Low-dose fractionated radiation with induction chemotherapy for locally advanced head and neck cancer: 5 year results of a prospective phase II trial

被引:8
|
作者
Gleason, John F., Jr. [1 ]
Kudrimoti, Mahesh [1 ]
Van Meter, Emily M. [2 ]
Mohiuddin, Mohammed [3 ]
Regine, William F. [4 ]
Valentino, Joseph [5 ,6 ]
Kenady, Daniel [7 ]
Arnold, Susanne M. [8 ]
机构
[1] Univ Kentucky, Markey Canc Ctr, Dept Radiat Med, Lexington, KY USA
[2] Univ Kentucky, Markey Canc Ctr, Div Canc Biostat, Lexington, KY USA
[3] King Faisal Specialist Hosp & Res Ctr, Riyadh, Saudi Arabia
[4] Univ Maryland, Dept Radiat Oncol, Baltimore, MD 21201 USA
[5] Univ Kentucky, Markey Canc Ctr, Dept Otolaryngol HNS, Lexington, KY USA
[6] Univ Kentucky, Markey Canc Ctr, Dept Surg, Lexington, KY USA
[7] Univ Kentucky, Markey Canc Ctr, Dept Surg, Div Gen Surg, Lexington, KY USA
[8] Markey Canc Ctr, Dept Internal Med, Div Med Oncol, Cc445,800 Rose St, Lexington, KY 40536 USA
关键词
Low-dose; Radiation; Induction; Chemotherapy;
D O I
10.1007/s13566-012-0074-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective This study aims to report the long-term outcomes of a novel treatment approach utilizing induction low-dose fractionated radiation therapy (LDFRT) and chemotherapy for locally advanced squamous cell carcinoma of head and neck (SCCHN). Methods We prospectively enrolled 40 patients with locally advanced SCCHN (77 % stage IV) on a phase II clinical trial and treated with induction paclitaxel (225 mg/m2), carboplatin (AUC 6), and LDFRT (80 cGy BID on days 1 and 2) every 21 days for two cycles. Results Forty patients enrolled; 39 were evaluable. The acute toxicity and response data have been previously reported; overall response rate (RR) was 82 %. After induction, definitive therapy was concurrent chemoradiation (CRT) in 51 %, XRT alone in 39 %, surgery in 5 %, and surgery and XRT in 5 %. The long-term outcomes are now reported with a median follow-up of 83 months. Locoregional control (LRC) is 80 % and distant control (DC) is 77 %. Five-year overall survival (OS), disease-specific survival, and progression-free survival (PFS) are 62 %, 66 %, and 58 %, respectively. Conclusion Induction chemotherapy with LDFRT has a high initial RR, comparable toxicity to two-drug induction regimens, but adds a third novel and effective agent, LDFRT. Five-year follow-up shows favorable outcomes compared to historical controls and excellent compliance with definitive therapy. This novel treatment approach is now planned for phase 3 trial evaluation.
引用
收藏
页码:35 / 42
页数:8
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