Assessing Adherence to Adjuvant Hormone Therapy in Breast Cancer Patients in Routine Clinical Practice.

IF 2.1 Q3 ONCOLOGY World Journal of Oncology Pub Date : 2023-08-01 DOI:10.14740/wjon1647
Natalia Camejo, Cecilia Castillo, Clara Tambasco, Noelia Strazzarino, Nicolas Requena, Silvina Peraza, Anna Boronat, Guadalupe Herrera, Patricia Esperon, Mauricio Cuello, Gabriel Krygier
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Abstract

Background: Adjuvant hormone therapy (HT) in patients with hormone receptor-positive breast cancer (BC) increases overall survival (OS). A lack of adherence to adjuvant endocrine therapy is common, 31.0-73.0% of women discontinue endocrine treatment before 5 years. The aim of the study was to assess adherence to HT in routine clinical practice in patients assisted at the Clinical Oncology Department of the Hospital de Clinicas - Universidad de la Republica, Uruguay.

Methods: Patients treated with HT for stage 0-III BC between 2017 and 2019 were included. The medication possession (MPR) rate was calculated using pharmacy records, and the Morisky-Green Scale was applied to assess adherence. Adherent patients were those with MPR ≥ 0.80 and who correctly answered the Morisky-Green treatment adherence questionnaire. The association of adherence with polypharmacy, treatment, and patient characteristics was assessed using simple logistic models. The associations between qualitative variables and adherence were assessed using simple logistic regression model or Fisher's exact test. The association between quantitative variables and adherence was assessed using the Student's t-test. The odds ratio (OR) for non-adherence to treatment and its 95% confidence interval were estimated.

Results: Totally, 118 patients were included; 65.2% were treated with aromatase inhibitors (AIs), 36.0% presenting polypharmacy. The adherence rate at the end of 2 years was 81.0 %; and it was associated with age (P = 0.03, OR = 0.96 for non-adherence), with adherent and non-adherent patients having a mean age of 65.0 and 60.3 years, respectively; however, adherence was not associated with polypharmacy, territory of origin, marital status, living alone, level of education, occupation, or stage. The adherence profile was similar for both drugs, but homemakers and retired women showed greater adherence to AI.

Conclusions: Adherence to HT was assessed in real life, with 19.0% of the patients not adhering to the treatment, despite the known benefit for OS, being a well-tolerated treatment, and being provided free of charge. Older patients were associated with being more adherent. The results show the need of the Pharmacy Service and Department of Clinical Oncology Medical Oncology combining efforts to develop coordinated strategies and interventions to increase adherence, given the impact that this may have on patients' OS.

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在常规临床实践中评估乳腺癌患者对辅助激素治疗的依从性。
背景:激素受体阳性乳腺癌(BC)患者的辅助激素治疗(HT)可提高总生存率(OS)。缺乏对辅助内分泌治疗的坚持是很常见的,31.0-73.0%的妇女在5岁前停止内分泌治疗。该研究的目的是评估乌拉圭共和国大学临床医院临床肿瘤科辅助患者在常规临床实践中对HT的依从性。方法:纳入2017年至2019年接受HT治疗的0-III期BC患者。使用药房记录计算药物持有率(MPR),采用Morisky-Green量表评估依从性。依从性患者为MPR≥0.80且正确回答Morisky-Green治疗依从性问卷的患者。使用简单逻辑模型评估依从性与多种药物、治疗和患者特征的关系。使用简单逻辑回归模型或Fisher精确检验评估定性变量与依从性之间的关系。定量变量与依从性之间的关系采用学生t检验进行评估。估计治疗不依从的优势比(OR)及其95%置信区间。结果:共纳入118例患者;65.2%的患者采用芳香酶抑制剂(AIs)治疗,36.0%的患者采用多药治疗。2年后依从率为81.0%;与年龄相关(P = 0.03,未依从组OR = 0.96),依从组和非依从组患者的平均年龄分别为65.0岁和60.3岁;然而,依从性与多种药物、原籍地、婚姻状况、独居、教育水平、职业或阶段无关。两种药物的依从性相似,但家庭主妇和退休妇女对AI的依从性更高。结论:在现实生活中对HT的依从性进行了评估,尽管已知对OS有好处,但19.0%的患者没有坚持治疗,这是一种耐受性良好的治疗方法,并且是免费提供的。年龄越大的患者依从性越强。结果表明,考虑到可能对患者OS产生的影响,药学服务和临床肿瘤医学肿瘤科需要联合努力,制定协调的策略和干预措施,以提高依从性。
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来源期刊
CiteScore
6.10
自引率
15.40%
发文量
37
期刊介绍: World Journal of Oncology, bimonthly, publishes original contributions describing basic research and clinical investigation of cancer, on the cellular, molecular, prevention, diagnosis, therapy and prognosis aspects. The submissions can be basic research or clinical investigation oriented. This journal welcomes those submissions focused on the clinical trials of new treatment modalities for cancer, and those submissions focused on molecular or cellular research of the oncology pathogenesis. Case reports submitted for consideration of publication should explore either a novel genomic event/description or a new safety signal from an oncolytic agent. The areas of interested manuscripts are these disciplines: tumor immunology and immunotherapy; cancer molecular pharmacology and chemotherapy; drug sensitivity and resistance; cancer epidemiology; clinical trials; cancer pathology; radiobiology and radiation oncology; solid tumor oncology; hematological malignancies; surgical oncology; pediatric oncology; molecular oncology and cancer genes; gene therapy; cancer endocrinology; cancer metastasis; prevention and diagnosis of cancer; other cancer related subjects. The types of manuscripts accepted are original article, review, editorial, short communication, case report, letter to the editor, book review.
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