首页> 外文期刊>Radiotherapy and oncology: Journal of the European Society for Therapeutic Radiology and Oncology >EORTC 24051: Unexpected side effects in a phase i study of TPF induction chemotherapy followed by chemoradiation with lapatinib, a dual EGFR/ErbB2 inhibitor, in patients with locally advanced resectable larynx and hypopharynx squamous cell carcinoma
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EORTC 24051: Unexpected side effects in a phase i study of TPF induction chemotherapy followed by chemoradiation with lapatinib, a dual EGFR/ErbB2 inhibitor, in patients with locally advanced resectable larynx and hypopharynx squamous cell carcinoma

机译:EORTC 24051:在局部晚期可切除的喉和下咽鳞状细胞癌患者中,TPF诱导化学疗法随后用拉帕替尼(一种EGFR / ErbB2双重抑制剂)进行化学放疗的I期研究中出现了意外的副作用

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Background: In this phase I/II study, the addition of lapatinib (LAP) was investigated in combination with the sequential use of both approaches TPF induction chemotherapy (ICT) followed by chemoradiation (CRT) in locally advanced larynx or hypopharynx squamous cell carcinoma. Patients and methods: Objectives were to assess maximum tolerated dose, dose-limiting toxicity (DLT) and to recommend a safe dose of LAP when administered with 4 cycles of TPF followed by CRT. Results: Seven male patients were included. Three patients were included in the first cohort, at dose level 1 (LAP 500 mg daily plus TPF). Renal toxicity was observed among these three patients (grade 3 [n = 1], grade 2 [n = 1] and grade 1 [n = 1]), with 1 DLT, leading to treatment interruption in this group. Nephrotoxicity was reversible after stopping LAP and hydration of the patients. In a second cohort of four patients administering docetaxel from the second cycle, 3 more DLTs were observed (grade 2 renal toxicity and grade 3 diarrhea, grade 3 anorexia and grade 3 stomatitis, and grade 4 neutropenia). Based on the occurrence of 4 DLTs at the first dose level of LAP, patient recruitment was closed. Conclusion: These data indicate that LAP cannot be combined safely with full dose TPF.
机译:背景:在这一I / II期研究中,研究了在局部晚期喉癌或下咽鳞状细胞癌中联合使用拉帕替尼(LAP)和依次使用两种方法TPF诱导化疗(ICT),然后进行化学放射(CRT)的情况。患者和方法:目的是评估最大耐受剂量,剂量限制性毒性(DLT)并建议在4个周期的TPF继之以CRT的情况下给予LAP安全剂量。结果:包括7名男性患者。第一组包括三名患者,剂量水平为1(每天LAP 500 mg加TPF)。在这三例患者中观察到肾毒性(3级[n = 1],2级[n = 1]和1级[n = 1]),其中1例DLT导致了该组患者的治疗中断。停止LAP和水合作用后,肾毒性是可逆的。从第二个周期开始服用多西他赛的四名患者的第二个队列中,又观察到3种DLT(2级肾毒性和3级腹泻,3级厌食症和3级口腔炎以及4级中性粒细胞减少症)。基于在LAP的第一个剂量水平出现4个DLT,患者招募结束。结论:这些数据表明LAP不能与全剂量TPF安全地组合。

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