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病理报告滤泡性淋巴瘤1-2级
就诊医院北京协和
目前状态康复10-20年
最后登录2025-6-10
  
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发表于 2023-7-6 16:28:23
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来自: 中国北京
在NCCN指南2023版中,关于伯基特淋巴瘤的治疗是这么说的:
CODOX-M/IVAC (originally published in 1998) is a highly effective regimen with a 1-year event-free survival (EFS) rate of 85% in pediatric and adult patients with previously untreated BL or Burkitt-like lymphoma. Patients with high-risk disease received 4 alternating treatments (ABAB) of CODOX-M(A) and IVAC(B), and those with low-risk disease received 3 cycles of CODOX-M. Both cycles included intrathecal chemotherapy (cytarabine or methotrexate) for CNS prophylaxis in addition to high-dose systemic cytarabine and methotrexate.
Subsequent phase II and retrospective studies have confirmed the efficacy of this regimen, and a “modified” regimen (inclusion of rituximab and dose-modified to decrease toxicity).
The efficacy of modified CODOX-M/IVAC regimen (modified slightly with vincristine dose capped at 2 mg) in adult patients with BL was confirmed in an international phase II study (n =52; 12 patients had low-risk disease; patients had high-risk disease). The overall 2-year EFS and OS rates were 65% and 73%, respectively.
CODOX-M/IVAC在儿童和成年患者中1年的无进展生存率是85%。高危患者接受4个周期的ABAB交替治疗。改良的CODOX-M/IVAC方案(加入利妥昔单抗,降低化疗剂量)在II期临床研究中2年无事件生存率是65%,总生存率是73%。
关于一线治疗后CR患者,是这么说的:
Patients with CR to induction therapy should be followed up every 2 to 3 months for 1 year then every 3 months for the next 1 year, and then every 6 months thereafter. Disease relapse after 2 years is rare following CR to induction therapy, and follow-up should be individualized according to patient characteristics. Consolidation therapy in the context of a clinical trial may be considered for high-risk patients with CR to induction therapy. Patients with less than CR to induction therapy should be treated in the context of a clinical trial.
诱导治疗后CR的患者第一年每两三个月复查一次,第二年每三个月复查一次,之后每六个月复查一次。两年后复发的患者非常罕见。CR的高危患者可以在临床试验的前提下考虑巩固治疗。未能CR的患者应该参加临床试验。
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