Salvage Therapy with Mitomycin and Ifosfamide in Patients with Gemcitabine-Resistant Metastatic Pancreatic Cancer: A Phase II Trial

被引:15
作者
Cereda, Stefano
Reni, Michele [1 ]
Rognone, Alessia
Fugazza, Clara
Ghidini, Michele
Ceraulo, Domenica
Brioschi, Matteo
Nicoletti, Roberto [2 ]
Villa, Eugenio
机构
[1] S Raffaele Sci Inst, Dept Oncol, Med Oncol Unit, IT-20132 Milan, Italy
[2] S Raffaele Sci Inst, Dept Radiol, IT-20132 Milan, Italy
关键词
Pancreatic cancer; Gemcitabine resistance; Mitomycin/ifosfamide therapy; CELL LUNG-CANCER; COOPERATIVE-ONCOLOGY-GROUP; 2ND-LINE THERAPY; RANDOMIZED-TRIAL; CLINICAL-TRIALS; ADENOCARCINOMA; CISPLATIN; CHEMOTHERAPY; MULTICENTER; OXALIPLATIN;
D O I
10.1159/000324865
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: At the time of upfront treatment failure, over half of the patients with advanced pancreatic cancer are candidates for further treatment. Methods: Patients with metastatic gemcitabine-resistant pancreatic cancer were treated with mitomycin 8 mg/m(2) on day 1, ifosfamide 2,500 mg/m(2) and mesna 3,000 mg/m(2) on days 1-3 every 28 days until progressive disease. A positive responder was defined as a patient who was progression free at 6 months from trial enrolment. According to the Fleming design, a sample size of 34 patients was estimated assuming p0 = 0.05 and p1 = 0.20. Results: Between May 2006 and December 2007, 21 patients (median age 56 years; median Karnofsky performance score 80) were enrolled. One patient died before receiving any treatment. Eighteen patients interrupted chemotherapy due to progressive disease (n = 15), toxicity (n = 2) or refusal (n = 1). Grade >2 toxicity consisted of neutropenia in 80% of patients, thrombocytopenia and fatigue in 20% and anemia in 10%. Only 1 patient was progression free at 6 months (5%). One patient had a partial response (5%) and 2 patients had stable disease (10%). Median survival was 3.7 months. Conclusion: Based on the poor outcome observed and on the high level of grade 3-4 toxicity, the trial was prematurely stopped and the mitomycin and ifosfamide regimen was considered insufficiently active in gemcitabine-pretreated advanced pancreatic cancer. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:156 / 161
页数:6
相关论文
共 48 条
[1]   Hypoxic regulation of glucose transport, anaerobic metabolism and angiogenesis in cancer: Novel pathways and targets for anticancer therapeutics [J].
Airley, Rachel E. ;
Mobasheri, Ali .
CHEMOTHERAPY, 2007, 53 (04) :233-256
[2]   IFOSFAMIDE AND MESNA - MARGINALLY ACTIVE IN PATIENTS WITH ADVANCED-CARCINOMA OF THE PANCREAS [J].
AJANI, JA ;
ABBRUZZESE, JL ;
GOUDEAU, P ;
FAINTUCH, JS ;
YEOMANS, AC ;
BOMAN, BM ;
NICAISE, C ;
LEVIN, B .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (11) :1703-1707
[3]   COMPREHENSIVE CRITERIA FOR ASSESSING THERAPY-INDUCED TOXICITY [J].
AJANI, JA ;
WELCH, SR ;
RABER, MN ;
FIELDS, WS ;
KRAKOFF, IH .
CANCER INVESTIGATION, 1990, 8 (02) :147-159
[4]   Phase III study of gemcitabine in combination with fluorouracil versus gemcitabine alone in patients with advanced pancreatic carcinoma: Eastern Cooperative Oncology Group Trial E2297 [J].
Berlin, JD ;
Catalano, P ;
Thomas, JP ;
Kugler, JW ;
Haller, DG ;
Benson, AB .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (15) :3270-3275
[5]   Second-line chemotherapy with pemetrexed after gemcitabine failure in patients with advanced pancreatic cancer:: a multicenter phase II trial [J].
Boeck, S. ;
Weigang-Koehler, K. ;
Fuchs, M. ;
Kettner, E. ;
Quietzsch, D. ;
Trojan, J. ;
Stoetzer, O. ;
Zeuzem, S. ;
Lordick, F. ;
Koehne, C. -H. ;
Kroening, H. ;
Steinmetz, T. ;
Depenbrock, H. ;
Heinemann, V. .
ANNALS OF ONCOLOGY, 2007, 18 (04) :745-751
[6]   Oral capecitabine in gemcitabine-pretreated patients with advanced pancreatic cancer [J].
Boeck, Stefan ;
Wilkowski, Ralf ;
Bruns, Christiane J. ;
Issels, Rolf D. ;
Schulz, Christoph ;
Moosmann, Nicolas ;
Laessig, Dorit ;
Haas, Michael ;
Golf, Alexander ;
Heinemann, Volker .
ONCOLOGY, 2007, 73 (3-4) :221-227
[7]  
BUKOWSKI RM, 1983, CANCER-AM CANCER SOC, V52, P1577, DOI 10.1002/1097-0142(19831101)52:9<1577::AID-CNCR2820520906>3.0.CO
[8]  
2-8
[9]   Phase II trial of oral rubitecan in previously treated pancreatic cancer patients [J].
Burris, HA ;
Rivkin, S ;
Reynolds, R ;
Harris, J ;
Wax, A ;
Gerstein, H ;
Mettinger, KL ;
Staddon, A .
ONCOLOGIST, 2005, 10 (03) :183-190
[10]   Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: A randomized trial [J].
Burris, HA ;
Moore, MJ ;
Andersen, J ;
Green, MR ;
Rothenberg, ML ;
Madiano, MR ;
Cripps, MC ;
Portenoy, RK ;
Storniolo, AM ;
Tarassoff, P ;
Nelson, R ;
Dorr, FA ;
Stephens, CD ;
VanHoff, DD .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (06) :2403-2413