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

Authors :
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
Source :
Annals of Hematology; Sep2023, Vol. 102 Issue 9, p2459-2469, 11p
Publication Year :
2023

Abstract

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09395555
Volume :
102
Issue :
9
Database :
Complementary Index
Journal :
Annals of Hematology
Publication Type :
Academic Journal
Accession number :
170063081
Full Text :
https://doi.org/10.1007/s00277-023-05311-5