Dierssen-Sotos Trinidad, Gómez-Acebo Inés, de Pedro María, Pérez-Gómez Beatriz, Servitja Sonia, Moreno Víctor, Amiano Pilar, Fernandez-Villa Tania, Barricarte Aurelio, Tardon Adonina, Diaz-Santos Marian, Peiro-Perez Rosana, Marcos-Gragera Rafael, Lope Virginia, Gracia-Lavedan Esther, Alonso M Henar, Michelena-Echeveste Maria Jesus, Garcia-Palomo Andrés, Guevara Marcela, Castaño-Vinyals Gemma, Aragonés Nuria, Kogevinas Manolis, Pollán Marina, Llorca Javier
CIBER Epidemiologia y Salud Publica (CIBERESP), Madrid, Spain.
University of Cantabria - IDIVAL, Santander, Spain.
BMC Cancer. 2016 Aug 20;16(1):660. doi: 10.1186/s12885-016-2692-4.
The relationship between non-steroidal anti-inflammatory drug (NSAID) consumption and breast cancer has been repeatedly studied, although the results remain controversial. Most case-control studies reported that NSAID consumption protected against breast cancer, while most cohort studies did not find this effect. Most studies have dealt with NSAIDs as a whole group or with specific drugs, such aspirin, ibuprofen, or others, but not with NSAID subgroups according to the Anatomical Therapeutic Chemical Classification System; moreover, scarce attention has been paid to their effect on different tumor categories (i.e.: ductal/non-ductal, stage at diagnosis or presence of hormonal receptors).
In this case-control study, we report the NSAID - breast cancer relationship in 1736 breast cancer cases and 1895 healthy controls; results are reported stratifying by the women's characteristics (i.e.: menopausal status or body mass index category) and by tumor characteristics.
In our study, NSAID use was associated with a 24 % reduction in breast cancer risk (Odds ratio [OR] = 0.76; 95 % Confidence Interval [CI]: 0.64-0.89), and similar results were found for acetic acid derivatives, propionic acid derivatives and COXIBs, but not for aspirin. Similar results were found in postmenopausal and premenopausal women. NSAID consumption also protected against hormone + or HER2+ cancers, but not against triple negative breast cancers. The COX-2 selectivity showed an inverse association with breast cancer (i.e. OR < 1), except in advanced clinical stage and triple negative cancers.
Most NSAIDs, but not aspirin, showed an inverse association against breast cancer; this effect seems to be restricted to hormone + or HER2+ cancers.
非甾体抗炎药(NSAID)的使用与乳腺癌之间的关系已被反复研究,但其结果仍存在争议。大多数病例对照研究报告称,服用NSAID可预防乳腺癌,而大多数队列研究未发现这种效果。大多数研究将NSAID作为一个整体或特定药物(如阿司匹林、布洛芬或其他药物)进行研究,而未根据解剖治疗化学分类系统对NSAID亚组进行研究;此外,人们很少关注它们对不同肿瘤类型(即导管癌/非导管癌、诊断时的分期或激素受体的存在)的影响。
在这项病例对照研究中,我们报告了1736例乳腺癌病例和1895例健康对照中NSAID与乳腺癌的关系;结果按女性特征(即绝经状态或体重指数类别)和肿瘤特征进行分层报告。
在我们的研究中,使用NSAID与乳腺癌风险降低24%相关(优势比[OR]=0.76;95%置信区间[CI]:0.64-0.89),乙酸衍生物、丙酸衍生物和COXIBs也有类似结果,但阿司匹林没有。绝经后和绝经前女性也有类似结果。服用NSAID也可预防激素阳性或HER2阳性癌症,但对三阴性乳腺癌无效。COX-2选择性与乳腺癌呈负相关(即OR<1),晚期临床分期和三阴性癌症除外。
大多数NSAID(但不包括阿司匹林)与乳腺癌呈负相关;这种效应似乎仅限于激素阳性或HER2阳性癌症。