Consolidative high-dose chemotherapy after conventional-dose chemotherapy as first salvage treatment for male patients with metastatic germ cell tumours

被引:4
作者
Beausoleil, Michel [1 ]
Ernst, D. Scott [2 ,3 ]
Stitt, Larry [4 ]
Winquist, Eric [2 ,3 ]
机构
[1] Univ Toronto, Fac Med, Toronto, ON, Canada
[2] Univ Western Ontario, Dept Oncol, Div Med Oncol, London, ON, Canada
[3] London Hlth Sci Ctr, London, ON, Canada
[4] Univ Western Ontario, Dept Epidemiol & Biostat, London, ON, Canada
来源
CUAJ-CANADIAN UROLOGICAL ASSOCIATION JOURNAL | 2012年 / 6卷 / 02期
关键词
BONE-MARROW-TRANSPLANTATION; IFOSFAMIDE; CISPLATIN; CANCER; CARBOPLATIN; ETOPOSIDE; TRIAL; PACLITAXEL; THERAPY;
D O I
10.5489/cuaj.11233
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Some men with metastatic germ cell tumours that have progressed after response to initial cisplatin-based combination chemotherapy are cured with conventional dose first salvage chemotherapy (CDCT) however, many are not. High-dose chemotherapy with autologous stem cell rescue (HDCT) may be of value in these patients. Prognosis has recently been better defined by International Prognostic Factor Study Group (IPFSG) prognostic factors. HDCT after response to CDCT has been offered at our institution over the past two decades. We retrospectively assessed the validity of the IPFSG prognostic factors in our patients and evaluated the value of HDCT. Methods: We identified eligible men with metastatic germ cell tumour progressed after at least 3 cycles of cisplatin-based chemotherapy and treated with cisplatin-based CDCT alone or with carboplatin-based HDCT. We also collected their clinical data. Patients were classified into risk groups using IPFSG factors, and progression-free and overall survival factors were analyzed and compared in patients treated with CDCT alone and with HDCT. Results: We identified 38 eligible first salvage patients who had received a median of 4 cycles (range, 1 to 7 cycles) of CDCT. Twenty patients received CDCT alone and 18 patients received CDCT plus HDCT. The overall median progression- free survival was 24.6 months (95%Cl, 7.3 to 28.7 months) and overall median overall survival was 34.6 months (95%Cl, 17.2 to 51.3 months). Distribution by IPFSG category and 2-year progression- free survival and 3-year overall survival rates within each risk category were very similar to the IPFSG results. There were two toxic deaths with CDCT and none with HDCT. Overall, patients treated with CDCT plus HDCT had improved progression- free survival and overall survival. Conclusions: The IPFSG prognostic risk factors appeared valid in our patient population. The safety of HDCT with etoposide and carboplatin was confirmed. HDCT was associated with improved progression- free survival and overall survival outcomes, consistent with observations of the IPFSG group. Ideally, the value of optimal HDCT should be determined in comparison to optimal CDCT as first salvage therapy in men with metastatic germ cell tumour with a randomized trial.
引用
收藏
页码:111 / 116
页数:6
相关论文
共 50 条
  • [21] Long-term outcome of salvage high-dose chemotherapy in patients with germ cell tumor with poor prognostic features
    De Giorgi, Ugo
    Rosti, Giovanni
    Salvioni, Roberto
    Papiani, Giorgio
    Ballardini, Michela
    Pizzocaro, Giorgio
    Marangolo, Maurizio
    UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2011, 29 (03) : 284 - 290
  • [22] The role of high-dose chemotherapy in the management of germ cell tumors
    Bastos, Diogo A.
    Feldman, Darren R.
    CURRENT OPINION IN ONCOLOGY, 2014, 26 (03) : 284 - 293
  • [23] Survival Outcomes After High-dose Chemotherapy and Stem Cell Transplantation in the Salvage Setting for Relapsed or Refractory Germ Cell Cancers
    Sharma, Anand
    Babra, Deshveer S.
    Joshi, Priya, V
    Hall, Marcia
    Gogbashian, Andrew
    Vasdev, Nikhil
    Joseph, Magdalene
    Yazdan, Amir
    Kanfer, Edward
    IN VIVO, 2020, 34 (06): : 3675 - 3679
  • [24] High-dose sequential chemotherapy (HDS) versus PEB chemotherapy as first-line treatment of patients with poor prognosis germ-cell tumors: mature results of an Italian randomized phase II study
    Necchi, A.
    Mariani, L.
    Di Nicola, M.
    Lo Vullo, S.
    Nicolai, N.
    Giannatempo, P.
    Raggi, D.
    Fare, E.
    Magni, M.
    Piva, L.
    Matteucci, P.
    Catanzaro, M.
    Biasoni, D.
    Torelli, T.
    Stagni, S.
    Bengala, C.
    Barone, C.
    Schiavetto, I.
    Siena, S.
    Carlo-Stella, C.
    Pizzocaro, G.
    Salvioni, R.
    Gianni, A. M.
    ANNALS OF ONCOLOGY, 2015, 26 (01) : 167 - 172
  • [25] High-dose chemotherapy as salvage treatment in germ-cell cancer: when, in whom and how
    Lorch, Anja
    Beyer, Jorg
    WORLD JOURNAL OF UROLOGY, 2017, 35 (08) : 1177 - 1184
  • [26] High Dose Chemotherapy as Salvage Treatment for Unresectable Late Relapse Germ Cell Tumors
    Lorch, Anja
    Rick, Oliver
    Wuendisch, Thomas
    Hartmann, Joerg-Thomas
    Bokemeyer, Carsten
    Beyer, Joerg
    JOURNAL OF UROLOGY, 2010, 184 (01) : 168 - 173
  • [27] High dose chemotherapy and germ cell tumor
    Massard, Christophe
    Flechon, Aude
    Fizazi, Karim
    Droz, Jean-Pierre
    BULLETIN DU CANCER, 2011, 98 (08) : 945 - 949
  • [28] High-Dose Chemotherapy for Recurrent Ovarian Germ Cell Tumors
    Ammakkanavar, Natraj Reddy
    Matei, Daniela
    Abonour, Rafat
    Einhorn, Lawrence H.
    JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (02) : 226 - U148
  • [29] High-dose chemotherapy followed by stem cell rescue for high-risk germ cell tumors: the Stanford experience
    Agarwal, R.
    Dvorak, C. C.
    Stockerl-Goldstein, K. E.
    Johnston, L.
    Srinivas, S.
    BONE MARROW TRANSPLANTATION, 2009, 43 (07) : 547 - 552
  • [30] High-dose chemotherapy in nonseminomatous germ cell cancer
    Kollmannsberger, Christian
    Beyer, Joerg
    Bokemeyer, Carsten
    BJU INTERNATIONAL, 2009, 104 (9B) : 1398 - 1403