Preoperative chemotherapy and radiotherapy concomitant to cetuximab in resectable stage IIIB NSCLC: a multicentre phase 2 trial (SAKK 16/08)

被引:7
|
作者
Curioni-Fontecedro, Alessandra L. [1 ]
Perentes, Jean Yannis [2 ]
Gelpke, Hans [3 ]
Xyrafas, Alexandros [4 ]
Bouchaab, Hasna [2 ]
Mach, Nicolas [5 ]
Matzinger, Oscar [6 ]
Stojcheva, Nina [2 ]
Frueh, Martin [7 ,8 ]
Weder, Walter [1 ]
Cathomas, Richard [9 ]
Gargiulo, Piera [4 ]
Bubendorf, Lukas [10 ]
Pless, Miklos [3 ]
Betticher, Daniel [11 ]
Peters, Solange [2 ]
机构
[1] Univ Hosp Zurich, Zurich, Switzerland
[2] Univ Hosp Vaud, Lausanne, Switzerland
[3] Cantonal Hosp Winterthur, Winterthur, Switzerland
[4] SAKK Coordinating Ctr, Bern, Switzerland
[5] Univ Hosp Geneva, Geneva, Switzerland
[6] Hosp Riviera Chablais Vaud Valais, Vevey, Switzerland
[7] Cantonal Hosp St Gallen, St Gallen, Switzerland
[8] Univ Bern, Bern, Switzerland
[9] Cantonal Hosp Graubunden, Chur, Switzerland
[10] Univ Hosp Basel, Basel, Switzerland
[11] Cantonal Hosp Fribourg, Fribourg, Switzerland
关键词
CELL LUNG-CANCER; GROWTH-FACTOR RECEPTOR; INDUCTION CHEMORADIATION; NEOADJUVANT CHEMOTHERAPY; CLINICAL GUIDELINES; SURGICAL RESECTION; PLUS CHEMOTHERAPY; OPEN-LABEL; SURGERY; THERAPY;
D O I
10.1038/s41416-019-0447-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Neoadjuvant chemotherapy (CT) followed by radiotherapy (RT) and surgery showed a median survival of 28.7 months in resectable stage IIIB non-small-cell lung cancer (NSCLC) patients (pts). Here, we evaluate the impact of concomitant cetuximab to the same neoadjuvant chemo-radiotherapy (CRT) in selected patients (pts) with NSCLC, stage IIIB. METHODS: Resectable stage IIIB NSCLC received three cycles of CT (cisplatin 100 mg/m(2) and docetaxel 85 mg/m(2) d1, q3w) followed by RT (44 Gy in 22 fractions) with concomitant cetuximab (250 mg/m(2), q1w) and subsequent surgery. The primary endpoint was 1-year progression-free survival (PFS). RESULTS: Sixty-nine pts were included in the trial. Fifty-seven (83%) pts underwent surgery, with complete resection (R0) in 42 (74%) and postoperative 30 day mortality of 3.5%. Responses were: 57% after CT-cetuximab and 64% after CRT-cetuximab. Oneyear PFS was 50%. Median PFS was 12.0 months (95% CI: 9.0-15.6), median OS was 21.3 months, with a 2- and 3-yr survival of 41% and 30%, respectively. CONCLUSIONS: This is one of the largest prospective phase 2 trial to investigate the role of induction CRT and surgery in resectable stage IIIB disease, and the first adding cetuximab to the neoadjuvant strategy. This trial treatment is feasible with promising response and OS rates, supporting an aggressive approach in selected pts.
引用
收藏
页码:968 / 974
页数:7
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