Literature DB >> 11291829

Phase I study of irofulven (MGI 114), an acylfulvene illudin analog, in patients with acute leukemia.

F Giles1, J Cortes, G Garcia-Manero, S Kornblau, E Estey, M Kwari, A Murgo, H Kantarjian.   

Abstract

Irofulven (MGI 114, 6-hydroxymethylacylfulvene, HMAF) is a semisynthetic illudin analog with broad in vitro anti-neoplastic activity. In this leukemia phase I study, we investigated the toxicity profile and activity of Irofulven in patients with primary refractory or relapsed acute myeloid leukemia (AML), acute lymphocytic leukemia (ALL), or myelodysplastic syndromes (MDS). Irofulven was given as an intravenous infusion over five minutes daily for five days. The starting dose was 10 mg/m2/day (50 mg/m2/course). Courses were scheduled to be given every 3-4 weeks according to toxicity and antileukemic efficacy. Twenty patients [AML: 17 patients; MDS: one patient; ALL: one patient; mixed lineage acute leukemia: one patient] were treated. Nausea, vomiting, hepatic dysfunction, weakness, renal dysfunction, and pulmonary edema were dose limiting toxicities, occurring in two of five patients treated at 20 mg/m2/day and two of three patients treated at 12.5 mg/m2/day. The MTD was defined as 10 mg/m2/day for five days. One patient with primary resistant AML achieved complete remission. Proposed phase II studies will further define the activity of Irofulven in patients with better prognosis AML and in other hematological malignancies, both as a single agent and in combination regimens, particularly with topoisomerase 1 inhibitors.

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Year:  2001        PMID: 11291829     DOI: 10.1023/a:1006432012394

Source DB:  PubMed          Journal:  Invest New Drugs        ISSN: 0167-6997            Impact factor:   3.850


  45 in total

1.  Clinical trials referral resource. Clinical trials of MGI-114.

Authors:  A Murgo; D J Cannon; G Blatner; B D Cheson
Journal:  Oncology (Williston Park)       Date:  1999-02       Impact factor: 2.990

2.  FUNGAL METABOLITES. THE STRUCTURES OF THE NOVEL SESQUITERPENOIDS ILLUDIN-S AND -M.

Authors:  T C MCMORRIS; M ANCHEL
Journal:  J Am Chem Soc       Date:  1965-04-05       Impact factor: 15.419

Review 3.  Platinum-DNA adduct, nucleotide excision repair and platinum based anti-cancer chemotherapy.

Authors:  E Reed
Journal:  Cancer Treat Rev       Date:  1998-10       Impact factor: 12.111

4.  Effect of diagnosis (refractory anemia with excess blasts, refractory anemia with excess blasts in transformation, or acute myeloid leukemia [AML]) on outcome of AML-type chemotherapy.

Authors:  E Estey; P Thall; M Beran; H Kantarjian; S Pierce; M Keating
Journal:  Blood       Date:  1997-10-15       Impact factor: 22.113

5.  Effects on DNA integrity and apoptosis induction by a novel antitumor sesquiterpene drug, 6-hydroxymethylacylfulvene (HMAF, MGI 114).

Authors:  J M Woynarowski; C Napier; S K Koester; S F Chen; D Troyer; W Chapman; J R MacDonald
Journal:  Biochem Pharmacol       Date:  1997-12-01       Impact factor: 5.858

6.  Phase I and pharmacodynamic study of the topoisomerase I-inhibitor topotecan in patients with refractory acute leukemia.

Authors:  E K Rowinsky; A Adjei; R C Donehower; S D Gore; R J Jones; P J Burke; Y C Cheng; L B Grochow; S H Kaufmann
Journal:  J Clin Oncol       Date:  1994-10       Impact factor: 44.544

7.  Efficacy of Acylfulvene Illudin analogues against a metastatic lung carcinoma MV522 xenograft nonresponsive to traditional anticancer agents: retention of activity against various mdr phenotypes and unusual cytotoxicity against ERCC2 and ERCC3 DNA helicase-deficient cells.

Authors:  M J Kelner; T C McMorris; L Estes; R J Starr; M Rutherford; M Montoya; K M Samson; R Taetle
Journal:  Cancer Res       Date:  1995-11-01       Impact factor: 12.701

8.  Four decades of therapy for AML.

Authors:  E J Freireich
Journal:  Leukemia       Date:  1998-09       Impact factor: 11.528

9.  Topotecan in the treatment of hematologic malignancies.

Authors:  M Beran; H Kantarjian
Journal:  Semin Hematol       Date:  1998-07       Impact factor: 3.851

10.  A new water-soluble camptothecin derivative, DX-8951f, exhibits potent antitumor activity against human tumors in vitro and in vivo.

Authors:  I Mitsui; E Kumazawa; Y Hirota; M Aonuma; M Sugimori; S Ohsuki; K Uoto; A Ejima; H Terasawa; K Sato
Journal:  Jpn J Cancer Res       Date:  1995-08
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