Comparing the risk of cardiovascular disease between degarelix and gonadotropin-releasing hormone agonists:a systematic review and meta-analysis.
메타분석
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
065 patients.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
However, degarelix reduced the risk of heart failure (HR=0.56, 95% CI: 0.36-0.88; P=0.01). [CONCLUSION] Further clarification on the effects of different androgen deprivation therapy modalities on cardiovascular disease is needed from future and larger prospective randomized controlled trials.
[BACKGROUND] Regarding the comparison of cardiovascular disease risk between gonadotropin-releasing hormone (GnRH) antagonists and GnRH agonists, there are discrepancies in results from different stud
- p-value P=0.01
- 95% CI 0.62-1.27
- HR 0.89
- 연구 설계 meta-analysis
APA
Liu W, Liu Z, et al. (2025). Comparing the risk of cardiovascular disease between degarelix and gonadotropin-releasing hormone agonists:a systematic review and meta-analysis.. Frontiers in oncology, 15, 1523794. https://doi.org/10.3389/fonc.2025.1523794
MLA
Liu W, et al.. "Comparing the risk of cardiovascular disease between degarelix and gonadotropin-releasing hormone agonists:a systematic review and meta-analysis.." Frontiers in oncology, vol. 15, 2025, pp. 1523794.
PMID
41103953 ↗
Abstract 한글 요약
[BACKGROUND] Regarding the comparison of cardiovascular disease risk between gonadotropin-releasing hormone (GnRH) antagonists and GnRH agonists, there are discrepancies in results from different studies. Therefore, this meta-analysis was conducted to investigate whether degarelix could reduce cardiovascular disease risk.
[METHODS] We systematically searched the PubMed, Embase, Web of Science, and Cochrane Library databases with a search time limit of up to December 2023 for articles focusing on the use of degarelix, a GnRH antagonist, in prostate cancer, with an emphasis on articles comparing degarelix to GnRH agonists. Study endpoints included major adverse cardiovascular events, stroke, all-cause mortality, myocardial infarction, heart failure, and arrhythmia.
[RESULTS] A total of 1320 articles were retrieved, of which eight met our inclusion criteria and involved 138-065 patients. The pooled results showed no difference in the risk of major adverse cardiovascular events (hazard ratio [HR]=0.94, 95% confidence interval [CI]: 0.65-1.35; P=0.73), stroke (HR=0.89, 95% CI: 0.62-1.27; P=0.52), myocardial infarction (HR=0.98, 95% CI: 0.70-1.37; P=0.91), all-cause mortality (HR=1.09, 95% CI: 0.73-1.65; P=0.67), and arrhythmia (risk ratio=0.64, 95% CI: 0.15-2.76; P=0.55) between degarelix and GnRH agonists. However, degarelix reduced the risk of heart failure (HR=0.56, 95% CI: 0.36-0.88; P=0.01).
[CONCLUSION] Further clarification on the effects of different androgen deprivation therapy modalities on cardiovascular disease is needed from future and larger prospective randomized controlled trials.
[METHODS] We systematically searched the PubMed, Embase, Web of Science, and Cochrane Library databases with a search time limit of up to December 2023 for articles focusing on the use of degarelix, a GnRH antagonist, in prostate cancer, with an emphasis on articles comparing degarelix to GnRH agonists. Study endpoints included major adverse cardiovascular events, stroke, all-cause mortality, myocardial infarction, heart failure, and arrhythmia.
[RESULTS] A total of 1320 articles were retrieved, of which eight met our inclusion criteria and involved 138-065 patients. The pooled results showed no difference in the risk of major adverse cardiovascular events (hazard ratio [HR]=0.94, 95% confidence interval [CI]: 0.65-1.35; P=0.73), stroke (HR=0.89, 95% CI: 0.62-1.27; P=0.52), myocardial infarction (HR=0.98, 95% CI: 0.70-1.37; P=0.91), all-cause mortality (HR=1.09, 95% CI: 0.73-1.65; P=0.67), and arrhythmia (risk ratio=0.64, 95% CI: 0.15-2.76; P=0.55) between degarelix and GnRH agonists. However, degarelix reduced the risk of heart failure (HR=0.56, 95% CI: 0.36-0.88; P=0.01).
[CONCLUSION] Further clarification on the effects of different androgen deprivation therapy modalities on cardiovascular disease is needed from future and larger prospective randomized controlled trials.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
같은 제1저자의 인용 많은 논문 (5)
- Neutrophils in nasopharyngeal carcinoma: from mechanisms to therapeutics.
- The application of mixed reality navigation system in robot-assisted radical prostatectomy for high-risk prostate cancer: a propensity score‑matched cohort study.
- CD146 pericyte-like lung cancer brain metastatic stem cells promote tumor angiogenesis through dual regulatory effects on the VEGF/VEGFR axis.
- Pharmacovigilance analysis of infliximab in inflammatory bowel disease: novel safety signals and sex-specific adverse event profiles from the FAERS database (2004-2024).
- Is a PERK-Regulated Long Non-Coding RNA That Fine-Tunes UPR Signalling and Inhibits Endoplasmic Reticulum Stress-Induced Cell Death.
🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반
- Association between polygenic risk scores and cardiovascular events in prostate cancer patients receiving androgen deprivation therapy in Han Chinese.
- Real-world Treatment Selection and Shared Decision-making in De Novo Metastatic Castration-sensitive Prostate Cancer in Japan.
- Latin American Consensus for the Diagnosis and Treatment of Metastatic Castration-Sensitive Prostate Cancer.
- Impact of androgen deprivation therapy on sexual health in patients who underwent brachytherapy for prostate cancer.
- PARP Inhibition in Prostate Cancer: Current Status, Resistance Mechanisms, and Clinical Challenges.
- GSTA1 deficiency drives neuroendocrine differentiation via TNFRSF13B/c-FOS/CHGA axis in prostate cancer.