Literature DB >> 35505116

Determining the suitability of definitive radiation therapy in patients with metastatic nasopharyngeal carcinoma based on PET/CT: a large cohort study.

Zhen-Chong Yang1,2, Ying-Ying Hu1,3, Li-Ting Liu1,2, Shan-Shan Guo1,2, Chao-Chao Du1,2, Yu-Jing Liang1,2, Qiu-Yan Chen4,5, Hai-Qiang Mai6,7.   

Abstract

OBJECTIVES: To determine patients with de novo metastatic nasopharyngeal carcinoma (mNPC) who would benefit from receiving definitive radiation therapy (DRT) along with their pre-existing palliative chemotherapy (PCT) by evaluating their post-PCT Deauville scores and EBV DNA.
METHODS: A total of 570 mNPC patients, treated with PCT or PCT+DRT, were studied. EBV DNA levels, along with post-PCT Deauville scores, were used to stratify risk based on the recursive partitioning analysis (RPA).
RESULTS: Significant differences were observed in the survival rates of patients with Deauville scores of 1-3 and 4-5 (2-year progression-free survival (PFS): 23.4% versus 8.5%, p < 0.001; 2-year overall survival (OS): 56.8% versus 18.8%, p < 0.001). RPA yielded three distinct groups in the increasing order of risk (Deauville scores of all RPA I-II were within the range of 1-3): (1) RPA I: EBV DNA levels at a pretreatment concentration ≤ 4000 copies/mL and undetectable post-PCT; (2) RPA II: EBV DNA levels either at a pretreatment concentration > 4000 copies/mL or at a pretreatment concentration ≤ 4000 copies/mL and detectable post-PCT; (3) RPA III: Deauville scores 4-5. While patients in RPA I and RPA II had significantly PFS rates when treated with PCT+DRT than when treated with PCT alone (RPA I: 72.7% versus 13.4%, RPA II: 37.8% versus 6.3%), those in RPA III did not experience such PFS benefits (6.5% versus 9.7%).
CONCLUSION: PCT+DRT might improve the survival rates in mNPC patients in the low- and mid-risk strata but not those of patients in the high-risk strata. KEY POINTS: We use the Deauville scores and the concentrations of the Epstein-Barr virus (EBV) DNA to determine those patients with de novo metastatic NPC who would benefit from radiation therapy.
© 2022. The Author(s), under exclusive licence to European Society of Radiology.

Entities:  

Keywords:  Deauville score; Nasopharyngeal carcinoma; Radiation therapy

Year:  2022        PMID: 35505116     DOI: 10.1007/s00330-022-08814-3

Source DB:  PubMed          Journal:  Eur Radiol        ISSN: 0938-7994            Impact factor:   5.315


  4 in total

1.  Not Yet Time to Abandon the Deauville Criteria in Diffuse Large B-Cell Lymphoma.

Authors:  Sally F Barrington; Jakoba J Eertink; Henrika C W de Vet; N George Mikhaeel; Otto S Hoekstra; Josee M Zijlstra
Journal:  J Nucl Med       Date:  2021-04-23       Impact factor: 11.082

2.  Prognostic factors in nasopharyngeal carcinoma with synchronous liver metastasis: a retrospective study for the management of treatment.

Authors:  Yun-Ming Tian; Lei Zeng; Feng-Hua Wang; Shuai Liu; Ying Guan; Tai-Xiang Lu; Fei Han
Journal:  Radiat Oncol       Date:  2013-11-19       Impact factor: 3.481

3.  Risk stratification for nasopharyngeal carcinoma: a real-world study based on locoregional extension patterns and Epstein-Barr virus DNA load.

Authors:  Lu-Lu Zhang; Meng-Yao Huang; Ke-Xin Wang; Di Song; Ting Wang; Li-Yue Sun; Jian-Yong Shao
Journal:  Ther Adv Med Oncol       Date:  2020-06-12       Impact factor: 8.168

4.  Prognostic Value of 2-Deoxy-2-[18F]fluoro-D-glucose Positron Emission Tomography/Computed Tomography after Autologous Hematopoietic Stem Cell Transplantation in Lymphoma Using Deauville Scores.

Authors:  Na Dai; Yeye Zhou; Shengming Deng; Shibiao Sang; Yiwei Wu
Journal:  Contrast Media Mol Imaging       Date:  2021-04-15       Impact factor: 3.161

  4 in total
  1 in total

1.  Prognostic value of mesorectal package area in patients with locally advanced rectal cancer following neoadjuvant chemoradiotherapy: A retrospective cohort study.

Authors:  Bingjie Guan; Xinmin Huang; Huang Xia; Guoxian Guan; Benhua Xu
Journal:  Front Oncol       Date:  2022-10-03       Impact factor: 5.738

  1 in total

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