First‐ versus second‐generation Bruton tyrosine kinase inhibitors in Waldenström's Macroglobulinemia: A systematic review and meta‐analysis
暂无分享,去创建一个
M. Zangari | F. van Rhee | H. Abushukair | S. Thanendrarajan | C. Schinke | Samer Al Hadidi | A. Qarqash | S. Syaj | O. Ababneh
[1] M. Dimopoulos,et al. Ibrutinib Plus Rituximab Versus Placebo Plus Rituximab for Waldenström's Macroglobulinemia: Final Analysis From the Randomized Phase III iNNOVATE Study , 2021, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[2] S. Treon,et al. Long-term follow-up of ibrutinib monotherapy in treatment-naive patients with Waldenstrom macroglobulinemia , 2021, Leukemia.
[3] M. Dimopoulos,et al. Single-Agent Ibrutinib for Rituximab-Refractory Waldenström Macroglobulinemia: Final Analysis of the Substudy of the Phase III InnovateTM Trial , 2021, Clinical Cancer Research.
[4] Shu Cheng,et al. A Phase II Trial of the Bruton Tyrosine-Kinase Inhibitor Zanubrutinib (BGB-3111) in Patients with Relapsed/Refractory Waldenström Macroglobulinemia , 2021, Clinical Cancer Research.
[5] E. Mayo-Wilson,et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews , 2021, BMJ.
[6] M. Kersten,et al. WhiMSICAL: A global Waldenström's Macroglobulinemia patient‐derived data registry capturing treatment and quality of life outcomes , 2021, American journal of hematology.
[7] M. Gertz. Waldenström macroglobulinemia: 2021 update on diagnosis, risk stratification, and management , 2020, American journal of hematology.
[8] M. Dimopoulos,et al. Zanubrutinib for the treatment of MYD88 wild-type Waldenström macroglobulinemia: a substudy of the phase 3 ASPEN trial. , 2020, Blood advances.
[9] C. Buske,et al. CXCR4 in Waldenström’s Macroglobulinema: chances and challenges , 2020, Leukemia.
[10] H. Heslop,et al. Assessment and reporting of quality-of-life measures in pivotal clinical trials of hematological malignancies. , 2020 .
[11] R. Advani,et al. Long-Term Follow-Up of Ibrutinib Monotherapy in Symptomatic, Previously Treated Patients With Waldenström Macroglobulinemia , 2020, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[12] E. Mayo-Wilson,et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews , 2020, BMJ.
[13] M. Dimopoulos,et al. A RANDOMIZED PHASE 3 TRIAL OF ZANUBRUTINIB VERSUS IBRUTINIB IN SYMPTOMATIC WALDENSTRÖM MACROGLOBULINEMIA:THE ASPEN STUDY. , 2020, Blood.
[14] W. Novotny,et al. Zanubrutinib for the treatment of patients with Waldenström macroglobulinemia: three years of follow-up. , 2020, Blood.
[15] S. Iida,et al. A multicenter, open‐label, phase II study of tirabrutinib (ONO/GS‐4059) in patients with Waldenström’s macroglobulinemia , 2020, Cancer science.
[16] W. Novotny,et al. Three-year follow-up of treatment-naïve and previously treated patients with Waldenström macroglobulinemia (WM) receiving single-agent zanubrutinib. , 2020 .
[17] S. Treon,et al. Genomic Landscape of Waldenström Macroglobulinemia and Its Impact on Treatment Strategies. , 2020, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[18] Sun Ku Lee,et al. Acalabrutinib monotherapy in patients with Waldenström macroglobulinemia: a single-arm, multicentre, phase 2 study. , 2019, The Lancet. Haematology.
[19] S. Treon,et al. CXCR4 mutation subtypes impact response and survival outcomes in patients with Waldenström macroglobulinaemia treated with ibrutinib , 2019, British journal of haematology.
[20] Natalie S Blencowe,et al. RoB 2: a revised tool for assessing risk of bias in randomised trials , 2019, BMJ.
[21] M. Dimopoulos,et al. Patient-reported outcomes (PROs) with ibrutinib-rituximab in Waldenström macroglobulinemia (WM): Results from iNNOVATE. , 2019, Journal of Clinical Oncology.
[22] M. Palomba,et al. First-Generation and Second-Generation Bruton Tyrosine Kinase Inhibitors in Waldenström Macroglobulinemia. , 2018, Hematology/oncology clinics of North America.
[23] R. Advani,et al. Long-Term Follow-up of Previously Treated Patients Who Received Ibrutinib for Symptomatic Waldenstrom's Macroglobulinemia: Update of Pivotal Clinical Trial , 2017 .
[24] A. Roberts,et al. BRUTON'S TYROSINE KINASE (BTK) INHIBITOR BGB‐3111 DEMONSTRATES HIGH VERY GOOD PARTIAL RESPONSE (VGPR) RATE IN PATIENTS WITH WALDENSTRÖM MACROGLOBULINEMIA (WM) , 2017 .
[25] M. Dimopoulos,et al. Ibrutinib for patients with rituximab-refractory Waldenström's macroglobulinaemia (iNNOVATE): an open-label substudy of an international, multicentre, phase 3 trial. , 2017, The Lancet. Oncology.
[26] M. Hernán,et al. ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions , 2016, British Medical Journal.
[27] Zhiwei Wang,et al. Abstract 2597: BGB-3111 is a novel and highly selective Bruton's tyrosine kinase (BTK) inhibitor , 2015 .
[28] R. Advani,et al. Ibrutinib in previously treated Waldenström's macroglobulinemia. , 2015, The New England journal of medicine.
[29] S. Treon,et al. CXCR4 WHIM‐like frameshift and nonsense mutations promote ibrutinib resistance but do not supplant MYD88L265P‐directed survival signalling in Waldenström macroglobulinaemia cells , 2015, British journal of haematology.
[30] A. Roccaro,et al. C1013G/CXCR4 acts as a driver mutation of tumor progression and modulator of drug resistance in lymphoplasmacytic lymphoma. , 2014, Blood.
[31] S. Rodig,et al. The WHIM-like CXCR4S338X somatic mutation activates AKT and ERK, and promotes resistance to ibrutinib and other agents used in the treatment of Waldenstrom’s Macroglobulinemia , 2014, Leukemia.
[32] S. Treon,et al. Somatic mutations in MYD88 and CXCR4 are determinants of clinical presentation and overall survival in Waldenstrom macroglobulinemia. , 2014, Blood.
[33] E. Kimby,et al. Response assessment in Waldenström macroglobulinaemia: update from the VIth International Workshop , 2013, British journal of haematology.
[34] P. Gobbi,et al. Prognostic factors in symptomatic Waldenstrom's macroglobulinemia. , 2003, Seminars in oncology.
[35] R Core Team,et al. R: A language and environment for statistical computing. , 2014 .