Reinisch Mattea, Marschner Norbert, Otto Thorsten, Korfel Agnieszka, Stoffregen Clemens, Wöckel Achim
Interdisziplinäres Brustzentrum/Senologie, Kliniken Essen-Mitte, Essen, Germany.
Praxis für Interdisziplinäre Onkologie und Hämatologie, Freiburg, Germany.
Breast Care (Basel). 2021 Oct;16(5):491-499. doi: 10.1159/000513139. Epub 2021 Jan 25.
Integration of patient preferences into shared decision making improves disease-related outcomes, but such data from patients with advanced breast cancer (aBC) are limited. The objective of this study was to demonstrate the relative importance of overall survival (OS) and progression-free survival (PFS) in relation to quality of life (QoL) and therapy-associated side effects from the perspective of patients with aBC.
Postmenopausal patients with hormone receptor-positive, human epidermal growth factor receptor 2-negative aBC receiving first- or second-line treatment were recruited throughout Germany. Patient-relevant attributes for aBC therapy assessment were collected using a stepwise multimodal approach. A conjoint matrix was developed, resulting in 2 attributes for therapy goals (OS and PFS), 4 for QoL, and 6 for side effects. An online quantitative survey was then performed using adaptive choice-based conjoint (ACBC) methodology.
The quantitative survey included 104 patients: 67 (64.4%) receiving first-line treatment and 37 (35.6%) receiving second-line treatment. The QoL attribute "physical agility and mobility" received the highest utility score (19.4 of 100%), reflecting the greatest importance to patients, followed by treatment goals (OS [15.2%] and PFS [14.4%]). Therapy-related side effects were less important, with nausea/vomiting being the most important (9.3%), followed by infection (6.4%) and hair loss (5.0%). The McFadden pseudo (0.805), the root likelihood (0.864), and the χ test (2,809.041; < 0.0001) indicated a very good fit of the statistical model.
Using ACBC analysis, it appears that QoL, OS, and PFS are most important to postmenopausal patients with aBC in relation to cancer treatment. Side effects seem to be less important if OS or PFS are prolonged and the QoL is maintained. Thus, QoL, OS, and PFS should be considered equally when making treatment decisions in aBC.
将患者偏好纳入共同决策可改善疾病相关结局,但晚期乳腺癌(aBC)患者的此类数据有限。本研究的目的是从aBC患者的角度证明总生存期(OS)和无进展生存期(PFS)相对于生活质量(QoL)和治疗相关副作用的相对重要性。
在德国各地招募接受一线或二线治疗的激素受体阳性、人表皮生长因子受体2阴性的绝经后aBC患者。采用逐步多模式方法收集与aBC治疗评估相关的患者属性。开发了一个联合矩阵,产生了2个治疗目标属性(OS和PFS)、4个QoL属性和6个副作用属性。然后使用基于自适应选择的联合分析(ACBC)方法进行在线定量调查。
定量调查包括104名患者:67名(64.4%)接受一线治疗,37名(35.6%)接受二线治疗。QoL属性“身体敏捷性和活动能力”获得最高效用得分(100%中的19.4%),反映出对患者最重要,其次是治疗目标(OS[15.2%]和PFS[14.4%])。治疗相关副作用不太重要,恶心/呕吐最重要(9.3%),其次是感染(6.4%)和脱发(5.0%)。麦克法登伪R²(0.805)、根似然值(0.864)和χ²检验(2809.041;P<0.0001)表明统计模型拟合度非常好。
使用ACBC分析,对于绝经后aBC患者,QoL、OS和PFS在癌症治疗方面似乎最为重要。如果OS或PFS延长且QoL得以维持,副作用似乎不太重要。因此,在aBC治疗决策时应同等考虑QoL、OS和PFS。