Prospective International Cohort Study Demonstrates Inability of Interim PET to Predict Treatment Failure in Diffuse Large B-Cell Lymphoma

被引:66
作者
Carr, Robert [1 ]
Fanti, Stefano [2 ]
Paez, Diana [3 ]
Cerci, Juliano [4 ]
Gyoerke, Tamas [5 ,6 ]
Redondo, Francisca [7 ]
Morris, Tim P. [8 ]
Meneghetti, Claudio [9 ]
Auewarakul, Chirayu [10 ,11 ]
Nair, Reena [12 ]
Gorospe, Charity [13 ]
Chung, June-Key [14 ]
Kuzu, Isinsu [15 ]
Celli, Monica [2 ]
Gujral, Sumeet [16 ]
Padua, Rose Ann [17 ]
Dondi, Maurizio [3 ]
机构
[1] Kings Coll London, Guys & St Thomas Hosp, Dept Haematol, London SE1 9RT, England
[2] Univ Bologna, Policlin S Orsola Malpighi, Bologna, Italy
[3] IAEA, Dept Nucl Sci & Applicat, Div Human Hlth, A-1400 Vienna, Austria
[4] Quanta Diagnost & Terapia, Sao Paulo, Brazil
[5] ScanoMed Med Diagnost Ltd, Budapest, Hungary
[6] Semmelweis Univ, Dept Nucl Med, H-1085 Budapest, Hungary
[7] Fdn Arturo Lopez Perez, Oncol Clin, Santiago, Chile
[8] UCL, MRC, Clin Trials Unit, London, England
[9] Univ Sao Paulo, Hosp Clin, Sao Paulo, Brazil
[10] Chulabhorn Canc Ctr, Bangkok, Thailand
[11] Siriraj Hosp, Fac Med, Bangkok, Thailand
[12] Tata Mem Hosp, Dept Med Oncol, Mumbai 400012, Maharashtra, India
[13] St Lukes Med Ctr, Manila, Philippines
[14] Seoul Natl Univ Hosp, Seoul 110744, South Korea
[15] Ankara Univ, Sch Med, Dept Pathol, TR-06100 Ankara, Turkey
[16] Tata Mem Hosp, Dept Pathol, Mumbai 400012, Maharashtra, India
[17] Univ Paris Diderot, Hop St Louis, Inst Hematol, UMRS 940, Paris, France
关键词
diffuse large B-cell lymphoma; positron emission tomography; prospective observational study; risk stratification; risk-adapted therapy; POSITRON-EMISSION-TOMOGRAPHY; NON-HODGKINS-LYMPHOMA; CHEMOTHERAPY PLUS RITUXIMAB; PROGNOSTIC VALUE; CRITERIA; SCANS; SURVIVAL; CYCLES; SUVMAX; TRIALS;
D O I
10.2967/jnumed.114.145326
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
The International Atomic Energy Agency sponsored a large, multinational, prospective study to further define PET for risk stratification of diffuse large B-cell lymphoma and to test the hypothesis that international biological diversity or diversity of healthcare systems may influence the kinetics of treatment response as assessed by interim PET (I-PET). Methods: Cancer centers in Brazil, Chile, Hungary, India, Italy, the Philippines, South Korea, and Thailand followed a common protocol based on treatment with R-CHOP (cyclophosphamide, hydroxyadriamycin, vincristine, prednisolone with rituximab), with I-PET after 2-3 cycles of chemotherapy and at the end of chemotherapy scored visually. Results: Two-year survivals for all 327 patients (median follow-up, 35 mo) were 79% (95% confidence interval [CI], 74%-83%) for event-free survival (EFS) and 86% (95% CI, 81%-89%) for overall survival (OS). Two hundred ten patients (64%) were I-PET-negative, and 117 (36%) were I-PET-positive. Two-year EFS was 90% (95% CI, 85%-93%) for I-PET-negative and 58% (95% CI, 48%-66%) for I-PET-positive, with a hazard ratio of 5.31 (95% CI, 3.29-8.56). Two-year OS was 93% (95% CI, 88%-96%) for I-PET-negative and 72% (95% CI, 63%-80%) for I-PET-positive, with a hazard ratio of 3.86 (95% CI, 2.12-7.03). On sequential monitoring, 192 of 312 (62%) patients had complete response at both I-PET and end-of-chemotherapy PET, with an EFS of 97% (95% CI, 92%-98%); 110 of these with favorable clinical indicators had an EFS of 98% (95% CI, 92%-100%). In contrast, the 107 I-PET-positive cases segregated into 2 groups: 58 (54%) achieved PET-negative complete remission at the end of chemotherapy (EFS, 86%; 95% CI, 73%-93%); 46% remained PET-positive (EFS, 35%; 95% CI, 22%-48%). Heterogeneity analysis found no significant difference between countries for outcomes stratified by I-PET. Conclusion: This large international cohort delivers 3 novel findings: treatment response assessed by I-PET is comparable across disparate healthcare systems, secondly a negative I-PET findings together with good clinical status identifies a group with an EFS of 98%, and thirdly a single I-PET scan does not differentiate chemoresistant lymphoma from complete response and cannot be used to guide risk-adapted therapy.
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页码:1936 / 1944
页数:9
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