Prospective study on warfarin and regional chemotherapy in patients with pancreatic carcinoma

被引:0
作者
Nakchbandi, Wes [3 ]
Mueller, Herwart [3 ]
Singer, Manfred V. [4 ]
Loehr, J. Matthias [4 ]
Nakchbandi, Inaam A. [1 ,2 ]
机构
[1] Univ Heidelberg, D-69120 Heidelberg, Germany
[2] Max Planck Inst Biochem, Heidelberg, Germany
[3] Carl Von Hess Hosp, Dept Surg Oncol, Hammelburg, Germany
[4] Univ Heidelberg, Dept Med 2, D-6800 Mannheim, Germany
关键词
pancreatic carcinoma; warfarin; regional chemotherapy;
D O I
暂无
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aims: The aim is to prospectively examine the effect of regional gemcitabine and mitomycin-C with systemic gemcitabine together with warfarin in patients with inoperable pancreatic carcinoma, and compare the effect to systemic gemcitabine alone. Methods: Seventeen patients received 1.25 mg of warfarin daily, gemcitabine 800 mg/m(2) on day I and mitomycin-C 8 mg/m(2) on day 2 regionally and gemcitabine 800 mg/m(2) on day 14 peripherally. The cycle was repeated every 4 weeks. Results: Median survival since presentation was 6.8 months, while median total survival was 9.6 months. Excluding the 3 patients who died before receiving any therapy, the median survival since presentation resulted in 10.7 months and the median total Survival, 12.7 months. One patient developed bleeding that required transfusion and 2 patients developed anemia (Grades III/IV). Comparing these data to historical controls of large cohorts supports the notion that this regimen offers a viable alternative to systemic gemcitabine alone. Conclusion: A regimen consisting of regional gemcitabine and mitomycin-C with systemic gemcitabine and low-dose warfarin compares favorably to the gold standard of systemic gemcitabine. These data suggest the feasibility of a large prospective study on the use of warfarin and combined regional and systemic chemotherapy in patients with pancreatic carcinoma.
引用
收藏
页码:285 / 290
页数:6
相关论文
共 41 条
  • [1] ANDRENSANDBERG A, 1992, CANCER-AM CANCER SOC, V69, P2884, DOI 10.1002/1097-0142(19920615)69:12<2884::AID-CNCR2820691204>3.0.CO
  • [2] 2-S
  • [3] [Anonymous], COMMON TOXICITY CRIT
  • [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
    Berlin, JD
    Catalano, P
    Thomas, JP
    Kugler, JW
    Haller, DG
    Benson, AB
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (15) : 3270 - 3275
  • [5] Anticoagulant drugs increase natural killer cell activity in lung cancer
    Bobek, V
    Boubelik, M
    Fiserová, A
    L'uptovcová, M
    Vannucci, L
    Kacprzak, G
    Kolodzej, J
    Majewski, AM
    Hoffman, RM
    [J]. LUNG CANCER, 2005, 47 (02) : 215 - 223
  • [6] Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: A randomized trial
    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
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (06) : 2403 - 2413
  • [7] CELLO JP, 1998, SLEISENGER FORDTRANS, P863
  • [8] CHEN HSG, 1980, CANCER TREAT REP, V64, P31
  • [9] PHARMACOLOGIC RATIONALE FOR REGIONAL DRUG DELIVERY
    COLLINS, JM
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1984, 2 (05) : 498 - 504
  • [10] Dawson-Saunders B., 1994, Basic and clinical biostatistics, V2