Induction Chemotherapy with Docetaxel and Cisplatin Followed by Concomitant Chemoradiotherapy in Patients with Inoperable Non-nasopharyngeal Carcinoma of the Head and Neck

被引:0
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作者
Fountzilas, George [1 ]
Bamias, Aristotelis [2 ]
Kalogera-Fountzila, Anna [1 ]
Karayannopoulou, Georgia [1 ]
Bobos, Mattheos [1 ]
Athanassiou, Eleni [3 ]
Kalogeras, Konstantine T. [1 ,4 ]
Tolis, Christos [5 ]
Tsekeris, Periklis [5 ]
Papakostas, Pavlos [6 ]
Vamvouka, Chrysanthi [7 ]
Zaramboukas, Thomas [1 ]
Kosmidis, Paris [8 ]
Zamboglou, Nikolaos [9 ]
Misailidou, Despina [1 ]
机构
[1] Aristotle Univ Thessaloniki, Sch Med, GR-54006 Thessaloniki, Greece
[2] Univ Athens, Sch Med, Dept Clin Therapeut, GR-11527 Athens, Greece
[3] Agios Savvas Canc Hosp, Dept Radiat Therapy, Athens, Greece
[4] Data Off, Hellen Cooperat Oncol Grp, Athens, Greece
[5] Ioannina Univ Hosp, Dept Med Oncol, Ioannina, Greece
[6] Hippokrateion Hosp, Dept Med Oncol, Athens, Greece
[7] Evangelismos Med Ctr, Dept Pathol, Athens, Greece
[8] Hygeia Hosp, Dept Med Oncol 2, Athens, Greece
[9] Klinikum Offenbach, Dept Radiotherapy, Offenbach, Germany
关键词
Head and neck cancer; chemotherapy; radiation therapy; docetaxel; ERCC1; SQUAMOUS-CELL CARCINOMA; GROWTH-FACTOR RECEPTOR; LOCALLY ADVANCED HEAD; PHASE-II; IMMUNOHISTOCHEMICAL EVIDENCE; CHEMORADIATION PARADIGM; PROTEIN OVEREXPRESSION; PTEN EXPRESSION; LUNG-CANCER; COPY NUMBER;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Induction chemotherapy (IC) followed by concomitant chemoradiotherapy (CCRT) has the potential of being an ideal multi-modality approach for improving the prognosis of patients with squamous cell carcinoma of the head and neck (SSCHN). Patients and Methods: Thirty-four patients with locally advanced SCCHN were treated with 3 cycles of IC, consisting of docetaxel 75 mg/m(2) and cisplatin 75 mg/m(2) even 3 weeks, followed 3-4 weeks later by definitive radiotherapy (70 Gy) and concomitant weekly cisplatin 40 mg/m(2). Results: After a median follow-up of 27.7 months, 6-month progression-free survival (PFS), the primary study end-point, was 84%. The median PFS was 16.4 months and median overall survival 24.4 months. The majority of the patients completed 3 cycles of IC with mild to moderate toxicity. Anemia, nausea/vomiting and mucositis were the prominent toxicities during CCRT Retrospective analysis of a panel of biomarkers suggested that excision repair cross-complementation group 1 (ERCC1) protein expression was associated with shorter PFS. Conclusion: IC followed by CCRT as administered in the present study, is a feasible and well-tolerated therapeutic approach. However, its real impact on the prognosis of SCCHN patients has to be demonstrated in a randomized study comparing this treatment to CCRT alone.
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收藏
页码:529 / 538
页数:10
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