| Literature DB >> 32080345 |
Xiao-Peng Tian1,2, Dan Xie1, Wei-Juan Huang3, Shu-Yun Ma1,2, Liang Wang4,5, Yan-Hui Liu6, Xi Zhang7, Hui-Qiang Huang2, Tong-Yu Lin2, Hui-Lan Rao8, Mei Li8, Fang Liu9, Fen Zhang6, Li-Ye Zhong10, Li Liang11, Xiao-Liang Lan12, Juan Li13, Bing Liao14, Zhi-Hua Li15, Qiong-Lan Tang15, Qiong Liang16, Chun-Kui Shao16, Qiong-Li Zhai17, Run-Fen Cheng17, Qi Sun18, Kun Ru17, Xia Gu19, Xi-Na Lin19, Kun Yi20, Yue-Rong Shuang21, Xiao-Dong Chen22, Wei Dong23, Wei Sang24, Cai Sun25, Hui Liu25, Zhi-Gang Zhu26, Jun Rao7, Qiao-Nan Guo27, Ying Zhou28, Xiang-Ling Meng29, Yong Zhu30, Chang-Lu Hu31, Yi-Rong Jiang32, Ying Zhang33, Hong-Yi Gao34, Wen-Jun He35, Zhong-Jun Xia36, Xue-Yi Pan37, Hai Lan38, Guo-Wei Li39, Lu Liu40, Hui-Zheng Bao40, Li-Yan Song3, Tie-Bang Kang1, Qing-Qing Cai41,42.
Abstract
We aimed to establish a discriminative gene-expression-based classifier to predict survival outcomes of T-cell lymphoblastic lymphoma (T-LBL) patients. After exploring global gene-expression profiles of progressive (n = 22) vs. progression-free (n = 28) T-LBL patients, 43 differentially expressed mRNAs were identified. Then an eleven-gene-based classifier was established using LASSO Cox regression based on NanoString quantification. In the training cohort (n = 169), high-risk patients stratified using the classifier had significantly lower progression-free survival (PFS: hazards ratio 4.123, 95% CI 2.565-6.628; p < 0.001), disease-free survival (DFS: HR 3.148, 95% CI 1.857-5.339; p < 0.001), and overall survival (OS: HR 3.790, 95% CI 2.237-6.423; p < 0.001) compared with low-risk patients. The prognostic accuracy of the classifier was validated in the internal testing (n = 84) and independent validation cohorts (n = 360). A prognostic nomogram consisting of five independent variables including the classifier, lactate dehydrogenase levels, ECOG-PS, central nervous system involvement, and NOTCH1/FBXW7 status showed significantly greater prognostic accuracy than each single variable alone. The addition of a five-miRNA-based signature further enhanced the accuracy of this nomogram. Furthermore, patients with a nomogram score ≥154.2 significantly benefited from the BFM protocol. In conclusion, our nomogram comprising the 11-gene-based classifier may make contributions to individual prognosis prediction and treatment decision-making.Entities:
Mesh:
Year: 2020 PMID: 32080345 DOI: 10.1038/s41375-020-0757-5
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528