Reutfors Johan, Wingård Louise, Brandt Lena, Wang Yiting, Qiu Hong, Kieler Helle, Bahmanyar Shahram
Centre for Pharmacoepidemiology, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Centre for Pharmacoepidemiology, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Schizophr Res. 2017 Apr;182:98-103. doi: 10.1016/j.schres.2016.10.035. Epub 2016 Nov 4.
Several antipsychotics, especially risperidone, are known to increase serum prolactin. Hyperprolactinemia has been linked to the development of mammary gland tumors in animal studies. We therefore investigated the risk of breast cancer in a nationwide cohort of women using risperidone or other antipsychotics.
All women, 18years or older, who initiated treatment with risperidone or any other antipsychotic between 2006 and 2012 were identified in Swedish nationwide registers. Patients with two consecutive dispensations of the same antipsychotic within 3months, no previous cancer diagnosis, and no previous dispensations of paliperidone were included. The final cohort consisted of 55976 women of whom 22908, 24524, and 8544 were exposed to risperidone, other atypical antipsychotics, and typical antipsychotics, respectively. A Cox regression model was used to estimate the hazard ratio (HR) and 95% confidence interval (CI) for the association between antipsychotics and breast cancer.
Patients were followed prospectively, the mean follow-up time ranging from 2.4 to 2.8years between treatment groups. After adjusting for age, there was no increased risk for breast cancer among risperidone users compared to patients exposed to another atypical antipsychotic (HR 0.94, 95% CI 0.72-1.22) or a typical antipsychotic (HR 1.25, 95% CI 0.94-1.66). Analyses stratified by tumor stage, using active treatment follow-up time, or including only treatment naïve patients did not reveal any noteworthy change in the results.
Risperidone use does not confer an increased short-term risk of breast cancer compared to other antipsychotic agents.
已知几种抗精神病药物,尤其是利培酮,会增加血清催乳素水平。在动物研究中,高催乳素血症与乳腺肿瘤的发生有关。因此,我们在全国范围内对使用利培酮或其他抗精神病药物的女性队列进行了乳腺癌风险调查。
在瑞典全国登记处识别出所有在2006年至2012年间开始使用利培酮或任何其他抗精神病药物治疗的18岁及以上女性。纳入在3个月内连续两次配药使用同一抗精神病药物、既往无癌症诊断且既往未使用过帕利哌酮的患者。最终队列包括55976名女性,其中22908名、24524名和8544名分别暴露于利培酮、其他非典型抗精神病药物和典型抗精神病药物。使用Cox回归模型估计抗精神病药物与乳腺癌之间关联的风险比(HR)和95%置信区间(CI)。
对患者进行前瞻性随访,各治疗组的平均随访时间为2.4至2.8年。在调整年龄后,与暴露于另一种非典型抗精神病药物(HR 0.94,95%CI 0.72 - 1.22)或典型抗精神病药物(HR 1.25,95%CI 0.94 - 1.66)的患者相比,使用利培酮的患者患乳腺癌的风险没有增加。按肿瘤分期分层分析、使用积极治疗随访时间分析或仅纳入初治患者分析,结果均未显示出任何值得注意的变化。
与其他抗精神病药物相比,使用利培酮不会增加短期患乳腺癌的风险。