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Outcome and risk prediction of early progression in patients with extranodal natural killer/T cell lymphoma from the CLCG study

Recently, progression-free survival at 24 months (PFS24) was defined as clinically relevant for patients with extranodal NK/T cell lymphoma. Herein, the clinical data from two independent random cohorts (696 patients each in the primary and validation datasets) were used to develop and validate a ri...

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Detalles Bibliográficos
Autores principales: Li, Jia-Ying, Hou, Xiao-Rong, Chen, Si-Ye, Liu, Xin, Zhong, Qiu-Zi, Qian, Li-Ting, Qiao, Xue-Ying, Wang, Hua, Zhu, Yuan, Cao, Jian-Zhong, Wu, Jun-Xin, Wu, Tao, Zhu, Su-Yu, Shi, Mei, Zhang, Hui-Lai, Zhang, Xi-Mei, Su, Hang, Song, Yu-Qin, Zhu, Jun, Zhang, Yu-Jing, Huang, Hui-Qiang, Wang, Ying, He, Xia, Zhang, Li-Ling, Qu, Bao-Lin, Yang, Yong, Hu, Chen, Deng, Min, Wang, Shu-Lian, Qi, Shu-Nan, Li, Ye-Xiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10444649/
https://www.ncbi.nlm.nih.gov/pubmed/37306711
http://dx.doi.org/10.1007/s00277-023-05311-5
Descripción
Sumario:Recently, progression-free survival at 24 months (PFS24) was defined as clinically relevant for patients with extranodal NK/T cell lymphoma. Herein, the clinical data from two independent random cohorts (696 patients each in the primary and validation datasets) were used to develop and validate a risk index for PFS24 (PFS24-RI), and evaluate its ability to predict early progression. Patients achieving PFS24 had a 5-year overall survival (OS) of 95.8%, whereas OS was only 21.2% in those failing PFS24 (P<0.001). PFS24 was an important predictor of subsequent OS, independent of risk stratification. The proportion of patients achieving PFS24 and 5-year OS rates correlated linearly among risk-stratified groups. Based on multivariate analysis of the primary dataset, the PFS24-RI included five risk factors: stage II or III/IV, elevated lactate dehydrogenase, Eastern Cooperative Oncology Group score ≥2, primary tumor invasion, and extra-upper aerodigestive tract. PFS24-RI stratified the patients into low-risk (0), intermediate-risk (1–2), high-risk (≥3) groups with different prognoses. Harrell’s C-index of PFS24-RI for PFS24 prediction was 0.667 in the validation dataset, indicating a good discriminative ability. PFS24-RI calibration indicated that the actual observed and predicted probability of failing PFS24 agreed well. PFS24-RI provided the probability of achieving PFS24 at an individual patient level. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00277-023-05311-5.