Lonidamine significantly increases the activity of epirubicin in patients with advanced breast cancer: Results from a multicenter prospective randomized trial

被引:57
|
作者
Dogliotti, L
Berruti, A
Buniva, T
Zola, P
Bau, MG
Farris, A
Sarobba, MG
Bottini, A
Alquati, P
Deltetto, F
Gosso, P
Monzeglio, C
Moro, G
Sussio, M
Perroni, D
机构
[1] UNIV TURIN,I-10149 TURIN,ITALY
[2] UNIV SASSARI,I-07100 SASSARI,ITALY
[3] IST OSPED CREMONA,CREMONA,ITALY
[4] OSPED MAURIZIANO UMBERTO 1,TURIN,ITALY
[5] OSPED MARTINI,TURIN,ITALY
[6] OSPED ALBA,ALBA,ITALY
[7] OSPED BIELLA,BIELLA,ITALY
[8] OSPED SAVIGLIANO,SAVIGLIANO,ITALY
[9] OSPED CUNEO,CUNEO,ITALY
关键词
D O I
10.1200/JCO.1996.14.4.1165
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Some evidence in vitro and in vivo shows that lonidamine (LND) can positively modulate the activity of doxorubicin and epirubicin (EPI). On this basis, a multicenter prospective randomized trial was performed in patients with advanced breast cancer (BC) to determine if the addition of LND to EPI could increase the response rate of EPI alone. Patients and Methods: From May 1991 to May 1993, 207 patients were enrolled onto this study and randomized to receive intravenous (IV) EPI (60 mg/m(2) on days 1 and 2) alone or with LND (600 mg orally daily). EPI administration was repeated every 21 days until tumor progression or for a maximum of eight cycles. LND was administered continuously until chemotherapy withdrawal. Results: Response rate was significantly superior for the EPI plus LND scheme compared with the single-agent EPI either considering assessable patients (60.0% v 39.8%; P < .01) or including all registered patients according to an intention-to-treat analysis (55.3% v 37.5%; P < .02). The distribution of the response rate according to the site of disease did not show any significant difference between the treatment arms, except for the patient subgroup with liver metastases in which the combination EPI plus LND resulted in a significant improvement of responses than EPI alone. Toxicity was moderate, and except for myalgia, no adjunctive side effects were observed in the EPI plus LND arm. Overall survival and time to progression were similar in both groups. Conclusion: This study confirms in vivo that the activity of EPI is enhanced by the concomitant LND administration. (C) 1996 by American Society of Clinical Oncology.
引用
收藏
页码:1165 / 1172
页数:8
相关论文
共 50 条
  • [31] Safety and efficacy of first-line epirubicin-docetaxel versus epirubicin-cyclophosphamide: updated results of a multicenter randomized phase III trial in metastatic breast cancer.
    Blohmer, JU
    Houschild, M
    Hilfrich, J
    Kleine-Tebbe, A
    Lichtenegger, W
    BREAST CANCER RESEARCH AND TREATMENT, 2004, 88 : S199 - S199
  • [32] A randomized, multicenter trial of epirubicin, oxaliplatin, and capecitabine (EOC) plus panitumumab in advanced esophagogastric cancer (REAL3).
    Waddell, Tom Samuel
    Chau, Ian
    Barbachano, Yolanda
    de Castro, David Gonzalez
    Wotherspoon, Andrew
    Saffery, Claire
    Middleton, Gary William
    Wadsley, Jonathan
    Ferry, David Raymond
    Mansoor, Wasat
    Crosby, Tom David Lewis
    Coxon, Fareeda Y.
    Smith, David
    Waters, Justin S.
    Iveson, Timothy
    Falk, Stephen
    Slater, Sarah
    Okines, Alicia Frances Clare
    Cunningham, David
    JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (15)
  • [33] Safety of aprotinin in CABG patients: Results of the VA multicenter prospective randomized ROOBY trial
    Zenati, Marco
    Sonel, Ali
    Bjerke, Richard
    Shroyer, Laurie
    Collins, Joseph
    CIRCULATION, 2007, 116 (16) : 396 - 396
  • [34] Maintenance treatment with medroxyprogesterone acetate in patients with advanced breast cancer responding to chemotherapy: results of a randomized trial
    O. Kloke
    U. Klaassen
    C. Oberhoff
    G. Hartwich
    J. Szanto
    E. Wolf
    M. Heckmann
    R. Huhn
    L. Stephan
    U. Schnepper
    G.‐M. Donsbach
    C. Bechtel
    R. Rudolph
    A. Berke
    D. Borquez
    I.rtwich Hawig
    H. Hirche
    A.E. Schindler
    S. Seeber
    R. Becher
    Breast Cancer Research and Treatment, 1999, 55 : 51 - 59
  • [35] Maintenance treatment with medroxyprogesterone acetate in patients with advanced breast cancer responding to chemotherapy: results of a randomized trial
    Kloke, O
    Klaassen, U
    Oberhoff, C
    Hartwich, G
    Szanto, J
    Wolf, E
    Heckmann, M
    Huhn, R
    Stephan, L
    Schnepper, U
    Donsbach, GM
    Bechtel, C
    Rudolph, R
    Berke, A
    Borquez, D
    Hawig, I
    Hirche, H
    Schindler, AE
    Seeber, S
    Becher, R
    BREAST CANCER RESEARCH AND TREATMENT, 1999, 55 (01) : 51 - 59
  • [36] Sentinel node biopsy in breast cancer: The first results of the randomized multicenter ALMANAC trial
    Mansel, RE
    Goyal, A
    Fallowfield, L
    Newcombe, RG
    JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (14) : 4S - 4S
  • [37] DOSE-RESPONSE RELATIONSHIP OF EPIRUBICIN-BASED 1ST-LINE CHEMOTHERAPY FOR ADVANCED BREAST-CANCER - A PROSPECTIVE RANDOMIZED TRIAL
    FOCAN, C
    ANDRIEN, JM
    CLOSON, MT
    DICATO, M
    DRIESSCHAERT, P
    FOCANHENRARD, D
    LEMAIRE, M
    LOBELLE, JP
    LONGREE, L
    RIES, F
    JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (07) : 1253 - 1263
  • [38] Clinical utility of systematic biopsy of first metastatic event in breast cancer: Results from a prospective multicenter trial
    Comte, A.
    Sigal-Zafrani, B.
    Belin, L.
    Bieche, I.
    Callens, C.
    Dieras, V.
    Bidard, F-C
    Mariani, O.
    Servois, V.
    Szwarc, D.
    Vincent-Salomon, A.
    Brain, E. C. G.
    Cottu, P. H.
    CANCER RESEARCH, 2016, 76
  • [39] Front line treatment of advanced breast cancer with docetaxel and epirubicin: Results from India.
    Doval, DC
    Pavithran, K
    Vaid, AK
    Rashmi, S
    Talwar, V
    BREAST CANCER RESEARCH AND TREATMENT, 2002, 76 : S89 - S89
  • [40] Final results of a randomized phase III trial comparing cyclophosphamide, epirubicin, and fluorouracil with a dose-intensified epirubicin and cyclophosphamide plus filgrastim as neoadjuvant treatment in locally advanced breast cancer: An EORTC-NCIC-SAKK multicenter study
    Therasse, P
    Mauriac, L
    Welnicka-Jaskiewicz, M
    Bruning, P
    Cufer, T
    Bonnefoi, H
    Tomiak, E
    Pritchard, KI
    Hamilton, A
    Piccart, MJ
    JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (05) : 843 - 850