Literature DB >> 3040920

Platinum analogue combination chemotherapy: cisplatin and carboplatin--a phase I trial with pharmacokinetic assessment of the effect of cisplatin administration on carboplatin excretion.

D L Trump, J L Grem, K D Tutsch, J K Willson, K J Simon, D Alberti, B Storer, D C Tormey.   

Abstract

Cisplatin (NSC 119875) and carboplatin (NSC 241240) are platinum (II) analogues with very different spectra of toxicity. Cisplatin dose is limited by nausea and vomiting, renal dysfunction, and dose-related peripheral neuropathy, whereas carboplatin is myelosuppressive. There are also clinical and laboratory data that suggest that these drugs may not be completely cross-resistant. Therefore, the following phase I trial of combination therapy with cisplatin and carboplatin was undertaken. Since carboplatin toxicity is enhanced in the presence of renal impairment, carboplatin excretion was also evaluated in selected patients at the maximum tolerated dose. Thirty-three patients received 50 mg/m2 cisplatin and doses of carboplatin between 160 mg/m2 and 400 mg/m2. Sequential 20-minute infusions of carboplatin and then cisplatin were able to be administered at the standard doses of carboplatin (320 and 400 mg/m2) with thrombocytopenia to the degree expected if carboplatin alone had been given. However, 280 mg/m2 carboplatin followed by 25 mg/m2 cisplatin/d X 3 caused unexpectedly severe thrombocytopenia in seven of eight patients (median platelet nadir 45,000/microL; range, 12 to 321,000/microL; nadir was less than 90,000 in seven of eight patients). In three patients treated with 280 mg/m2 carboplatin plus 25 mg/m2/d X 3 cisplatin, pharmacokinetics of carboplatin were compared during consecutive monthly cycles without and with cisplatin. Modestly increased areas under the curve (AUC) for carboplatin (15% and 35%) with cisplatin were seen in the two patients who experienced more pronounced platelet suppression with combination therapy. No other limiting or unusual toxicity was seen with this combination. Responses, primarily in "platinum responsive" tumors, were seen. The combination of cisplatin plus carboplatin is feasible and merits further study.

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Year:  1987        PMID: 3040920     DOI: 10.1200/JCO.1987.5.8.1281

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  10 in total

Review 1.  Clinical pharmacokinetics and dose optimisation of carboplatin.

Authors:  S B Duffull; B A Robinson
Journal:  Clin Pharmacokinet       Date:  1997-09       Impact factor: 6.447

2.  In vitro interactions between platinum analogues in human ovarian-carcinoma cell lines.

Authors:  R P Perez; K M Perez; L M Handel; T C Hamilton
Journal:  Cancer Chemother Pharmacol       Date:  1992       Impact factor: 3.333

Review 3.  Clinical pharmacokinetics of carboplatin.

Authors:  W J van der Vijgh
Journal:  Clin Pharmacokinet       Date:  1991-10       Impact factor: 6.447

4.  Carboplatin combined with carmustine and etoposide in the treatment of glioblastoma.

Authors:  A Boiardi; A Silvani; I Milanesi; M Botturi; G Broggi
Journal:  Ital J Neurol Sci       Date:  1992-12

Review 5.  Carboplatin. A preliminary review of its pharmacodynamic and pharmacokinetic properties and therapeutic efficacy in the treatment of cancer.

Authors:  A J Wagstaff; A Ward; P Benfield; R C Heel
Journal:  Drugs       Date:  1989-02       Impact factor: 9.546

6.  Long-term pharmacokinetic behavior of platinum after cisplatin administration.

Authors:  E Gamelin; P Allain; P Maillart; A Turcant; R Delva; A Lortholary; F Larra
Journal:  Cancer Chemother Pharmacol       Date:  1995       Impact factor: 3.333

7.  Phase I/II study of a short course of weekly cisplatin in patients with advanced solid tumours.

Authors:  A S Planting; M E van der Burg; M de Boer-Dennert; G Stoter; J Verweij
Journal:  Br J Cancer       Date:  1993-10       Impact factor: 7.640

8.  Pharmacokinetics of carboplatin at a dose of 750 mg m-2 divided over three consecutive days.

Authors:  P O Mulder; E G de Vries; D R Uges; A H Scaf; D T Sleijfer; N H Mulder
Journal:  Br J Cancer       Date:  1990-03       Impact factor: 7.640

9.  Advantages in combination chemotherapy using cisplatin and its analogues for human testicular tumor xenografts.

Authors:  S Hida; K Okada; O Yoshida
Journal:  Jpn J Cancer Res       Date:  1990-04

10.  Histological vis-a-vis biochemical assessment on the toxic level and antineoplastic efficacy of a synthetic drug Pt-ATP on experimental animal models.

Authors:  Shipra Pal; Arpita Sengupta Sadhu; Swarup Patra; Kalyan K Mukherjea
Journal:  J Exp Clin Cancer Res       Date:  2008-11-12
  10 in total

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