cancer
Lab requirements
Blood counts
platelet count > 50,000 cells/mm3 and an absolute neutrophil count (ANC) > 500 cells/mm3
Kidney function
measured creatinine clearance >70 ml/min/1.73 m2 or normal radioisotope glomerular filtration rate (GFR)
Adequate organ function, including: a) adequate renal function, defined as a measured creatinine clearance >70 ml/min/1.73 m2 or normal radioisotope glomerular filtration rate (GFR); and b) adequate hematologic function, defined as a platelet count > 50,000 cells/mm3 and an absolute neutrophil count (ANC) > 500 cells/mm3
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- The Johns Hopkins SKCCC · Baltimore, Maryland
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