首页> 外文期刊>Annals of King Edward Medical University. >A phase ii study of doxorubicin, vincristine, cyclophosphamide, prednisolone (CHOP) chemotherapy with intathecal (IT) methotrexate and prophylactic cranial irradiation in a patients with high grade non Hodgkin`s lymphoma (NHL)
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A phase ii study of doxorubicin, vincristine, cyclophosphamide, prednisolone (CHOP) chemotherapy with intathecal (IT) methotrexate and prophylactic cranial irradiation in a patients with high grade non Hodgkin`s lymphoma (NHL)

机译:高度非霍奇金淋巴瘤(NHL)患者中阿霉素,长春新碱,环磷酰胺,泼尼松龙(CHOP)化疗与inthethetal(IT)甲氨蝶呤和预防性颅脑放疗的ii期研究

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Objective: The objective of this phase II study was to evaluate the efficacy and toxicity of (CHOP) chemotherapy with intrathecal methotrexate and prophylactic cranial irradiation in patients with high-grade Non Hodgkin`s lymphoma. Method: From January 2002 to December 2002 tewenty consecutive patients with histopathologically and immunohistochemically confirmed high grade NHL with Ann Arbor stage III & IV were enrolled. ECOG performance status of 0 or 1 was required. Written informed consent was obtained from all patients. Patients with symptomatic meningeal or brain involvement were excluded from the study. Cyclophosphamide 750 mg /m2, vincristine 1.4 mg / m2 (maximum 2 mg), doxorubicin 50 mg / m2 was given I/V on D1 and prednisolone 100 mg PO was given from D1 - D5. Cycles were repeated after every 21 days. Intrathecal methotrexate was given at a dose of 12 mg once during 3rd week, twice weekly on 5th & 6th week and once during 7th week. A total dose of 1800 cGy was given to whole brain in 10 fraction s with a daily tumor dose of 180 cGy using a Cobalt 60. Common Toxicity Criteria was used for evaluation of toxicity and WHO criteria for response evaluation. Result: All 20 patients were able to complete the planned therapy. Grade IV neutropenia was observed in 45% (9/20) of patients. Episodes of febrile neutropenia were seen in 20%(4/20). Grade II diarrhea was seen in 25%(05/20). 20%(4/20) had grade II cutaneous toxicity. No immediate radiation related toxicity was seen except grade II nausea and vomiting. Overall response was found in 75%(15/20) of patients, CR in 60%(12/20) and PR in 15%(03/20). 15%(03/20) patients showed stable disease and 10%(02/20) had progressive disease. Conclusion: This combined modality treatment of CHOP chemotherapy with intrathecal methotrexate and prophylactic cranial irradiation has been feasible and effective with acceptable toxicity in this group of patients with high-grade Non Hodgkin`s lymphoma.
机译:目的:该II期研究的目的是评估鞘内注射甲氨蝶呤和预防性颅脑放疗的(CHOP)化疗对严重非霍奇金淋巴瘤患者的疗效和毒性。方法:从2002年1月至2002年12月,连续纳入20例经组织病理学和免疫组化证实为Ann Arbor III和IV期高级别NHL的患者。要求ECOG性能状态为0或1。所有患者均获得书面知情同意书。有症状的脑膜或脑部受累的患者被排除在研究之外。在D1上给予I / V环磷酰胺750 mg / m2,长春新碱1.4 mg / m2(最大2 mg),阿霉素50 mg / m2,D1-D5给予泼尼松龙100 mg PO。每隔21天重复一次循环。鞘内注射甲氨蝶呤的剂量为12毫克,第3周一次,第5周和第6周每周两次,第7周一次。使用Cobalt 60在整整10 s内向全脑给予1800 cGy的总剂量,每日肿瘤剂量为180 cGy。使用通用毒性标准评估毒性,并使用WHO标准进行反应评估。结果:全部20例患者均能完成计划的治疗。在45%(9/20)的患者中观察到IV级中性粒细胞减少。发热性中性粒细胞减少症的发作率占20%(4/20)。观察到II级腹泻的发生率为25%(05/20)。 20%(4/20)具有II级皮肤毒性。除II级恶心和呕吐外,未观察到直接的辐射相关毒性。总体缓解率为75%(15/20),CR为60%(12/20),PR为15%(03/20)。 15%(03/20)患者病情稳定,10%(02/20)患者病情进展。结论:CHOP化疗联合鞘内注射甲氨蝶呤和预防性颅脑放疗的联合治疗在该组高级别非霍奇金淋巴瘤患者中是可行和有效的,并且具有可接受的毒性。

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