First-in-human phase I study of the DNA-repair inhibitor DT01 in combination with radiotherapy in patients with skin metastases from melanoma

被引:28
作者
Le Tourneau, C. [1 ,2 ,3 ]
Dreno, B. [4 ]
Kirova, Y. [5 ]
Grob, J. J. [6 ]
Jouary, T. [7 ]
Dutriaux, C. [7 ]
Thomas, L. [8 ]
Lebbe, C. [9 ]
Mortier, L. [10 ]
Saiag, P. [11 ]
Avril, M. F. [12 ]
Maubec, E. [13 ]
Joly, P. [14 ]
Bey, P. [15 ]
Cosset, J. M. [5 ]
Sun, J. S. [16 ]
Asselain, B. [17 ]
Devun, F. [16 ,18 ]
Marty, M. E. [9 ]
Dutreix, M. [18 ,19 ]
机构
[1] Inst Curie, Dept Med Oncol, F-75005 Paris, France
[2] Inst Curie, Dept Med Oncol, F-75005 St Cloud, France
[3] Versailles St Quentin En Yvelines Univ, EA7285, F-78000 Versailles, France
[4] Hop Hotel Dieu, CHU Nantes, F-44093 Nantes, France
[5] Inst Curie, Dept Radiotherapy, F-75005 Paris, France
[6] Aix Marseille Univ, Hop Enfants La Timone, AP HM, F-13385 Marseille, France
[7] CHU Bordeaux, St Andreas Hosp, Dept Dermatol, F-33000 Bordeaux, France
[8] Univ Lyon 1, Lyon Sud Hosp Ctr, F-69495 Pierre Benite, France
[9] Hop St Louis, AP HP, F-75010 Paris, France
[10] CHRU Lille, Dept Dermatol, F-59037 Lille, France
[11] Hop Ambroise Pare, F-92104 Boulogne Billancourt, France
[12] Cochin Hosp, AP HP, F-75014 Paris, France
[13] Hop Xavier Bichat, F-75877 Paris, France
[14] CHU Rouen, F-76000 Rouen, France
[15] Inst Curie, F-75005 Paris, France
[16] DNA Therapeut, F-91058 Evry, France
[17] Inst Curie, Dept Biostat, F-75005 Paris, France
[18] Inst Curie, F-91405 Orsay, France
[19] Univ Paris 11, CNRS, INSERM, UMR3347,U1021, F-91405 Orsay, France
关键词
phase I trial; DT01; DNA repair; radiotherapy; melanoma; skin metastases; MALIGNANT-MELANOMA; COLORECTAL-CANCER; RADIATION-THERAPY; SURVIVAL; DBAIT; TEMOZOLOMIDE; PATHWAYS;
D O I
10.1038/bjc.2016.120
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: DT01 is a DNA-repair inhibitor preventing recruitment of DNA-repair enzymes at damage sites. Safety, pharmacokinetics and preliminary efficacy through intratumoural and peritumoural injections of DT01 were evaluated in combination with radiotherapy in a first-in-human phase I trial in patients with unresectable skin metastases from melanoma. Methods: Twenty-three patients were included and received radiotherapy (30 Gy in 10 sessions) on all selected tumour lesions, comprising of two lesions injected with DT01 three times a week during the 2 weeks of radiotherapy. DT01 dose levels of 16, 32, 48, 64 and 96mg were used, in a 3+3 dose escalation design, with an expansion cohort at 96 mg. Results: The median follow-up was 180 days. All patients were evaluable for safety and pharmacokinetics. No dose-limiting toxicity was observed and the maximum-tolerated dose was not reached. Most frequent adverse events were reversible grades 1 and 2 injection site reactions. Pharmacokinetic analyses demonstrated a systemic passage of DT01. Twenty-one patients were evaluable for efficacy on 76 lesions. Objective response was observed in 45 lesions (59%), including 23 complete responses (30%). Conclusions: Intratumoural and peritumoural DT01 in combination with radiotherapy is safe and pharmacokinetic analyses suggest a systemic passage of DT01.
引用
收藏
页码:1199 / 1205
页数:7
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