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Romidepsin Plus CHOP Versus CHOP in Patients With Previously Untreated Peripheral T-Cell Lymphoma: Results of the Ro-CHOP Phase III Study (Conducted by LYSA)

Authors
Bachy, E.[Bachy, E.]Camus, V.[Camus, V.]Thieblemont, C.[Thieblemont, C.]Sibon, D.[Sibon, D.]Casasnovas, R.-O.[Casasnovas, R.-O.]Ysebaert, L.[Ysebaert, L.]Damaj, G.[Damaj, G.]Guidez, S.[Guidez, S.]Pica, G.M.[Pica, G.M.]Kim, W.S.[Kim, W.S.]Lim, S.T.[Lim, S.T.]André, M.[André, M.]García-Sancho, A.M.[García-Sancho, A.M.]Penarrubia, M.J.[Penarrubia, M.J.]Staber, P.B.[Staber, P.B.]Trotman, J.[Trotman, J.]Hüttmann, A.[Hüttmann, A.]Stefoni, V.[Stefoni, V.]Re, A.[Re, A.]Gaulard, P.[Gaulard, P.]Delfau-Larue, M.-H.[Delfau-Larue, M.-H.]de, Leval L.[de, Leval L.]Meignan, M.[Meignan, M.]Li, J.[Li, J.]Morschhauser, F.[Morschhauser, F.]Delarue, R.[Delarue, R.]
Issue Date
20-Jan-2022
Publisher
NLM (Medline)
Citation
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, v.40, no.3, pp.242 - 251
Indexed
SCIE
SCOPUS
Journal Title
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Volume
40
Number
3
Start Page
242
End Page
251
URI
https://scholarx.skku.edu/handle/2021.sw.skku/96663
DOI
10.1200/JCO.21.01815
ISSN
0732-183X
Abstract
PURPOSE: Romidepsin, a histone deacetylase inhibitor, has demonstrated activity in relapsed or refractory peripheral T-cell lymphoma (PTCL) as a single agent. Cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) therapy is widely used as first-line treatment of PTCL; however, it has limited efficacy. Results from a phase Ib and II study showed the feasibility of combining romidepsin with CHOP (Ro-CHOP). METHODS: This study is a randomized phase III study of Ro-CHOP versus CHOP in adult patients with previously untreated PTCL. All patients received CHOP in 3-week cycles for six cycles. Romidepsin, 12 mg/m2, was administered intravenously over a 4-hour period on days 1 and 8 of each 3-week cycle for six cycles. The primary end point was progression-free survival (PFS) according to International Working Group 1999 criteria. RESULTS: Between January 2013 and December 2017, 421 patients were enrolled (Ro-CHOP, n = 211; CHOP, n = 210). The median PFS for Ro-CHOP versus CHOP was 12.0 months (95% CI, 9.0 to 25.8) versus 10.2 months (95% CI, 7.4 to 13.2) with a hazard ratio of 0.81 (P = .096). In the Ro-CHOP versus CHOP arms, the median overall survival was 51.8 versus 42.9 months and the objective response rate was 63% versus 60% with complete response plus unconfirmed complete response rates of 41% versus 37% (P > .1 in all comparisons), respectively. Grade 3 or 4 treatment-emergent adverse events occurring in ≥ 30% of patients in the Ro-CHOP arm included thrombocytopenia (50% v 10% in the Ro-CHOP v CHOP arms, respectively), neutropenia (49% v 33%), anemia (47% v 17%), and leukopenia (32% v 20%). CONCLUSION: The addition of romidepsin to CHOP did not improve PFS, response rates, nor overall survival and increased the frequency for grade ≥ 3 treatment-emergent adverse events. Ro-CHOP does not represent a significant advance in the standard of care for patients with previously untreated PTCL.
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