Yoon Jean, Malin Jennifer L, Tao May Lin, Tisnado Diana M, Adams John L, Timmer Martha J, Ganz Patricia A, Kahn Katherine L
School of Public Health, Health Services, University of California at Los Angeles, Box 951772, Los Angeles, CA 90095-1722, USA.
Breast Cancer Res Treat. 2008 Mar;108(2):153-65. doi: 10.1007/s10549-007-9599-3. Epub 2007 May 10.
This study examines the burden of symptoms by treatment type and patient characteristics in a population-based sample of newly diagnosed breast cancer patients.
Using the Los Angeles County SEER Registry Rapid Case Ascertainment, we identified a cohort of breast cancer patients in 2000 and conducted telephone surveys in English and Spanish among participants.
We completed interviews of 1,219 breast cancer patients and found almost half (46%) had at least one severe symptom (any of the following: nausea/vomiting, arm problems, hot flashes, vaginal dryness, difficulty sleeping) that interfered with her daily functioning or mood. Multi-variate analysis controlling for patient characteristics and treatment showed that older (OR=0.90; P<0.000), black (OR=0.50; P<0.000), Hispanic Spanish-speaking (OR=0.37; P<0.000), widowed or never married (OR=0.68; P=0.049), and working (OR=0.72; P=0.024) women were less likely to report severe symptoms than other women. Number of comorbid conditions (OR=1.21; P<0.000) and receipt of chemotherapy (OR=1.48; P=0.040) were positively associated with reporting symptoms.
These findings estimate the prevalence of several mutable symptoms in breast cancer patients that can be addressed by appropriate treatments. Comorbidity is a significant predictor of symptoms, especially amongst those receiving chemotherapy. Variation in symptom reporting occurred by race/ethnicity and other sociodemographic characteristics, raising questions of different thresholds for reporting symptoms or truly fewer symptoms for some sociodemographic groups. Population-based estimates of the probability of symptoms in women with incident breast cancer can be used to provide patient education about potential outcomes following the treatment of breast cancer.
本研究在基于人群的新诊断乳腺癌患者样本中,按治疗类型和患者特征检查症状负担。
利用洛杉矶县监测、流行病学和最终结果(SEER)登记处的快速病例确定方法,我们确定了2000年的一组乳腺癌患者,并对参与者进行了英语和西班牙语的电话调查。
我们完成了对1219名乳腺癌患者的访谈,发现近一半(46%)的患者至少有一种严重症状(以下任何一种:恶心/呕吐、手臂问题、潮热、阴道干燥、睡眠困难),这些症状会干扰其日常功能或情绪。控制患者特征和治疗的多变量分析表明,年龄较大(比值比[OR]=0.90;P<0.000)、黑人(OR=0.50;P<0.000)、说西班牙语的西班牙裔(OR=0.37;P<0.000)、丧偶或未婚(OR=0.68;P=0.049)以及在职(OR=0.72;P=0.024)的女性报告严重症状的可能性低于其他女性。合并症数量(OR=1.21;P<0.000)和接受化疗(OR=1.48;P=0.040)与报告症状呈正相关。
这些发现估计了乳腺癌患者中几种可通过适当治疗解决的可变症状的患病率。合并症是症状的重要预测因素,尤其是在接受化疗的患者中。症状报告因种族/民族和其他社会人口学特征而异,这引发了关于不同症状报告阈值或某些社会人口学群体症状确实较少的问题。基于人群的新发乳腺癌女性症状发生概率估计可用于为患者提供关于乳腺癌治疗后潜在结果的教育。