Argiris Athanassios, Brockstein Bruce E, Haraf Daniel J, Stenson Kerstin M, Mittal Bharat B, Kies Merrill S, Rosen Fred R, Jovanovic Borko, Vokes Everett E
The Feinberg School of Medicine and the Robert H Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL 60611, USA.
Clin Cancer Res. 2004 Mar 15;10(6):1956-62. doi: 10.1158/1078-0432.ccr-03-1077.
The purpose of this retrospective analysis was to evaluate the emergence of second primary malignancies and the contribution of different causes of death to the outcome of patients with locoregionally advanced head and cancer receiving primary chemoradiotherapy.
We studied 324 patients with stage IV squamous cell head and neck cancer who were enrolled on five consecutive multicenter Phase II studies of concurrent chemoradiotherapy. All of the regimens included concurrent 5-fluorouracil and hydroxyurea on an alternate week schedule with radiotherapy, either alone (FHX) or with cisplatin (C-FHX) or paclitaxel (T-FHX). The cumulative incidence of second primary tumors or death from any cause was estimated using methods of competing risk analysis.
Median follow-up of surviving patients was 5.2 years (2-10.6 years). The 5-year overall survival and progression-free survival of the cohort were 46% and 65%, respectively. Causes of death and median time of occurrence were as follows: disease (n = 88; 1.5 years), treatment-associated acute or late complications (n = 30; 4 months), second primary tumors (n = 18; 3.5 years), comorbidities (n = 41; 1.9 years), and unknown (n = 20; 5.1 years). Predominant causes of death from comorbidities were cardiac and respiratory illnesses. Twenty-six patients (8%) developed a second primary tumor at a median time of 2.8 years (4 months to 10 years). The cumulative incidence of second primary tumors was 5%, 7%, and 13% at 3, 5, and 10 years, respectively. The most frequent site of second primaries was the lung (n = 13), followed by the esophagus (n = 3) and head and neck (n = 2)
Patients with locoregionally advanced head and neck cancer treated with concurrent chemoradiotherapy are potentially curable but face significant risks of mortality from causes other than disease progression. Ameliorating toxicity, and implementing secondary screening and chemoprevention strategies are major goals in the management of head and neck cancer.
本回顾性分析的目的是评估第二原发性恶性肿瘤的出现情况,以及不同死亡原因对接受原发性放化疗的局部晚期头颈癌患者预后的影响。
我们研究了324例IV期头颈鳞状细胞癌患者,这些患者参加了连续五项同步放化疗的多中心II期研究。所有方案均包括在放疗的交替周方案中同时使用5-氟尿嘧啶和羟基脲,单独使用(FHX)或与顺铂(C-FHX)或紫杉醇(T-FHX)联合使用。使用竞争风险分析方法估计第二原发性肿瘤或任何原因导致的死亡的累积发生率。
存活患者的中位随访时间为5.2年(2 - 10.6年)。该队列的5年总生存率和无进展生存率分别为46%和65%。死亡原因及中位发生时间如下:疾病(n = 88;1.5年)、治疗相关的急性或晚期并发症(n = 30;4个月)、第二原发性肿瘤(n = 18;3.5年)、合并症(n = 41;1.9年)和不明原因(n = 20;5.1年)。合并症导致死亡的主要原因是心脏和呼吸系统疾病。26例患者(8%)在中位时间2.8年(4个月至10年)时发生了第二原发性肿瘤。第二原发性肿瘤的累积发生率在3年、5年和10年时分别为5%、7%和13%。第二原发性肿瘤最常见的部位是肺(n = 13),其次是食管(n = 3)和头颈(n = 2)。
接受同步放化疗的局部晚期头颈癌患者有可能治愈,但面临疾病进展以外原因导致的显著死亡风险。改善毒性,实施二级筛查和化学预防策略是头颈癌管理的主要目标。