Second-line high-dose chemotherapy in patients with mediastinal and retroperitoneal primary non-seminomatous germ cell tumors: the EBMT experience

被引:60
|
作者
De Giorgi, U
Demirer, T
Wandt, H
Taverna, C
Siegert, W
Bornhauser, M
Kozak, T
Papiani, G
Ballardini, M
Rosti, G
机构
[1] Santa Maria Croci Hosp, Dept Hematol & Oncol, Ist Oncol Romagnolo, I-48100 Ravenna, Italy
[2] Ankara Univ, Sch Med, TR-06100 Ankara, Turkey
[3] Klinikum Nuremberg, Nurnberg, Germany
[4] Univ Hosp, Zurich, Switzerland
[5] Charite Humboldt Univ, Berlin, Germany
[6] Univ Hosp, Dresden, Germany
[7] Univ Hosp, Prague, Czech Republic
[8] Ist Oncol Romagnolo, Forli, Italy
关键词
EBMT; extragonadal; high-dose chemotherapy; non-seminomatous germ cell tumor; second-line chemotherapy;
D O I
10.1093/annonc/mdi017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Results of second-line chemotherapy in patients with extragonadal non-seminomatous germ cell tumor (NSGCT) appear inferior to results in testicular NSGCT. Patients with retroperitoneal NSGCT achieve a comparable long-term survival rate of 30%, but the salvage rates of patients with mediastinal primary are less than 10%. We conducted a retrospective analysis on patients with mediastinal and retroperitoneal NSGCT treated with second-line high-dose chemotherapy (HDCT) registered with the European Group for Blood and Marrow Transplantation (EBMT). Patients and methods: Between 1987 and 1999, 59 registered patients with retroperitoneal (n = 37) and mediastinal (n=22) primary NSGCT, median age 28 years (range 18-60). were treated with second-line HDCT. All had received cisplatin-containing chemotherapy as first-fine treatment. Results: Toxic death occurred in three cases (5%). With a median follow-up of 58 months (range 14-114), 18/59 patients (30%) continue to be disease-free. Of three patients who had a disease recurrence after HDCT, one patient achieved a disease-free status with further chemotherapy and surgery. In total, 19 patients (32%) are currently disease-free. Sixteen of 37 patients (43%) with retroperitoneal NSGCT, and three of 22 patients (14%) with mediastinal NSGCT are currently alive and disease-free. Conclusions: Second-line HDCT might represent a possible option for patients with retroperitoneal primary NSGCT. New salvage strategies are needed for patients with mediastinal NSGCT.
引用
收藏
页码:146 / 151
页数:6
相关论文
共 50 条
  • [31] POST CHEMOTHERAPY ROBOTIC RETROPERITONEAL LYMPH NODE DISSECTION FOR NON-SEMINOMATOUS GERM CELL TUMOR
    Porter, James
    Heulitt, Gerald
    JOURNAL OF UROLOGY, 2017, 197 (04): : E679 - E679
  • [32] Surgical outcomes in patients with primary mediastinal non-seminomatous germ cell tumours and elevated post-chemotherapy serum tumour markers
    De Latour, Bertrand
    Fadel, Elie
    Mercier, Olaf
    Mussot, Sacha
    Fabre, Dominique
    Fizazi, Karim
    Dartevelle, Philippe
    EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2012, 42 (01) : 66 - 71
  • [33] Antitumor activity of paclitaxel after failure of high-dose chemotherapy in a patient with late relapse of a non-seminomatous germ cell tumor
    Gerl, A
    Wilmanns, W
    ANTI-CANCER DRUGS, 1996, 7 (06) : 716 - 718
  • [34] CHEMOTHERAPY OF NON-SEMINOMATOUS GERM-CELL TUMORS WITH A RELATIVE LOW-DOSE OF CIS-PLATINUM
    STEINKE, B
    HEIDEMANN, E
    OSTENDORF, P
    WILMS, K
    WALLER, HD
    ONKOLOGIE, 1983, 6 (03): : 144 - 147
  • [35] Resection of Primary Mediastinal Non-Seminomatous Germ Cell Tumors A 28-Year Experience at Memorial Sloan-Kettering Cancer Center
    Sarkaria, Inderpal S.
    Bains, Manjit S.
    Sood, Shelly
    Sima, Camelia S.
    Reuter, Victor E.
    Flores, Raja M.
    Motzer, Robert J.
    Bosl, George J.
    Rusch, Valerie W.
    JOURNAL OF THORACIC ONCOLOGY, 2011, 6 (07) : 1236 - 1241
  • [36] Approach to chemotherapy for high-risk, stage 1, non-seminomatous, germ cell testicular tumors
    Anand, Madhur
    INDIAN JOURNAL OF UROLOGY, 2021, 37 (02) : 197 - 198
  • [37] NON-SEMINOMATOUS GERM-CELL TUMORS OF THE TESTIS - ANALYSIS OF CEA PRODUCTION IN PRIMARY TUMORS AND IN RETROPERITONEAL LYMPH-NODE METASTASES AFTER PVB CHEMOTHERAPY
    SUURMEIJER, AJH
    OOSTERHUIS, JW
    MARRINK, J
    OCKHUIZEN, T
    SLEIJFER, DT
    KOOPS, HS
    FLEUREN, GJ
    EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1984, 20 (05): : 601 - 608
  • [38] INTENSIVE INDUCTION CHEMOTHERAPY FOR POOR RISK NON-SEMINOMATOUS GERM-CELL TUMORS
    HORWICH, A
    BRADA, M
    NICHOLLS, J
    JAY, G
    HENDRY, WF
    DEARNALEY, D
    PECKHAM, MJ
    EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1989, 25 (02): : 177 - 184
  • [39] FLT-PET for monitoring chemotherapy in patients with metastatic non-seminomatous testicular germ cell tumors
    Been, LB
    Cobben, DC
    Hoekstra, HJ
    Jager, PL
    Gietema, JA
    Elsinga, PH
    Suurmeijer, AJ
    ANNALS OF SURGICAL ONCOLOGY, 2006, 13 (02) : 80 - 80
  • [40] Is high-dose chemotherapy after primary chemotherapy a therapeutic option for patients with primary mediastinal nonseminomatous germ cell tumor?
    Banna, Giuseppe Luigi
    De Giorgi, Ugo
    Ferrari, Benvenuto
    Castagna, Luca
    Alloisio, Marco
    Marangolo, Maurizio
    Rosti, Giovanni
    Santoro, Armando
    BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2006, 12 (10) : 1085 - 1091