| Literature DB >> 33651099 |
Lale Kostakoglu1, Maurizio Martelli2, Laurie H Sehn3, David Belada4, Angelo-Michele Carella5, Neil Chua6, Eva Gonzalez-Barca7, Xiaonan Hong8, Antonio Pinto9, Yuankai Shi10, Yoichi Tatsumi11, Andrea Knapp12, Federico Mattiello12, Tina Nielsen12, Deniz Sahin12, Gila Sellam12, Mikkel Z Oestergaard12, Umberto Vitolo13, Marek Trněný14.
Abstract
GOYA was a randomized phase 3 study comparing obinutuzumab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) vs standard-of-care rituximab plus CHOP in patients with previously untreated diffuse large B-cell lymphoma (DLBCL). This retrospective analysis of GOYA aimed to assess the association between progression-free survival (PFS) and overall survival (OS) with positron emission tomography (PET)-based complete response (CR) status. Overall, 1418 patients were randomly assigned to receive 8 21-day cycles of obinutuzumab (n = 706) or rituximab (n = 712) plus 6 or 8 cycles of CHOP. Patients received a mandatory fluoro-2-deoxy-d-glucose-PET/computed tomography scan at baseline and end of treatment. After a median follow-up of 29 months, the numbers of independent review committee-assessed PFS and OS events in the entire cohort were 416 (29.3%) and 252 (17.8%), respectively. End-of-treatment PET CR was highly prognostic for PFS and OS according to Lugano 2014 criteria (PFS: hazard ratio [HR], 0.26; 95% confidence interval [CI], 0.19-0.38; P < .0001; OS: HR, 0.12; 95% CI, 0.08-0.17; P < .0001), irrespective of international prognostic index score and cell of origin. In conclusion, the results from this prospectively acquired large cohort corroborated previously published data from smaller sample sizes showing that end-of-treatment PET CR is an independent predictor of PFS and OS and a promising prognostic marker in DLBCL. Long-term survival analysis confirmed the robustness of these data over time. Additional meta-analyses including other prospective studies are necessary to support the substitution of PET CR for PFS as an effective and practical surrogate end point. This trial was registered at www.clinicaltrials.gov as #NCT01287741.Entities:
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Year: 2021 PMID: 33651099 PMCID: PMC7948296 DOI: 10.1182/bloodadvances.2020002690
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529