Influence of non-measurable disease on progression-free survival in patients with metastatic breast cancer

被引:3
|
作者
Goldvaser, Hadar [1 ,2 ,3 ]
Ribnikar, Domen [1 ,2 ]
Fazelzad, Rouhi [1 ,2 ]
Seruga, Bostjan [4 ]
Templeton, Arnoud J. [5 ]
Ocana, Alberto [6 ]
Amir, Eitan [1 ,2 ]
机构
[1] Univ Toronto, Div Med Oncol, 610 Univ Ave, Toronto, ON M5G 2M9, Canada
[2] Princess Margaret Canc Ctr, 610 Univ Ave,700 Univ Ave,7-721, Toronto, ON M5G 2M9, Canada
[3] Tel Aviv Univ, Sackler Fac Med, POB 39040, IL-6997801 Tel Aviv, Israel
[4] Inst Oncol Ljubljana, Dept Med Oncol, 2 Zaloska Cesta, Ljubljana 1000, Slovenia
[5] Univ Basel, Dept Oncol & Hematol, St Claraspital, Fac Med, Kleinriehenstr 30, CH-4058 Basel, Switzerland
[6] Univ Castilla La Mancha, Translat Res Unit, Ctr Reg Invest Biomed, Albacete Univ Hosp, Calle Francisco Javier de Moya, Albacete 02006, Spain
关键词
Bone-only disease; Measurable disease; Endpoints; Metastatic breast cancer; Progression-free survival; PHASE-III TRIAL; PEGYLATED LIPOSOMAL DOXORUBICIN; POSTMENOPAUSAL WOMEN; 1ST-LINE THERAPY; SOLID TUMORS; BEVACIZUMAB; FULVESTRANT; LETROZOLE; COMBINATION; EXEMESTANE;
D O I
10.1016/j.ctrv.2017.06.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The presence of non-measurable disease is common in metastatic breast cancer. It is unknown whether treatment effect on progression free survival (PFS) is consistent among patients with measurable and non-measurable disease. Methods: A systematic literature search identified phase III randomized controlled trials (RCTs) in metastatic breast cancer that reported outcomes in patients with non-measurable and measurable disease. Hazard ratios (HRs) and 95% confidence intervals were computed to compare the individual trial treatment effect on PFS in non-measurable versus measurable disease. Analyses were repeated for bone only compared to non-bone-only disease and based on drug mechanism of action. Results: Among 82 RCTs that enrolled patients with non-measurable disease, data were available from 16 trials comprising 8516 patients. Treatment effect on PFS was similar in patients with non-measurable and measurable disease (HR for intra-study comparison = 1.01, p = 0.82). However, compared to non-bone only disease, a significantly greater effect on PFS was seen in those with bone-only disease (HR 0.83, p = 0.03). Compared to patients with measurable disease, there was a greater effect on PFS in those with non-measurable disease in RCTs of signal transduction inhibitors and endocrine therapy (HR 0.74, p = 0.01) and a lesser effect on PFS in RCTs of antiangiogenic drugs (HR 1.34, p = 0.02). Comparable effect on PFS was shown in RCTs evaluating endocrine therapy (HR 1.13, p = 0.23) and chemotherapy (HR 0.73, p = 0.22). Conclusions: There is variability in treatment effect on PFS in patients with measurable and non measurable disease, especially those with bone-only disease. Standardization of PFS determination in these patients is warranted. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:46 / 53
页数:8
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