Increased risk of pseudoprogression among pediatric low-grade glioma patients treated with proton versus photon radiotherapy

被引:26
作者
Ludmir, Ethan B. [1 ]
Mahajan, Anita [1 ,2 ]
Paulino, Arnold C. [1 ,3 ]
Jones, Jeremy Y. [3 ,4 ]
Ketonen, Leena M. [1 ]
Su, Jack M. [3 ]
Grosshans, David R. [1 ]
McAleer, Mary Frances [1 ]
McGovern, Susan L. [1 ]
Lassen-Ramshad, Yasmin A. [5 ]
Adesina, Adekunle M. [3 ]
Dauser, Robert C. [3 ]
Weinberg, Jeffrey S. [1 ]
Chintagumpala, Murali M. [3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[2] Mayo Clin, Rochester, MN USA
[3] Baylor Coll Med, Texas Childrens Canc Ctr, Houston, TX 77030 USA
[4] Nationwide Childrens Hosp, Columbus, OH USA
[5] Aarhus Univ Hosp, Aarhus, Denmark
关键词
low-grade glioma; pediatric malignancy; proton beam therapy; pseudoprogression; radiotherapy; RADIATION-THERAPY; PHASE-II; CHILDREN; CHEMOTHERAPY; TEMOZOLOMIDE; ADOLESCENTS; PROGRESSION; DIAGNOSIS; ONCOLOGY; NECROSIS;
D O I
10.1093/neuonc/noz042
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Pseudoprogression (PsP) is a recognized phenomenon after radiotherapy (RT) for high-grade glioma but is poorly characterized for low-grade glioma (LGG). We sought to characterize PsP for pediatric LGG patients treated with RT, with particular focus on the role of RT modality using photon-based intensity-modulated RT (IMRT) or proton beam therapy (PBT). Methods. Serial MRI scans from 83 pediatric LGG patients managed at 2 institutions between 1998 and 2017 were evaluated. PsP was scored when a progressive lesion subsequently decreased or stabilized for at least a year without therapy. Results. Thirty-two patients (39%) were treated with IMRT, and 51 (61%) were treated with PBT. Median RT dose for the cohort was 50.4 Gy(RBE) (range, 45-59.4 Gy[RBE]). PsP was identified in 31 patients (37%), including 8/32 IMRT patients (25%) and 23/51 PBT patients (45%). PBT patients were significantly more likely to have post-RT enlargement (hazard ratio [HR] 2.15, 95% CI: 1.06-4.38, P = 0.048). RT dose >50.4 Gy(RBE) similarly predicted higher rates of PsP (HR 2.61, 95% CI: 1.20-5.68, P = 0.016). Multivariable analysis confirmed the independent effects of RT modality (P = 0.03) and RT dose (P = 0.01) on PsP incidence. Local progression occurred in 10 patients: 7 IMRT patients (22%) and 3 PBT patients (6%), with a trend toward improved local control for PBT patients (HR 0.34, 95% CI: 0.10-1.18, P = 0.099). Conclusions. These data highlight substantial rates of PsP among pediatric LGG patients, particularly those treated with PBT. PsP should be considered when assessing response to RT in LGG patients within the first year after RT.
引用
收藏
页码:686 / 695
页数:10
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