Phase II study of triapinea® in patients with metastatic renal cell carcinoma:: A trial of the national cancer institute of canada clinical trials group (NCIC IND.161)

被引:134
作者
Knox, Jennifer J.
Hotte, Sebastien J.
Kollmannsberger, Christian
Winquist, Eric
Fisher, Bryn
Eisenhauer, Elizabeth A.
机构
[1] Univ Hlth Network OCI Princess Margaret Hosp, Dept Med Oncol, Toronto, ON M5G 2M9, Canada
[2] Juravinski Canc Ctr Hamilton Hlth Sci, Hamilton, ON, Canada
[3] British Columbia Canc Agcy, Vancouver Canc Ctr, Vancouver, BC V5Z 4E6, Canada
[4] London Hlth Sci Ctr, London, ON, Canada
[5] Queens Univ, NCIC Clin Trails Grp, Kingston, ON, Canada
关键词
kidney cancer; phase II; ribonucleotide reductase; renal cell; Triapine;
D O I
10.1007/s10637-007-9044-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triapine((R)) is a novel small molecule ribonucleotide reductase inhibitor that showed activity in renal cell carcinoma (RCC) cell lines. Evaluating new agents with novel mechanisms remains of interest for patients with incurable RCC. This was a single-arm, multicentre phase II trial where Triapine was given at a schedule of 96 mg/m(2) 2-h infusion daily x 4 repeated every 2 weeks in patients with recurrent RCC. A median of four cycles of Triapine was administered to 19 eligible patients. One response was seen (7%.) Median time to progression was 3.6 months. Common adverse events (AEs) were grade 1-2, with fatigue in 74%, nausea in 68% and vomiting in 58%. However grade 3/4 neutropenia was seen in 79% and acute reactions of hypoxia, hypotension, methemoglobinemia were seen. Dose reductions/delays due to AEs were common with only 47% of patients receiving > 90% of planned dose intensity. The study closed, at the end of stage 1 as it did not meet the minimal efficacy criteria to proceed. Further evaluation of Triapine at this dose and schedule in patients with advanced kidney cancer is not recommended.
引用
收藏
页码:471 / 477
页数:7
相关论文
共 29 条
  • [1] ATIEH DM, 2004, P AM SOC CLIN, V24
  • [2] COPPIN C, 2007, IMMUNOTHERAPY ADV RE, V1
  • [3] Cory J.G., 1989, INHIBITORS RIBONUCLE, P1
  • [4] INHIBITORS OF RIBONUCLEOTIDE REDUCTASE - COMPARATIVE EFFECTS OF AMINO-SUBSTITUTED AND HYDROXY-SUBSTITUTED PYRIDINE-2-CARBOXALDEHYDE THIOSEMICARBAZONES
    CORY, JG
    CORY, AH
    RAPPA, G
    LORICO, A
    LIU, MC
    LIN, TS
    SARTORELLI, AC
    [J]. BIOCHEMICAL PHARMACOLOGY, 1994, 48 (02) : 335 - 344
  • [5] CORY JG, 1989, INHIBITORS RIBONUCLE, P245
  • [6] Application of a new multinomial phase II stopping rule using response and early progression
    Dent, S
    Zee, B
    Dancey, J
    Hanauske, A
    Wanders, J
    Eisenhauer, E
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (03) : 785 - 791
  • [7] ELFORD HL, 1970, J BIOL CHEM, V245, P5228
  • [8] Escudier B, 2005, J CLIN ONCOL, V23, p380S, DOI 10.1200/jco.2005.23.16_suppl.lba4510
  • [9] Phase I and pharmacokinetic study of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP) using a single intravenous dose schedule
    Feun, L
    Modiano, M
    Lee, K
    Mao, J
    Marini, A
    Savaraj, N
    Plezia, P
    Almassian, B
    Colacino, E
    Fischer, J
    MacDonald, S
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2002, 50 (03) : 223 - 229
  • [10] Triapine (3-aminopyridine-2-carboxaldehydethiosemicarbazone): A potent inhibitor of ribonucleotide reductase activity with broad spectrum antitumor activity
    Finch, RA
    Liu, MC
    Grill, SP
    Rose, WC
    Loomis, R
    Vasquez, KM
    Cheng, YC
    Sartorelli, AC
    [J]. BIOCHEMICAL PHARMACOLOGY, 2000, 59 (08) : 983 - 991