Polatuzumab vedotin plus bendamustine and rituximab or obinutuzumab in relapsed/refractory follicular lymphoma: a phase Ib/II study
Jazyk angličtina Země Itálie Médium electronic
Typ dokumentu randomizované kontrolované studie, klinické zkoušky, fáze I, časopisecké články, práce podpořená grantem
Grantová podpora
P30 CA008748
NCI NIH HHS - United States
PubMed
37767550
PubMed Central
PMC10985435
DOI
10.3324/haematol.2023.283557
Knihovny.cz E-zdroje
- MeSH
- bendamustin hydrochlorid škodlivé účinky MeSH
- difúzní velkobuněčný B-lymfom * etiologie MeSH
- folikulární lymfom * farmakoterapie etiologie MeSH
- humanizované monoklonální protilátky * MeSH
- imunokonjugáty * škodlivé účinky MeSH
- lidé MeSH
- monoklonální protilátky * MeSH
- protokoly protinádorové kombinované chemoterapie škodlivé účinky MeSH
- rituximab škodlivé účinky MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze I MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- bendamustin hydrochlorid MeSH
- humanizované monoklonální protilátky * MeSH
- imunokonjugáty * MeSH
- monoklonální protilátky * MeSH
- obinutuzumab MeSH Prohlížeč
- polatuzumab vedotin MeSH Prohlížeč
- rituximab MeSH
Follicular lymphoma (FL) is the most common type of indolent non-Hodgkin lymphoma. Despite treatment advances that have improved outcomes for patients with relapsed or refractory (R/R) FL, many patients still die from progressive disease or treatment-related toxicities. In the phase Ib/II GO29365 study (clinicaltrials.gov 02257567), the safety and efficacy of polatuzumab vedotin plus bendamustine and rituximab (Pola-BR) versus bendamustine and rituximab (BR) alone, and polatuzumab vedotin plus bendamustine and obinutuzumab (Pola-BG) as a single-arm cohort were evaluated in patients with R/R FL. Following the phase Ib safety run-in, patients were randomized 1:1 to receive Pola-BR or BR alone in the phase II stage; a separate non-randomized Pola-BG cohort was examined in the phase Ib/II expansion stage. Primary endpoints included safety and tolerability (phase Ib) and positron emission tomography complete response (PET-CR) rate by independent review committee (phase II). Overall, 112 patients were enrolled (phase Ib safety run-in: Pola-BR, N=6; phase II randomized cohort: Pola-BR, N=39; BR, N=41; phase Ib/II expansion cohort: Pola-BG, N=26). PET-CR rates were 66.7% (phase Ib safety run-in, Pola-BR); 69.2% (phase II randomized, Pola-BR); 63.4% (phase II randomized, BR); and 65.4% (phase Ib/II expansion Pola-BG). There was a higher occurrence of cytopenias with Pola-BR and Pola-BG than with BR; serious adverse events were more frequent with Pola-BR (61.4%) and Pola-BG (46.2%) than with BR (29.3%). Overall, this analysis does not demonstrate a benefit of adding Pola to BR or BG regimens for patients with R/R FL.
BC Cancer Centre for Lymphoid Cancer and The University of British Columbia Vancouver BC
Center for Clinical Haematology Nottingham University Hospitals NHS Trust Nottingham
Charles University General Hospital Prague Czech Republic
City of Hope Medical Centre Duarte CA
Clinical Haematology Monash Health and Monash University Clayton
Genentech Inc South San Francisco CA
Jewish General Hospital Montreal QC
Memorial Sloan Kettering Cancer Center New York NY
Prince of Wales Hospital and University of NSW Sydney
Semmelweiss University Budapest Hungary
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