Adjuvant chemotherapy with paclitaxel and carboplatin in patients with advanced carcinoma of the upper urinary tract: A study by the Hellenic Cooperative Oncology Group

被引:67
作者
Bamias, A
Deliveliotis, C
Fountzilas, G
Gika, D
Anagnostopoulos, A
Zorzou, MP
Kastritis, E
Constantinides, C
Kosmidis, P
Dimopoulos, MA
机构
[1] Univ Athens, Dept Clin Therapeut, Sch Med, Athens, Greece
[2] Univ Athens, Dept Urol, Sch Med, Athens, Greece
[3] Univ Thessaloniki, AHEPA Hosp, Dept Med Oncol, Sch Med, Athens, Greece
关键词
D O I
10.1200/JCO.2004.09.043
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose. Radical surgery represents the treatment of choice for carcinoma of the upper urinary tract. Nevertheless, approximately 50% of patients with stage T greater than or equal to 3 or lymph node involvement die from their disease, mainly as a result of the development of distant metastases. Therefore, there is a need for effective adjuvant systemic treatment. We prospectively studied a cohort of patients who underwent surgery for high-risk carcinoma of the upper urinary tract to assess the feasibility of the combination of paclitaxel and carboplatin as adjuvant treatment. Patients and Methods. Thirty-six patients with tumor stage greater than or equal to 3 or lymph node involvement were treated with four cycles of paclitaxel at 175 mg/m(2) and carboplatin (area under the curve 5, Calvert Formula) every 3 weeks following surgery. Results. Median follow-up was 40.6 months. Chemotherapy was well tolerated with 32 patients (89%) receiving full carboplatin and paclitaxel doses without delays. The most frequent grade 3/4 toxicity was neutropenia (39%) which was complicated with fever in only one case (3%). Nonhematologic grade 3 or 4 toxicities were reported in only one case. Five-year survival was 62% (95% Cl, 35% to 69%), while 5-year disease-free survival was 40.2% (95% Cl, 15.8% to 64.6%). Local failure rate was 30%, as opposed to 17% of patients who developed distant metastases. No patients with grade 2 tumors relapsed during follow-up, as opposed to 60% of patients with grade 3 tumors, Conclusion. Adjuvant chemotherapy with paclitaxel and carboplatin is feasible and may reduce the risk of distant metastases in high-risk upper urinary tract carcinoma. (C) 2004 by American Society of Clinical Oncology.
引用
收藏
页码:2150 / 2154
页数:5
相关论文
共 38 条
  • [1] Abol-Enein H, 2003, LANCET, V361, P1927
  • [2] [Anonymous], 1997, Acta Urol Ital
  • [3] COMBINATION NEPHROURETERECTOMY AND POSTOPERATIVE RADIOTHERAPY FOR INFILTRATIVE URETERAL CARCINOMA
    BABAIAN, RJ
    JOHNSON, DE
    CHAN, RC
    [J]. INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1980, 6 (09): : 1229 - 1232
  • [4] Long-term survival in metastatic transitional-cell carcinoma and prognostic factors predicting outcome of therapy
    Bajorin, DF
    Dodd, PM
    Mazumdar, M
    Fazzari, M
    McCaffrey, JA
    Scher, HI
    Herr, H
    Higgins, G
    Boyle, MG
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (10) : 3173 - 3181
  • [5] PRIMARY CARCINOMA OF URETER - A REPORT OF 102 NEW CASES
    BLOOM, NA
    [J]. JOURNAL OF UROLOGY, 1970, 103 (05) : 590 - +
  • [6] THE POSTOPERATIVE IRRADIATION OF TRANSITIONAL CELL-CARCINOMA OF THE RENAL PELVIS AND URETER
    BROOKLAND, RK
    RICHTER, MP
    [J]. JOURNAL OF UROLOGY, 1985, 133 (06) : 952 - 955
  • [7] TRANSITIONAL CELL-CARCINOMA OF THE UPPER URINARY-TRACT - EVALUATION OF PROGNOSTIC FACTORS BY HISTOPATHOLOGY AND FLOW CYTOMETRIC ANALYSIS
    CORRADO, F
    FERRI, C
    MANNINI, D
    CORRADO, G
    BERTONI, F
    BACCHINI, P
    LELLI, G
    LIEBER, MM
    SONG, JM
    [J]. JOURNAL OF UROLOGY, 1991, 145 (06) : 1159 - 1163
  • [8] TRANSITIONAL-CELL CARCINOMA OF THE RENAL PELVIS OR URETER - PATTERNS OF FAILURE
    COZAD, SC
    SMALLEY, SR
    AUSTENFELD, M
    NOBLE, M
    JENNINGS, S
    RAYMOND, R
    [J]. UROLOGY, 1995, 46 (06) : 796 - 800
  • [9] DEIWIT R, 2003, CANCER, V97, P2120
  • [10] Role of adjuvant chemotherapy in the treatment of invasive carcinoma of the urinary bladder
    Dimopoulos, MA
    Moulopoulos, LA
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (04) : 1601 - 1612