| Literature DB >> 33710337 |
Reid W Merryman1, Robert A Redd2, Taiga Nishihori3, Julio Chavez3, Yago Nieto4, Justin M Darrah5,6, Uttam Rao7, Michael T Byrne7, David A Bond8, Kami J Maddocks8, Michael A Spinner9, Ranjana H Advani9, Hatcher J Ballard10, Jakub Svoboda10, Anurag K Singh11, Joseph P McGuirk11, Dipenkumar Modi12, Radhakrishnan Ramchandren13, Jason Romancik14, Jonathon B Cohen14, Matthew J Frigault15, Yi-Bin Chen15, Anthony V Serritella16, Justine Kline16, Stephen Ansell17, Sunita Nathan18, Maryam Rahimian19, Robin M Joyce19, Mansi Shah20, Kevin A David20, Steven Park21, Anne W Beaven22, Alma Habib23, Veronika Bachanova23, Shazia Nakhoda24, Nadia Khan24, Ryan C Lynch25, Stephen D Smith25, Vincent T Ho1, Ann LaCasce1, Philippe Armand1, Alex F Herrera5.
Abstract
Autologous stem cell transplantation (ASCT) can be curative for patients with relapsed/refractory Hodgkin lymphoma (HL). Based on studies suggesting that anti-PD-1 monoclonal antibodies (mAbs) can sensitize patients to subsequent chemotherapy, we hypothesized that anti-PD-1 therapy before ASCT would result in acceptable outcomes among high-risk patients who progressed on or responded insufficiently to ≥1 salvage regimen, including chemorefractory patients who are traditionally considered poor ASCT candidates. We retrospectively identified 78 HL patients who underwent ASCT after receiving an anti-PD-1 mAb (alone or in combination) as third-line or later therapy across 22 centers. Chemorefractory disease was common, including 42 patients (54%) refractory to ≥2 consecutive systemic therapies immediately before anti-PD-1 treatment. Fifty-eight (74%) patients underwent ASCT after anti-PD-1 treatment, while 20 patients (26%) received additional therapy after PD-1 blockade and before ASCT. Patients received a median of 4 systemic therapies (range, 3-7) before ASCT, and 31 patients (41%) had a positive pre-ASCT positron emission tomography (PET) result. After a median post-ASCT follow-up of 19.6 months, the 18-month progression-free survival (PFS) and overall survival were 81% (95% CI, 69-89) and 96% (95% confidence interval [CI], 87-99), respectively. Favorable outcomes were observed for patients who were refractory to 2 consecutive therapies immediately before PD-1 blockade (18-month PFS, 78%), had a positive pre-ASCT PET (18-month PFS, 75%), or received ≥4 systemic therapies before ASCT (18-month PFS, 73%), while PD-1 nonresponders had inferior outcomes (18-month PFS, 51%). In this high-risk cohort, ASCT after anti-PD-1 therapy was associated with excellent outcomes, even among heavily pretreated, previously chemorefractory patients.Entities:
Mesh:
Year: 2021 PMID: 33710337 PMCID: PMC7993097 DOI: 10.1182/bloodadvances.2020003556
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529