FOLFOX 4与改良FOLFOX 6在伊朗结直肠癌患者治疗毒性的比较研究

Amir Shahram Yousefi Kashi, A. Razzaghdoust, A. Rakhsha
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引用次数: 6

摘要

背景:结直肠癌癌症是癌症患者的主要健康问题和癌症相关死亡原因之一,在伊朗等国家,大多数病例诊断为晚期。目的:评价两种不同方案奥沙利铂和5-氟尿嘧啶加亚叶酸(FOLFOX)联合治疗癌症患者的毒性反应发生率和严重程度,并对其进行比较。方法:回顾2005年至2014年收治的458例癌症大肠癌患者的病历资料。对96名符合条件的患者的数据进行了分析。56名患者(58.3%)接受FOLFOX 4治疗,40名患者(41.7%)接受改良FOLFOX 6治疗。结果:该研究包括96名患者,其中39人为男性(40.6%),57人为女性(59.4%)。中位年龄为62岁(范围:38-87岁)。随访时间为16-109个月,中位数为62个月。FOLFOX 4和改良FOLFOX 6作为两种方案,腹泻≥1级毒性与胃肠道(GI)毒性的发生率具有统计学意义(P=0.034),FOLFOX 4和改良FOLFOX 6两种方案的中性粒细胞减少症≥1级毒性作为血液学毒性的发生率具有高度统计学意义(P<0.001),但我们没有观察到两种方案之间血液毒性的血小板减少症≥1级的统计学显著差异(P=0.063)。FOLFOX 4和改良FOLFOX 6作为两种方案的神经毒性≥1级发生率具有统计学显著性(P=0.017)FOLFOX6。一些血液学和非血液学并发症比FOLFOX4多,值得关注。
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A Comparative Study of Treatment Toxicities Between FOLFOX 4 and Modified FOLFOX 6 in Iranian Colorectal Cancer Patients
Background: Colorectal cancer is one major health problem and cancer-related cause of death in cancer patients in countries such as Iran where the most cases are diagnosed in advanced stages. Objectives: To evaluate the incidence and severity of toxic effects in colorectal cancer patients who have been treated with two different schedules of combination of oxaliplatin and bolus/infusional 5-fluorouracil with leucovorin (FOLFOX) and to compare them. Methods: Medical records of 458 patients with colorectal cancer treated with FOLFOX 4 and modified FOLFOX 6 regimen between 2005 and 2014 were reviewed. Data from 96 eligible patients were analyzed. Fifty-six patients (58.3%) received FOLFOX 4 and 40 patients (41.7%) received modified FOLFOX 6. Results: The study included 96 patients, 39 of whom were males (40.6%) and 57 of whom were females (59.4%). The median age was 62 years (range: 38 - 87 years). The follow up duration was between 16 - 109 months with a median of 62 months. There was a statistically significant incidence rate of grade ≥ 1 toxicity of diarrhea as gastrointestinal (GI) toxicity between FOLFOX 4 and modified FOLFOX 6 as the two regimens (P = 0.034), but there was not a statistically significant incidence rate of grade ≥ 1 toxicity of stomatitis as GI toxicity between the two regimens (P = 0.27). We observed a highly statistically significant incidence rate of grade ≥ 1 toxicity of neutropenia as hematologic toxicity between FOLFOX 4 and modified FOLFOX 6 as the two regimens (P < 0.001), but we did not observe any statistically significant differences of grade ≥ 1 of thrombocytopenia as hematologic toxicity between the two regimens (P = 0.063). There was a statistically significant incidence rate of grade ≥ 1 neurotoxicity between FOLFOX 4 and modified FOLFOX 6 as the two regimens (P = 0.017). Conclusions: We showed that in colorectal cancer patients treated with modified FOLFOX6. Some of hematological and non-hematological complications were more than FOLFOX4 and they can be concerned.
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