{"title":"不孕妇女使用促卵巢药物与卵巢肿瘤风险的meta分析","authors":"Hong Li, Zhonghua Hu, Yuyan Fan, Yingying Hao","doi":"10.1016/j.ijgc.2024.100046","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To explore whether ovarian-stimulating drugs increase the risk of ovarian cancer in infertile women.</p><p><strong>Methods: </strong>This meta-analysis involved searching PubMed, Cochrane Library, Web of Science, and Embase. The methodological quality of observational studies was assessed using the modified Newcastle-Ottawa Scale. Data were summarized as OR with 95% CIs. The primary objective was to assess the effect of ovarian-stimulating drugs on ovarian tumors and the secondary objective was to assess this effect in different sub-groups.</p><p><strong>Results: </strong>Forty studies were eligible for this meta-analysis. Overall, compared with unexposed infertile women and unexposed general population, ovarian-stimulating drugs increased the risk of invasive ovarian cancer (OR 1.23, 95% CI 1.14 to 1.32, p =.001) and borderline cancer (OR = 1.32, 95% CI 1.19 to 1.47, p < .001) in women receiving any fertility drugs. Our sub-group analysis showed a higher risk of both invasive and borderline ovarian cancer in infertile women using ovarian-stimulating drugs compared to infertile women with no exposure and the general unexposed population. An increased risk of ovarian cancer was observed in nulliparous women, but not in parous women. In addition, a cumulative clomiphene dose of <900 mg and a number of gonadotropin cycles ≥6 were factors that increased the risk of invasive ovarian cancer. Combined treatment with clomiphene and gonadotropin was associated with an increased risk of borderline cancer. Risk analyses further revealed that prolonged use of oral contraceptives (>60 months) and a family history of ovarian cancer significantly increased the odds of developing ovarian cancer among women treated with ovarian-stimulating drugs.</p><p><strong>Conclusion: </strong>Our study showed that ovarian-stimulating drugs increased the risk of ovarian tumors.</p>","PeriodicalId":14097,"journal":{"name":"International Journal of Gynecological Cancer","volume":"35 2","pages":"100046"},"PeriodicalIF":4.1000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ovarian-stimulating drug use and risk of ovarian tumor in infertile women: a meta-analysis.\",\"authors\":\"Hong Li, Zhonghua Hu, Yuyan Fan, Yingying Hao\",\"doi\":\"10.1016/j.ijgc.2024.100046\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To explore whether ovarian-stimulating drugs increase the risk of ovarian cancer in infertile women.</p><p><strong>Methods: </strong>This meta-analysis involved searching PubMed, Cochrane Library, Web of Science, and Embase. 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An increased risk of ovarian cancer was observed in nulliparous women, but not in parous women. In addition, a cumulative clomiphene dose of <900 mg and a number of gonadotropin cycles ≥6 were factors that increased the risk of invasive ovarian cancer. Combined treatment with clomiphene and gonadotropin was associated with an increased risk of borderline cancer. 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引用次数: 0
摘要
目的:探讨促卵巢药物是否会增加不孕妇女患卵巢癌的风险。方法:meta分析包括检索PubMed、Cochrane Library、Web of Science和Embase。观察性研究的方法学质量采用改良的纽卡斯尔-渥太华量表进行评估。数据汇总为OR, 95% ci。主要目的是评估促卵巢药物对卵巢肿瘤的影响,次要目的是评估不同亚组的效果。结果:40项研究符合此荟萃分析。总的来说,与未服用任何生育药物的不孕妇女和未服用任何生育药物的普通人群相比,卵巢刺激药物增加了接受任何生育药物的妇女患侵袭性卵巢癌(OR = 1.23, 95% CI 1.14至1.32,p = 0.001)和边缘性癌症(OR = 1.32, 95% CI 1.19至1.47,p < 0.001)的风险。我们的亚组分析显示,使用促卵巢药物的不孕妇女患侵袭性和交界性卵巢癌的风险高于未使用促卵巢药物的不孕妇女和未使用促卵巢药物的一般人群。在未生育妇女中观察到卵巢癌的风险增加,但在已生育妇女中没有。此外,服用克罗米芬累计剂量为60个月和有卵巢癌家族史的妇女在接受促卵巢药物治疗时患卵巢癌的几率显著增加。结论:本研究表明促卵巢药物增加卵巢肿瘤发生的风险。
Ovarian-stimulating drug use and risk of ovarian tumor in infertile women: a meta-analysis.
Objective: To explore whether ovarian-stimulating drugs increase the risk of ovarian cancer in infertile women.
Methods: This meta-analysis involved searching PubMed, Cochrane Library, Web of Science, and Embase. The methodological quality of observational studies was assessed using the modified Newcastle-Ottawa Scale. Data were summarized as OR with 95% CIs. The primary objective was to assess the effect of ovarian-stimulating drugs on ovarian tumors and the secondary objective was to assess this effect in different sub-groups.
Results: Forty studies were eligible for this meta-analysis. Overall, compared with unexposed infertile women and unexposed general population, ovarian-stimulating drugs increased the risk of invasive ovarian cancer (OR 1.23, 95% CI 1.14 to 1.32, p =.001) and borderline cancer (OR = 1.32, 95% CI 1.19 to 1.47, p < .001) in women receiving any fertility drugs. Our sub-group analysis showed a higher risk of both invasive and borderline ovarian cancer in infertile women using ovarian-stimulating drugs compared to infertile women with no exposure and the general unexposed population. An increased risk of ovarian cancer was observed in nulliparous women, but not in parous women. In addition, a cumulative clomiphene dose of <900 mg and a number of gonadotropin cycles ≥6 were factors that increased the risk of invasive ovarian cancer. Combined treatment with clomiphene and gonadotropin was associated with an increased risk of borderline cancer. Risk analyses further revealed that prolonged use of oral contraceptives (>60 months) and a family history of ovarian cancer significantly increased the odds of developing ovarian cancer among women treated with ovarian-stimulating drugs.
Conclusion: Our study showed that ovarian-stimulating drugs increased the risk of ovarian tumors.
期刊介绍:
The International Journal of Gynecological Cancer, the official journal of the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology, is the primary educational and informational publication for topics relevant to detection, prevention, diagnosis, and treatment of gynecologic malignancies. IJGC emphasizes a multidisciplinary approach, and includes original research, reviews, and video articles. The audience consists of gynecologists, medical oncologists, radiation oncologists, radiologists, pathologists, and research scientists with a special interest in gynecological oncology.