Induction chemotherapy with the EXTREME regimen in frail patients with locally advanced head and neck squamous cell carcinoma

被引:2
|
作者
Cochin, Valerie [1 ,2 ]
de Mones, Erwan [3 ]
Digue, Laurence [1 ]
Garcia-Ramirez, Muriel [4 ]
Dupin, Charles [5 ]
Majoufre, Claire [2 ,6 ]
Fernandez, Philipe [2 ,7 ]
Daste, Amaury [1 ]
机构
[1] CHU Bordeaux, Bordeaux Univ Hosp, Hop St Andre, Dept Med Oncol, 1 Rue Jean Burguet, F-33000 Bordeaux, France
[2] Univ Bordeaux, Bordeaux, France
[3] CHU Bordeaux, Univ Hosp, Pellegrin Hosp, Dept Otolaryngol Head & Neck Surg, Bordeaux, France
[4] Robert Boulin Hosp, Dept Radiat Therapy, Libourne, France
[5] CHU Bordeaux, Univ Hosp, Haut Leveque Hosp, Dept Radiat Therapy, Bordeaux, France
[6] CHU Bordeaux, Univ Hosp, Pellegrin Hosp, Dept Oral & Maxillofacial Surg, Bordeaux, France
[7] CHU Bordeaux, Univ Hosp, Pellegrin Hosp, Dept Nucl Med, Bordeaux, France
关键词
PHASE-III; CONCURRENT CHEMORADIOTHERAPY; CISPLATIN; CETUXIMAB; FLUOROURACIL; DOCETAXEL; CANCER; TRIAL; PACLITAXEL;
D O I
10.1007/s11523-018-0552-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Induction chemotherapy (IC) with TPF (docetaxel, cisplatin, 5FU) for locally advanced head and neck squamous cell carcinoma (LAHNSCC) is limited to fit patients. We conducted a retrospective cohort study to assess the use of the EXTREME regimen (platinum-based therapy, 5FU, cetuximab) as IC in frail patients with LAHNSCC. Retrospective analysis of all consecutive patients with unresectable LAHNSCC treated with the EXTREME regimen, with or without 5FU as IC, from two French centers from 2008 to 2015. We assessed the rate of completed sequence defined as at least two cycles of IC and definitive radiation therapy. We included 34 patients with a median age of 56 years [44-70]. The primary site of tumor development was the oropharynx (67%, n=23, all HPV negative), hypopharynx (21%, n=7) and the oral cavity (12%, n=4). At inclusion, patients presented: T4 76, 5% (n=26), N2c 41% (n=14), N3 26% (n=9), stage disease IVa 62% (n=21), IVb 38% (n=13), ECOG PS2 38% (n=13), decreased weight (10% in one month or 15% in 6 months) 74% (n=25). The sequence was achieved for 76% (n=26) of patients and 80% (n=27) presented a clinical response after the chemotherapy course with notably increased weight (40%, n=11) or general status (75%, n=26). Median PFS and OS were 5.7 and 15.5 months, respectively. Disease progression at 3 months was significantly associated with decreased median overall survival (13.6 versus 21.9 months, p=0.01). This is the first study to report the use of the EXTREME regimen as induction chemotherapy, and although this IC was used in a very frail population, the majority completed the sequence with significant clinical benefit.
引用
收藏
页码:247 / 252
页数:6
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