Predictability of antitumor efficacy of cetuximab plus irinotecan based on skin rash severity according to observation period in patients with metastatic colorectal cancer following failure of fluorouracil, irinotecan and oxaliplatin

被引:3
作者
Horie, Yoshiki [1 ,2 ]
Yamazaki, Kentaro [2 ]
Funakoshi, Taro [2 ]
Hamauchi, Satoshi [2 ]
Taniguchi, Hiroya [2 ]
Tsushima, Takahiro [2 ]
Todaka, Akiko [2 ]
Machida, Nozomu [2 ]
Taku, Keisei [2 ]
Fukutomi, Akira [2 ]
Onozawa, Yusuke [2 ]
Yasui, Hirofumi [2 ]
Mizukami, Takuro [1 ]
Izawa, Naoki [1 ]
Hirakawa, Mami [1 ]
Tsuda, Takashi [1 ]
Nakajima, Takako [1 ]
Boku, Narikazu [1 ]
机构
[1] St Marianna Univ, Sch Med, Dept Clin Oncol, Kawasaki, Kanagawa 2168511, Japan
[2] Shizuoka Canc Ctr, Div Gastrointestinal Oncol, Shizuoka, Shizuoka 4118777, Japan
关键词
colorectal cancer; cetuximab; skin rash; predictability;
D O I
10.3892/mco.2015.586
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The efficacy of cetuximab correlates with the severity of skin toxicity, although its onset may vary. The aim of this retrospective study was to investigate the optimal observation period for skin rash as a predictor of the efficacy of cetuximab plus irinotecan. The subjects comprised 33 patients with KRAS wild-type metastatic colorectal cancer (mCRC) who had received prior chemotherapy with fluorouracil, irinotecan and oxaliplatin. The response rate (RR), progression-free survival (PFS) and overall survival (OS) were compared according to the presence or absence of >= grade 2 skin rash within 2, 4, 6, or 8 weeks following cetuximab initiation. The overall RR was 45% (15/33) and the median PFS and OS were 188 and 383 days, respectively. A total of 26 patients experienced >= grade 2 skin rash within 8 weeks. The proportion of responders among patients who developed >= grade 2 skin rash (severe group) decreased depending on the duration of the observation period (50% within 8 weeks), whereas the proportion of non-responders among patients with <grade 2 skin rash (mild group) increased (71% within 8 weeks). Similarly, the proportion of patients with an unfavorable prognosis (PFS <6 months, OS <1 year) in the mild group increased (86%for PFS and 71% for OS within 8 weeks), whereas the proportion of those with a favorable prognosis in the severe group remained stable (73% for PFS and 62% for OS within 8 weeks). Therefore, the absence of >= grade 2 skin rash within 8 weeks may be predictive of unfavorable efficacy of cetuximab plus irinotecan in mCRC patients.
引用
收藏
页码:1029 / 1034
页数:6
相关论文
共 10 条
[1]   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
[2]   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
[3]   Survival of patients with advanced colorectal cancer improves with the availability of fluorouracil-leucovorin, irinotecan, and oxaliplatin in the course of treatment [J].
Grothey, A ;
Sargent, D ;
Goldberg, RM ;
Schmoll, HJ .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (07) :1209-1214
[4]   A Japanese Post-marketing Surveillance of Cetuximab (Erbitux) in Patients with Metastatic Colorectal Cancer [J].
Ishiguro, Megumi ;
Watanabe, Toshiaki ;
Yamaguchi, Kensei ;
Satoh, Taroh ;
Ito, Hideyuki ;
Seriu, Taku ;
Sakata, Yuh ;
Sugihara, Kenichi .
JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2012, 42 (04) :287-294
[5]   Cetuximab for the treatment of colorectal cancer [J].
Jonker, Derek J. ;
O'Callaghan, Chris J. ;
Karapetis, Christos S. ;
Zalcberg, John R. ;
Tu, Dongsheng ;
Au, Heather-Jane ;
Berry, Scott R. ;
Krahn, Marianne ;
Price, Timothy ;
Simes, R. John ;
Tebbutt, Niall C. ;
van Hazel, Guy ;
Wierzbicki, Rafal ;
Langer, Christiane ;
Moore, Malcolm J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (20) :2040-2048
[6]   Skin Toxicity Evaluation Protocol With Panitumumab (STEPP), a Phase II, Open-Label, Randomized Trial Evaluating the Impact of a Pre-Emptive Skin Treatment Regimen on Skin Toxicities and Quality of Life in Patients With Metastatic Colorectal Cancer [J].
Lacouture, Mario E. ;
Mitchell, Edith P. ;
Piperdi, Bilal ;
Pillai, Madhavan V. ;
Shearer, Heather ;
Iannotti, Nicholas ;
Xu, Feng ;
Yassine, Mohamed .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (08) :1351-1357
[7]   Status of epidermal growth factor receptor antagonists in the biology and treatment of cancer [J].
Mendelsohn, J ;
Baselga, J .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (14) :2787-2799
[8]   EPIC:: Phase III trial of cetuximab plus irinotecan after fluoropyrimidine and oxaliplatin failure in patients with metastatic colorectal cancer [J].
Sobrero, Alberto F. ;
Maurel, Joan ;
Fehrenbacher, Louis ;
Scheithauer, Werner ;
Abubakr, Yousif A. ;
Lutz, Manfred P. ;
Vega-Villegas, M. Eugenia ;
Eng, Cathy ;
Steinhauer, Ernst U. ;
Prausova, Jana ;
Lenz, Heinz-Josef ;
Borg, Christophe ;
Middleton, Gary ;
Kroening, Hendrik ;
Luppi, Gabriele ;
Kisker, Oliver ;
Zubel, Angela ;
Langer, Christiane ;
Kopit, Justin ;
Burris, Howard A., III .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (14) :2311-2319
[9]  
Van Cutsem E, 2007, JOP, V10, P361
[10]   Cetuximab and Chemotherapy as Initial Treatment for Metastatic Colorectal Cancer [J].
Van Cutsem, Eric ;
Koehne, Claus-Henning ;
Hitre, Erika ;
Zaluski, Jerzy ;
Chien, Chung-Rong Chang ;
Makhson, Anatoly ;
D'Haens, Geert ;
Pinter, Tamas ;
Lim, Robert ;
Bodoky, Gyoergy ;
Roh, Jae Kyung ;
Folprecht, Gunnar ;
Ruff, Paul ;
Stroh, Christopher ;
Tejpar, Sabine ;
Schlichting, Michael ;
Nippgen, Johannes ;
Rougier, Philippe .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (14) :1408-1417