Literature DB >> 10597204

Management of intermediate-prognosis germ-cell cancer: results of a phase I/II study of Taxol-BEP.

R de Wit1, M Louwerens, P H de Mulder, J Verweij, S Rodenhuis, J Schornagel.   

Abstract

The standard chemotherapy regimen in metastatic germ-cell cancer is bleomycin, etoposide and cisplatin (BEP). Chemotherapy studies testing cisplatin dosage and the substitution of ifosfamide for bleomycin have not shown this to be superior to BEP. Paclitaxel (Taxol) has demonstrated promising activity as a second-line treatment in patients with relapsing or cisplatin-refractory germ-cell cancer. Hence, the potential of incorporating paclitaxel in first-line chemotherapy should be investigated. We assessed the feasibility of the addition of paclitaxel to BEP (T-BEP) in a phase I/II study in patients with intermediate- or poor-prognosis germ-cell cancer or with carcinoma of unknown primary (CUP). Paclitaxel was investigated at dose levels of 75, 125, 175 and 200 mg/m2 given as a 3 hr infusion on day 1, before the start of BEP. BEP comprised etoposide at a dose of either 120 mg/m2 on days 1, 3 and 5 or 100 mg/m2 on days 1-5. To deliver the highest possible dose of paclitaxel into BEP, all patients received filgrastim (G-CSF). Thirty patients were entered, 14 of whom had intermediate- (n = 7) or poor- (n = 7) prognosis germ-cell cancer. Paclitaxel up to 200 mg/m2 and BEP at 360 mg/m2 was well tolerated. There was minimal neurosensory and no neuromotor toxicity with the use of 4 T-BEP cycles. More pronounced myelotoxicity and diarrhea at the higher dose level of etoposide resulted in a recommended dose level for multicenter phase II/III testing of paclitaxel 175 mg/m2 and BEP 500 mg/m2. Of the 13 evaluable patients with intermediate- or poor-prognosis germ-cell cancer, all achieved complete response. With a median follow-up of 18 months, none of these patients has relapsed. We conclude that T-BEP is a well-tolerated induction regimen that should be further tested for its therapeutic potential. A randomized phase II/III study of T-BEP vs. BEP has been started as an EORTC trial in patients with intermediate-prognosis disease.

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Year:  1999        PMID: 10597204     DOI: 10.1002/(sici)1097-0215(19991210)83:6<831::aid-ijc24>3.0.co;2-o

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  7 in total

1.  Early experience with chemotherapy intensification for poor-prognosis metastatic germ cell cancer and unfavorable tumor marker decline.

Authors:  Anupam Batra; Scott Ernst; Kylea Potvin; Ricardo Fernandes; Nicholas Power; James Vanhie; Eric Winquist
Journal:  Can Urol Assoc J       Date:  2019-07-23       Impact factor: 1.862

Review 2.  Advanced testis cancer.

Authors:  J P Droz; M Rivoire
Journal:  Curr Treat Options Oncol       Date:  2001-10

Review 3.  [Stage-specific treatment for testicular germ cell tumours].

Authors:  A Heidenreich; C Bokemeyer; R Souchon
Journal:  Urologe A       Date:  2009-04       Impact factor: 0.639

4.  Intensive induction chemotherapy with C-BOP/BEP for intermediate- and poor-risk metastatic germ cell tumours (EORTC trial 30948).

Authors:  S D Fosså; B Paluchowska; A Horwich; G Kaiser; P H M de Mulder; O Koriakine; A T van Oosterom; L de Prijck; L Collette; R de Wit
Journal:  Br J Cancer       Date:  2005-11-28       Impact factor: 7.640

5.  Randomized phase III study comparing paclitaxel-bleomycin, etoposide, and cisplatin (BEP) to standard BEP in intermediate-prognosis germ-cell cancer: intergroup study EORTC 30983.

Authors:  Ronald de Wit; Iwona Skoneczna; Gedske Daugaard; Maria De Santis; August Garin; Nina Aass; Alfred J Witjes; Peter Albers; Jeffery D White; José R Germa-Lluch; Sandrine Marreaud; Laurence Collette
Journal:  J Clin Oncol       Date:  2012-01-23       Impact factor: 44.544

6.  Paclitaxel-containing high-dose chemotherapy for relapsed or refractory testicular germ cell tumours.

Authors:  I A McNeish; E J Kanfer; R Haynes; C Giles; S J Harland; D Driver; G J S Rustin; E S Newlands; M J Seckl
Journal:  Br J Cancer       Date:  2004-03-22       Impact factor: 7.640

7.  Bleomycin, vincristine, cisplatin/bleomycin, etoposide, cisplatin chemotherapy: an alternating, dose intense regimen producing promising results in untreated patients with intermediate or poor prognosis malignant germ-cell tumours.

Authors:  D A Anthoney; M J McKean; J T Roberts; A W Hutcheon; J Graham; W Jones; J Paul; S B Kaye
Journal:  Br J Cancer       Date:  2004-02-09       Impact factor: 7.640

  7 in total

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