Ibrutinib and rituximab plus cyclophosphamide, doxorubicin, vincristine and prednisone in patients with previously untreated non‐germinal centre B‐cell‐like diffuse large B‐cell lymphoma: A Chinese subgroup analysis of the phase III PHOENIX trial. Issue 4 (30th August 2022)
- Record Type:
- Journal Article
- Title:
- Ibrutinib and rituximab plus cyclophosphamide, doxorubicin, vincristine and prednisone in patients with previously untreated non‐germinal centre B‐cell‐like diffuse large B‐cell lymphoma: A Chinese subgroup analysis of the phase III PHOENIX trial. Issue 4 (30th August 2022)
- Main Title:
- Ibrutinib and rituximab plus cyclophosphamide, doxorubicin, vincristine and prednisone in patients with previously untreated non‐germinal centre B‐cell‐like diffuse large B‐cell lymphoma: A Chinese subgroup analysis of the phase III PHOENIX trial
- Authors:
- Zhu, Jun
Hong, Xiaonan
Song, Yu Qin
Hodkinson, Brendan
Balasubramanian, Sriram
Wang, Songbai
Zhang, Qingyuan
Shi, Yuankai
Huang, Huiqiang
Zhang, Huilai
Zhu, Yan
Shreeve, Stephen Martin
Sun, Steven
Wang, Ze
Wang, Xiaocan
Fan, Yue
Wilson, Wyndham
Vermeulen, Jessica - Abstract:
- Abstract: In this post hoc subgroup analysis of 200 patients enrolled in China from the phase III PHOENIX trial ( N = 838, NCT01855750), addition of ibrutinib to rituximab plus cyclophosphamide, doxorubicin, vincristine and prednisone (R‐CHOP) did not improve event‐free survival (EFS) versus placebo+R‐CHOP in the intent‐to‐treat (ITT; n = 200, hazard ratio [HR] = 0.83, 95% confidence interval [CI]: 0·509–1.349; p = 0.4495) or activated B‐cell‐like (ABC; n = 141 [based on available gene‐expression profiling data], HR = 0.86, 95% CI: 0.467–1.570; p = 0.6160) subpopulations. However, ibrutinib+R‐CHOP improved EFS (HR = 0·50, 95% CI: 0.251–1.003) and progression‐free survival (PFS; HR = 0.48, 95% CI: 0.228–1.009) versus placebo+R‐CHOP in patients aged <60 but not ≥60 years. Grade ≥3 serious treatment‐emergent adverse events occurred more with ibrutinib+R‐CHOP (45·6% vs. 31·3%). The percentage of patients receiving ≥6 cycles of R‐CHOP was similar across treatment arms in those <60 years. A numerical trend was seen towards improved EFS and PFS with ibrutinib+R‐CHOP versus placebo+R‐CHOP in patients with MYC ‐high/ BCL2 ‐high co‐expression. In this slightly younger Chinese subgroup, ibrutinib+R‐CHOP did not improve EFS in the ITT and ABC subpopulations but improved outcomes with manageable safety in patients <60 years, consistent with overall PHOENIX study outcomes.
- Is Part Of:
- EJHaem. Volume 3:Issue 4(2022)
- Journal:
- EJHaem
- Issue:
- Volume 3:Issue 4(2022)
- Issue Display:
- Volume 3, Issue 4 (2022)
- Year:
- 2022
- Volume:
- 3
- Issue:
- 4
- Issue Sort Value:
- 2022-0003-0004-0000
- Page Start:
- 1154
- Page End:
- 1164
- Publication Date:
- 2022-08-30
- Subjects:
- China -- DLBCL -- ibrutinib -- previously untreated
Hematology -- Periodicals
616.15 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
https://onlinelibrary.wiley.com/journal/26886146 ↗ - DOI:
- 10.1002/jha2.517 ↗
- Languages:
- English
- ISSNs:
- 2688-6146
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24626.xml