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本文引用的文献

1
Low-intensity therapy in adults with Burkitt's lymphoma.成人伯基特淋巴瘤的低强度治疗。
N Engl J Med. 2013 Nov 14;369(20):1915-25. doi: 10.1056/NEJMoa1308392.
2
A multicenter phase II study incorporating high-dose rituximab and liposomal doxorubicin into the CODOX-M/IVAC regimen for untreated Burkitt's lymphoma.一项多中心 II 期研究将高剂量利妥昔单抗和脂质体多柔比星纳入 CODOX-M/IVAC 方案,用于未经治疗的伯基特淋巴瘤。
Ann Oncol. 2013 Dec;24(12):3076-81. doi: 10.1093/annonc/mdt414. Epub 2013 Oct 20.
3
High cure rates in Burkitt lymphoma and leukemia: a Northern Italy Leukemia Group study of the German short intensive rituximab-chemotherapy program.在意北部白血病协作组对德国短期强化利妥昔单抗化疗方案的研究中,伯基特淋巴瘤和白血病的治愈率高。
Haematologica. 2013 Nov;98(11):1718-25. doi: 10.3324/haematol.2013.086827. Epub 2013 Jun 10.
4
Safety and activity of a new intensive short-term chemoimmunotherapy in HIV-positive patients with Burkitt lymphoma.一种新型强化短期化疗免疫疗法在HIV阳性伯基特淋巴瘤患者中的安全性及活性
Br J Haematol. 2012 Oct;159(2):252-5. doi: 10.1111/bjh.12020. Epub 2012 Aug 25.
5
Brief intensive therapy for older adults with newly diagnosed Burkitt or atypical Burkitt lymphoma/leukemia.老年新发伯基特或非典型伯基特淋巴瘤/白血病患者的强化短程治疗。
Leuk Lymphoma. 2013 Mar;54(3):483-90. doi: 10.3109/10428194.2012.715346. Epub 2012 Aug 17.
6
The Bruton tyrosine kinase inhibitor PCI-32765 thwarts chronic lymphocytic leukemia cell survival and tissue homing in vitro and in vivo.布鲁顿酪氨酸激酶抑制剂 PCI-32765 可阻止慢性淋巴细胞白血病细胞在体外和体内的存活和组织归巢。
Blood. 2012 Feb 2;119(5):1182-9. doi: 10.1182/blood-2011-10-386417. Epub 2011 Dec 16.
7
RD-CODOX-M/IVAC with rituximab and intrathecal liposomal cytarabine in adult Burkitt lymphoma and 'unclassifiable' highly aggressive B-cell lymphoma.RD-CODOX-M/IVAC 联合利妥昔单抗和鞘内脂质体阿糖胞苷治疗成人伯基特淋巴瘤和“未分类”高度侵袭性 B 细胞淋巴瘤。
Br J Haematol. 2012 Jan;156(2):234-44. doi: 10.1111/j.1365-2141.2011.08947.x. Epub 2011 Nov 21.
8
Targeted therapy with the T-cell-engaging antibody blinatumomab of chemotherapy-refractory minimal residual disease in B-lineage acute lymphoblastic leukemia patients results in high response rate and prolonged leukemia-free survival.针对化疗耐药的 B 系急性淋巴细胞白血病患者微小残留病灶的 T 细胞结合抗体blinatumomab 的靶向治疗可带来高缓解率和延长无白血病生存。
J Clin Oncol. 2011 Jun 20;29(18):2493-8. doi: 10.1200/JCO.2010.32.7270. Epub 2011 May 16.
9
Bruton tyrosine kinase represents a promising therapeutic target for treatment of chronic lymphocytic leukemia and is effectively targeted by PCI-32765.布鲁顿酪氨酸激酶是治疗慢性淋巴细胞白血病的一个很有前途的治疗靶点,它可以被 PCI-32765 有效靶向。
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10
Evaluation of the addition of rituximab to CODOX-M/IVAC for Burkitt's lymphoma: a retrospective analysis.评估利妥昔单抗联合 CODOX-M/IVAC 方案治疗伯基特淋巴瘤的疗效:一项回顾性分析。
Ann Oncol. 2011 Aug;22(8):1859-64. doi: 10.1093/annonc/mdq677. Epub 2011 Feb 21.

美罗华联合短程、高强度化疗联合粒细胞集落刺激因子支持治疗伯基特或侵袭性淋巴瘤的疗效改善:癌症和白血病组 B 研究 10002。

Improved efficacy using rituximab and brief duration, high intensity chemotherapy with filgrastim support for Burkitt or aggressive lymphomas: cancer and Leukemia Group B study 10 002.

机构信息

Department of Medicine, Duke University Medical Center, Durham, NC, USA.

出版信息

Br J Haematol. 2014 Apr;165(1):102-11. doi: 10.1111/bjh.12736. Epub 2014 Jan 15.

DOI:10.1111/bjh.12736
PMID:24428673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3996561/
Abstract

To improve long-term outcomes for Burkitt leukaemia/lymphoma (BL) or aggressive lymphomas in adults, we assessed the benefit of adding rituximab and filgrastim support to a dose-dense modified chemotherapy regimen from the Cancer and Leukemia Group B (CALGB) 9251 trial. One hundred and five patients (aged 19-79 years) were enrolled; 27% were >60 years old; 47% had high or high-intermediate risk by International Prognostic Index (IPI) criteria. Common severe toxicities included stomatitis/upper gastrointestinal toxicity (69%), renal insufficiency (10%), neurological events (25%) and pulmonary events (18%). Seven died from treatment-related causes (one central nervous system bleed, four infections, two respiratory failure); five were >60 years old. Results in this adult population are encouraging as complete response (CR) was observed in 83% and 4-year event-free (EFS) and overall survivals (OS) were 74% and 78%, respectively. Results compare favourably to our prior chemotherapy alone study (CALGB 9251) but despite this, high-risk patients still had worse outcomes. In conclusion, short duration, intensive chemo-immunotherapy is feasible and should be considered in adults with BL as it results in high remission rates and durable remissions.

摘要

为了改善伯基特白血病/淋巴瘤(BL)或成人侵袭性淋巴瘤的长期预后,我们评估了在癌症和白血病组 B(CALGB)9251 试验中的剂量密集改良化疗方案中添加利妥昔单抗和非格司亭支持的益处。共纳入 105 例患者(年龄 19-79 岁);27%的患者年龄>60 岁;47%的患者按国际预后指数(IPI)标准属于高危或中高危。常见的严重毒性包括口腔炎/上消化道毒性(69%)、肾功能不全(10%)、神经事件(25%)和肺部事件(18%)。7 例患者死于治疗相关原因(1 例中枢神经系统出血,4 例感染,2 例呼吸衰竭);5 例患者年龄>60 岁。该成年人群的结果令人鼓舞,完全缓解(CR)率为 83%,4 年无事件生存(EFS)和总生存(OS)率分别为 74%和 78%。结果与我们之前单独化疗的研究(CALGB 9251)相比更为有利,但尽管如此,高危患者的结局仍较差。总之,短疗程、强化化疗免疫治疗是可行的,并且应该在 BL 成人患者中考虑使用,因为它可以带来高缓解率和持久缓解。