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本文引用的文献

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Randomized phase II study of pemetrexed, carboplatin, and thoracic radiation with or without cetuximab in patients with locally advanced unresectable non-small-cell lung cancer: Cancer and Leukemia Group B trial 30407.培美曲塞、卡铂和胸部放疗联合或不联合西妥昔单抗治疗局部晚期不可切除非小细胞肺癌的随机 II 期研究:癌症和白血病组 B 试验 30407。
J Clin Oncol. 2011 Aug 10;29(23):3120-5. doi: 10.1200/JCO.2010.33.4979. Epub 2011 Jul 11.
2
Epidermal growth factor receptor inhibitor gefitinib added to chemoradiotherapy in locally advanced head and neck cancer.表皮生长因子受体抑制剂吉非替尼联合放化疗治疗局部晚期头颈部肿瘤。
J Clin Oncol. 2010 Jul 10;28(20):3336-43. doi: 10.1200/JCO.2009.27.0397. Epub 2010 May 24.
3
Pemetrexed plus cetuximab in patients with recurrent non-small cell lung cancer (NSCLC): a phase I/II study from the Hoosier Oncology Group.培美曲塞联合西妥昔单抗治疗复发性非小细胞肺癌(NSCLC)患者的Ⅰ/Ⅱ期研究:印第安纳肿瘤协作组的研究结果。
J Thorac Oncol. 2009 Nov;4(11):1420-4. doi: 10.1097/JTO.0b013e3181b624ae.
4
Meta-analysis of chemotherapy in head and neck cancer (MACH-NC): an update on 93 randomised trials and 17,346 patients.头颈部癌化疗的荟萃分析(MACH-NC):93项随机试验及17346例患者的最新情况
Radiother Oncol. 2009 Jul;92(1):4-14. doi: 10.1016/j.radonc.2009.04.014. Epub 2009 May 14.
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Randomized phase II and pharmacogenetic study of pemetrexed compared with pemetrexed plus carboplatin in pretreated patients with advanced non-small-cell lung cancer.培美曲塞与培美曲塞加卡铂用于晚期非小细胞肺癌经治患者的随机II期及药物遗传学研究
J Clin Oncol. 2009 Apr 20;27(12):2038-45. doi: 10.1200/JCO.2008.19.1650. Epub 2009 Mar 23.
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C677T and A1298C MTHFR polymorphisms, a challenge for antifolate and fluoropyrimidine-based therapy personalisation.C677T和A1298C亚甲基四氢叶酸还原酶(MTHFR)基因多态性:基于抗叶酸和氟嘧啶治疗个体化的一项挑战
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Phase III study comparing cisplatin plus gemcitabine with cisplatin plus pemetrexed in chemotherapy-naive patients with advanced-stage non-small-cell lung cancer.一项III期研究,比较顺铂加吉西他滨与顺铂加培美曲塞用于初治晚期非小细胞肺癌患者的化疗效果。
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8
Head and neck cancer.头颈癌
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9
Phase I study of bevacizumab added to fluorouracil- and hydroxyurea-based concomitant chemoradiotherapy for poor-prognosis head and neck cancer.一项关于在氟尿嘧啶和羟基脲基础上的同步放化疗中加入贝伐单抗用于预后不良头颈癌的I期研究。
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10
Phase II study of low-dose paclitaxel and cisplatin in combination with split-course concomitant twice-daily reirradiation in recurrent squamous cell carcinoma of the head and neck: results of Radiation Therapy Oncology Group Protocol 9911.低剂量紫杉醇和顺铂联合分程同步每日两次再照射治疗复发性头颈部鳞状细胞癌的II期研究:放射治疗肿瘤学组9911方案的结果
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头颈部癌症患者中培美曲塞联合西妥昔单抗和顺铂同期放化疗的 I 期临床试验。

Phase I trial of pemetrexed in combination with cetuximab and concurrent radiotherapy in patients with head and neck cancer.

机构信息

University of Pittsburgh Cancer Institute; Division of Hematology-Oncology, Department of Medicine, University of Pittsburgh School of Medicine; Department of Otolaryngology.

Division of Hematology-Oncology, Department of Medicine, University of Pittsburgh School of Medicine.

出版信息

Ann Oncol. 2011 Nov;22(11):2482-2488. doi: 10.1093/annonc/mdr002. Epub 2011 Mar 1.

DOI:10.1093/annonc/mdr002
PMID:21363880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3200222/
Abstract

BACKGROUND

We studied the combination of pemetrexed, a multi-targeted antifolate, and cetuximab, an mAb against the epidermal growth factor receptor, with radiotherapy in poor prognosis head and neck cancer.

PATIENTS AND METHODS

Patients received pemetrexed on days 1, 22, and 43 on a dose-escalation scheme with starting level (0) 350 mg/m(2) (level -1, 200 mg/m(2); level +1, 500 mg/m(2)) with concurrent radiotherapy (2 Gy/day) and cetuximab in two separate cohorts, not previously irradiated (A) and previously irradiated (B), who received 70 and 60-66 Gy, respectively. Genetic polymorphisms of thymidylate synthase and methylenetetrahydrofolate reductase were evaluated.

RESULTS

Thirty-two patients were enrolled. The maximum tolerated dose of pemetrexed was 500 mg/m(2) in cohort A and 350 mg/m(2) in cohort B. Prophylactic antibiotics were required. In cohort A, two dose-limiting toxicities (DLTs) occurred (febrile neutropenia), one each at levels 0 and +1. In cohort B, two DLTs occurred at level +1 (febrile neutropenia; death from perforated duodenal ulcer and sepsis). Grade 3 mucositis was common. No association of gene polymorphisms with toxicity or efficacy was evident.

CONCLUSION

The addition of pemetrexed 500 mg/m(2) to cetuximab and radiotherapy is recommended for further study in not previously irradiated patients.

摘要

背景

我们研究了培美曲塞(一种多靶点抗叶酸药物)联合西妥昔单抗(一种针对表皮生长因子受体的单抗)与放射疗法在预后不良的头颈部癌症中的应用。

患者和方法

患者采用剂量递增方案接受培美曲塞治疗,在两个单独的队列中,未接受过放疗的患者(A 队列)和已接受过放疗的患者(B 队列),分别在第 1、22 和 43 天接受培美曲塞治疗(起始剂量为 0 时为 350 mg/m2(水平-1 为 200 mg/m2;水平+1 为 500 mg/m2)),同时接受放射治疗(2 Gy/天)和西妥昔单抗治疗。评估了胸苷酸合成酶和亚甲基四氢叶酸还原酶的遗传多态性。

结果

共纳入 32 例患者。在 A 队列中,培美曲塞的最大耐受剂量为 500 mg/m2,在 B 队列中为 350 mg/m2。需要预防性使用抗生素。在 A 队列中,有两例剂量限制性毒性(DLT)发生(发热性中性粒细胞减少症),分别发生在 0 水平和+1 水平。在 B 队列中,有两例 DLT 发生在+1 水平(发热性中性粒细胞减少症;十二指肠穿孔溃疡伴败血症死亡)。3 级黏膜炎较为常见。基因多态性与毒性或疗效无明显相关性。

结论

建议进一步研究培美曲塞 500 mg/m2 联合西妥昔单抗和放射疗法在未接受过放疗的患者中的应用。