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Phase Ib Study of Gemcitabine Plus Cisplatin or Carboplatin Plus Dovitinib in Patients With Advanced Solid Tumors

Phase 1
Terminated
Conditions
Solid Tumors
Bladder Cancer
Interventions
Registration Number
NCT01496534
Lead Sponsor
Matthew Galsky
Brief Summary

This is a phase Ib dose escalation study of dovitinib given in combination with either gemcitabine plus cisplatin or carboplatin in patients with advanced solid tumors. Patients with advanced solid tumors, for whom treatment with gemcitabine plus cisplatin or carboplatin would otherwise be warranted, will be enrolled. The dose of dovitinib will be escalated in successive cohorts using standard "3+3" dose escalation rules. Patients will continue treatment, in the absence of prohibitive toxicity, until disease progression. The study will define the recommended phase II dose of these combination regimens.

Detailed Description

This is a phase Ib study of dovitinib given in combination with gemcitabine plus cisplatin or carboplatin in patients with advanced solid tumors. This study will utilize standard 3+3 dose escalation rules to define the recommended phase II dose. Dose escalation will proceed independently in the two cohorts (cisplatin cohort: gemcitabine + cisplatin + dovitinib; carboplatin cohort: gemcitabine + carboplatin + dovitinib). Patients will receive treatment for up to 6 cycles, in the absence of toxicity, until disease progression

Primary Objective:

To determine the recommended phase II dose of dovitinib given in combination with gemcitabine plus cisplatin or carboplatin.

Secondary Objectives:

* To determine the response rate to treatment as per Response Evaluation Criteria in Solid Tumors (RECIST)

* To determine the toxicity of treatment at per the Common Terminology for Adverse Events (CTCAE v4)

* To determine the pharmacokinetics of dovitinib in combination with gemcitabine plus cisplatin or carboplatin.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
14
Inclusion Criteria
  • Written informed consent and HIPAA authorization for release of personal health information.

  • Age ≥ 18 years at the time of consent.

  • Karnofsky Performance Status of ≥ 70%.

  • Advanced/metastatic solid tumor for which treatment with gemcitabine plus carboplatin or gemcitabine plus cisplatin would otherwise be warranted.

  • Prior treatment with chemotherapy is permitted. Patients must not have received more than three prior chemotherapeutic regimens.

  • Adequate organ function as determined by the following laboratory values:

    • Hemoglobin (Hgb) ≥ 9 g/dL
    • Platelets ≥ 100 x 109/L
    • Absolute neutrophil count (ANC) ≥ 1.5 x 109/L
    • Creatinine of ≤ 1.5 OR Calculated creatinine clearance of ≥ 60 cc/min for the cisplatin cohort.

Calculated creatinine clearance of ≥ 30 cc/min for the carboplatin cohort.

  • Bilirubin ≤ 1.5 x ULN
  • Aspartate aminotransferase (AST, SGOT) ≤ 1.5 ULN
  • Alanine Aminotransferase (ALT, SGPT) < 1.5 ULN
  • INR ≤ 1.5 and a PTT within normal limits
  • LVEF assessed by 2-D echocardiogram (ECHO) > 50% or lower limit of normal or multiple gated acquisition scan (MUGA) > 45% or lower limit of normal
Exclusion Criteria
  • Prior treatment with more than three prior chemotherapy regimens.
  • Has had major surgery within 30 days of starting the study treatment
  • Have active CNS metastases.
  • No treatment with any investigational agent within 30 days prior to being registered for protocol therapy.
  • Prior cancer treatment must be completed at least 30 days prior to being registered for protocol therapy and the subject must have recovered from the acute toxic effects of the regimen.
  • Prior radiation therapy must be completed at least 30 days prior to being registered for protocol therapy.
  • Pregnant or breastfeeding.
  • Clinically significant infections as judged by the treating investigator.
  • Impaired cardiac function or clinically significant cardiac diseases
  • Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of dovitinib (e.g. ulcerative diseases, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection)
  • Patients who are currently receiving anticoagulation treatment with therapeutic doses of warfarin
  • Women of child-bearing potential, who are biologically able to conceive, not employing two forms of highly effective contraception.
  • Fertile males not willing to use contraception

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
CarboplatinCarboplatinGemcitabine 1000 mg/m2 IV on days 1 + 8 Carboplatin AUC 5 IV day 1 Dovitinib given orally on days 1-5, 8-12 and 15-19. Treatment will be recycled every 21-days. The dose of dovitinib will be escalated in successive cohorts.
CisplatinCisplatinGemcitabine 1000 mg/m2 IV on days 1 + 8 Cisplatin 70 mg/m2 IV day 1 Dovitinib given orally on days 1-5, 8-12 and 15-19. Treatment will be recycled every 21-days. The dose of dovitinib will be escalated in successive cohorts.
Primary Outcome Measures
NameTimeMethod
Recommended phase II dose of combination regimenWithin the first 21 days of treatment

The primary objectives of this study are to determine the recommended phase II dose of dovitinib given in combination with gemcitabine plus carboplatin or cisplatin.

Secondary Outcome Measures
NameTimeMethod
Antitumor activityAfter every 2 cycles (42 days) of combination therapy up to 3 years

A CT scan of the chest, abdomen, and pelvis will be performed after every 2 cycles (or sooner if there is evidence of disease progression) while on combination therapy until disease progression (eg, after cycle 2, after cycle 4, and after cycle 6). Response to treatment will be determined using RECIST.

Trial Locations

Locations (1)

Icahn School of Medicine at Mount Sinai

🇺🇸

New York, New York, United States

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