Szturz Petr, Specenier Pol, Van Laer Carl, Van Den Weyngaert Danielle, Corthouts Bob, Carp Laurens, Van Marck Eric, Vanderveken Olivier, Vermorken Jan B
Department of Medical Oncology, Antwerp University Hospital, Wilrijkstraat 10, 2650, Edegem, Belgium.
Department of Internal Medicine, Hematology and Oncology, School of Medicine, University Hospital Brno and Masaryk University, Brno, Czech Republic.
Eur Arch Otorhinolaryngol. 2016 Jun;273(6):1629-36. doi: 10.1007/s00405-015-3673-y. Epub 2015 Jun 5.
In recurrent head and neck squamous cell carcinoma ineligible for resection or irradiation, treatment aims primarily at symptom control and quality of life enhancement with an expected outcome of 6-12 months.
In 2005, a male patient, born in 1944, with a second local recurrence of human papillomavirus negative tonsil cancer was enrolled in the EXTREME trial, and randomized to platinum/5-fluorouracil/cetuximab arm resulting in partial remission with progression-free survival of 12 months. The second-line systemic therapy comprised 5 cycles of 3-weekly docetaxel/cisplatin/5-fluorouracil regimen plus weekly cetuximab.
As confirmed on imaging and repeated biopsies, complete response was achieved with disease-free survival of 8 years and follow-up period of 12 years. Severe acute toxicities during the taxane-based chemotherapy plus cetuximab included grade 4 anorexia and grade 3 febrile neutropenia.
Poor tumor differentiation, no weight loss, oropharyngeal location, white race, and particularly the induced complete response were most likely the key favorable prognostic factors in the reported patient. The possibility of a synergistic interaction between taxanes and cetuximab should be further explored.
在无法进行手术切除或放疗的复发性头颈部鳞状细胞癌中,治疗主要旨在控制症状和提高生活质量,预期生存期为6至12个月。
2005年,一名1944年出生的男性患者,患有人乳头瘤病毒阴性扁桃体癌并出现第二次局部复发,被纳入EXTREME试验,并随机分配至铂类/5-氟尿嘧啶/西妥昔单抗组,结果达到部分缓解,无进展生存期为12个月。二线全身治疗包括每3周进行5个周期的多西他赛/顺铂/5-氟尿嘧啶方案加每周一次的西妥昔单抗。
经影像学检查和重复活检证实,患者实现了完全缓解,无病生存期为8年,随访期为12年。基于紫杉烷的化疗加西妥昔单抗期间的严重急性毒性包括4级厌食和3级发热性中性粒细胞减少。
肿瘤分化差、无体重减轻、口咽部位、白种人,尤其是诱导的完全缓解,很可能是该报告患者的关键有利预后因素。应进一步探索紫杉烷与西妥昔单抗之间协同相互作用的可能性。