First-cycle rash and survival in patients with advanced non-small-cell lung cancer receiving cetuximab in combination with first-line chemotherapy: a subgroup analysis of data from the FLEX phase 3 study

被引:93
作者
Gatzemeier, Ulrich [1 ]
von Pawel, Joachim [2 ]
Vynnychenko, Ihor [3 ]
Zatloukal, Petr [4 ,5 ]
de Marinis, Filippo [6 ]
Eberhardt, Wilfried E. E. [7 ]
Paz-Ares, Luis [8 ,9 ]
Schumacher, Karl-Maria [10 ]
Goddemeier, Thomas [10 ]
O'Byrne, Kenneth J. [11 ]
Pirker, Robert [12 ]
机构
[1] Hosp Grosshansdorf, Dept Thorac Oncol, Hamburg, Germany
[2] Zentrum Onkol, Gauting, Germany
[3] Sumy Reg Oncol Ctr, Sumy, Ukraine
[4] Charles Univ Prague, Fac Med 3, Prague, Czech Republic
[5] Fac Hosp Bulovka, Prague, Czech Republic
[6] San Camillo Forlanini Hosp, Oncol Pulm Unit 1, Rome, Italy
[7] Univ Duisburg Essen, W German Tumour Ctr, Essen, Germany
[8] Inst Biomed Sevilla, Seville, Spain
[9] Hosp Univ Virgen Rocio, Seville, Spain
[10] Merck KGaA, Darmstadt, Germany
[11] St James Hosp, Dublin, Ireland
[12] Med Univ Vienna, Dept Med 1, Vienna, Austria
关键词
GROWTH-FACTOR RECEPTOR; METASTATIC COLORECTAL-CANCER; ANTIBODY CETUXIMAB; DOSE-ESCALATION; II MULTICENTER; SKIN REACTIONS; MANAGEMENT; INHIBITORS; TRIAL; HEAD;
D O I
10.1016/S1470-2045(10)70278-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The randomised phase 3 First-Line Erbitux in Lung Cancer (FLEX) study showed that the addition of cetuximab to cisplatin and vinorelbine significantly improved overall survival compared with chemotherapy alone in the first-line treatment of advanced non-small-cell lung cancer (NSCLC). The main cetuximab-related side-effect was acne-like rash. Here, we assessed the association of this acne-like rash with clinical benefit. Methods We did a subgroup analysis of patients in the FLEX study, which enrolled patients with advanced NSCLC whose tumours expressed epidermal growth factor receptor. Our landmark analysis assessed if the development of acne-like rash in the first 21 days of treatment (first-cycle rash) was associated with clinical outcome, on the basis of patients in the intention-to-treat population alive on day 21. The FLEX study is registered with ClinicalTrials.gov, number NCT00148798. Findings 518 patients in the chemotherapy plus cetuximab group-290 of whom had first-cycle rash and 540 patients in the chemotherapy alone group were alive on day 21. Patients in the chemotherapy plus cetuximab group with first-cycle rash had significantly prolonged overall survival compared with patients in the same treatment group without first-cycle rash (median 15.0 months [95% CI 12.8-16.4] vs 8.8 months [7.6-11.1]; hazard ratio [HR] 0.631 [0.515-0.774]; p<0.0001). Corresponding significant associations were also noted for progression-free survival (median 5.4 months [5.2-5.7] vs 4.3 months [4.1-5.3]; HR 0.741 [0.607-0.905]; p=0.0031) and response (rate 44.8% [39.0-50.8] vs 32.0% [26.0-38.5]; odds ratio 1.703 [1.186-2.448]; p=0.0039). Overall survival for patients without first-cycle rash was similar to that of patients that received chemotherapy alone (median 8.8 months [7.6-11.1] vs 10.3 months [9.6-11.3]; HR 1.085 [0.910-1.293]; p=0.36). The significant overall survival benefit for patients with first-cycle rash versus without was seen in all histology subgroups: adenocarcinoma (median 16.9 months, [14.1-20.6] vs 9.3 months [7.7-13.2]; HR 0.614 [0.453-0.832]; p=0.0015), squamous-cell carcinoma (median 13.2 months [10.6-16.0] vs 8.1 months [6.7-12.6]; HR 0.659 [0.472-0.921]; p=0.014), and carcinomas of other histology (median 12.6 months [9.2-16.4] vs 6.9 months [5.2-11.0]; HR 0.616 [0.392-0.966]; p=0.033). Interpretation First-cycle rash was associated with a better outcome in patients with advanced NSCLC who received cisplatin and vinorelbine plus cetuximab as a first-line treatment. First-cycle rash might be a surrogate clinical marker that could be used to tailor cetuximab treatment for advanced NSCLC to those patients who would be most likely to derive a significant benefit.
引用
收藏
页码:30 / 37
页数:8
相关论文
共 27 条
[1]   American Society of Clinical Oncology Clinical Practice Guideline Update on Chemotherapy for Stage IV Non-Small-Cell Lung Cancer [J].
Azzoli, Christopher G. ;
Baker, Sherman, Jr. ;
Temin, Sarah ;
Pao, William ;
Aliff, Timothy ;
Brahmer, Julie ;
Johnson, David H. ;
Laskin, Janessa L. ;
Masters, Gregory ;
Milton, Daniel ;
Nordquist, Luke ;
Pfister, David G. ;
Piantadosi, Steven ;
Schiller, Joan H. ;
Smith, Reily ;
Smith, Thomas J. ;
Strawn, John R. ;
Trent, David ;
Giaccone, Giuseppe .
JOURNAL OF ONCOLOGY PRACTICE, 2010, 6 (01) :39-43
[2]   Phase II multicenter study of the antiepidermal growth factor receptor monoclonal antibody cetuximab in combination with platinum-based chemotherapy in patients with platinum-refractory metastatic and/or recurrent squamous cell carcinoma of the head and neck [J].
Baselga, J ;
Trigo, JM ;
Bourhis, J ;
Tortochaux, J ;
Cortés-Funes, H ;
Hitt, R ;
Gascón, P ;
Arnellal, N ;
Harstrick, A ;
Eckardt, A .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (24) :5568-5577
[3]   Fluorouracil, Leucovorin, and Oxaliplatin With and Without Cetuximab in the First-Line Treatment of Metastatic Colorectal Cancer [J].
Bokemeyer, Carsten ;
Bondarenko, Igor ;
Makhson, Anatoly ;
Hartmann, Joerg T. ;
Aparicio, Jorge ;
de Braud, Filippo ;
Donea, Serban ;
Ludwig, Heinz ;
Schuch, Gunter ;
Stroh, Christopher ;
Loos, Anja H. ;
Zubel, Angela ;
Koralewski, Piotr .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (05) :663-671
[4]   Radiotherapy plus cetuximab for locoregionally advanced head and neck cancer: 5-year survival data from a phase 3 randomised trial, and relation between cetuximab-induced rash and survival [J].
Bonner, James A. ;
Harari, Paul M. ;
Giralt, Jordi ;
Cohen, Roger B. ;
Jones, Christopher U. ;
Sur, Ranjan K. ;
Raben, David ;
Baselga, Jose ;
Spencer, Sharon A. ;
Zhu, Junming ;
Youssoufian, Hagop ;
Rowinsky, Eric K. ;
Ang, K. Kian .
LANCET ONCOLOGY, 2010, 11 (01) :21-28
[5]   Phase III randomized trial of cisplatin plus placebo compared with cisplatin plus cetuximab in metastatic/recurrent head and neck cancer: An eastern cooperative oncology group study [J].
Burtness, B ;
Goldwasser, MA ;
Flood, W ;
Mattar, B ;
Forastiere, AA .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (34) :8646-8654
[6]   Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer [J].
Cunningham, D ;
Humblet, Y ;
Siena, S ;
Khayat, D ;
Bleiberg, H ;
Santoro, A ;
Bets, D ;
Mueser, M ;
Harstrick, A ;
Verslype, C ;
Chau, I ;
Van Cutsem, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (04) :337-345
[7]   An interdisciplinary consensus on managing skin reactions associated with human epidermal growth factor receptor inhibitors [J].
Eaby, Beth ;
Culkin, Ann ;
Lacouture, Mario E. .
CLINICAL JOURNAL OF ONCOLOGY NURSING, 2008, 12 (02) :283-290
[8]   Phase II multicenter study of the epidermal growth factor receptor antibody cetuximab and cisplatin for recurrent and refractory squamous cell carcinoma of the head and neck [J].
Herbst, RS ;
Arquette, M ;
Shin, DM ;
Dicke, K ;
Vokes, EE ;
Azarnia, N ;
Hong, WK ;
Kies, MS .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (24) :5578-5587
[9]   Cutaneous side effects of epidermal growth factor receptor inhibitors: Clinical presentation, pathogenesis, and management [J].
Hu, Jenny C. ;
Sadeghi, Parrish ;
Pinter-Brown, Lauren C. ;
Yashar, Sharona ;
Chin, Melvin W. .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2007, 56 (02) :317-326
[10]   Cetuximab dose-escalation in patients (pts) with metastatic colorectal cancer (mCRC) with no or slight skin reactions on standard treatment: pharmacokinetic (PK), pharmacodynamic (PD) and efficacy data from the EVEREST study [J].
Humblet, Y. ;
Peeters, M. ;
Gelderblom, H. ;
Vermorken, J. B. ;
Viret, F. ;
Glimelius, B. ;
Ciardiello, F. ;
Gallerani, E. ;
Kisker, O. ;
Van Cutsem, E. .
EJC SUPPLEMENTS, 2007, 5 (04) :240-240