Raguse Jan-Dirk, Gath Hans Joachim, Bier Jürgen, Riess Hanno, Oettle Helmut
Klinik für Mund-, Kiefer- und Gesichtschirurgie, klinische Navigation und Robotik Plastische Operationen, Charité Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburgerplatz 1, 13353 Berlin, Germany.
Oral Oncol. 2004 Feb;40(2):228-30. doi: 10.1016/j.oraloncology.2003.08.003.
The suppression and eradication of malignant tumours by targeting the endothelial cells of the tumour is one of the rapidly evolving new approaches to cancer therapy. Head and neck tumours, because of their high levels of vascularization, present themselves as ideal candidates for such antiangiogenic strategies. We report a heavily pretreated patient with a tumour 15 cm in diameter representing fourth relapse of squamous cell carcinoma, which had its origin in the upper left jaw. The patient was treated with the antiangiogenetic, cyclic peptide, EMD 121974 [cilengitide] (600 mg/m2 over 60 minutes i.v.) on day 1 and 4 in combination with gemcitabine (1000 mg/m2 over 30 minutes) administered days 1 and 8 every 3 weeks for five months, and a partial remission was achieved. This resulted in a clinical improvement in the ability of the patient to eat and smell. The patient remained stable for 12 months on cilengitide mainenance therapy, with no tendency towards spontaneous bleeding. This clinical case demonstrates the clinical efficacy of the antiangiogenetic agent cilengitide, in combination with gemcitabine, in inhibiting rapid growth of highly vascularized tumour and highlights the potential of this new therapeutic agent
通过靶向肿瘤内皮细胞来抑制和根除恶性肿瘤是癌症治疗中迅速发展的新方法之一。头颈部肿瘤由于血管化程度高,成为此类抗血管生成策略的理想候选对象。我们报告了一名经过多次治疗的患者,其肿瘤直径达15厘米,为左上颌起源的鳞状细胞癌第四次复发。该患者在第1天和第4天接受抗血管生成环肽EMD 121974西仑吉肽治疗,同时每3周在第1天和第8天联合使用吉西他滨(1000毫克/平方米,静脉滴注30分钟),持续五个月,实现了部分缓解。这使患者的进食和嗅觉能力得到了临床改善。患者在西仑吉肽维持治疗下保持稳定12个月,无自发出血倾向。该临床病例证明了抗血管生成药物西仑吉肽与吉西他滨联合使用在抑制高血管化肿瘤快速生长方面的临床疗效,并突出了这种新治疗药物的潜力