2019
DOI: 10.1002/hon.2687
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Event free survival at 24 months is a strong surrogate prognostic endpoint of peripheral T cell lymphoma

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… Show more

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Cited by 12 publications
(6 citation statements)
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References 29 publications
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“…Maurer et al [ 12 ] reported that patients with PTCL who remain event-free at 24 months have longer subsequent OS, even if it is shorter than the survival rate of the general population. Similarly, Wudhikarn et al [ 13 ] showed that EFS24 is an independent predictor of OS for PTCL.…”
Section: Discussionmentioning
confidence: 93%
See 1 more Smart Citation
“…Maurer et al [ 12 ] reported that patients with PTCL who remain event-free at 24 months have longer subsequent OS, even if it is shorter than the survival rate of the general population. Similarly, Wudhikarn et al [ 13 ] showed that EFS24 is an independent predictor of OS for PTCL.…”
Section: Discussionmentioning
confidence: 93%
“…Recent data showed that EFS24 achievement could predict favorable subsequent outcomes in PTCL patients [ 12 , 13 ]. There is no study for predictors of achieving EFS24 in PTCL.…”
Section: Introductionmentioning
confidence: 99%
“…In the neoadjuvant setting, or for hematologic malignancies or other settings where interventions such as drugs, biologics, radiation therapy, or surgery would be used to render a patient free of detectable disease after a well-defined induction/neo-adjuvant period, a logical extension of the validated concept of DFS would be a time-to-event endpoint, with failure defined to be the earliest of the occurrence of: (a) failure to achieve disease-free status locally at the end of the induction and surgery period; (b) detection of recurrence of disease (either local post induction or distal) by CT; or (c) death. 6,[11][12][13] Figure 1 provides a graphical summary of this definition of EFS. This composite endpoint, which is a novel formulation of DFS applied in the neoadjuvant setting, seems particularly well suited to be a key measure of efficacy for therapeutic strategies in settings such as LAPC that may involve neoadjuvant treatment followed by surgery, with the goal of rendering such patients disease-free (locally and systemically).…”
Section: Formulating a Novel Event-free Survival Endpoint For Lapcmentioning
confidence: 99%
“…In the neoadjuvant setting, or for hematologic malignancies or other settings where interventions such as drugs, biologics, radiation therapy, or surgery would be used to render a patient free of detectable disease after a well-defined induction/neo-adjuvant period, a logical extension of the validated concept of DFS would be a time-to-event endpoint, with failure defined to be the earliest of the occurrence of: (a) failure to achieve disease-free status locally at the end of the induction and surgery period; (b) detection of recurrence of disease (either local post induction or distal) by CT; or (c) death. 6,1113 Figure 1 provides a graphical summary of this definition of EFS.…”
Section: Formulating a Novel Event-free Survival Endpoint For Lapcmentioning
confidence: 99%
“…In Asia, the prevalence of the three most common T-cell lymphomas is quite different, with a nearly equal distribution of PTCL-NOS, NK/T-cell lymphomas, and adult T-cell leukemia / lymphoma (ATLL). The latter two are up to twenty-five times more frequent in Asia than in North America or Europe [15][16][17][18].…”
Section: Introductionmentioning
confidence: 97%