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改良 R-CODOX-M/IVAC 化疗方案治疗未经治疗的散发性伯基特淋巴瘤中国患者。

Modified R-CODOX-M/IVAC chemotherapy regimens in Chinese patients with untreated sporadic Burkitt lymphoma.

机构信息

Department of Medical Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou 510060, China.

Senior Ward/Phase I Clinical Trial Ward, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610041, China.

出版信息

Cancer Biol Med. 2021 Aug 15;18(3):833-40. doi: 10.20892/j.issn.2095-3941.2020.0314.

Abstract

OBJECTIVE

To characterize modified R-CODOX-M/IVAC-based chemotherapy to lower the severe adverse events in Chinese adult patients with sporadic Burkitt lymphoma.

METHODS

We enrolled a retrospective cohort including 123 adult patients with untreated sporadic Burkitt lymphoma from August 2008 to September 2019 at Sun Yat-sen University Cancer Center. We studied a dose-modified and long-course R-CODOX-M/IVAC regimen utilizing a low dose of 1.0 g/m/cycle cyclophosphamide, 2 g/m/cycle methotrexate, 4,500 mg/m/cycle ifosfamide, and 4.0 g/m/cycle cytarabine. Forty-nine patients with low risk disease underwent 4-6 cycles of dose-modified R-CODOX-M-based chemotherapy. Seventy-four patients with high risk disease underwent 6-8 cycles of dose-modified alternating R-CODOX-M/IVAC regimens.

RESULTS

The objective remission was 87.0%. The event-free survival rate and overall survival at 3 years were 81.2% and 92.1%, respectively. Major grade 3-4 adverse events included leukopenia (91.9%), anemia (58.5%), thrombocytopenia (73.2%), and febrile neutropenia (48.8%). A total of 26.0% and 37.4% of patients received red blood cell and platelet transfusions, respectively. We observed 4 cases (3.3%) of septic shock after chemotherapy. Two treatment-related deaths occurred from severe infection.

CONCLUSIONS

The modified R-CODOX-M/IVAC chemotherapy regimen was effective for sporadic Burkitt lymphoma in the Chinese population, with a lower toxicity than standard regimens.

摘要

目的

描述改良后的 R-CODOX-M/IVAC 化疗方案,以降低中国成人散发型伯基特淋巴瘤患者的严重不良事件。

方法

我们纳入了 2008 年 8 月至 2019 年 9 月中山大学肿瘤防治中心收治的 123 例未经治疗的散发型伯基特淋巴瘤成人患者的回顾性队列。我们研究了一种剂量改良的长疗程 R-CODOX-M/IVAC 方案,该方案使用低剂量的 1.0 g/m/周期环磷酰胺、2 g/m/周期甲氨蝶呤、4500 mg/m/周期异环磷酰胺和 4.0 g/m/周期阿糖胞苷。49 例低危疾病患者接受了 4-6 个周期的剂量改良 R-CODOX-M 为基础的化疗。74 例高危疾病患者接受了 6-8 个周期的剂量改良交替 R-CODOX-M/IVAC 方案。

结果

客观缓解率为 87.0%。3 年无事件生存率和总生存率分别为 81.2%和 92.1%。主要的 3-4 级不良事件包括白细胞减少症(91.9%)、贫血症(58.5%)、血小板减少症(73.2%)和发热性中性粒细胞减少症(48.8%)。分别有 26.0%和 37.4%的患者接受了红细胞和血小板输注。我们观察到 4 例(3.3%)患者在化疗后发生感染性休克。2 例治疗相关死亡是由严重感染引起的。

结论

改良后的 R-CODOX-M/IVAC 化疗方案对中国人群中的散发型伯基特淋巴瘤有效,毒性低于标准方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df37/8330526/2e9a0af68887/cbm-18-833-g001.jpg

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