High-dose chemotherapy (HDCT) as second-salvage treatment in patients with multiple relapsed or refractory germ-cell tumors

被引:54
|
作者
Lorch, A. [3 ,4 ]
Neubauer, A. [3 ,4 ]
Hackenthal, M. [1 ,2 ]
Dieing, A. [5 ,6 ]
Hartmann, J. T. [7 ,8 ]
Rick, O. [9 ,10 ]
Bokemeyer, C. [11 ,12 ,13 ]
Beyer, J. [1 ,2 ]
机构
[1] Vivantes Klinikum Urban, Dept Hematol, D-10967 Berlin, Germany
[2] Vivantes Klinikum Urban, Dept Oncol, D-10967 Berlin, Germany
[3] Univ Klinikum Giessen & Marburg GmbH, Dept Hematol, Marburg, Germany
[4] Univ Klinikum Giessen & Marburg GmbH, Dept Oncol, Marburg, Germany
[5] Charite Campus Mitte, Dept Hematol, Berlin, Germany
[6] Charite Campus Mitte, Dept Oncol, Berlin, Germany
[7] SW German Comprehens Canc Ctr, Dept Hematol, Tubingen, Germany
[8] SW German Comprehens Canc Ctr, Dept Oncol, Tubingen, Germany
[9] Klin Reinhardshohe, Dept Hematol, Bad Wildungen, Germany
[10] Klin Reinhardshohe, Dept Oncol, Bad Wildungen, Germany
[11] UCCH Univ Med Ctr Hamburg Eppendorf, Hubertus Wald Tumorzentrum, Sect Pneumol, Dept Oncol, Hamburg, Germany
[12] UCCH Univ Med Ctr Hamburg Eppendorf, Hubertus Wald Tumorzentrum, Sect Pneumol, Dept Hematol, Hamburg, Germany
[13] UCCH Univ Med Ctr Hamburg Eppendorf, Hubertus Wald Tumorzentrum, Sect Pneumol, Dept BMT, Hamburg, Germany
关键词
autologous transplantation; chemotherapy; germ-cell tumor; retrospective study; salvage therapy; testicular cancer; SALVAGE CHEMOTHERAPY; TESTICULAR-CANCER; PHASE-I/II; IFOSFAMIDE; PACLITAXEL; CISPLATIN; ETOPOSIDE; CARBOPLATIN; RESCUE; TRIAL;
D O I
10.1093/annonc/mdp366
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Survival after high-dose chemotherapy (HDCT) as second-salvage treatment (SST) in multiple relapsed germ-cell tumors (GCTs). Patients and methods: Existing databases in Berlin and Marburg of HDCT trials from 1989 to 2008 were retrospectively screened. Among 534 patients, 71 of 534 (13%) patients were scheduled for HDCT having failed previous conventional-dose first-line and first-salvage chemotherapy regimens; those 49 patients who had received at least cisplatin plus etoposide first-line as well as conventional-dose cisplatin-based first-salvage regimens and were diagnosed after 1 January 1990 were further analyzed. Results: Median age at SST was 32 years (range 19-52 years). Median follow-up for surviving patients was 4 years (range 1.7-8.5 years). Three of 49 (6%) patients either progressed or died before scheduled HDCT; the remaining 46 of 49 (94%) received either single or sequential HDCT. The rate of favorable responses to HDCT was 27 of 49 (55%). Nine patients remain alive and free of progression. One additional patient was lost to follow without progression at 4 years. The projected overall survival rate at 5 years was 17% (95% confidence intervals 7% to 30%). Conclusion: HDCT can induce remissions in patients with multiple relapsed GCTs with a long-term survival rate of similar to 17%.
引用
收藏
页码:820 / 825
页数:6
相关论文
共 50 条
  • [1] High-dose chemotherapy (HDCT) as second salvage treatment in patients with multiple relapsed or refractory germ cell tumors
    Beyer, J.
    Hackenthal, M.
    Lorch, A.
    Neubauer, A.
    Dieing, A.
    Rick, O.
    Hartmann, J. T.
    Bokemeyer, C.
    JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (15)
  • [2] Salvage high-dose chemotherapy (HDCT) for relapsed primary mediastinal nonseminomatous germ-cell tumors (PMNSGCT).
    Taza, Fadi
    Abonour, Rafat
    Althouse, Sandra K.
    Ashkar, Ryan
    Abu Zaid, Mohammad Issam
    Hanna, Nasser H.
    Kessler, Kenneth A.
    Adra, Nabil
    Einhorn, Lawrence H.
    JOURNAL OF CLINICAL ONCOLOGY, 2022, 40 (16)
  • [3] Prognostic factors for high-dose chemotherapy (HDCT) as salvage treatment in germ cell tumors (GCT)
    Beyer, J
    Kramar, A
    Mandanas, R
    Linkesch, W
    Greinix, A
    Droz, JP
    Pico, JL
    Diehl, A
    Bokemeyer, C
    Schmoll, HJ
    Nichols, CR
    Einhorn, LH
    Siegert, W
    BONE MARROW TRANSPLANTATION, 1998, 22 : S10 - S10
  • [4] Maintenance Oral Etoposide After High-Dose Chemotherapy (HDCT) for Patients With Relapsed Metastatic Germ-Cell Tumors (mGCT)
    Taza, Fadi
    Abonour, Rafat
    Zaid, Mohammad Abu
    Althouse, Sandra K.
    Anouti, Bilal
    Akel, Reem
    Hanna, Nasser H.
    Adra, Nabil
    Einhorn, Lawrence H.
    CLINICAL GENITOURINARY CANCER, 2023, 21 (02) : 213 - 220
  • [5] Is high-dose chemotherapy effective in patients with relapsed or refractory germ cell tumors?
    Feldman, Darren R.
    Motzer, Robert J.
    Bajorin, Dean F.
    NATURE CLINICAL PRACTICE UROLOGY, 2008, 5 (02): : 78 - 79
  • [6] Is high-dose chemotherapy effective in patients with relapsed or refractory germ cell tumors?
    Darren R Feldman
    Robert J Motzer
    Dean F Bajorin
    Nature Clinical Practice Urology, 2008, 5 : 78 - 79
  • [7] HIGH-DOSE CARBOPLATIN AND ETOPOSIDE FOR SALVAGE CHEMOTHERAPY OF GERM-CELL TUMORS
    LAMPE, H
    DEARNALEY, DP
    PRICE, A
    MEHTA, J
    POWLES, R
    NICHOLLS, J
    HORWICH, A
    EUROPEAN JOURNAL OF CANCER, 1995, 31A (05) : 717 - 723
  • [8] Management of progressive brain metastases in patients (pts) with relapsed germ-cell tumor (GCT) treated with salvage high-dose chemotherapy (HDCT).
    King, Jennifer
    Abonour, Rafat
    Hassoun, Rebecca
    Althouse, Sandra K.
    Salous, Tareq
    Hanna, Nasser H.
    Einhorn, Lawrence H.
    Adra, Nabil
    JOURNAL OF CLINICAL ONCOLOGY, 2024, 42 (16)
  • [9] Salvage high-dose chemotherapy in female patients with relapsed/refractory germ cell tumors: The EBMT experience.
    De Giorgi, Ugo
    Richard, Sandrine
    Badoglio, Manuela
    Kanfer, Edward
    Bourrhis, Jean Henri
    Nicolas-Virelizier, Emmanuelle
    Liouret, Bruno
    Vettenranta, Kim
    Martin, Sonja
    Dreger, Peter
    Schuler, Markus Kajo
    Scarpi, Emanuela
    Rosti, Giovanni
    Selle, Frederic
    Lanza, Francesco
    Bregni, Marco
    JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (15)
  • [10] Single versus sequential high-dose chemotherapy (HOCT) in patients with relapsed or refractory germ-cell tumors (GCT).
    Lorch, A.
    Rick, O.
    Hartmann, J. T.
    Kollmannsberger, C.
    Metzner, B.
    Schmidt-Wolf, I.
    Berdel, W. E.
    Schirren, R.
    Beyer, J.
    Bokemeyer, C.
    JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (18) : 219S - 219S