Nab-paclitaxel-based compared to docetaxel-based induction chemotherapy regimens for locally advanced squamous cell carcinoma of the head and neck

被引:20
|
作者
Schell, Amy [1 ]
Ley, Jessica [1 ]
Wu, Ningying [2 ]
Trinkaus, Kathryn [2 ]
Wildes, Tanya Marya [1 ,3 ]
Michel, Loren [1 ,3 ]
Thorstad, Wade [3 ,4 ]
Gay, Hiram [3 ,4 ]
Lewis, James [5 ,6 ]
Rich, Jason [3 ,6 ]
Diaz, Jason [3 ,6 ]
Paniello, Randal C. [3 ,6 ]
Nussenbaum, Brian [3 ,6 ]
Adkins, Douglas R. [1 ,3 ]
机构
[1] Washington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Div Biostat, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Alvin J Siteman Canc Ctr, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Radiat Oncol, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Div Surg Pathol, Dept Pathol & Immunol, St Louis, MO 63110 USA
[6] Washington Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, St Louis, MO 63110 USA
来源
CANCER MEDICINE | 2015年 / 4卷 / 04期
关键词
Docetaxel; head and neck cancer; induction chemotherapy; nab-paclitaxel; p16; TUMOR RESPONSE; PHASE-III; CISPLATIN; CETUXIMAB; FLUOROURACIL; TRIAL; CHEMORADIOTHERAPY; PROGNOSIS; SURVIVAL; PATHWAY;
D O I
10.1002/cam4.382
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We previously reported that nab-paclitaxel-based induction chemotherapy (IC) and concurrent chemoradiotherapy resulted in low relapse rates (13%) and excellent survival in head and neck squamous cell carcinoma (HNSCC). We compare the disease-specific survival (DSS) and overall survival (OS) between patients given nab-paclitaxel, cisplatin, and fluorouracil with cetuximab (APF-C) and historical controls given docetaxel, cisplatin, and fluorouracil with cetuximab (TPF-C). Patients with locally advanced HNSCC were treated with APF-C (n=30) or TPF-C (n=38). After 3 cycles of IC, patients were scheduled to receive cisplatin concurrent with definitive radiotherapy. T and N classification and smoking history were similar between the two groups and within p16-positive and p16-negative subsets. The median duration of follow-up for living patients in the APF-C group was 43.5 (range: 30-58)months versus 52 (range: 13-84)months for TPF-C. The 2-year DSS for patients treated with APF-C was 96.7% [95% Confidence Interval (CI): 85.2%, 99.8%] and with TPF-C was 77.6% (CI: 62.6%, 89.7%) (P=0.0004). Disease progression that resulted in death was more frequent in the TPF-C group (39%) compared with the APF-C group (3%) when adjusted for competing risks of death from other causes (Gray's test, P=0.0004). In p16 positive OPSCC, the 2-year DSS for APF-C was 100% and for TPF-C was 74.6% (CI: 47.4%, 94.6%) (P=0.0019) and the 2-year OS for APF-C was 94.1% (CI: 65.0%, 99.2%) and for TPF-C was 74.6% (CI: 39.8%, 91.1%) (P=0.013). In p16 negative HNSCC, the 2-year DSS for APF-C was 91.7% (CI: 67.6%, 99.6%) and for TPF-C was 82.6% (CI: 64.4%, 94.8%) (P=0.092). A 2-year DSS and OS were significantly better with a nab-paclitaxel-based IC regimen (APF-C) compared to a docetaxel-based IC regimen (TPF-C) in p16-positive OPSCC.
引用
收藏
页码:481 / 489
页数:9
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