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奥沙利铂联合雷替曲塞及术前放疗用于T3-T4期腹膜外直肠癌:一项剂量探索性研究。

Oxaliplatin with raltitrexed and preoperative radiotherapy in T3-T4 extraperitoneal rectal cancer. A dose finding study.

作者信息

Lupattelli Marco, Bellavita Rita, Natalini Giovanni, Giovenali Paolo, Sidoni Angelo, Castagnoli Paolo, Corgna Enrichetta, Draghini Lorena, Trippolini Romano, Aristei Cynthia

机构信息

Radiation Oncology Center, University and Hospital of Perugia, Perugia, Italy.

出版信息

Tumori. 2006 Nov-Dec;92(6):474-80. doi: 10.1177/030089160609200602.

Abstract

AIMS AND BACKGROUND

The availability of new drugs offers the opportunity to improve the outcome of locally advanced rectal cancer. Raltitrexed and oxaliplatin are effective in advanced colorectal cancer with acceptable toxicity and can act as radiation enhancers as shown in phase I-II studies. The aim of the study was thus to determine the recommended dose of oxaliplatin concomitantly administered with raltitrexed and concurrent preoperative radiotherapy in patients with stage II-III extraperitoneal rectal cancer.

METHODS

From September 2001 to September 2002, 18 consecutive patients with T3/T4 rectal cancer were treated at our Institution with preoperative chemoradiation followed by surgery after 6-8 weeks. Pelvic radiotherapy was delivered at a dose of 45 Gy in 25 fractions in 5 weeks followed by a 5.4 Gy boost at 1.8 Gy daily. Concomitant chemotherapy consisted of 3 mg/m2/i.v. of raltitrexed on days 1, 19, 38 of radiotherapy treatment with incremental doses of oxaliplatin according to dose finding rules (4 dose levels: 65, 85, 110, 130 mg/m2). Dose-limiting toxicity for oxaliplatin was defined as either grade 3-4 hematological or grade 3-4 gastrointestinal or neurological toxicity. We studied a minimum of 3 patients at each dose level.

RESULTS

Three patients were treated at 65, 85, and 110 mg/m2/i.v., respectively, while 9 patients were recruited at the last dose level. Neither grade 3-4 gastrointestinal nor neurological toxicity were documented. Dose-limiting toxicity was documented in 2/9 subjects at the 130 mg/m2 level consisting of grade 3 transient asymptomatic leukopenia. Thirteen patients developed transient increase of one or more liver enzymes (grade 3-4) and 2 patients developed grade 3 perineal dermatitis. All patients received the programmed dose of radiotherapy. The chemotherapy regimen was not completed in 4 cases due to grade 2 protracted leukopenia.

CONCLUSIONS

The maximum tolerated dose of oxaliplatin was not reached at the maximum dose level (i.v.); 130 mg/m2 can therefore be defined as the recommended dose. The combination of oxaliplatin with raltitrexed and radiotherapy can be considered feasible and well tolerated.

摘要

目的与背景

新型药物的出现为改善局部晚期直肠癌的治疗效果提供了契机。雷替曲塞和奥沙利铂对晚期结直肠癌有效,毒性可接受,且如I - II期研究所示,可作为放疗增敏剂。因此,本研究的目的是确定II - III期腹膜外直肠癌患者在接受雷替曲塞和同期术前放疗时奥沙利铂的推荐剂量。

方法

2001年9月至2002年9月,我院连续收治了18例T3/T4期直肠癌患者,先行术前放化疗,6 - 8周后进行手术。盆腔放疗剂量为45 Gy,分25次在5周内完成,随后每日1.8 Gy追加剂量5.4 Gy。同步化疗方案为放疗第1、19、38天静脉注射雷替曲塞3 mg/m²,并根据剂量探索规则递增奥沙利铂剂量(4个剂量水平:65、85、110、130 mg/m²)。奥沙利铂的剂量限制性毒性定义为3 - 4级血液学毒性或3 - 4级胃肠道或神经毒性。每个剂量水平至少研究3例患者。

结果

分别有3例患者接受了65、85和110 mg/m²静脉注射剂量的治疗,而最后一个剂量水平纳入了9例患者。未记录到3 - 4级胃肠道或神经毒性。在130 mg/m²剂量水平的9例患者中有2例记录到剂量限制性毒性,表现为3级短暂无症状白细胞减少。13例患者出现一种或多种肝酶短暂升高(3 - 4级),2例患者出现3级会阴皮炎。所有患者均接受了计划的放疗剂量。4例患者因2级持续性白细胞减少未完成化疗方案。

结论

在最大剂量水平(静脉注射)未达到奥沙利铂的最大耐受剂量;因此,130 mg/m²可定义为推荐剂量。奥沙利铂与雷替曲塞及放疗联合应用可认为是可行的且耐受性良好。

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