Department of Radiation Oncology, Medical University of South Carolina, Charleston, South Carolina 29414, USA.
Laryngoscope. 2010 Feb;120(2):236-42. doi: 10.1002/lary.20536.
OBJECTIVES/HYPOTHESIS: The optimal concurrent chemoradiotherapy regimen for definitive treatment of locoregionally advanced head and neck cancer remains to be determined. The present investigation reports toxicities, disease control, patterns of failure, and survival outcomes in a large mature cohort of patients treated with low-dose weekly platinum-based concurrent chemoradiotherapy.
Retrospective single-institution series.
Toxicity and outcome data for locoregionally advanced head and neck cancer patients treated with low-dose weekly platinum-based chemotherapy concurrent with standard fractionation radiotherapy were retrospectively collected and analyzed from a clinical database. Survival analysis methods, including Kaplan-Meier estimation and competing risks analysis, were used to assess locoregional disease control, freedom from failure, and overall survival.
Ninety-six patients were eligible for the present analysis. Nearly all patients had American Joint Committee on Cancer clinical stage III to IVB disease (99%). Severe acute toxicities included grade 3 mucositis (61%), grade 3/4 nausea (27%/1%), and grade 3 neutropenia (8%). Thirty-seven patients (38%) required hospitalization for a median of 7 days (range, 1-121). Ninety-two percent of patients completed the fully prescribed course of radiotherapy, and 87% completed >or=6 cycles of chemotherapy. At a median survivor follow-up of 40 months (range, 8-68), 47% of patients were without evidence of disease recurrence. The estimated 4-year freedom from failure and overall survival were 48% and 58%, respectively. Initial site(s) of disease failure were locoregional for 22 patients, locoregional and distant (five patients), and distant only (14 patients).
Weekly low-dose platinum-based chemotherapy with full-dose daily radiotherapy is a tolerable alternative regimen for locoregionally advanced head and neck cancers, with comparable efficacy and patterns of failure to alternative regimens.
目的/假设:局部晚期头颈部癌症的确定性治疗的最佳同期放化疗方案仍有待确定。本研究报告了大例成熟队列患者接受低剂量每周铂类同期放化疗的毒性、疾病控制、失败模式和生存结果。
回顾性单机构系列。
从临床数据库中回顾性收集和分析局部晚期头颈部癌症患者接受低剂量每周铂类化疗联合标准分割放疗的毒性和结局数据。生存分析方法,包括 Kaplan-Meier 估计和竞争风险分析,用于评估局部区域疾病控制、无失败自由和总生存。
96 例患者符合本分析条件。几乎所有患者均患有美国癌症联合委员会临床分期 III 至 IVB 期疾病(99%)。严重的急性毒性包括 3 级黏膜炎(61%)、3/4 级恶心(27%/1%)和 3 级中性粒细胞减少症(8%)。37 例患者(38%)需要住院治疗,中位数为 7 天(范围为 1-121 天)。92%的患者完成了全剂量放疗的全疗程,87%的患者完成了>或=6 个周期的化疗。在中位数为 40 个月(范围为 8-68 个月)的幸存者随访中,47%的患者无疾病复发证据。估计的 4 年无失败和总生存率分别为 48%和 58%。初始疾病失败部位为局部区域 22 例,局部区域和远处(5 例),远处(14 例)。
全剂量每日放疗联合每周低剂量铂类化疗是局部晚期头颈部癌症的一种可耐受的替代方案,与其他方案的疗效和失败模式相当。