机构:[1]Department of Hematology, The First Affiliated Hospital of Zhejiang University College of Medicine, Hangzhou, Zhejiang, China浙江大学医学院附属第一医院[2]Key Laboratory of Hematologic Malignancies, Diagnosis and Treatment, Hangzhou, Zhejiang, China[3]Department of Chemotherapy, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan[4]Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea[5]Division of Hematology–Oncology, Chang Gung Memorial Hospital-Linkou, Chang Gung University, Taoyuan, Taiwan[6]Department of Lymphoma, Peking University Cancer Hospital & Institute, Beijing, China[7]Division of Hematology, Department of Internal Medicine, West China Hospital, Sichuan University, Chengdu, Sichuan, China四川大学华西医院[8]Lymphoma and GIGI Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China[9]Janssen Research & Development, LLC , Raritan, NJ, USA[10]Janssen Research & Development, High Wycombe, Buckinghamshire, UK[11]Oncology Clinical Research, Millennium Pharmaceuticals, Inc., Boston, MA, USA[12]Department of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China
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.
基金:
Janssen Global Services LLC and Millennium (Takeda Oncology)
第一作者机构:[1]Department of Hematology, The First Affiliated Hospital of Zhejiang University College of Medicine, Hangzhou, Zhejiang, China[2]Key Laboratory of Hematologic Malignancies, Diagnosis and Treatment, Hangzhou, Zhejiang, China
通讯作者:
通讯机构:[12]Department of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China[*1]Ward 4, Internal Medicine, Sun Yat-sen University Cancer Center, 651 East Dongfeng Road, Guangzhou, Guangdong 510060, China
推荐引用方式(GB/T 7714):
Jin Jie,Okamoto Rumiko,Yoon Sung-Soo,et al.Bortezomib-based therapy for transplant-ineligible East Asian patients with newly diagnosed mantle-cell lymphoma[J].OncoTargets and therapy.2018,11:3869-3882.doi:10.2147/OTT.S150339.
APA:
Jin, Jie,Okamoto, Rumiko,Yoon, Sung-Soo,Shih, Lee-Yung,Zhu, Jun...&Huang, Huiqiang.(2018).Bortezomib-based therapy for transplant-ineligible East Asian patients with newly diagnosed mantle-cell lymphoma.OncoTargets and therapy,11,
MLA:
Jin, Jie,et al."Bortezomib-based therapy for transplant-ineligible East Asian patients with newly diagnosed mantle-cell lymphoma".OncoTargets and therapy 11.(2018):3869-3882