Literature DB >> 8519676

Carboplatin combined with amifostine, a bone marrow protectant, in the treatment of non-small-cell lung cancer: a randomised phase II study.

D C Betticher1, H Anderson, M Ranson, K Meely, W Oster, N Thatcher.   

Abstract

Amifostine (WR-2721), a thiol compound, has been shown to protect normal tissue from alkylating agents and cisplatin-induced toxicity without loss of anti-tumour effects. To confirm this result, we conducted a phase II randomised trial to determine if the addition of amifostine reduces the toxicity of carboplatin without loss of anti-tumour activity in patients with inoperable non-small-cell lung cancer (NSCLC). After the first course of carboplatin (600 mg m-2 i.v. infusion), 21 patients were randomised to receive three cycles of carboplatin alone (C arm) or three infusions of amifostine at 910 mg m-2 (CA arm) at 28 day intervals. The amifostine was given 20 min before and at 2 and 4 h after carboplatin. Since the 910 mg m-2 amifostine infusion led to hypotension in six patients, the dosage was reduced by 25%, to 683 mg m-2 t.i.d., in the other four patients. Amifostine was well tolerated at this dose level. Five patients in the CA arm and three in the C arm had their planned treatment discontinued owing to progressive disease (n = 3), amifostine side-effects (hypotension, sneezing and sickness, n = 4), and carboplatin-induced thrombocytopenia (n = 1). Bone marrow and renal function at study entry and after the first course of carboplatin before randomisation were similar in both treatment arms. Twenty courses of carboplatin+amifostine have been compared with 25 courses of carboplatin alone. Although there was no statistically significant difference with respect to haematological values comparing both arms, the median time to platelet recovery (> 100 x 10(9) l-1) (13.5 days vs 21 days; P = 0.04) and the need for hospitalisation for i.v. antibiotic and other supportive treatment tended to be reduced in the CA arm (0/20 vs 6/25 patient courses; P = 0.06). Response rates and median survival (14 vs 9 months) were no different, excluding tumour protection activity by amifostine. These results with a small number of patients suggest that amifostine given with carboplatin may reduce the duration of thrombocytopenia and hospitalisation.

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Year:  1995        PMID: 8519676      PMCID: PMC2034079          DOI: 10.1038/bjc.1995.546

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  23 in total

1.  WR-2721 and high-dose cisplatin: an active combination in the treatment of metastatic melanoma.

Authors:  D Glover; J H Glick; C Weiler; K Fox; D Guerry
Journal:  J Clin Oncol       Date:  1987-04       Impact factor: 44.544

2.  WR-2721 protects against the hematologic toxicity of cyclophosphamide: a controlled phase II trial.

Authors:  D Glover; J H Glick; C Weiler; S Hurowitz; M M Kligerman
Journal:  J Clin Oncol       Date:  1986-04       Impact factor: 44.544

Review 3.  Carboplatin: the clinical spectrum to date.

Authors:  R Canetta; M Rozencweig; S K Carter
Journal:  Cancer Treat Rev       Date:  1985-09       Impact factor: 12.111

Review 4.  Cisplatin rescue therapy: experience with sodium thiosulfate, WR2721, and diethyldithiocarbamate.

Authors:  D R Gandara; V J Wiebe; E A Perez; R W Makuch; M W DeGregorio
Journal:  Crit Rev Oncol Hematol       Date:  1990       Impact factor: 6.312

5.  Human pharmacokinetics of WR-2721.

Authors:  L M Shaw; A T Turrisi; D J Glover; H S Bonner; A L Norfleet; C Weiler; M M Kligerman
Journal:  Int J Radiat Oncol Biol Phys       Date:  1986-08       Impact factor: 7.038

6.  Randomized clinical trial of mitomycin-C with or without pretreatment with WR-2721 in patients with advanced colorectal cancer.

Authors:  E A Poplin; P LoRusso; J J Lokich; J J Gullo; P D Leming; J J Schulz; S R Veach; W McCulloch; L Baker; P Schein
Journal:  Cancer Chemother Pharmacol       Date:  1994       Impact factor: 3.333

7.  Effects of the modulating agent WR2721 on myelotoxicity and antitumour activity in carboplatin-treated mice.

Authors:  M Treskes; E Boven; A A van de Loosdrecht; J F Wijffels; J Cloos; G J Peters; H M Pinedo; W J van der Vijgh
Journal:  Eur J Cancer       Date:  1994       Impact factor: 9.162

8.  Cisplatin neuropathy. Risk factors, prognosis, and protection by WR-2721.

Authors:  J E Mollman; D J Glover; W M Hogan; R E Furman
Journal:  Cancer       Date:  1988-06-01       Impact factor: 6.860

9.  Carboplatin dosage: prospective evaluation of a simple formula based on renal function.

Authors:  A H Calvert; D R Newell; L A Gumbrell; S O'Reilly; M Burnell; F E Boxall; Z H Siddik; I R Judson; M E Gore; E Wiltshaw
Journal:  J Clin Oncol       Date:  1989-11       Impact factor: 44.544

10.  Treatment of tumours with the combination of WR-2721 and cis-dichlorodiammineplatinum (II) or cyclophosphamide.

Authors:  J M Yuhas; J M Spellman; S W Jordan; M C Pardini; S M Afzal; F Culo
Journal:  Br J Cancer       Date:  1980-10       Impact factor: 7.640

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  11 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.  Phase I/II dose escalation study of docetaxel and carboplatin combination supported with amifostine and GM-CSF in patients with incomplete response following docetaxel chemo-radiotherapy: additional chemotherapy enhances regression of residual cancer.

Authors:  M I Koukourakis; A Giatromanolaki; S Kakolyris; M Froudarakis; V Georgoulias; G Retalis; N Bahlitzanakis
Journal:  Med Oncol       Date:  2000-05       Impact factor: 3.064

Review 3.  Chemoprotectants: a review of their clinical pharmacology and therapeutic efficacy.

Authors:  M Links; C Lewis
Journal:  Drugs       Date:  1999-03       Impact factor: 9.546

Review 4.  A risk-benefit assessment of amifostine in cytoprotection.

Authors:  M Mabro; S Faivre; E Raymond
Journal:  Drug Saf       Date:  1999-11       Impact factor: 5.606

Review 5.  Amifostine: an update on its clinical status as a cytoprotectant in patients with cancer receiving chemotherapy or radiotherapy and its potential therapeutic application in myelodysplastic syndrome.

Authors:  C R Culy; C M Spencer
Journal:  Drugs       Date:  2001       Impact factor: 9.546

6.  Protective effect of amifostine against toxicity of paclitaxel and carboplatin in non-small cell lung cancer: a single center randomized study.

Authors:  Ozkan Kanat; Turkkan Evrensel; Ibrahim Baran; Hakan Coskun; Mehmet Zarifoglu; Omer Faruk Turan; Ender Kurt; Mutlu Demiray; Guzin Gonullu; Osman Manavoglu
Journal:  Med Oncol       Date:  2003       Impact factor: 3.064

7.  Amifostine protects against cisplatin-induced ototoxicity in children with average-risk medulloblastoma.

Authors:  Maryam Fouladi; Murali Chintagumpala; David Ashley; Stewart Kellie; Sridharan Gururangan; Tim Hassall; Lindsey Gronewold; Clinton F Stewart; Dana Wallace; Alberto Broniscer; Gregory A Hale; Kimberly A Kasow; Thomas E Merchant; Brannon Morris; Matthew Krasin; Larry E Kun; James M Boyett; Amar Gajjar
Journal:  J Clin Oncol       Date:  2008-08-01       Impact factor: 44.544

Review 8.  Amifostine. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential as a radioprotector and cytotoxic chemoprotector.

Authors:  C M Spencer; K L Goa
Journal:  Drugs       Date:  1995-12       Impact factor: 9.546

9.  Influence of single and multiple doses of amifostine on the efficacy and the pharmacokinetics of carboplatin in mice.

Authors:  A E Korst; E Boven; M L van der Sterre; A M Fichtinger-Schepman; W J van der Vijgh
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

10.  In vitro effect of amifostine on haematopoietic progenitors exposed to carboplatin and non-alkylating antineoplastic drugs: haematoprotection acts as a drug-specific progenitor rescue.

Authors:  L Pierelli; G Scambia; A Fattorossi; G Bonanno; A Battaglia; A Perillo; G Menichella; P B Panici; G Leone; S Mancuso
Journal:  Br J Cancer       Date:  1998-10       Impact factor: 7.640

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