Literature DB >> 2306797

Efficacy and safety of high-dose cisplatin and cyclophosphamide with glutathione protection in the treatment of bulky advanced epithelial ovarian cancer.

F Di Re1, S Bohm, S Oriana, G B Spatti, F Zunino.   

Abstract

Recent efforts to improve the response rates in advanced ovarian cancer with the use of high-dose cisplatin have been limited by unacceptable toxicity. Based on experimental and clinical studies indicating that reduced glutathione (GSH) is a protective agent against cisplatin-induced toxicity, a new high-dose regimen including GSH as a chemoprotector was designed in an attempt to improve the efficacy and therapeutic index of cisplatin. A total of 40 consecutive patients with stage III (bulky) and IV ovarian carcinoma were treated with cisplatin (40 mg/m2 daily for 4 consecutive days) and cyclophosphamide (600 mg/m2 i.v. on day 4). The treatment was repeated every 3-4 weeks for five courses unless progression or severe toxicity occurred. Before each cisplatin administration, patients received GSH (1,500 mg/m2) i.v. over 15 min, with a standard i.v. hydration (2,000 ml fluid) without diuretics. Debulking surgery was initially attempted in 18 patients and, after 2-3 courses, in 16 patients; it could not be carried out in 6 patients. Three patients were not evaluable for response because they prematurely discontinued their treatment. In all, 23 patients (62%) achieved complete clinical remission (negative second-look laparotomy in 16), with an overall (complete + partial) response rate of 86%; 2 patients achieved disease-free status following second surgery. Nausea/vomiting was the most severe acute toxic effect; myelosuppression was acceptable. Renal impairment was effectively prevented by GSH. Neurotoxicity that was not associated with motor dysfunction was the most significant cumulative toxicity in patients (24/32) receiving 4-5 courses. The results of this study indicate that the use of GSH is a safe new method for high-dose cisplatin administration. This regimen is well-tolerated and very effective in ovarian cancer patients with bulky disease and warrants further evaluation.

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Year:  1990        PMID: 2306797     DOI: 10.1007/bf00686237

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  20 in total

Review 1.  Chemotherapy of ovarian cancer.

Authors:  R F Ozols; R C Young
Journal:  Semin Oncol       Date:  1984-09       Impact factor: 4.929

2.  High-dose cisplatin therapy for cancer of the ovary: neurotoxicity.

Authors:  C M Bagley; R H Rudolph; S E Rivkin; J L Yon
Journal:  Ann Intern Med       Date:  1985-05       Impact factor: 25.391

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Authors:  A Wendel; P Cikryt
Journal:  FEBS Lett       Date:  1980-11-03       Impact factor: 4.124

4.  Phase I study of cis-diamminedichloroplatinum(II) administered as a constant 5-day infusion.

Authors:  J J Lokich
Journal:  Cancer Treat Rep       Date:  1980 Aug-Sep

Review 5.  High-dose cisplatin therapy in ovarian cancer.

Authors:  R F Ozols; R C Young
Journal:  Semin Oncol       Date:  1985-12       Impact factor: 4.929

Review 6.  Chemotherapy for advanced or recurrent gynecologic cancer.

Authors:  T Thigpen; R Vance; B Lambuth; L Balducci; T Khansur; J Blessing; R McGehee
Journal:  Cancer       Date:  1987-10-15       Impact factor: 6.860

7.  Hypomagnesemia, renal dysfunction, and Raynaud's phenomenon in patients treated with cisplatin, vinblastine, and bleomycin.

Authors:  N J Vogelzang; J L Torkelson; B J Kennedy
Journal:  Cancer       Date:  1985-12-15       Impact factor: 6.860

8.  Selective modification of glutathione metabolism.

Authors:  A Meister
Journal:  Science       Date:  1983-04-29       Impact factor: 47.728

9.  High dose cisplatin compared with high dose cyclophosphamide in the management of advanced epithelial ovarian cancer (FIGO stages III and IV): report from the North Thames Cooperative Group.

Authors:  H E Lambert; R J Berry
Journal:  Br Med J (Clin Res Ed)       Date:  1985-03-23

10.  A preliminary clinical experience with reduced glutathione as protector against cisplatin-toxicity.

Authors:  S Oriana; S Böhm; G Spatti; F Zunino; F Di Re
Journal:  Tumori       Date:  1987-08-31
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  16 in total

1.  Experimental cisplatin neuronopathy in rats and the effect of retinoic acid administration.

Authors:  G Tredici; S Tredici; D Fabbrica; C Minoia; G Cavaletti
Journal:  J Neurooncol       Date:  1998-01       Impact factor: 4.130

Review 2.  Cytoprotection: concepts and challenges.

Authors:  F M Muggia
Journal:  Support Care Cancer       Date:  1994-11       Impact factor: 3.603

Review 3.  Systematic review: generating evidence-based guidelines on the concurrent use of dietary antioxidants and chemotherapy or radiotherapy.

Authors:  Akiko Nakayama; Karen P Alladin; Obianuju Igbokwe; Jeffrey D White
Journal:  Cancer Invest       Date:  2011-12       Impact factor: 2.176

4.  Protection by ebselen against cisplatin-induced nephrotoxicity: antioxidant system.

Authors:  K Husain; C Morris; C Whitworth; G L Trammell; L P Rybak; S M Somani
Journal:  Mol Cell Biochem       Date:  1998-01       Impact factor: 3.396

5.  Application of a neuroprotective ACTH(4-9) analog to affect cisplatin ototoxicity: an electrocochleographic study in guinea pigs.

Authors:  F P Hamers; S F Klis; W H Gispen; G F Smoorenburg
Journal:  Eur Arch Otorhinolaryngol       Date:  1994       Impact factor: 2.503

6.  Evaluation by somatosensory evoked potentials of the neurotoxicity of cisplatin alone or in combination with glutathione.

Authors:  G Bogliun; L Marzorati; G Cavaletti; L Frattola
Journal:  Ital J Neurol Sci       Date:  1992-11

7.  Weekly 5-fluorouracil and folinic acid plus escalating doses of cisplatin with glutathione protection in patients with advanced head and neck cancer.

Authors:  V Gebbia; R Valenza; A Testa; G Zerillo; S Restivo; G Cupido; F Ingria; G Spadafora; C Barbaccia; G Cannata
Journal:  Med Oncol Tumor Pharmacother       Date:  1992

Review 8.  WR2721 as a modulator of cisplatin- and carboplatin-induced side effects in comparison with other chemoprotective agents: a molecular approach.

Authors:  M Treskes; W J van der Vijgh
Journal:  Cancer Chemother Pharmacol       Date:  1993       Impact factor: 3.333

9.  Influence of glutathione administration on the disposition of free and total platinum in patients after administration of cisplatin.

Authors:  R Leone; M E Fracasso; E Soresi; G Cimino; M Tedeschi; D Castoldi; V Monzani; L Colombi; T Usari; A Bernareggi
Journal:  Cancer Chemother Pharmacol       Date:  1992       Impact factor: 3.333

10.  Glutathione restores normal cell activation and cell cycle progression in cis-platinum treated human lymphocytes.

Authors:  M Kubbies; B Goller; B Schetters; I Bartosek; W Albert
Journal:  Br J Cancer       Date:  1991-11       Impact factor: 7.640

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