Phase I dose-escalating study of TAS-106 in combination with carboplatin in patients with solid tumors

Invest New Drugs. 2014 Feb;32(1):154-9. doi: 10.1007/s10637-013-9964-5. Epub 2013 Apr 23.

Abstract

Background: TAS-106 was designed to inhibit RNA synthesis by blocking RNA polymerases I, II, and III.

Methods: This was a single-center, open-label, phase I study to identify the maximum tolerated dose (MTD), pharmacokinetics, and biologic effects of the combination of TAS-106 and carboplatin, following a standard 3 + 3 design. This phase I trial was comprised of a regimen of a 60-min IV infusion of carboplatin on day 1 of each 21-day cycle followed by a 24-h infusion of TAS-106, also on day 1 of each cycle.

Results: 39 patients were treated (21 male, 18 female, median age 62 years, range 21-80 years). Median number of prior therapies was 4. Maximum Tolerated Dose (MTD) was 3 mg/m(2) TAS-106 with AU 4 carboplatin. Dose-limiting toxicities were neutropenia and thrombocytopenia, with and without growth factor support. While no patients achieved a complete or partial response, four patients had stable disease lasting ≥4 months, including one patient each with ovarian, non-small cell lung, basal cell and colorectal cancer.

Conclusions: In summary, the combination of TAS-106 and carboplatin was well-tolerated, and further studies in non-small cell lung and ovarian cancer are warranted to assess the efficacy of this drug combination.

Publication types

  • Clinical Trial, Phase I
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / pharmacokinetics
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Carboplatin / administration & dosage*
  • Carboplatin / adverse effects
  • Carboplatin / pharmacokinetics
  • Carboplatin / therapeutic use*
  • Cytidine / administration & dosage
  • Cytidine / adverse effects
  • Cytidine / analogs & derivatives*
  • Cytidine / pharmacokinetics
  • Cytidine / therapeutic use
  • Demography
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Male
  • Maximum Tolerated Dose
  • Middle Aged
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Nervous System / pathology
  • Young Adult

Substances

  • 1-(3-C-ethynylribopentofuranosyl)cytosine
  • Cytidine
  • Carboplatin