Literature DB >> 20072801

Phase II study of combination chemotherapy with irinotecan and cetuximab for pretreated metastatic colorectal cancer harboring wild-type KRAS.

Kohei Shitara1, Tomoya Yokota, Daisuke Takahari, Takashi Shibata, Takashi Ura, Setsuo Utsunomiya, Yoshitaka Inaba, Hidekazu Yamaura, Yozo Sato, Mina Najima, Hiroki Kawai, Masahiro Tajika, Akira Sawaki, Yasushi Yatabe, Kei Muro.   

Abstract

The aim of this study was to prospectively evaluate the efficacy of combination irinotecan and cetuximab chemotherapy in patients with pretreated metastatic colorectal cancer harboring wild-type KRAS. Patients with metastatic colorectal cancer that had progressed after chemotherapy with irinotecan, oxaliplatin, and fluoropyrimidine were included. KRAS status was evaluated using the Cycleave PCR method; only patients without KRAS mutations were included. Cetuximab was administered initially at 400 mg/m² followed by weekly 250 mg/m² infusions. Irinotecan was administered biweekly. From October 2008 to April 2009, a total of 30 patients were enrolled. The objective response rate was 30.0% (95% confidence interval [CI], 14.7-49.4%) and the disease control rate (complete response, partial response, or stable disease) was 80.0% (95% CI, 61.4-92.3%). Among the 15 patients with stable disease, 11 patients experienced >10% tumor shrinkage. Median progression-free survival was 5.8 months (95% CI, 4.1-7.6). Median overall survival was not reached at a median follow-up of 10.1 months. Grade 2 skin toxicity was observed in 23 patients, while no grade 3 skin toxicity was observed. Combined irinotecan and cetuximab is effective for pretreated metastatic wild-type KRAS colorectal cancer.

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Year:  2010        PMID: 20072801     DOI: 10.1007/s10637-009-9382-x

Source DB:  PubMed          Journal:  Invest New Drugs        ISSN: 0167-6997            Impact factor:   3.850


  16 in total

1.  New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada.

Authors:  P Therasse; S G Arbuck; E A Eisenhauer; J Wanders; R S Kaplan; L Rubinstein; J Verweij; M Van Glabbeke; A T van Oosterom; M C Christian; S G Gwyther
Journal:  J Natl Cancer Inst       Date:  2000-02-02       Impact factor: 13.506

2.  Multicenter phase II and translational study of cetuximab in metastatic colorectal carcinoma refractory to irinotecan, oxaliplatin, and fluoropyrimidines.

Authors:  Heinz-Josef Lenz; Eric Van Cutsem; Shirin Khambata-Ford; Robert J Mayer; Philip Gold; Philip Stella; Barry Mirtsching; Allen L Cohn; Andrew W Pippas; Nozar Azarnia; Zenta Tsuchihashi; David J Mauro; Eric K Rowinsky
Journal:  J Clin Oncol       Date:  2006-10-20       Impact factor: 44.544

3.  PI3KCA/PTEN deregulation contributes to impaired responses to cetuximab in metastatic colorectal cancer patients.

Authors:  F Perrone; A Lampis; M Orsenigo; M Di Bartolomeo; A Gevorgyan; M Losa; M Frattini; C Riva; S Andreola; E Bajetta; L Bertario; E Leo; M A Pierotti; S Pilotti
Journal:  Ann Oncol       Date:  2008-07-31       Impact factor: 32.976

4.  Cetuximab for the treatment of colorectal cancer.

Authors:  Derek J Jonker; Chris J O'Callaghan; Christos S Karapetis; John R Zalcberg; Dongsheng Tu; Heather-Jane Au; Scott R Berry; Marianne Krahn; Timothy Price; R John Simes; Niall C Tebbutt; Guy van Hazel; Rafal Wierzbicki; Christiane Langer; Malcolm J Moore
Journal:  N Engl J Med       Date:  2007-11-15       Impact factor: 91.245

5.  PTEN expression and KRAS mutations on primary tumors and metastases in the prediction of benefit from cetuximab plus irinotecan for patients with metastatic colorectal cancer.

Authors:  Fotios Loupakis; Luca Pollina; Irene Stasi; Annamaria Ruzzo; Mario Scartozzi; Daniele Santini; Gianluca Masi; Francesco Graziano; Chiara Cremolini; Eliana Rulli; Emanuele Canestrari; Niccola Funel; Gaia Schiavon; Iacopo Petrini; Mauro Magnani; Giuseppe Tonini; Daniela Campani; Irene Floriani; Stefano Cascinu; Alfredo Falcone
Journal:  J Clin Oncol       Date:  2009-04-27       Impact factor: 44.544

6.  PIK3CA mutation/PTEN expression status predicts response of colon cancer cells to the epidermal growth factor receptor inhibitor cetuximab.

Authors:  Minaxi Jhawer; Sanjay Goel; Andrew J Wilson; Cristina Montagna; Yi-He Ling; Do-Sun Byun; Shannon Nasser; Diego Arango; Joongho Shin; Lidija Klampfer; Leonard H Augenlicht; Roman Perez-Soler; Roman Perez Soler; John M Mariadason
Journal:  Cancer Res       Date:  2008-03-15       Impact factor: 12.701

7.  K-ras mutations and benefit from cetuximab in advanced colorectal cancer.

Authors:  Christos S Karapetis; Shirin Khambata-Ford; Derek J Jonker; Chris J O'Callaghan; Dongsheng Tu; Niall C Tebbutt; R John Simes; Haji Chalchal; Jeremy D Shapiro; Sonia Robitaille; Timothy J Price; Lois Shepherd; Heather-Jane Au; Christiane Langer; Malcolm J Moore; John R Zalcberg
Journal:  N Engl J Med       Date:  2008-10-23       Impact factor: 91.245

8.  Disproportionate representation of KRAS gene mutation in atypical adenomatous hyperplasia, but even distribution of EGFR gene mutation from preinvasive to invasive adenocarcinomas.

Authors:  H Sakamoto; J Shimizu; Y Horio; R Ueda; T Takahashi; T Mitsudomi; Y Yatabe
Journal:  J Pathol       Date:  2007-07       Impact factor: 7.996

9.  Wild-type BRAF is required for response to panitumumab or cetuximab in metastatic colorectal cancer.

Authors:  Federica Di Nicolantonio; Miriam Martini; Francesca Molinari; Andrea Sartore-Bianchi; Sabrina Arena; Piercarlo Saletti; Sara De Dosso; Luca Mazzucchelli; Milo Frattini; Salvatore Siena; Alberto Bardelli
Journal:  J Clin Oncol       Date:  2008-11-10       Impact factor: 44.544

10.  Clinical relevance of KRAS mutation detection in metastatic colorectal cancer treated by Cetuximab plus chemotherapy.

Authors:  F Di Fiore; F Blanchard; F Charbonnier; F Le Pessot; A Lamy; M P Galais; L Bastit; A Killian; R Sesboüé; J J Tuech; A M Queuniet; B Paillot; J C Sabourin; F Michot; P Michel; T Frebourg
Journal:  Br J Cancer       Date:  2007-03-20       Impact factor: 7.640

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  4 in total

1.  Biweekly cetuximab plus irinotecan as second-line chemotherapy for patients with irinotecan-refractory and KRAS wild-type metastatic colorectal cancer according to epidermal growth factor receptor expression status.

Authors:  Myoung Joo Kang; Yong Sang Hong; Kyu-pyo Kim; Sun Young Kim; Ji Yeon Baek; Min-Hee Ryu; Jae-Lyun Lee; Heung Moon Chang; Mi-Jung Kim; Hee Jin Chang; Yoon-Koo Kang; Tae Won Kim
Journal:  Invest New Drugs       Date:  2011-06-25       Impact factor: 3.850

2.  Phase II study of combination chemotherapy with biweekly cetuximab and irinotecan for wild-type KRAS metastatic colorectal cancer refractory to irinotecan, oxaliplatin, and fluoropyrimidines.

Authors:  Kohei Shitara; Satoshi Yuki; Motoki Yoshida; Daisuke Takahari; Setsuo Utsunomiya; Tomoya Yokota; Yozo Sato; Yoshitaka Inaba; Masahiro Tajika; Hiroki Kawai; Hidekazu Yamaura; Mina Kato; Kentaro Yamazaki; Yoshito Komatsu; Kei Muro
Journal:  Invest New Drugs       Date:  2010-12-22       Impact factor: 3.850

3.  A systematic review of salvage therapies in refractory metastatic colorectal cancer.

Authors:  Fausto Petrelli; Gianluca Perego; Antonio Ghidini; Michele Ghidini; Karen Borgonovo; Cinzia Scolari; Renata Nozza; Valentina Rampulla; Antonio Costanzo; Antonio Varricchio; Emanuele Rausa; Filippo Pietrantonio; Alberto Zaniboni
Journal:  Int J Colorectal Dis       Date:  2020-03-26       Impact factor: 2.571

4.  Is there an efficacy-effectiveness gap between randomized controlled trials and real-world studies in colorectal cancer: a systematic review and meta-analysis.

Authors:  Xiao Zhang; Shihui Fu; Rui Meng; Yu Ren; Ye Shang; Lei Tian
Journal:  Transl Cancer Res       Date:  2020-11       Impact factor: 1.241

  4 in total

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