Bortezomib-based therapy for transplant-ineligible East Asian patients with newly diagnosed mantle-cell lymphoma

被引:3
|
作者
Jin, Jie [1 ,2 ]
Okamoto, Rumiko [3 ]
Yoon, Sung-Soo [4 ]
Shih, Lee-Yung [5 ]
Zhu, Jun [6 ]
Liu, Ting [7 ]
Hong, Xiaonan [8 ]
Pei, Lixia [9 ]
Rooney, Brendan [10 ]
van de Velde, Helgi [11 ]
Huang, Huiqiang [12 ]
机构
[1] Zhejiang Univ, Dept Hematol, Affiliated Hosp 1, Coll Med, Hangzhou, Zhejiang, Peoples R China
[2] Key Lab Hematol Malignancies Diag & Treatment, Hangzhou, Zhejiang, Peoples R China
[3] Komagome Hosp, Dept Chemotherapy, Tokyo Metropolitan Canc & Infect Dis Ctr, Tokyo, Japan
[4] Seoul Natl Univ, Dept Internal Med, Coll Med, Seoul, South Korea
[5] Chang Gung Univ, Div Hematol Oncol, Chang Gung Mem Hosp Linkou, Taoyuan, Taiwan
[6] Peking Univ, Dept Lymphoma, Canc Hosp & Inst, Beijing, Peoples R China
[7] Sichuan Univ, Div Hematol, Dept Internal Med, West China Hosp, Chengdu, Sichuan, Peoples R China
[8] Fudan Univ, Lymphoma & GI Med Oncol, Shanghai Canc Ctr, Shanghai, Peoples R China
[9] Janssen Res & Dev LLC, Raritan, NJ USA
[10] Janssen Res & Dev, High Wycombe, Bucks, England
[11] Millennium Pharmaceut Inc, Oncol Clin Res, Boston, MA USA
[12] Sun Yat Sen Univ, Dept Med Oncol, Canc Ctr, Guangzhou, Guangdong, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2018年 / 11卷
关键词
mantle-cell lymphoma; bortezomib; VR-CAP; R-CHOP; MULTIPLE-MYELOMA; MALIGNANT-LYMPHOMAS; 1ST-LINE TREATMENT; RANDOMIZED-TRIALS; RESPONSE RATES; RITUXIMAB; MULTICENTER; VINCRISTINE; EXPERIENCE; CHOP;
D O I
10.2147/OTT.S150339
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: This subgroup analysis of the LYM-3002 Phase III study (NCT00722137) investigated whether substituting bortezomib for vincristine in frontline R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone) therapy could improve outcomes in East Asian patients with newly diagnosed mantle-cell lymphoma (MCL). Materials and methods: A total of 121 East Asian patients from China, Taiwan, Japan, and the Republic of Korea with stage II-IV MCL who were ineligible or not considered for stem-cell transplantation were enrolled to six to eight 21-day cycles of R-CHOP or VR-CAP (R-CHOP with bortezomib replacing vincristine). Results: The primary end point was progression-free survival. After a median follow-up of 42.4 months, median progression-free survival in East Asian patients was 13.9 (R-CHOP) versus 28.6 (VR-CAP) months (HR 0.7, P=0.157; 43% improvement with VR-CAP). Secondary end points (R-CHOP vs VR-CAP), including complete response rate (47% vs 63%), duration of complete response (median 16.6 vs 46.7 months), and treatment-free interval (median 21 vs 46.5 months), were improved with VR-CAP. VR-CAP was associated with increased but manageable toxicity. The most frequent adverse events were hematologic toxicities. Conclusion: VR-CAP was effective in East Asian patients with newly diagnosed MCL, and could be considered for patients in whom stem-cell transplantation is not an option.
引用
收藏
页码:3869 / 3882
页数:14
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