Cetuximab combined with paclitaxel or paclitaxel alone for patients with recurrent or metastatic head and neck squamous cell carcinoma progressing after EXTREME

被引:11
作者
Chevalier, Thomas [1 ]
Daste, Amaury [2 ]
Saada-Bouzid, Esmaa [3 ]
Loundou, Anderson [4 ]
Peyraud, Florent [2 ]
Lambert, Tiphaine [5 ,6 ]
Le Tourneau, Christophe [5 ,6 ]
Peyrade, Frederic [3 ]
Dupuis, Charlotte [1 ]
Alfonsi, Marc [7 ]
Fayette, Jerome [8 ]
Reure, Juliette [8 ]
Huguet, Florence [9 ]
Fakhry, Nicolas [10 ]
Toullec, Clemence [11 ]
Salas, Sebastien [1 ]
机构
[1] CHU Timone, AP HM, Dept Med Oncol, Marseille, France
[2] Bordeaux Univ Hosp CHU, Hop St Andre, Dept Med Oncol, Bordeaux, France
[3] Ctr Antoine Lacassagne, Dept Med Oncol, Nice, France
[4] Aix Marseille Univ, Self Perceived Hlth Assessment Res Unit, EA3279, Marseille, France
[5] Paris Saclay Univ, Dept Drug Dev & Innovat D3i, Inst Curie, Paris, France
[6] Paris Saclay Univ, Dept Drug Dev & Innovat D3i, Inst Curie, St Cloud, France
[7] Clin St Catherine, Dept Radiat Oncol, Avignon, France
[8] Univ Lyon, Leon Berard Ctr, Dept Med Oncol, Lyon, France
[9] Paris Sorbonne Univ, Tenon Hosp, Assistance Publ Hop Paris, Dept Radiat Oncol, Paris, France
[10] Aix Marseille Univ, AP HM, Dept Otorhinolaryngol Head & Neck Surg, Marseille, France
[11] Clin St Catherine, Dept Med Oncol, Avignon, France
关键词
cetuximab; chemotherapy; EXTREME; paclitaxel; Recurrent; metastatic head and neck squamous cell carcinoma; CHEMOTHERAPY PLUS CETUXIMAB; PLATINUM-BASED CHEMOTHERAPY; RECURRENT/METASTATIC HEAD; SALVAGE CHEMOTHERAPY; PHASE-II; COMBINATION; INHIBITORS; EXPRESSION; EFFICACY; EVALUATE;
D O I
10.1002/cam4.3953
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND Prognosis of recurrent or metastatic (R/M) head and neck squamous cell carcinoma (HNSCC) remains poor. The addition of cetuximab, to platinum and fluorouracil chemotherapy (EXTREME regimen) has been shown to improve patients' outcomes in first-line settings. METHODS We conducted a retrospective, multicenter study, including HNSCC that progressed after a first line of platinum-based chemotherapy and cetuximab, treated either by paclitaxel + cetuximab (PC) or paclitaxel alone (P), between January 2010 and April 2018. The end points were overall survival (OS), progression-free survival (PFS), and overall response rates (ORR). Patients were matched according to their propensity scores, estimated with a logistic regression model. The secondary objectives were to study the safety profile and to look for prognostic and predictive factors of effectiveness. RESULTS Of the 340 identified patients, 262 were included in the analysis, 165 received PC, and 97 received P. In unmatched population, ORR was 16.4% with PC and 6.2% for P. Median PFS was 2.9 months [95% Confidence Interval 2.7-3.0] for PC versus 2.5 months [2.2-2.7] for P, hazard ratio (HR) = 0.770 [0.596-0.996]. Median OS was 5.5 months [4.4-6.9] for PC versus 4.2 months [3.4-4.8] for P, HR = 0.774 [0.590-1.015]. In multivariate analysis, PC was associated with better PFS and OS. These results were consistent in matched-paired population. Previous cetuximab maintenance for more than 3 months was predictive of better OS with PC. CONCLUSION Although the continuation of cetuximab in combination with paclitaxel after EXTREME provides moderate benefit, it could be an interesting option for selected patients.
引用
收藏
页码:3952 / 3963
页数:12
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