Methotrexate plus or minus cetuximab as first-line treatment in a recurrent or metastatic (R/M) squamous cell carcinoma population of the head and neck (SCCHN), unfit for cisplatin combination treatment, a phase Ib-randomized phase II study Commence

被引:11
|
作者
Ham, Janneke C. [1 ]
van Meerten, Esther [2 ]
Fiets, W. Edward [3 ]
Beerepoot, Laurens V. [4 ]
Jeurissen, Frank J. F. [5 ]
Slingerland, Marije [6 ]
Jonker, Marianne A. [7 ]
Husson, Olga [8 ,9 ]
van der Graaf, Winette T. A. [1 ,10 ]
van Herpen, Carla M. L. [1 ]
机构
[1] Radboud Univ Nijmegen, Dept Med Oncol, Med Ctr, Nijmegen HB, Netherlands
[2] Erasmus MC, Dept Med Oncol, Inst Canc, Rotterdam GD, Netherlands
[3] Med Ctr Leeuwarden, Dept Internal Med, Leeuwarden AD, Netherlands
[4] Elisabeth TweeSteden Hosp, Dept Internal Med, Tilburg AD, Netherlands
[5] Med Ctr Haaglanden, Dept Internal Med, The Hague VA, Netherlands
[6] Leiden Univ, Dept Med Oncol, Med Ctr, Leiden ZA, Netherlands
[7] Radboud Univ Nijmegen, Radboud Inst Hlth Sci, Biostat, Med Ctr, Nijmegen HB, Netherlands
[8] Netherlands Canc Inst, Dept Psychosocial Res & Epidemiol, Amsterdam CX, Netherlands
[9] Inst Canc Res, Div Clin Studies, London, England
[10] Netherlands Canc Inst, Dept Med Oncol, Amsterdam CX, Netherlands
关键词
cetuximab; first-line; methotrexate; palliative treatment; recurrent or metastatic squamous cell carcinoma of the head and neck; QUALITY-OF-LIFE; EUROPEAN-ORGANIZATION; OPEN-LABEL; CANCER; TRIAL; FLUOROURACIL; GEFITINIB;
D O I
10.1002/hed.26053
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background Methotrexate in recurrent or metastatic (R/M) squamous cell carcinoma of the head and neck (SCCHN) has limited progression-free survival (PFS) benefit. We hypothesized that adding cetuximab to methotrexate improves PFS. Methods In the phase-Ib-study, patients with R/M SCCHN received methotrexate and cetuximab as first-line treatment. The primary objective was feasibility. In the phase-II-study patients were randomized to this combination or methotrexate alone (2:1). The primary endpoint was PFS. Secondary endpoints were overall survival (OS), toxicity, and quality of life (QoL). Results In six patients in the phase-Ib-study, no dose limiting toxicities were observed. In the phase II study, 30 patients received the combination and 15 patients methotrexate. In the phase-II-study median PFS was 4.5 months in the combination group vs 2.0 months in the methotrexate group (HR 0.37; P = .002). OS, toxicity, and QoL were not significantly different. Conclusion Cetuximab with methotrexate improved PFS without increased toxicity in R/M SCCHN-patients.
引用
收藏
页码:828 / 838
页数:11
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