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. 2022 Jun 3;26(4):722–729. doi: 10.1038/s41391-022-00555-0

Table 3.

Risk of MACE and composite CV events in patients on GnRH antagonists compared with patients on GnRH agonists by pre-existing cardiovascular disease.

MACE Composite CV eventsa
No. of events aHRb (95% CI) P value No. of events aHRc (95% CI) P value
All
  GnRH antagonist (n = 499) 136 0.97 (0.81–1.17) 0.7665 24 0.34 (0.21–0.55) <0.0001
  GnRH agonist (n = 15,127) 5105 2001
Pre-existing CVDd
  GnRH antagonist (n = 167) 39 0.67 (0.46–0.96) 0.0299 5 0.16 (0.05–0.50) 0.0017
  GnRH agonist (n = 3348) 1046 462
No pre-existing CVD
  GnRH antagonist (n = 332) 97 1.23 (0.91–1.40) 0.2901 19 0.44 (0.26–0.74) 0.0019
  GnRH agonist (n = 11,779) 4059 1539

aHR adjusted hazard ratio, CV cardiovascular, CVD, cardiovascular disease(s), GnRH gonadotropin-releasing hormone, MACE major adverse cardiovascular event (ischemic heart disease, stroke, congestive heart failure or all cause deaths), occurring ≥90 days after ADT initiation, whichever came first.

aComposite CV events: ischemic heart disease, stroke, congestive heart failure or CV deaths occurring ≥90 days after ADT initiation, whichever came first.

bAdjusted hazard ratios were estimated using cox model adjusted for age, cancer stage, receiving chemotherapy, radiation therapy, antiandrogen, abiraterone, and enzalutamide.

cAdjusted hazard ratios were estimated using the Fine and Gray competing risk model adjusted for age, cancer stage, receiving chemotherapy, radiation therapy, antiandrogen, abiraterone, and enzalutamide.

dPre-existing CVD: receiving cardiac therapy, diagnosis of ischemic heart diseases, stroke, or congestive heart failure 1 year before androgen deprivation therapy initiation.