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Pharmacometabolomic of Trabectedin in Soft Tissue Patients

Completed
Conditions
Sarcoma
Registration Number
NCT04394728
Lead Sponsor
Centro di Riferimento Oncologico - Aviano
Brief Summary

This perspective, mono institutional study is addressed to find potential serum and urine biomarkers predictive of the pharmacokinetic and pharmacodynamic profile of soft tissue sarcomas patients treated with trabectedin.

Detailed Description

This investigation enrolled patients with unresectable and/or metastatic soft tissue sarcoma not responsive to the first-line treatment based on anthracycline/ifosfamide. Patients underwent trabectedin monotherapy that was administered intravenously at the dose of 1.3 mg/m2 every 21 days.

Single overnight fasting urine and blood samples were collected on day-1 of the first trabectedin administration.

Plasma pharmacokinetics was performed during cycle 1. Blood samples, drawn from a site separate from the drug infusion site, were obtained prior to the infusion (basal) at 2, 8, 24 (end of infusion) and 0.5, 1.0, 4.0, 8.0, 24.0 after the end of the infusion. Plasma concentrations of trabectedin were measured by liquid chromatography, tandem mass spectrometry assay (LC-MS/MS) and the pharmacokinetic parameters (Cmax, Clearance, AUC and T1/2) were calculated from the concentration-time curve using a non-compartmental model.

Metabolomics profiles were explored by LC-MS/MS in predose urine and serum and encompassed a total of 192: a) 45 amino acid derivatives, virtually involved in a wide set of biochemical pathways; b) 40 different acylcarnitines, principally involved in the cellular energy metabolism; c) 15 lysophosphatidylcholine metabolites, 77 phosphatidylcholine derivatives, and 15 sphingomyelins, involved in fatty acid metabolism and cellular signaling. The identification of predictive metabolomics biomarkers is performed using univariate and multivariate statistical analyses.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
44
Inclusion Criteria
  • Advanced Soft Tissues Sarcoma STSs (unresectable and/or metastatic disease).
  • One previous systemic treatment with ananthracycline ± ifosfamide.
  • Measurable disease, as defined by RECIST criteria.
  • ECOG PS ≤2.
  • Age ≥18 years.
  • A minimum of 3 weeks since prior tumor directed therapy
  • Recovery from toxic effects of prior therapies to NCI CTC Grade 1 or lower.
  • Adequate haematological, renal liver function.
  • Ability and willingness to provide informed consent
Exclusion Criteria
  • Pregnant or breast-feeding women
  • Prior exposure to Trabectedin.
  • Peripheral neuropathy, Grade 2 or higher.
  • Known CNS metastases.
  • Active viral hepatitis or chronic liver disease.
  • Unstable cardiac condition, including congestive heart failure or angina pectoris, myocardial infarction within one year before enrolment, uncontrolled arterial hypertension or arrhythmias.
  • Active major infection.
  • Other serious concomitant illnesses.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Area Under Curve (AUC)0-48 hours

Pharmacokinetics profile of Trabectedin for 24 hours intravenous infusion

Cmax0-48 hours

Maximum plasma concentration of Trabectedin

Metabolomics profile0 hours ( pre-dose)

Predose metabolomic profile in serum and urine

Secondary Outcome Measures
NameTimeMethod
Treatment Toxicitythrough study completion, an average of 1 year

Hematologic and non-hematologic toxicity according to WHO

Progression free survival2 years

From the first day of treatment to progression or death due to any cause

Overall survival2 years

The time from the first course of trabectedin to death from any cause or to the last follow-up

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