Early 18F-FDG PET/CT Response Predicts Survival in Relapsed or Refractory Hodgkin Lymphoma Treated with Nivolumab

被引:38
作者
Chen, Aiping [1 ,2 ]
Mokrane, Fatima-Zohra [1 ,3 ]
Schwartz, Lawrence H. [1 ]
Morschhauser, Franck [4 ]
Stamatoullas, Apasia [5 ]
de Colella, Jean-Marc Schiano [6 ]
Vercellino, Laetitia [7 ]
Casasnovas, Olivier [8 ]
Chauchet, Adrien [9 ]
Delmer, Alain [10 ]
Nicolas-Virelizier, Emmanuelle [11 ]
Ghesquieres, Herve [12 ]
Moles-Moreau, Marie-Pierre [13 ]
Schmitt, Anna [14 ]
Dulery, Remy [15 ]
Bouabdallah, Krimo [16 ]
Borel, Cecile [17 ]
Touati, Mohamed [18 ]
Deau-Fischer, Benedicte [19 ]
Peyrade, Frederic [20 ]
Seban, Romain-David [21 ]
Manson, Guillaume [22 ,23 ]
Armand, Philippe [24 ]
Houot, Roch [22 ,23 ]
Dercle, Laurent [1 ,25 ]
机构
[1] Columbia Univ, New York Presbyterian Hosp, Dept Radiol, Med Ctr, 68 Bradhurst Ave, New York, NY 10039 USA
[2] Nanjing Med Univ, Dept Radiol, Affiliated Hosp 1, Nanjing, Peoples R China
[3] Rangueil Univ Hosp, Radiol Dept, Toulouse, France
[4] Univ Lille, CHU Lille, EA 7365, GRITA Grp Rech Formes Injectables & Technol Assoc, Lille, France
[5] Ctr Henri Becquerel, Dept Hematol, Rouen, France
[6] Paoli Calmette Inst, Dept Hematol, Marseille, France
[7] St Louis Hosp, AP HP, Dept Nucl Med, Paris, France
[8] Univ Hosp Dijon, Dept Hematol, Dijon, France
[9] Univ Hosp Besancon, Dept Hematol, Besancon, France
[10] Univ Hosp Reims, Dept Hematol, Reims, France
[11] Leon Berard Ctr, Dept Hematol, Lyon, France
[12] Univ Hosp Lyon, Dept Hematol, Lyon, France
[13] Univ Hosp Angers, Dept Hematol, Angers, France
[14] Bergonie Inst, Dept Hematol, Bordeaux, France
[15] St Antoine Hosp, AP HP, Dept Hematol, Paris, France
[16] Univ Hosp Bordeaux, Dept Hematol, Bordeaux, France
[17] Inst Univ Canc Toulouse Oncopole, Dept Hematol, Toulouse, France
[18] Univ Hosp Limoges, Dept Hematol, Limoges, France
[19] Cochin Hosp, AP HP, Dept Hematol, Paris, France
[20] Ctr Antoine Lacassagne, Nice, France
[21] Inst Curie, Dept Nucl Med, Paris, France
[22] Univ Hosp Rennes, Dept Hematol, Rennes, France
[23] INSERM, U1236, Rennes, France
[24] Dana Farber Canc Inst, Med Oncol, Boston, MA 02115 USA
[25] Univ Paris Saclay, Inst Gustave Roussy, INSERM, UMR1015, Villejuif, France
关键词
anti-PD-1; immunotherapy; nivolumab; Hodgkin lymphoma; F-18-FDG PET; BRENTUXIMAB VEDOTIN; CELL TRANSPLANTATION; PD-1; BLOCKADE; INTERIM PET; PHASE-II; PEMBROLIZUMAB; CHEMOTHERAPY; MULTICOHORT; EFFICACY; ANTI-PD1;
D O I
10.2967/jnumed.119.232827
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
Monoclonal antibodies (mAbs) against programmed cell death 1 (PD-1), such as nivolumab and pembrolizumab, are associated with high response rates in patients with relapsed or refractory classic Hodgkin lymphoma (HL). To date, no prognostic factor for overall survival (OS) has been established with these agents in HL. We examined whether the first early response assessment evaluated using F-18-FDG PET/CT may be associated with OS in this setting. Methods: This retrospective study included 45 patients from 34 institutions. In a masked, centralized review, 3 independent radiologists classified PET/CT scans obtained at a median of 2.0 mo (interquartile range, 1.7-3.7 mo) after nivolumab initiation using existing criteria (i.e., 2014 Lugano classification and 2016 LYRIC). Patients were classified according to 4 possible response categories: complete metabolic response (CMR), partial metabolic response (PMR), no metabolic response (NMR), or progressive metabolic disease (PMD). Because the OS of patients with NMR and PMR was similar, they were grouped together. OS was estimated using the Kaplan-Meier method and compared between groups using log-rank testing. Results: Eleven patients (24%) died after a median follow-up of 21.2 mo. The classification was identical between Lugano and LYRIC because all 16 progression events classified as indeterminate response per LYRIC were confirmed on subsequent evaluations. Both Lugano and LYRIC classified patients as CMR in 13 cases (29%), PMD in 16 (36%), NMR in 4 (9%), and PMR in 12 (27%). The 2-y OS probability was significantly different in patients with PMD (0.53; 95% confidence interval [95%C1], 0.32-0.87), NMR or PMR (0.80; 95%Cl, 0.63-1.00), and CMR (1.00; 95%Cl, 1.00-1.00) in the overall population (P = 0.02, 45 patients), as well as according to a landmark analysis at 3 mo (P = 0.05, 32 patients). Conclusion: In relapsed or refractory HL patients treated with anti-PD-1 mAbs, the first early PET/CT assessment using either Lugano or LYRIC predicted OS and allowed early risk stratification, suggesting that PET/CT might be used to develop risk-adapted strategies.
引用
收藏
页码:649 / 654
页数:6
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