Important Group Differences on the Functional Assessment of Cancer Therapy-Kidney Symptom Index Disease-Related Symptoms in Patients with Metastatic Renal Cell Carcinoma

被引:7
作者
Cella, David [1 ]
Motzer, Robert J. [2 ]
Rini, Brian I. [3 ]
Cappelleri, Joseph C. [4 ]
Ramaswamy, Krishnan [5 ]
Hariharan, Subramanian [5 ]
Arondekar, Bhakti [6 ]
Bushmakin, Andrew G. [4 ]
机构
[1] Northwestern Univ, Dept Med Social Sci, 633 N St Clair,Suite 1900, Chicago, IL 60611 USA
[2] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[3] Cleveland Clin, Taussig Canc Inst, Cleveland, OH 44106 USA
[4] Pfizer Inc, Groton, CT 06340 USA
[5] Pfizer Inc, New York, NY USA
[6] Pfizer Inc, Collegeville, PA USA
关键词
clinically important difference; health-related quality of life; renal cell carcinoma; targeted therapy; QUALITY-OF-LIFE; MINIMALLY IMPORTANT DIFFERENCES; INTERFERON-ALPHA; PHASE-III; REPORTED OUTCOMES; SYSTEMIC THERAPY; SUNITINIB; SURVIVAL; SORAFENIB; AXITINIB;
D O I
10.1016/j.jval.2018.04.1371
中图分类号
F [经济];
学科分类号
02 ;
摘要
Background: The Functional Assessment of Cancer Therapy -Kidney Symptom Index Disease-Related Symptoms (FKSI-DRS) is important to gauge clinical benefit in metastatic renal cell carcinoma (mRCC). Objectives: To estimate important difference (ID) in FKSI-DRS scores that is considered to be meaningful when comparing treatment effect between groups, using mRCC trial data. Methods: Data were derived from two pivotal phase III mRCC trials comparing sunitinib versus interferon alfa (N = 750) in first-line mRCC, and axitinib versus sorafenib (N = 723) in second-line mRCC. The change from baseline in FKSI-DRS score was examined as a function of a set of anchors using the repeated-measures model. Several anchors were evaluated: FKSI item "I am bothered by side effects of treatment," EuroQol five-dimensional questionnaire utility score, and adverse events. Results: When the "I am bothered by side effects of treatment" score was used as an anchor, the ID ranged between 1.2 and 1.3 points. When change in the EuroQol five-dimensional questionnaire utility score was used as an anchor, the FKSI-DRS ID ranged between 0.62 and 0.63 points. Selecting the adverse events that corresponded to a maximum worsening in the FKSI-DRS score in either trial, the ID ranged between 0.62 and 0.74 points. Conclusions: Among patients undergoing treatment for mRCC, between-group differences in FKSI-DRS scores as low as 1 point might be meaningful.
引用
收藏
页码:1413 / 1418
页数:6
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