Radiotherapy for Atypical Teratoid/=Rhabdoid Tumor (ATRT) on the Pediatric Proton/Photon Consortium Registry (PPCR)

被引:2
|
作者
Roehrig, Andrew [1 ]
Indelicato, Daniel J. [2 ]
Paulino, Arnold C. [3 ]
Ermoian, Ralph [4 ]
Hartsell, William [5 ]
Perentesis, John [6 ]
Hill-Kayser, Christine [7 ]
Lee, Jae Y. [8 ]
Laack, Nadia N. [9 ]
Mangona, Victor [10 ]
MacEwan, Iain [11 ]
Eaton, Bree R. [12 ]
Gallotto, Sara [13 ]
Bajaj, Benjamin V. M. [13 ]
Aridgides, Paul D. [1 ]
Yock, Torunn I. [13 ]
机构
[1] SUNY Upstate Med Univ, 750 E Adams St, Syracuse, NY 13210 USA
[2] Univ Florida, Gainesville, FL USA
[3] Univ Texas MD Anderson Canc Ctr, Houston, TX USA
[4] Univ Washington, Seattle, WA USA
[5] Northwestern Med Chicago Proton Ctr, Warrenville, IL USA
[6] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH USA
[7] Univ Penn, Philadelphia, PA USA
[8] Princeton Radiat Oncol, ProCure Proton Therapy Ctr, Somerset, NJ USA
[9] Mayo Clin, Rochester, MN USA
[10] Texas Ctr Proton Therapy, Irving, TX USA
[11] Univ Calif San Diego, San Diego, CA USA
[12] Emory Univ, Proton Ctr, Atlanta, GA USA
[13] Massachusetts Gen Hosp, Boston, MA USA
关键词
ATRT; Atypical teratoid; rhabdoid tumor; Brain; Pediatric; Proton; Radiotherapy; CENTRAL-NERVOUS-SYSTEM; TERATOID RHABDOID TUMORS; HIGH-DOSE CHEMOTHERAPY; PROGENITOR-CELL RESCUE; MALIGNANT BRAIN-TUMORS; TERATOID/RHABDOID TUMOR; INTENSIVE CHEMOTHERAPY; SURVIVAL OUTCOMES; CHILDREN; THERAPY;
D O I
10.1007/s11060-023-04296-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeAtypical teratoid/rhabdoid tumors (ATRT) of the central nervous system (CNS) are rare tumors with a poor prognosis and variable use of either focal or craniospinal (CSI) radiotherapy (RT). Outcomes on the prospective Pediatric Proton/Photon Consortium Registry (PPCR) were evaluated according to RT delivered.MethodsPediatric patients receiving RT were prospectively enrolled on PPCR to collect initial patient, disease, and treatment factors as well as provide follow-up for patient outcomes. All ATRT patients with evaluable data were included. Kaplan-Meier analyses with log-rank p-values and cox proportional hazards regression were performed.ResultsThe PPCR ATRT cohort includes 68 evaluable ATRT patients (median age 2.6 years, range 0.71-15.40) from 2012 to 2021. Median follow-up was 40.8 months (range 3.4-107.7). Treatment included surgery (65% initial gross total resection or GTR), chemotherapy (60% with myeloablative therapy including stem cell rescue) and RT. For patients with M0 stage (n = 60), 50 (83%) had focal RT and 10 (17%) had CSI. Among patients with M + stage (n = 8), 3 had focal RT and 5 had CSI. Four-year overall survival (OS, n = 68) was 56% with no differences observed between M0 and M + stage patients (p = 0.848). Local Control (LC) at 4 years did not show a difference for lower primary dose (50-53.9 Gy) compared to >= 54 Gy (73.3% vs 74.7%, p = 0.83). For patients with M0 disease, four-year OS for focal RT was 54.6% and for CSI was 60% (Hazard Ratio 1.04, p = 0.95. Four-year event free survival (EFS) among M0 patients for focal RT was 45.6% and for CSI was 60% (Hazard Ratio 0.71, p = 0.519). For all patients, the 4-year OS comparing focal RT with CSI was 54.4% vs 60% respectively (p = 0.944), and the 4-year EFS for focal RT or CSI was 42.8% vs 51.4% respectively (p = 0.610).ConclusionThe PPCR ATRT cohort found no differences in outcomes according to receipt of either higher primary dose or larger RT field (CSI). However, most patients were M0 and received focal RT. A lower primary dose (50.4 Gy), regardless of patient age, is appealing for further study as part of multi-modality therapy.
引用
收藏
页码:353 / 362
页数:10
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