Table 2.
Trial | Regimen | Population | Design | Notes |
---|---|---|---|---|
NCT04301076 | lenalidomide + EPOCH | untreated acute, lymphoma, or poor-risk chronic subtype ATL | phase I | NCI sponsored, estimated completion 2023 |
NCT03264131 | BV-CHEP | untreated acute, lymphoma, or poor-risk chronic subtype ATL | pilot/phase I | interim results,33 showing 75% ORR in 8 patients |
NCT04502446 | CTX130 | R/R T-cell lymphoma, including ATL | phase I | anti-CD70 allogeneic CRISPR-Cas9-engineered T cells, interim results91 |
recombinant human IL-15 (rhIL-15) combinations (NCT02689453, NCT04185220) | rhIL-15 + mogamulizumab or alemtuzumab | R/R T-cell lymphoma, including ATL | phase I | NCI sponsored |
NCT04848046 | NK cell therapy + mogamulizumab | R/R ATL or CTCL | phase I | IL-21 expanded, off-the-shelf NK cell therapy |
NCT02737046 | belinostat + ZDV +/− IFN | aggressive ATL with persistent circulating disease after prior chemotherapy or ZDV/IFN | phase II | interim results of 6 patients reported, potential to achieve complete molecular CR92 |
NCT04703192 (VALENTINE-PTCL01) | valemetostat | R/R T-cell lymphoma, including ATL | phase II | enrollment complete, registration study |
JCOG1111C | IFN/AZT versus watchful waiting | indolent ATL (symptomatic smoldering or chronic w/o unfavorable features) | open-label, randomized phase III | led by Japanese Clinical Oncology Group (JCOG) |
BV, brentuximab vedotin; CR, complete response; CTCL, cutaneous T-cell lymphoma; EPOCH, etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin; IFN, interferon; NCI, National Cancer Institute; NK, natural killer; ORR, objective response rate; R/R, relapsed/refractory; ZDV, zidovudine.