PRRT neuroendocrine tumor response monitored using circulating transcript analysis: the NETest

被引:85
作者
Bodei, Lisa [1 ,2 ]
Kidd, Mark S. [3 ]
Singh, Aviral [4 ]
van der Zwan, Wouter A. [5 ]
Severi, Stefano [6 ,7 ]
Drozdov, Ignat A. [3 ]
Malczewska, Anna [8 ]
Baum, Richard P. [2 ,4 ]
Kwekkeboom, Dik J. [2 ,5 ]
Paganelli, Giovanni [6 ,7 ]
Krenning, Eric P. [2 ,5 ,9 ]
Modlin, Irvin M. [2 ,10 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiol, Mol Imaging & Therapy Serv, 1275 York Ave,Box 77, New York, NY 10065 USA
[2] LuGenIum Consortium, 54 Portland Pl, London W1B 1DY, England
[3] Wren Labs, Branford, CT USA
[4] Zent Klin Bad Berka, Theranost Ctr Mol Radiotherapy & Imaging, Bad Berka, Germany
[5] Erasmus MC, Dept Radiol & Nucl Med, Rotterdam, Netherlands
[6] Ist Sci Romagnolo Studio & Cura Tumori IRST IRCCS, Nucl Med Unit, Meldola, Italy
[7] Ist Sci Romagnolo Studio & Cura Tumori IRST IRCCS, Radiometab Units, Meldola, Italy
[8] Med Univ Silesia, Dept Endocrinol & Neuroendocrine Tumors, Katowice, Poland
[9] Erasmus MC, Cyclotron Rotterdam BV, Rotterdam, Netherlands
[10] Yale Sch Med, New Haven, CT USA
关键词
Biomarker; NETest; PPQ; Liquid biopsy; Neuroendocrine; PRRT; RECEPTOR RADIONUCLIDE THERAPY; DEFINES; PREDICT; LU-177-DOTATATE; BIOMARKERS; EFFICACY; DISEASE; BLOOD;
D O I
10.1007/s00259-019-04601-3
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose Peptide receptor radionuclide therapy (PRRT) is effective for metastatic/inoperable neuroendocrine tumors (NETs). Imaging response assessment is usually efficient subsequent to treatment completion. Blood biomarkers such as PRRT Predictive Quotient (PPQ) and NETest are effective in real-time. PPQ predicts PRRT efficacy; NETest monitors disease. We prospectively evaluated: (1) NETest as a surrogate biomarker for RECIST; (2) the correlation of NETest levels with PPQ prediction. Methods Three independent Lu-177-PRRT-treated GEP-NET and lung cohorts (Meldola, Italy: n = 72; Bad-Berka, Germany: n = 44; Rotterdam, Netherlands: n = 41). Treatment response: RECIST1.1 (responder (stable, partial, and complete response) vs non-responder). Blood sampling: pre-PRRT, before each cycle and follow-up (2-12 months). PPQ (positive/negative) and NETest (0-100 score) by PCR. Stable < 40; progressive > 40). CgA (ELISA) as comparator. Samples de-identified, measurement and analyses blinded. Kaplan-Meier survival and standard statistics. Results One hundred twenty-two of the 157 were evaluable. RECIST stabilization or response in 67%; 33% progressed. NETest significantly (p < 0.0001) decreased in RECIST "responders" (- 47 +/- 3%); in "non-responders," it remained increased (+ 79 +/- 19%) (p < 0.0005). NETest monitoring accuracy was 98% (119/122). Follow-up levels > 40 (progressive) vs stable (< 40) significantly correlated with mPFS (not reached vs. 10 months; HR 0.04 (95%CI, 0.02-0.07). PPQ response prediction was accurate in 118 (97%) with a 99% accurate positive and 93% accurate negative prediction. NETest significantly (p < 0.0001) decreased in PPQ-predicted responders (- 46 +/- 3%) and remained elevated or increased in PPQ-predicted non-responders (+ 75 +/- 19%). Follow-up NETest categories stable vs progressive significantly correlated with PPQ prediction and mPFS (not reached vs. 10 months; HR 0.06 (95%CI, 0.03-0.12). CgA did not reflect PRRT treatment: in RECIST responders decrease in 38% and in non-responders 56% (p = NS). Conclusions PPQ predicts PRRT response in 97%. NETest accurately monitors PRRT response and is an effective surrogate marker of PRRT radiological response. NETest decrease identified responders and correlated (> 97%) with the pretreatment PPQ response predictor. CgA was non-informative.
引用
收藏
页码:895 / 906
页数:12
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