A phase I study of bortezomib plus irinotecan in patients with advanced solid tumors

被引:51
作者
Ryan, David R.
O'Neil, Bell H.
Supko, Jeffrey G.
Lima, Carlo M. Rocha
Dees, E. Claire
Appleman, Leonard J.
Clark, Jeffrey
Fidias, Phinos
Orlowski, Robert Z.
Kashala, Oscar
Eder, Joseph R.
Cusack, James C., Jr.
机构
[1] Massachusetts Gen Hosp, Div Hematol Oncol, Ctr Canc, Boston, MA 02114 USA
[2] Univ N Carolina, Chapel Hill, NC 27515 USA
[3] Univ Miami, Miami, FL 33152 USA
[4] Sylvester Canc Ctr, Miami, FL 33152 USA
[5] Dana Farber Canc Inst, Boston, MA 02115 USA
[6] Millennium Pharmaceut Inc, Cambridge, MA USA
关键词
bortezomib; colorectal cancer; irinotecan; proteasome inhibitor; solid tumors;
D O I
10.1002/cncr.22280
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The authors conducted a Phase I dose-finding trial to study the use of combined bortezomib plus irinotecan in patients with advanced solid tumors. METHODS. Patients who had received >= 1 prior chemotherapy regimen were eligible. Patients received bortezomib (1.0 mg/m(2), 1.3 mg/m(2), or 1.5 mg/m2) on Days 1, 4, 8, and 11 and received irinotecan (from 50 mg/m(2) to 125 mg/m(2)) on Days 1 and 8 of each 21-day cycle for a maximum of 8 cycles. Bortezomib followed irinotecan on coadministration days in Cycle 1 and Cycles 3 through 8 but preceded irinotecan in Cycle 2 to assess the effect of administration sequence on bortezomib pharmacodynamics. RESULTS. Fifty-one enrolled patients with malignancies, including colorectal cancer (n = 23 patients), lung cancer (n 6 patients), gastroesophageal cancer (n = 6 patients), and pancreatic cancer (n 3 patients), received >= 1 dose of study drug. Nausea, vomiting, and diarrhea were the principal dose-limiting toxicities and led to the maximum tolerated doses of 1.3 mg/m(2) bortezomib and 125 mg/m(2) irinotecan. The most common grade >= 3 bortezomib-related nonhematologic adverse events were fatigue (n = 5 episodes), diarrhea (n = 4 episodes), and nausea (n = 4 episodes). grade >= 3 bortezomib-related hematologic adverse events included neutropenia (n = 6 episodes) and thrombocytopenia (n = 4 episodes) and rarely were dose limiting. Of 34 evaluable patients, no objective responses according to the Response Evaluation Criteria in Solid Tumors were seen; 10 patients achieved stable disease. The degree of proteasome inhibition in whole blood indicated that the biologic activity of bortezomib was unaffected by irinotecan coadministration. CONCLUSIONS. The results of this Phase I study in patients with solid tumors indicated that bortezomib at a dose of 1.3 mg/m(2) on Days 1, 4, 8, and 11 plus irinotecan at a dose of 125 mg/m(2) on Days I and 8 every 21 days were the recommended Phase 11 doses. Cancer 2006;107:2688-97. @ 2006 American Cancer Society.
引用
收藏
页码:2688 / 2697
页数:10
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