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:
- 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.