Progression-free and overall survival in metastatic castration-resistant prostate cancer treated with abiraterone acetate can be predicted with serial C11-acetate PET/CT

被引:3
作者
Farnebo, Jacob [1 ,2 ]
Wadelius, Agnes [3 ,4 ]
Sandstrom, Per [3 ,4 ]
Nilsson, Sten [3 ,4 ]
Jacobsson, Hans [1 ,2 ]
Blomqvist, Lennart [1 ,2 ]
Ullen, Anders [3 ,4 ]
机构
[1] Karolinska Univ Hosp, Dept Diagnost Radiol & Nucl Med, Stockholm, Sweden
[2] Dept Mol Med & Surg, Stockholm, Sweden
[3] Karolinska Univ Hosp, Dept Oncol, Stockholm, Sweden
[4] Karolinska Inst, Dept Pathol & Oncol, Stockholm, Sweden
关键词
abiraterone acetate; C11-acetate PET/CT; metastatic castration-resistant prostate cancer; FATTY-ACID SYNTHASE; F-18-FLUOROCHOLINE PET/CT; RECURRENCE; EXPRESSION;
D O I
10.1097/MD.0000000000004308
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this retrospective study, we evaluated the benefit of repeated carbon 11 (C11)-acetate positron emission tomography/computed tomography (PET/CT) to assess response in patients with metastatic castration-resistant prostate cancer (mCRPC) treated with abiraterone acetate (AA). A total of 30 patients with mCRPC were monitored with C11 -acetate PET/CT and PSA levels during their treatment with AA. Retrospective evaluation of their response was made after 102 days (median; range 70-155) of treatment. Statistical analyses were employed to detect predictors of progression-free survival (PFS) and overall survival (OS), and potential correlation between serum levels of PSA, standardized uptake values (SUVpeak), and bone lesion index measured from PC I were investigated. At follow-up 10 patients exhibited partial response (PR), 10 progressive disease (PD), and 10 stable disease (SD), as assessed by PET/CT. In survival analysis, both PR and PD were significantly associated with PFS and OS. CT response was also associated with OS, but only 19/30 patients demonstrated a lesion meeting target lesion criteria according to RECIST 1.1. No PET/CT baseline characteristic was significantly associated with PFS or OS. A PSA response (reduction in the level by >50%) could also predict PFS and OS. In the subgroup lacking a PSA response, those with PD had significantly shorter OS than those with PR or SD. PFS and OS in patients with mCRPC treated with AA can be predicted from repeated C11 -acetate PET/CT. This may be of particular clinical value in patients who do not exhibit a PSA response to treatment.
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页数:6
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