Health-related quality of life in survivors of locally advanced breast cancer: an international randomised controlled phase III trial

被引:42
作者
Bottomley, A [1 ]
Therasse, P
Piccart, M
Efficace, F
Coens, C
Gotay, C
Welnicka-Jaskiewicz, M
Mauriac, L
Dyczka, J
Cufer, T
Lichinitser, MR
Schornagel, JH
Bonnefoi, H
Shepherd, L
机构
[1] European Org Res Treatment Canc, EORTC, Ctr Data, Qual Life Unit, Brussels, Belgium
[2] Inst Jules Bordet, B-1000 Brussels, Belgium
[3] Univ Hawaii, Canc Res Ctr, Honolulu, HI 96822 USA
[4] Med Univ Gdansk, Gdansk, Poland
[5] Inst Bergonie, Bordeaux, France
[6] Med Acad Lodz, Lodz, Poland
[7] Inst Oncol, Ljubljana, Slovenia
[8] Canc Res Ctr, Moscow, Russia
[9] Univ Hosp Geneva, Geneva, Switzerland
[10] Swiss Grp Clin Canc Res, SAKK, Bern, Switzerland
[11] NCIC, Clin Trials Grp, Kingston, ON, Canada
关键词
D O I
10.1016/S1470-2045(05)70100-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Dose-intensive chemotherapy has generated much interest in the treatment of patients with locally advanced breast cancer because it might offer a survival benefit. We aimed to compare the effects of such an approach with those of standard chemotherapy on health-related quality of life (HRQOL). Methods 224 patients with locally advanced breast cancer were randomly assigned to 75 mg/m(2) cyclophosphamide given orally on days 1-14, and 60 mg/m(2) epirubicin and 500 mg/m(2) fluorouracil both given intravenously on days 1 and 8, for six cycles every 28 days (6 months' treatment; standard treatment) and 224 patients to 830 mg/m(2) cyclophosphamide and 120 mg/m(2) epirubicin both given intravenously on day 1, and 5 mu g/kg filgrastim per day given subcutaneously on days 2-13, for six cycles every 14 days (3 months' treatment; dose-intensive treatment). HRQOL was assessed by use of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30). Baseline assessments were done before randomisation; then once a month for the first 3 months; and at months 6, 9, 12, 18, 26, 34, 42, 48, and 54. The primary endpoint was progression-free survival; secondary endpoints were HRQOL, response, safety, overall response, and health economics. Analyses were by intention to treat. Findings Previously reported data showed that groups did not differ in progression-free survival. Patients assigned shorter, intensified treatment had a significantly lower overall HRQOL score during the first 3 months than did those assigned standard treatment (mean score at 3 months 41.8 [SD 1.78] vs 49.6 [1.64], p=0.0015). However, scores returned to near baseline, with no difference between groups, at 12 months (62.6 [1.97] vs 65.6 [2.04], p=0.3007). Over the remaining 2 years, the groups showed few significant differences in HRQOL. Interpretation Dose-intensive treatment only has a temporary effect on HRQOL, thus enabling more research on intensive treatment for patients with locally advanced breast cancer.
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收藏
页码:287 / 294
页数:8
相关论文
共 23 条
  • [1] THE EUROPEAN-ORGANIZATION-FOR-RESEARCH-AND-TREATMENT-OF-CANCER QLQ-C30 - A QUALITY-OF-LIFE INSTRUMENT FOR USE IN INTERNATIONAL CLINICAL-TRIALS IN ONCOLOGY
    AARONSON, NK
    AHMEDZAI, S
    BERGMAN, B
    BULLINGER, M
    CULL, A
    DUEZ, NJ
    FILIBERTI, A
    FLECHTNER, H
    FLEISHMAN, SB
    DEHAES, JCJM
    KAASA, S
    KLEE, M
    OSOBA, D
    RAZAVI, D
    ROFE, PB
    SCHRAUB, S
    SNEEUW, K
    SULLIVAN, M
    TAKEDA, F
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (05) : 365 - 376
  • [2] Age-specific detriments to quality of life among breast cancer patients one year after diagnosis
    Arndt, V
    Merx, H
    Stürmer, T
    Stegmaier, C
    Ziegler, H
    Brenner, H
    [J]. EUROPEAN JOURNAL OF CANCER, 2004, 40 (05) : 673 - 680
  • [3] The challenges and achievements involved in implementing Quality of Life research in cancer clinical trials
    Bottomley, A
    Vanvoorden, V
    Flechtner, H
    Therasse, P
    [J]. EUROPEAN JOURNAL OF CANCER, 2003, 39 (03) : 275 - 285
  • [4] Quality of life in patients undergoing systemic therapy for advanced breast cancer
    Bottomley, A
    Therasse, P
    [J]. LANCET ONCOLOGY, 2002, 3 (10) : 620 - 628
  • [5] Randomized trial of dose-dense versus conventionally scheduled and sequential versus concurrent combination chemotherapy as postoperative adjuvant treatment of node-positive primary breast cancer: First report of intergroup trial C9741/cancer and leukemia group B trial 9741
    Citron, ML
    Berry, DA
    Cirrincione, C
    Hudis, C
    Winer, EP
    Gradishar, WJ
    Davidson, NE
    Martino, S
    Livingston, R
    Ingle, JN
    Perez, EA
    Carpenter, J
    Hurd, D
    Holland, JF
    Smith, BL
    Sartor, CI
    Leung, EH
    Abrams, J
    Schilsky, RL
    Muss, HB
    Norton, L
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (08) : 1431 - 1439
  • [6] Summary measures and statistics in the analysis of quality of life data: an example from an EORTC-NCIC-SAKK locally advanced breast cancer study
    Curran, D
    Aaronson, N
    Standaert, B
    Molenberghs, G
    Therasse, P
    Ramirez, A
    Koopmanschap, M
    Erder, H
    Piccart, M
    [J]. EUROPEAN JOURNAL OF CANCER, 2000, 36 (07) : 834 - 844
  • [7] Beyond the development of health-related quality-of-life (HRQOL) measures: A checklist for evaluating HRQOL outcomes in cancer clinical trials - Does HRQOL evaluation in prostate cancer research inform clinical decision making?
    Efficace, F
    Bottomley, A
    Osoba, D
    Gotay, C
    Flechtner, H
    D'haese, S
    Zurlo, A
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (18) : 3502 - 3511
  • [8] Health-related quality of life parameters as prognostic factors in a nonmetastatic breast cancer population: An international multicenter study
    Efficace, F
    Therasse, P
    Piccart, MJ
    Coens, C
    Van Steen, K
    Welnicka-Jaskiewicz, M
    Cufer, T
    Dyczka, J
    Lichinitser, M
    Shepherd, L
    de Haes, H
    Sprangers, MA
    Bottomley, A
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (16) : 3381 - 3388
  • [9] Fairclough DL, 2002, Design and Analysis of Quality of Life Studies in Clinical Trials
  • [10] FAYERS P, 1998, EORTC Q1 Q C30 REF V