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SNUH Immune Checkpoint Inhibitor-induced Hypothyroidism Recovery Trial

SNUH Immune Checkpoint Inhibitor-induced Hypothyroidism Recovery Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07421869
Acronym
S-CORT
Enrollment
107
Registered
2026-02-19
Start date
2024-06-12
Completion date
2029-03-04
Last updated
2026-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypothyroidism

Keywords

Hypothyroidism, Immune checkpoint inhibitors, Thyroid hormones, Levothyroxine

Brief summary

The goal of this study is to find out whether hypothyroidism caused by immune checkpoint inhibitors (ICIs) can recover after stopping the ICIs. The study also aims to identify factors that can help predict which patients will be able to stop taking thyroid hormone replacement. The main questions the study will answer are: * What percentage of patients recover normal thyroid function and can stop levothyroxine after stopping ICIs? * What clinical or laboratory factors can predict successful withdrawal of levothyroxine? Participants will: * Be adult cancer patients who developed hypothyroidism during ICI treatment and are currently taking levothyroxine * Have already stopped ICI therapy * Gradually reduce their levothyroxine dose every 3 months if their thyroid function remains normal * Stop levothyroxine if thyroid function remains normal at low doses (≤0.025 mg) * Be monitored with thyroid function tests and clinical symptoms at each visit

Interventions

DRUGLevothyroxine tapering

Participants will undergo a gradual dose reduction of levothyroxine according to a standardized tapering protocol. The levothyroxine dose will be reduced every 3 months based on thyroid function test results. If thyroid function remains stable, the dose will be decreased by 0.025 mg (±0.0125 mg). If thyroid function remains stable at a low dose (≤0.025 mg), levothyroxine will be discontinued.

Sponsors

Seoul National University Bundang Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

This is a prospective, single-group, open-label study designed to evaluate the potential for recovery from immune checkpoint inhibitor (ICI)-induced hypothyroidism after discontinuation of ICI therapy. All participants will receive a standardized protocol for stepwise reduction of levothyroxine dosage based on thyroid function tests. No comparator group is included.

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged 19 years or older. * Patients with a history of treatment with immune checkpoint inhibitors (ICIs). * Developed hypothyroidism during ICI treatment and initiated levothyroxine after starting ICI therapy. * Discontinued ICI therapy prior to study enrollment.

Exclusion criteria

* Use of levothyroxine or antithyroid medications within 3 months prior to initiating ICI therapy. * History of thyroid surgery, radioactive iodine therapy, or neck radiation therapy. * Current levothyroxine dose ≥0.1 mg at the time of enrollment.

Design outcomes

Primary

MeasureTime frameDescription
Proportion of participants who maintain discontinuation of levothyroxine for at least 6 monthsUp to 6 months after levothyroxine discontinuationThe number and proportion of participants who are able to remain off levothyroxine for at least 6 consecutive months without requiring re-initiation of treatment due to abnormal thyroid function (serum TSH level ≥10 μIU/mL).

Secondary

MeasureTime frameDescription
Proportion of participants who can discontinue levothyroxineup to 3 years after study enrollmentThe number and proportion of participants who were able to discontinue levothyroxine after dose reduction during the study follow-up period, regardless of whether the discontinuation was sustained. This includes any participant who temporarily stopped levothyroxine for any duration, even if the medication was later resumed.
Proportion of participants who maintain discontinuation of levothyroxine for at least 12 monthsUp to 12 months after levothyroxine discontinuationThe number and proportion of participants who are able to remain off levothyroxine for at least 12 consecutive months without requiring re-initiation of treatment due to abnormal thyroid function (serum TSH level ≥10 μIU/mL).
Proportion of participants who maintain discontinuation of levothyroxine for at least 36 monthsUp to 36 months after levothyroxine discontinuationThe number and proportion of participants who are able to remain off levothyroxine for at least 36 consecutive months without requiring re-initiation of treatment due to abnormal thyroid function (serum TSH level ≥10 μIU/mL).

Countries

South Korea

Contacts

CONTACTMin Joo Kim, Professor
mjkim@snubh.org+82-31-787-7855

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026