Detailed Information on Publication Record
2023
Overall survival of patients with cHL who progress after autologous stem cell transplant: results in the novel agent era
DESAI, Sanjal H, Michael A SPINNER, Andrew M EVENS, Alice SYKOROVA, Veronika BACHANOVA et. al.Basic information
Original name
Overall survival of patients with cHL who progress after autologous stem cell transplant: results in the novel agent era
Authors
DESAI, Sanjal H, Michael A SPINNER, Andrew M EVENS, Alice SYKOROVA, Veronika BACHANOVA, Gaurav GOYAL, Brad KAHL, Kathleen DORRITIE, Jacues AZZI, Vaishalee P KENKRE, Cheryl CHANG, Jozef MICHALKA (703 Slovakia, belonging to the institution), Stephen M ANSELL, Brendon FUSCO, Nuttavut SUMRANSUB, Haris HATIC, Raya SABA, Uroosa IBRAHAM, Elyse I HARRIS, Harsh SHAH, Nina WAGNER-JOHNSTON, Sally ARAI, Grzegorz S NOWAKOWSKI, Heidi MOCIKOVA, Deepa JAGADEESH, Kristie A BLUM, Catherine DIEFENBACH, Siddharth IYENGAR, K C RAPPAZZO, Firas BAIDOUN, Yun CHOI, Vit PROCHAZKA, Ranjana H ADVANI and Ivana MICALLEF
Edition
Blood advances, AMSTERDAM, ELSEVIER, 2023, 2473-9529
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30205 Hematology
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 7.500 in 2022
RIV identification code
RIV/00216224:14110/23:00133402
Organization unit
Faculty of Medicine
UT WoS
001134654800001
Keywords in English
cHL; patients; survival; autologous stem cell transplant
Tags
International impact, Reviewed
Změněno: 2/2/2024 09:19, Mgr. Tereza Miškechová
Abstract
V originále
In the pre-novel agent era, the median postprogression overall survival (PPS) of patients with classic Hodgkin lymphoma (cHL) who progress after autologous stem cell transplant (ASCT) was 2 to 3 years. Recently, checkpoint inhibitors (CPI) and brentuximab vedotin (BV) have improved the depth and durability of response in this population. Here, we report the estimate of PPS in patients with relapsed cHL after ASCT in the era of CPI and BV. In this multicenter retrospective study of 15 participating institutions, adult patients with relapsed cHL after ASCT were included. Study objective was postprogression overall survival (PPS), defined as the time from posttransplant progression to death or last follow-up. Of 1158 patients who underwent ASCT, 367 had progressive disease. Median age was 34 years (range, 27-46) and 192 were male. Median PPS was 114.57 months (95% confidence interval [CI], 91-not achieved) or 9.5 years. In multivariate analysis, increasing age, progression within 6 months, and pre-ASCT positive positron emission tomography scan were associated with inferior PPS. When adjusted for these features, patients who received CPI, but not BV, as first treatment for post-ASCT progression had significantly higher PPS than the no CPI/no BV group (hazard ratio, 3.5; 95% CI, 1.6-7.8; P = .001). Receipt of allogeneic SCT (Allo-SCT) did not improve PPS. In the era of novel agents, progressive cHL after ASCT had long survival that compares favorably with previous reports. Patients who receive CPI as first treatment for progression had higher PPS. Receipt to Allo-SCT was not associated with PPS in this population.