Anti-epidermal growth factor receptor therapy in combination with chemoradiotherapy for the treatment of locally advanced anal canal carcinoma: Results of a phase I dose-escalation study with panitumumab (FFCD 0904)

被引:9
作者
Vendrely, Veronique [1 ]
Lemanski, Claire [2 ]
Gnep, Khemara [3 ]
Barbier, Emilie [4 ]
El Hajbi, Farid [5 ]
Lledo, Gerard [6 ]
Dahan, Laetitia [7 ]
Terrebonne, Eric [1 ]
Manfredi, Sylvain [3 ]
Mirabel, Xavier [5 ]
Mammar, Vincent [6 ]
Cowen, Didier [7 ]
Lepage, Come [8 ]
Aparicio, Thomas [9 ]
机构
[1] CHU Bordeaux, Pessac, France
[2] Inst Reg Canc Montpellier, Montpellier, France
[3] Ctr Eugene Marquis, Rennes, France
[4] Univ Burgundy & Franche Comte, Biostat, FFCD, EPICAD INSERM LNC UMR 1231, Dijon, France
[5] Ctr Oscar Lambret, Lille, France
[6] Hop Prive Jean Mermoz, Lyon, France
[7] CHU La Timone, Marseille, France
[8] Univ Burgundy & Franche Comte, EPICAD INSERM LNC UMR 1231, Dijon, France
[9] CHU APHP St Louis, Paris, France
关键词
Anal cancer; Squamous cell carcinoma; Epidermal growth factor receptor; Panitumumab; Chemoradiotherapy; Immunotherapy; CETUXIMAB PLUS CHEMORADIOTHERAPY; CLINICAL-PRACTICE GUIDELINES; SQUAMOUS-CELL CARCINOMA; CONVENTIONAL CHEMORADIOTHERAPY; PREOPERATIVE RADIATION; RANDOMIZED-TRIAL; MITOMYCIN-C; FOLLOW-UP; CANCER; RADIOTHERAPY;
D O I
10.1016/j.radonc.2019.05.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: Standard treatment of epidermoid anal cancer is 5-fluorouracil (5FU) and mitomycin C (MMC) based chemoradiotherapy (CRT). This phase I study aims to evaluate the addition of panitumumab (Pmab) to CRT and to determine the maximum tolerated dose (MTD) of Pmab and 5-FU in combination with CRT. Materials and methods: Immunocompetent patients with locally advanced tumour without metastases (Stage T2, T3 or T4, whatever N stage; Stage N1-N3 whatever T stage) followed two RT periods (45 Gy in 5 weeks and 20 Gy in 2 weeks, separated by a 2-week break) with concomitant CT sessions of 5FU/MMC at RT weeks 1, 5 and 8. Pmab was administered on RT weeks 1, 3, 5, 8 and 10 according to a predefined dose escalation schedule. Results: Ten patients were enroled. One was excluded due to unmet dose constraints respect. Three patients received dose level (DL) 0 (Pmab 3 mg/kg + 5FU 600 mg/m(2)/day) and six received DL-1 (Pmab 3 mg/kg + 5FU 400 mg/m(2)/day). Dose-limiting toxicities occurred in all patients at DL 0 and 2 at DL-1. Most common grade 3-4 toxicities observed at DL 0 were haematologic (100%), dermatitis (67%), and anaemia (67%). No death occurred. Four months after ending CRT, five and two patients had a local complete response and a partial response, respectively. One patient had a colostomy with abdomino-perineal amputation due to a tumour recurrence. Conclusions: The MTD is 5FU at 400 mg/m(2)/day, MMC at 10 mg/m(2) and Pmab at 3 mg/kg. The effect of the MTD on tumour response is evaluated in the phase 2 study. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 89
页数:6
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