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Title: | Event free survival at 24 months is a strong surrogate prognostic endpoint of peripheral T cell lymphoma |
Authors: | Wudhikarn K. Bunworasate U. Julamanee J. Lekhakula A. Ekwattanakit S. Khuhapinant A. Niparuck P. Chuncharunee S. Numbenjapon T. Prayongratana K. Kanitsap N. Wongkhantee S. Makruasri N. Wong P. Norasetthada L. Nawarawong W. Sirijerachai C. Chansung K. Suwanban T. Praditsuktavorn P. Intragumtornchai T. on behalf of Thai Lymphoma Study Group |
Keywords: | cyclophosphamide cyclophosphamide plus doxorubicin plus etoposide plus prednisolone plus vincristine dexamethasone doxorubicin lactate dehydrogenase prednisolone tumor marker vincristine antineoplastic agent advanced cancer aged Article blood toxicity cancer combination chemotherapy cancer mortality cancer prognosis cancer regression cancer survival controlled study disease severity drug dose reduction event free survival febrile neutropenia female human major clinical study male overall survival peripheral T cell lymphoma priority journal standardized mortality ratio systemic disease Thailand therapy delay adult disease free survival health survey Kaplan Meier method middle aged mortality peripheral T cell lymphoma prognosis treatment outcome Adult Antineoplastic Combined Chemotherapy Protocols Disease-Free Survival Female Humans Kaplan-Meier Estimate Lymphoma, T-Cell, Peripheral Male Middle Aged Prognosis Progression-Free Survival Public Health Surveillance Thailand Treatment Outcome |
Issue Date: | 2019 |
Abstract: | Event free survival at 24 months (EFS24) has been described as a powerful predictor for outcome in several subtypes of B cell lymphoma. However, it was limitedly described in T cell lymphoma. We explored the implication of EFS24 as a predictor marker for peripheral T cell lymphoma (PTCL). We reviewed 293 systemic PTCL patients at 13 nationwide major university hospitals in Thailand from 2007 to 2014. The median event free survival (EFS) and overall survival (OS) of PTCL patients in our cohort was 16.3 and 27.7 months with corresponding 2-year EFS and 2-year OS of 45.8% and 51.9%, respectively. A total of 118 patients achieved EFS24 (no events during the first 24 mo). Patients who achieved EFS24 had better OS than patients who did not (2-y OS 92% vs 18.8%; HR, 0.1; P <.001). The standardized mortality ratio of patients achieving EFS24 was 18.7 (95% CI, 14.6-22.8). Multivariable analysis demonstrated performance status, histologic subtype, remission status, and EFS24 achievement as independent predictors for OS. Our study affirmed the value of EFS24 as a powerful prognostic factor for PTCL. Further validation in prospective study setting is warranted. ©2019 John Wiley & Sons, Ltd. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/12248 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85075039642&doi=10.1002%2fhon.2687&partnerID=40&md5=2e82dd1fc922104cdac60ff7696daf52 |
ISSN: | 2780232 |
Appears in Collections: | Scopus 1983-2021 |
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