Literature DB >> 6366131

High-dose VP-16-213 and autologous bone marrow transplantation for refractory malignancies: a phase I study.

S N Wolff, M F Fer, C M McKay, K R Hande, J D Hainsworth, F A Greco.   

Abstract

VP-16-213, a congener of epipodophyllotoxin, is a useful chemotherapeutic agent especially against small-cell carcinoma of the lung, germ cell carcinoma, and lymphoma. The standard dose of this drug is limited by myelosuppression. Autologous transplantation of cryopreserved bone marrow assures the restoration of hematopoiesis after marrow ablative cytotoxic therapy. By using this technique, VP-16-213 was dose-escalated using a Fibonacci scheme from the previous highest dose administered to humans (1,500 mg/m2) to 2,700 mg/m2 (900 mg/m2 per day for three consecutive days). At 2,700 mg/m2, severe extramedullary toxicity of the mucous membranes was observed in three of three courses. At the next highest dose (2,400 mg/m2), two of 18 courses (11%, p less than 0.01) resulted in severe mucositis, thus defining this dose as the maximally tolerated dose based on extramedullary toxicities. As anticipated, myelotoxicity was severe but based on the kinetics of marrow recovery, VP-16-213 in these doses appeared not to be marrow ablative. Based on responses observed in this study, high-dose VP-16-213 should be explored in phase II studies or used in combination chemotherapy.

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Year:  1983        PMID: 6366131     DOI: 10.1200/JCO.1983.1.11.701

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


  15 in total

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2.  High-dose etoposide: from phase I to a component of curative therapy.

Authors:  Steven N Wolff; John D Hainsworth; F Anthony Greco
Journal:  J Clin Oncol       Date:  2008-10-06       Impact factor: 44.544

Review 3.  Etoposide. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in combination chemotherapy of cancer.

Authors:  J M Henwood; R N Brogden
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4.  The pharmacokinetics of high dose cyclophosphamide and high dose etoposide.

Authors:  D Cunningham; J Cummings; R B Blackie; L McTaggart; S W Banham; S B Kaye; M Soukop
Journal:  Med Oncol Tumor Pharmacother       Date:  1988

5.  The effect of dose on the bioavailability of oral etoposide.

Authors:  V J Harvey; M L Slevin; S P Joel; A Johnston; P F Wrigley
Journal:  Cancer Chemother Pharmacol       Date:  1986       Impact factor: 3.333

6.  Combination high-dose etoposide and vincristine infusion.

Authors:  D V Jackson; J M Cruz; D R White; H B Muss; A R Chauvenet
Journal:  Invest New Drugs       Date:  1990       Impact factor: 3.850

7.  Phase I study of high dose etoposide phosphatase with filgrastim (G-CSF) in the treatment of advanced refractory malignancies.

Authors:  J D Hainsworth; S M Utley; F A Greco
Journal:  Invest New Drugs       Date:  1997       Impact factor: 3.850

8.  Pharmacokinetics of high-dose etoposide after short-term infusion.

Authors:  P Köhl; H Köppler; L Schmidt; H W Fritsch; J Holz; K H Pflüger; H Jungclas
Journal:  Cancer Chemother Pharmacol       Date:  1992       Impact factor: 3.333

9.  In vitro pharmacodynamic evaluation of VP-16-213 and implications for chemotherapy.

Authors:  S N Wolff; W W Grosh; K Prater; K R Hande
Journal:  Cancer Chemother Pharmacol       Date:  1987       Impact factor: 3.333

10.  Assessment of toxicokinetics and toxicodynamics following intravenous administration of etoposide phosphate in beagle dogs.

Authors:  L N Igwemezie; S Kaul; R H Barbhaiya
Journal:  Pharm Res       Date:  1995-01       Impact factor: 4.200

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