What is the half-life of Human Chorionic Gonadotropin (HCG)?

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Last updated: March 3, 2025View editorial policy

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From the Guidelines

The half-life of human chorionic gonadotropin (hCG) is approximately 1 to 3 days. This information is crucial in diagnosing and monitoring the presence of tumors, determining prognosis, and assessing treatment outcome in patients with testicular cancer 1.

Key Points

  • The half-life of hCG is an important factor in understanding its role as a serum tumor marker.
  • hCG is produced by nonseminomatous cells, such as choriocarcinoma, and may be elevated in both seminomatous and nonseminomatous tumors.
  • The half-life of hCG is significantly shorter than that of alpha-fetoprotein (AFP), which has a half-life of approximately 5 to 7 days 1.

Clinical Implications

  • The short half-life of hCG means that its levels can fluctuate rapidly in response to changes in tumor burden or treatment.
  • This information can be used to monitor treatment response and adjust therapy as needed.
  • The half-life of hCG may vary slightly between individuals based on factors such as kidney function, but the approximate range of 1 to 3 days provides a useful guideline for clinical decision-making 1.

From the Research

Half-Life of Human Chorionic Gonadotropin (HCG)

  • The half-life of HCG can be described by two half-lives: an early and a late half-life, which follow a biexponential decay curve 2, 3.
  • The early half-life of HCG is dependent on the preoperative value of HCG, whereas the late half-life is independent 2.
  • Studies have reported the following half-lives for HCG:
    • Average half-life of 82.5 hours (±SD 50.2) in patients with steadily declining serum β-hCG levels 4.
    • Average half-life of 106.7 hours (±SD 72.0) in patients with primarily plateauing β-hCG levels in the declining phase 4.
    • Mean half-life of 2.32 days after exogenous administration of HCG 5.
  • The late half-life of HCG has been proposed as a parameter to follow ectopic pregnancies after treatment, as it can help identify patients with persistent trophoblastic activity 2, 3.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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