Wiegand Susanne, Wichmann Gunnar, Vogt Jeannette, Vogel Kathrin, Franke Annegret, Kuhnt Thomas, Lordick Florian, Scheuble Anne-Marie, Hambsch Peter, Brossart Peter, Bauernfeind Franz Georg, Kaftan Holger, Maschmeyer Georg, Paland Matthias, Münter Marc, Lewitzki Victor, Rotter Nicole, Stromberger Carmen, Beck Marcus, Dommerich Steffen, Gauler Thomas Christoph, Hapke Gunnar, Guntinas-Lichius Orlando, Schröder Ursula, Görner Martin, Hautmann Matthias G, Steger Felix, Tamaskovics Bálint, Schmiedeknecht Anett, Dietz Andreas
Department of Otolaryngology, Head and Neck Surgery, Leipzig University Medical Center, Leipzig, Germany.
Clinical Trial Centre Leipzig, University of Leipzig, Leipzig, Germany.
Front Oncol. 2023 Mar 21;13:1128176. doi: 10.3389/fonc.2023.1128176. eCollection 2023.
Most of the patients with head and neck squamous cell carcinoma (HNSCC) are diagnosed with locally advanced disease. Standards of care for curative-intent treatment of this patient group are either surgery and adjuvant radio(chemo)therapy (aRCT) or definitive chemoradiation. Despite these treatments, especially pathologically intermediate and high-risk HNSCC often recur. The ADRISK trial investigates in locally advanced HNSCC and intermediate and high risk after up-front surgery if the addition of pembrolizumab to aRCT with cisplatin improves event-free sur-vival compared to aRCT alone. ADRISK is a prospective, randomized controlled investiga-tor-initiated (IIT)-phase II multicenter trial within the German Interdisciplinary Study Group of German Cancer Society (IAG-KHT). Patients with primary resectable stage III and IV HNSCC of the oral cavity, oropharynx, hypopharynx and larynx with pathologic high (R1, extracapsular nodal extension) or intermediate risk (R0 <5 mm; N≥2) after surgery will be eligible. Two hun-dred forty patients will be randomly assigned (1:1) to either standard aRCT with cisplatin (standard arm) or aRCT with cisplatin + pembrolizumab (200 mg iv, in 3-week cycle, max. 12 months) (interventional arm). Endpoints are event-free and overall survival. Recruitment started in August 2018 and is ongoing.
大多数头颈部鳞状细胞癌(HNSCC)患者被诊断为局部晚期疾病。该患者群体根治性治疗的护理标准是手术和辅助放(化)疗(aRCT)或根治性放化疗。尽管有这些治疗方法,但尤其是病理上为中高危的HNSCC常常复发。ADRISK试验在局部晚期HNSCC以及 upfront手术(新辅助手术)后为中高危患者中研究,与单纯aRCT相比,在含顺铂的aRCT中加入帕博利珠单抗是否能改善无事件生存期。ADRISK是德国癌症协会德国跨学科研究小组(IAG-KHT)开展的一项前瞻性、随机对照研究者发起的(IIT)II期多中心试验。符合条件的患者为口腔、口咽、下咽和喉的原发性可切除III期和IV期HNSCC患者,术后病理为高风险(R1,包膜外淋巴结转移)或中风险(R0<5mm;N≥2)。240名患者将被随机分配(1:1)至含顺铂的标准aRCT(标准组)或含顺铂 + 帕博利珠单抗(200mg静脉注射,每3周1次,最长12个月)的aRCT(干预组)。终点指标为无事件生存期和总生存期。招募工作于2018年8月开始,目前仍在进行。