RecruitingPhase 2NCT01898416

Safety and Efficacy Study Using 5-ALA Oral Administration as an Adjuvant Therapy on the Rate of Local Tumor Recurrence in Patients Who Have Desmoids Tumors

A PHASE 2, SINGLE CENTRE, SINGLE ARM STUDY TO DETERMINE THE EFFICACY AND SAFETY OF 5- ALA POHOTODYNAMIC THERAPY AS ADJUVANT THERAPY AFTER SURGICAL DISSECTION IN PATIENTS WITH DESMOID TUMORS.


Sponsor

michal roll

Enrollment

140 participants

Start Date

Jun 1, 2013

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate the efficacy of preoperative 5-ALA oral administration and subsequently intraoperative tumor bed phototherapy with red light laser, as an adjuvant therapy on the 3 years rate of local tumor recurrence in patients with desmoid tumors. To evaluate the Safety of 5-ALA administration. 5 years local recurrence rate.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Patient has a resectable histologically confirmed desmoid tumor.
  • Previously treated (by chemotherapy, irradiation or surgery) patients are eligible.
  • Age > 18 years
  • Signed informed consent prior to patient recruitment. -

Exclusion Criteria11

  • Hepatic enzymes or bilirubin > 2X upper limit of normal.
  • Serum creatinine > 2.5 x upper limit of normal.
  • Suspected /documented metastatic disease.
  • Active or uncontrolled infections.
  • Active second malignant disease (excluding non-melanoma skin cancer, or in situ cervix or breast carcinoma) < 2 years prior to the study.
  • Use of other investigational agents < 30 days prior to the study.
  • Patients who are mentally or physically unable to comply with all aspects of the study.
  • Any serious medical condition, including the presence of laboratory abnormalities, which places the subject at an unacceptable risk if he or she participates in this study or confounds the experimental ability to interpret data from the study.
  • Pregnant or lactating females.
  • Known intolerance or allergy to 5-ALA
  • Suspicious or documented acute or chronic porphyria

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Interventions

DRUG5-AMINOLEVULINIC ACID (5-ALA), is a non fluorescent prodrug.

60 mg/kg 5-ALA prepared solution given orally, 3-5 hours before induction of anesthesia. Red light laser given by a Dye laser system, wave length of 635nm, in s dose of 150J/cm for 2000 seconds (33 minutes) will be given to tumor bed. In case of positive margins a second operation and 5-ALA administration or irradiation will be given.


Locations(2)

Tel Aviv sourasky medical center

Tel Aviv, Israel, Israel

The Aviv Sourasky Medical Center

Tel Aviv, Israel, Israel

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NCT01898416


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