Study to Evaluate the Safety and Efficacy of Sunitinib, in Subject With Refractory Solid Tumors

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Samsung Medical Center

Status and phase

Completed
Phase 4

Conditions

Refractory Solid Tumors

Treatments

Drug: Sunitinib

Study type

Interventional

Funder types

Other

Identifiers

NCT02691793
2016-02-098

Details and patient eligibility

About

This study is a single arm, pilot study of Sunitinib in patient with RET fusion positive, FGFR2 fusion/FGFR mutation Refractory solid tumor and/or specific sensitivity to Sunitinib by Avatar scan that has progressed following standard therapy or that has not responded to standard therapy or for which there is no standard therapy. To investigate the efficacy and safety of Sunitinib in patient with Refractory solid tumor.

Enrollment

1 patient

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Provision of fully informed consent prior to study specific procedures.

  • Patients must be >= 19 years of age

  • RET fusion positive or FGFR2 fusion/other FGFR mutation Refractory solid tumor and/or specific sensitivity to Sunitinib by Avatar scan that has progressed following standard therapy or that has not responded to standard therapy or for which there is no standard therapy.

  • ECOG Performance status0-2

  • Have measurable or evaluated disease based on RECIST 1.1 as determined by investigator.

  • Adequate Organ Function Laboratory values

    • Absolute neutrophil count >= 1.5 x 109/L, Hemoglobin >= 9g/dL, Platelets>=100 x 109/L Bilirubin <= 1.5 x upper limit of normal AST/ALT <= 2.5 X upper limit of normal(5.0 x upper limit of normal, for subject with liver metastases) Creatinine<= 1.5 X UNL
  • Patients of child-bearing potential should be using adequate contraceptive measures should not be breast feeding and must have a negative pregnancy test prior to start of dosing

  • Adequate heart function

Exclusion criteria

  • Patients with second primary cancer, except:adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix, or other solid tumor curatively treated with no evidence of disease for <= 5 years.
  • Has known active central nervous system(CNS) metastases
  • Has an active infection requiring systemic therapy
  • Pregnancy or breast feeding
  • Patients with cardiac problem
  • Any previous treatment with sunitinib

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

1 participants in 1 patient group

sunitinib
Experimental group
Description:
sunitinib 50 mg will be administered orally daily
Treatment:
Drug: Sunitinib

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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