Prospective Study of 3′-Deoxy-3′-18F-Fluorothymidine PET for Early Interim Response Assessment in Advanced-Stage B-Cell Lymphoma

被引:36
作者
Schoder, Heiko [1 ]
Zelenetz, Andrew D. [2 ]
Hamlin, Paul [2 ]
Gavane, Somali [1 ]
Horwitz, Steven [2 ]
Matasar, Matthew [2 ]
Moskowitz, Alison [2 ]
Noy, Ariela [2 ]
Palomba, Lia [2 ]
Portlock, Carol [2 ]
Straus, David [2 ]
Grewal, Ravinder [1 ]
Migliacci, Jocelyn C. [3 ]
Larson, Steven M. [1 ]
Moskowitz, Craig H. [2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiol, Mol Imaging & Therapy Serv, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med, Lymphoma Serv, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY 10065 USA
关键词
FLT PET; B-cell cell lymphoma; FDG PET; outcome; POSITRON-EMISSION-TOMOGRAPHY; CHEMOTHERAPY PLUS RITUXIMAB; RANDOMIZED CONTROLLED-TRIAL; METABOLIC TUMOR VOLUME; NON-HODGKIN-LYMPHOMA; SUVMAX REDUCTION; PROGNOSTIC VALUE; F-18-FDG PET; FDG-PET; R-CHOP;
D O I
10.2967/jnumed.115.166769
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
100231 [临床病理学]; 100902 [航空航天医学];
摘要
Current clinical and imaging tools remain suboptimal for early assessment of prognosis and treatment response in aggressive lymphomas. PET with 3'-deoxy-3'-F-18-fluorothymidine (F-18-FLT) can be used to measure tumor cell proliferation and treatment response. In a prospective study in patients with advanced-stage B-cell lymphoma, we investigated the prognostic and predictive value of F-18-FLT PET in comparison to standard imaging with F-18-FDG PET and clinical outcome. Methods: Sixty-five patients were treated with an induction/consolidation regimen consisting of 4 cycles of R-CHOP-14 (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone) followed by 3 cycles of ICE (ifosfamide, carboplatin, etoposide). F-18-FLT PET was performed at baseline and at interim (iPET) after 1-2 cycles of therapy. F-18-FDG PET was performed at baseline, after cycle 4, and at the end of therapy. The relationship between PET findings, progression free survival (PFS) and overall survival (OS) was investigated. Results: With a median follow-up of 51 mo, PFS and OS were 71% and 86%, respectively. F-18-FLT iPET, analyzed visually (using a 5-point score) or semiquantitatively (using SUV and Delta SUV) predicted both PFS and OS (P < 0.01 for all parameters). Residual F-18-FLT SUV. on iPEI was associated with an inferior PFS (hazard ratio, 1.26, P = 0.001) and OS (hazard ratio, 1.27, P = 0.002). When F-18-FDG PET was used, findings in the end of treatment scan were better predictors of PFS and OS than findings on the interim scan. Baseline PET imaging parameters, including SUV, proliferative volume, or metabolic tumor volume, did not correlate with outcome. Conclusion: F-18-FLT PET after 1-2 cycles of chemotherapy predicts PFS and OS, and a negative F-18-FLT iPET result may potentially help design risk-adapted therapies in patients with aggressive lymphomas. In contrast, the positive predictive value of F-18-FLT iPET remains too low to justify changes in patient management.
引用
收藏
页码:728 / 734
页数:7
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