Oxaliplatin, Irinotecan and Cetuximab in Advanced Gastric Cancer. A Multicenter Phase II Trial (Gastric-2) of the Arbeitsgemeinschaft Medikamentose Tumortherapie (AGMT)
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作者:
Woell, Ewald
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St Vinzenz Hosp Zams, Zams, AustriaSt Vinzenz Hosp Zams, Zams, Austria
Woell, Ewald
[1
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Greil, Richard
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III Med Univ Klin, Salzburg, AustriaSt Vinzenz Hosp Zams, Zams, Austria
Greil, Richard
[2
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Eisterer, Wolfgang
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Med Univ Innsbruck, Innsbruck, AustriaSt Vinzenz Hosp Zams, Zams, Austria
Eisterer, Wolfgang
[3
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Bechter, Oliver
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Med Univ Innsbruck, Innsbruck, AustriaSt Vinzenz Hosp Zams, Zams, Austria
Bechter, Oliver
[3
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Fridrik, Michael A.
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AKH Linz, Linz, AustriaSt Vinzenz Hosp Zams, Zams, Austria
Background: Patients suffering from advanced gastric cancer still have a poor prognosis and treatment options are limited. In our previous phase II trial (AGMT-Gastric-1), we showed that the combination of oxaliplatin and irinotecan was well tolerated and effective. The same chemotherapy regimen was now tested in combination with cetuximab in a multicenter phase II trial. Patients and Methods: Oxaliplatin at 85 mg/m(2) biweekly and irinotecan at 125 mg/m(2) biweekly were combined with cetuximab at 400 mg/m(2) loading dose and subsequent weekly infusions of 250 mg/m(2). Fifty-one patients with histologically proven unresectable and/or metastatic gastric adenocarcinoma were treated in the first line setting. The median age was 62 years. A single metastatic site was found in 24 patients, 27 patients had multiple metastatic sites. Results: Frequently reported adverse events (in more than 20% of patients) were predominantly grade 1 or 2 and included neutropenia (35%), thrombocytopenia (33%), anemia (73%), nausea (45%), diarrhea (57%), alopecia (22%), and fatigue (37%). Grade 3/4 toxicities included neutropenia in 9/1 patients., thrombocytopenia in 1/0 patients, anemia in 3/1 patients, nausea in 2/0 patients, and diarrhea in 7/2 patients. Sensory neuropathy occurred mostly as grade 1 and 2 in 37% of patients, grade 3 neurotoxicity was observed in 7 patients. Acne-like rash grades 1/2/3/4 were reported in 31%/20%/6%/2% of patients respectively. Thirteen patients discontinued the study due to neutropenia (n=5), nausea/vomiting (n=1), diarrhea (n=1), toxic colon (n=2), and allergic reaction to cetuximab at first (n=2), second (n=1) or third infusion (n=1). Thirty-five patients were assessable for response, with 1 patient (3%) showing a complete response, 21 patients (60%) a partial response, 7 patients (20%) a stable disease, and 6 patients (17%) a progressive disease respectively. The median time to progression was 24.8 weeks. median overall survival was 38.1 weeks. All patients tested had a wild type KRAS status. Conclusion: The combination of oxaliplatin and irinotecan with cetuximab is safe and its action established in advanced gastric cancer.
机构:
Univ Ulsan, Dept Pathol, Asan Med Ctr, Coll Med, Seoul 138736, South KoreaUniv Ulsan, Dept Oncol, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
Park, Young Soo
Park, Sook Ryun
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Univ Ulsan, Dept Oncol, Asan Med Ctr, Coll Med, Seoul 138736, South KoreaUniv Ulsan, Dept Oncol, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
Park, Sook Ryun
Han, Hye-Suk
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Chungbuk Natl Univ, Coll Med, Dept Internal Med, Cheongju, South KoreaUniv Ulsan, Dept Oncol, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
Han, Hye-Suk
Chung, Ik Joo
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Chonnam Natl Univ, Sch Med, Dept Internal Med, Kwangju, South KoreaUniv Ulsan, Dept Oncol, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
Chung, Ik Joo
Song, Eun-Kee
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Chonbuk Natl Univ, Sch Med, Dept Internal Med, Jeonju, South KoreaUniv Ulsan, Dept Oncol, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
Song, Eun-Kee
Lee, Kyung Hee
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Yeungnam Univ, Coll Med, Dept Internal Med, Med Ctr, Daegu, South KoreaUniv Ulsan, Dept Oncol, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
Lee, Kyung Hee
Kang, Seok Yun
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机构:
Ajou Univ, Dept Hematol Oncol, Sch Med, Suwon 441749, South KoreaUniv Ulsan, Dept Oncol, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
机构:
Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Chan, J. A.
Blaszkowsky, L. S.
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Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USA
Massachusetts Gen Hosp, Dept Med, Div Hematol Oncol, Boston, MA 02114 USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Blaszkowsky, L. S.
Enzinger, P. C.
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机构:
Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Enzinger, P. C.
Ryan, D. P.
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Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USA
Massachusetts Gen Hosp, Dept Med, Div Hematol Oncol, Boston, MA 02114 USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Ryan, D. P.
Abrams, T. A.
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Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Abrams, T. A.
Zhu, A. X.
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Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USA
Massachusetts Gen Hosp, Dept Med, Div Hematol Oncol, Boston, MA 02114 USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Zhu, A. X.
Temel, J. S.
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Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USA
Massachusetts Gen Hosp, Dept Med, Div Hematol Oncol, Boston, MA 02114 USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Temel, J. S.
Schrag, D.
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机构:
Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Schrag, D.
Bhargava, P.
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机构:
Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Bhargava, P.
Meyerhardt, J. A.
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Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Meyerhardt, J. A.
Wolpin, B. M.
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机构:
Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Wolpin, B. M.
Fidias, P.
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机构:
Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USA
Massachusetts Gen Hosp, Dept Med, Div Hematol Oncol, Boston, MA 02114 USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Fidias, P.
Zheng, H.
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机构:
Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USA
Massachusetts Gen Hosp, Ctr Biostat, Boston, MA 02114 USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Zheng, H.
Florio, S.
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Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Florio, S.
Regan, E.
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Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Regan, E.
Fuchs, C. S.
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机构:
Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Hematol Oncol, Boston, MA USADana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA