Association between end-induction response according to the revised International Neuroblastoma Response Criteria (INRC) and outcome in high-risk neuroblastoma patients

被引:7
作者
Barr, Erin K. [1 ]
Laurie, Kathryn [2 ]
Wroblewski, Kristen [3 ]
Applebaum, Mark A. [4 ]
Cohn, Susan L. [4 ]
机构
[1] Texas Tech Univ Hlth Sci, Dept Pediat, Lubbock, TX USA
[2] Ann & Robert H Lurie Childrens Hosp Chicago, Pediat Hematol Oncol & Stem Cell Transplantat, Chicago, IL 60611 USA
[3] Univ Chicago, Dept Publ Hlth Sci, Chicago, IL 60637 USA
[4] Univ Chicago, Dept Pediat, 900 E 57th St,KCBD 5100, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
International Neuroblastoma Response Criteria (INRC); neuroblastoma; outcome; CHILDRENS ONCOLOGY GROUP; STAGE; 4; NEUROBLASTOMA; EVENT-FREE SURVIVAL; METAIODOBENZYLGUANIDINE SCINTIGRAPHY; F-18-FDG PET; BONE-MARROW; DIAGNOSIS;
D O I
10.1002/pbc.28390
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The 1993 International Neuroblastoma Response Criteria (INRC) were revised in 2017 to include modern functional imaging studies and methods for quantifying disease in bone marrow. We hypothesized the 2017 INRC would enable more precise assessment of response to treatment and provide superior prognostic information compared with the 1993 criteria. Methods High-risk (HR) neuroblastoma patients from two institutions in Chicago diagnosed between 2006 and 2016 were identified. Patients were assessed post induction chemotherapy via the 1993 and 2017 INRC and classified as responder (>= mixed response [MXR] or >= minor response [MR], respectively) or nonresponder (< MXR or < MR). Event-free survival (EFS) and overall survival (OS) for responders versus nonresponders were determined from end induction and stratified by Cox regression. Patients with progressive disease at end induction were eliminated from the EFS analyses but included in the OS analysis. Results The 1993 criteria classified 52 of the 60 HR patients as responders, whereas 54 responders were identified using the 2017 criteria (Spearman correlationr = 0.82,P < 0.001). No statistically significant difference in EFS was observed for responders versus nonresponders using either criteria (P = 0.48 andP = 0.08). However, superior OS was observed for responders (P = 0.01) using either criteria. Both criteria were sensitive in identifying responders among those with good outcomes. The specificity to identify nonresponders among those with poor outcomes was poor. Conclusions In HR neuroblastoma, end-induction response defined by the 1993 or 2017 INRC is associated with survival. Larger cohorts are needed to determine if the 2017 INRC provides more precise prognostication.
引用
收藏
页数:8
相关论文
共 29 条
[1]   ANALYSIS OF SURVIVAL BY TUMOR RESPONSE [J].
ANDERSON, JR ;
CAIN, KC ;
GELBER, RD .
JOURNAL OF CLINICAL ONCOLOGY, 1983, 1 (11) :710-719
[2]   Assessment of Primary Site Response in Children With High-Risk Neuroblastoma: An International Multicenter Study [J].
Bagatell, Rochelle ;
McHugh, Kieran ;
Naranjo, Arlene ;
Van Ryn, Collin ;
Kirby, Chaim ;
Brock, Penelope ;
Lyons, Karen A. ;
States, Lisa J. ;
Rojas, Yesenia ;
Miller, Alexandra ;
Volchenboum, Sam L. ;
Simon, Thorsten ;
Krug, Barbara ;
Sarnacki, Sabine ;
Valteau-Couanet, Dominique ;
von Schweinitz, Dietrich ;
Kammer, Birgit ;
Granata, Claudio ;
Pio, Luca ;
Park, Julie R. ;
Nuchtern, Jed .
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (07) :740-+
[3]  
Biasotti S, 2000, MED PEDIATR ONCOL, V35, P153, DOI 10.1002/1096-911X(200008)35:2<153::AID-MPO18>3.0.CO
[4]  
2-7
[5]   REVISIONS OF THE INTERNATIONAL CRITERIA FOR NEUROBLASTOMA DIAGNOSIS, STAGING, AND RESPONSE TO TREATMENT [J].
BRODEUR, GM ;
PRITCHARD, J ;
BERTHOLD, F ;
CARLSEN, NLT ;
CASTEL, V ;
CASTLEBERRY, RP ;
DEBERNARDI, B ;
EVANS, AE ;
FAVROT, M ;
HEDBORG, F ;
KANEKO, M ;
KEMSHEAD, J ;
LAMPERT, F ;
LEE, REJ ;
LOOK, AT ;
PEARSON, ADJ ;
PHILIP, T ;
ROALD, B ;
SAWADA, T ;
SEEGER, RC ;
TSUCHIDA, Y ;
VOUTE, PA .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (08) :1466-1477
[6]   INTERNATIONAL CRITERIA FOR DIAGNOSIS, STAGING, AND RESPONSE TO TREATMENT IN PATIENTS WITH NEURO-BLASTOMA [J].
BRODEUR, GM ;
SEEGER, RC ;
BARRETT, A ;
BERTHOLD, F ;
CASTLEBERRY, RP ;
DANGIO, G ;
DEBERNARDI, B ;
EVANS, AE ;
FAVROT, M ;
FREEMAN, AI ;
HAASE, G ;
HARTMANN, O ;
HAYES, FA ;
HELSON, L ;
KEMSHEAD, J ;
LAMPERT, F ;
NINANE, J ;
OHKAWA, H ;
PHILIP, T ;
PINKERTON, CR ;
PRITCHARD, J ;
SAWADA, T ;
SIEGEL, S ;
SMITH, EI ;
TSUCHIDA, Y ;
VOUTE, PA .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (12) :1874-1881
[7]   Recommendations for the Standardization of Bone Marrow Disease Assessment and Reporting in Children With Neuroblastoma on Behalf of the International Neuroblastoma Response Criteria Bone Marrow Working Group [J].
Burchill, Susan A. ;
Beiske, Klaus ;
Shimada, Hiroyuki ;
Ambros, Peter F. ;
Seeger, Robert ;
Tytgat, Godelieve A. M. ;
Brock, Penelope R. ;
Haber, Michelle ;
Park, Julie R. ;
Berthold, Frank .
CANCER, 2017, 123 (07) :1095-1105
[8]   Prospective evaluation of the International Neuroblastoma Staging System (INSS) and the International Neuroblastoma Response Criteria (INRC) in a multicentre setting [J].
Castel, V ;
García-Miguel, P ;
Cañete, A ;
Melero, C ;
Navajas, A ;
Ruíz-Jiménez, JI ;
Navarro, S ;
Badal, MD .
EUROPEAN JOURNAL OF CANCER, 1999, 35 (04) :606-611
[9]   Iodine-123 Metaiodobenzylguanidine Scintigraphy Scoring Allows Prediction of Outcome in Patients With Stage 4 Neuroblastoma: Results of the Cologne Interscore Comparison Study [J].
Decarolis, Boris ;
Schneider, Christina ;
Hero, Barbara ;
Simon, Thorsten ;
Volland, Ruth ;
Roels, Frederik ;
Dietlein, Markus ;
Berthold, Frank ;
Schmidt, Matthias .
JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (07) :944-951
[10]   Sensitivity of Surveillance Studies for Detecting Asymptomatic and Unsuspected Relapse of High-Risk Neuroblastoma [J].
Kushner, Brian H. ;
Kramer, Kim ;
Modak, Shakeel ;
Cheung, Nai-Kong V. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (07) :1041-1046