TY - JOUR
T1 - Overall survival of patients with cHL who progress after autologous stem cell transplant
T2 - results in the novel agent era
AU - Desai, Sanjal H.
AU - Spinner, Michael A.
AU - Evens, Andrew M.
AU - Sykorova, Alice
AU - Bachanova, Veronika
AU - Goyal, Gaurav
AU - Kahl, Brad
AU - Dorritie, Kathleen
AU - Azzi, Jacues
AU - Kenkre, Vaishalee P.
AU - Chang, Cheryl
AU - Michalka, Jozef
AU - Ansell, Stephen M.
AU - Fusco, Brendon
AU - Sumransub, Nuttavut
AU - Hatic, Haris
AU - Saba, Raya
AU - Ibrahim, Uroosa
AU - Harris, Elyse I.
AU - Shah, Harsh
AU - Wagner-Johnston, Nina
AU - Arai, Sally
AU - Nowakowski, Grzegorz S.
AU - Mocikova, Heidi
AU - Jagadeesh, Deepa
AU - Blum, Kristie A.
AU - Diefenbach, Catherine
AU - Iyengar, Siddharth
AU - Rappazzo, K. C.
AU - Baidoun, Firas
AU - Choi, Yun
AU - Prochazka, Vit
AU - Advani, Ranjana H.
AU - Micallef, Ivana
N1 - Publisher Copyright:
© 2023 by The American Society of Hematology.
PY - 2023/12/12
Y1 - 2023/12/12
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85179822809&partnerID=8YFLogxK
U2 - 10.1182/bloodadvances.2023011205
DO - 10.1182/bloodadvances.2023011205
M3 - Article
C2 - 37729621
AN - SCOPUS:85179822809
SN - 2473-9529
VL - 7
SP - 7295
EP - 7303
JO - Blood Advances
JF - Blood Advances
IS - 23
ER -