@article{4c88ab1b84a94aa2b27cbb49a8cdfa6b,
title = "International assessment of event-free survival at 24 months and subsequent survival in peripheral T-cell lymphoma",
abstract = "Purpose: Peripheral T-cell lymphomas (PTCLs) have aggressive clinical behavior. We have previously shown that event-free survival (EFS) at 24 months (EFS24) is a clinically useful end point in diffuse large B-cell lymphoma. Here, we assess EFS24 and subsequent overall survival (OS) in large, multinational PTCL cohorts. Patients and Methods: Patients with systemic PTCL newly diagnosed from 2000 to 2012 and treated with curative intent were included from the United States and Sweden (initial cohorts) and from Canada (replication cohort). EFS was defined as time from date of diagnosis to progression after primary treatment, retreatment, or death. Subsequent OS was measured after achieving EFS24 or from the time of progression if it occurred within 24 months. OS rates were compared with the age-, sex-, and country-matched general population. Results: Seven hundred seventy-five patients were included in the study (the median age at diagnosis was 64 years; 63% were men). Results were similar in the initial and replication cohorts, and a combined analysis was undertaken. Sixty-four percent of patients progressed within the first 24 months and had a median OS of only 4.9 months (5-year OS, 11%). In contrast, median OS after achieving EFS24 was not reached (5-year OS, 78%), although relapses within 5 years of achieving EFS24 occurred in 23% of patients. Superior outcomes after achieving EFS24 were observed in younger patients (≤ 60 years of age: 5-year OS, 91%). Conclusion: EFS24 stratifies subsequent outcome in PTCL. Patients with PTCL with primary refractory disease or early relapse have extremely poor survival. However, more than one third of patients with PTCL remain in remission 2 years after diagnosis with encouraging subsequent OS, especially in younger patients. These marked differences in outcome suggest that EFS24 has utility for patient counseling, study design, and risk stratification in PTCL.",
author = "Maurer, {Matthew J.} and Fredrik Ellin and Line Srour and Mats Jerkeman and Bennani, {N. Nora} and Connors, {Joseph M.} and Slack, {Graham W.} and Smedby, {Karin E.} and Ansell, {Stephen M.} and Link, {Brian K.} and Cerhan, {James R.} and Thomas Relander and Savage, {Kerry J.} and Feldman, {Andrew L.}",
note = "Funding Information: An international cohort of patients with newly diagnosed PTCL treated with curative-intent combination chemotherapy regimens was assembled from the University of Iowa/Mayo Clinic Specialized Program of Research Excellence Molecular Epidemiology Resource (MER) and the Swedish Lymphoma Registry (SWE). Subtypes included were ALK-negative ALCL; AITL; PTCL NOS; enteropathy-associated T-cell lymphoma; extranodal NK/T-cell lymphoma, nasal type; and hepatosplenic T-cell lymphoma. Precursor T-cell malignancies, primary cutaneous lymphomas, leukemic T-cell neoplasms, and ALK-positive ALCL were excluded. Demographic and clinical data were recorded, including International Prognostic Index (IPI) risk factors. To validate the findings and increase sample size for subset analyses, a replication cohort was assembled from the BC Cancer Agency (BCCA). After confirming initial results, the cohorts were pooled for subsequent analyses. This study was reviewed and approved by the Human Subjects Institutional Review Boards at Mayo Clinic and the University of Iowa; the Regional Ethical Board, Lund, Sweden; and the University of British Columbia-BCCA Research Ethics Board. Research was conducted in accordance with the Declaration of Helsinki. Funding Information: Supported by Grants No. P50 CA97274 (University of Iowa/Mayo Clinic Lymphoma Specialized Programs of Research Excellence), R01 CA177734 (to A.L.F.), P30 CA15083 (Mayo Clinic Cancer Center), and U01 CA195568 (Lymphoma Epidemiology of Outcomes Cohort) from the National Cancer Institute and by the Terry Fox Research Institute and the British Columbia Cancer Foundation (BC Cancer Agency). Publisher Copyright: {\textcopyright} 2017 by American Society of Clinical Oncology.",
year = "2017",
month = dec,
day = "20",
doi = "10.1200/JCO.2017.73.8195",
language = "English (US)",
volume = "35",
pages = "4019--4026",
journal = "Journal of Clinical Oncology",
issn = "0732-183X",
publisher = "American Society of Clinical Oncology",
number = "36",
}