Efficacy of TopotectTM (Dexrazoxane) for Accidental Extravasation of Anthracyclines

Phase 2

Completed

• Conditions: Anthracycline Extravasation

• Registration Number: NCT00548561
• Lead Sponsor: Valerio Therapeutics

Brief Summary

The purpose of this study is to avoid surgical intervention following extravasation of anthracycline chemotherapy out of a vessel into the surrounding tissues.

Detailed Description

Accidental extravasation of anthracyclines including doxorubicin and its derivative epirubicin, may cause severe, progressive tissue necrosis requiring the surgical removal of any damaged tissue. Thus, the patient is subjected to major surgery causing substantial delay of the treatment of the primary cancer disease.

Tissue infiltration by anthracyclines may be detected by fluorescence microscopy. This test is performed at most hospitals in Denmark.

In a large preclinical trial, as well as 4 clinical cases, dexrazoxane has proven to prevent these severe tissue necroses. This trial will determine the effect of dexrazoxane as an acute treatment (acute antidote) in patients with anthracycline extravasation verified by fluorescence biopsy.

Purpose

Primary:

• To avoid surgical intervention following the accidental extravasation of anthracycline drug, and thus preventing the patient from sequelae.

Secondary:

* To avoid deleterious postponement of the cancer treatment itself.

* To evaluate and describe subjective and objective symptoms in the damaged area following treatment with TopotectTM.

* To evaluate tolerability/toxicity of TopotectTM used for this indication, according to the indicated schedule.

Trial Population 25 patients with accidental anthracycline extravasation confirmed by fluorescence microscopy

Trial Design Open-label clinical trial. Twenty-five consecutive patients with an acute (\<6 hours) history of anthracycline extravasation confirmed by fluorescence microscopy (who in general practice are candidates for acute plastic surgical intervention) will be included.

Effect Variables Response rates, presence of late sequelae, time to progression, and clinical consequence of progression.

Safety Features

* Any toxicity caused by TopotectTM will be studied by blood tests, systematic questioning regarding subjective discomfort, as well as by objective clinical examination.

* A systematic clinical evaluation of the marked area of skin covering the area of extravasation will be performed to assure prompt treatment should any deterioration occur.

* Sequential colour photographs of the involved skin area will be taken.

Study Timeline

• Study Start: 2001-06
• Primary Completion: 2003-07
• Study Completion: 2003-07
• Study First Submitted: 2007-10-23
• Study First Submitted QC: 2007-10-23
• Study First Posted: 2007-10-24
• Status Verified: 2013-11
• Last Update Submitted: 2015-10-20
• Last Update Posted: 2015-10-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 23

Inclusion Criteria

1. Cancer patients treated with anthracycline

2. Informed consent obtained from the patient.

3. Suspicion of anthracycline extravasation is defined as:

   A primary assessment by the physician on duty, which would activate the standard departmental procedure for treatment of anthracycline extravasation.

   The presence of at least one of the following:

   • pain
   • swelling
   • redness

4. The Topotect infusion must be started <6 hours after the accident.

5. The patient must be at least 18 years of age.

6. Performance status (PS) ≤2.

7. Suspicion of anthracycline extravasation from a central venous access device. -

Exclusion Criteria

1. Known allergy towards dexrazoxane.
2. Reasonable suspicion of extravasation by other compounds than anthracyclines through the same intravenous access, e.g. vincristine, mitomycin, and vinorelbine, all of which may cause ulceration.
3. AST, ALT, bilirubin, LDH, serum alkaline phosphatase >3 x upper normal value
4. Neutropenia and thrombocytopenia ≥ CTC grade 2
5. Pregnant or nursing women
6. Women of childbearing age and potential, where the patient does not agree to use an efficient contraceptive (e.g. birth control pill or an intra-uterine device for 3 months previous to start of the trial medication or diaphragm plus a spermicide).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
The rate of surgical resection necessity by progressing necrosis

Trial Locations

Locations (9)

Aalborg Hospital South; 🇩🇰 Aalborg, Denmark

Rigshospitalet; 🇩🇰 Copenhagen, Denmark

Herlev County Hospital; 🇩🇰 Herlev, Denmark

Herlev Hospital Hematological Department; 🇩🇰 Herlev, Denmark

Herning District Hospital; 🇩🇰 Herning, Denmark

Odense University Hospital; 🇩🇰 Odense, Denmark

Roskilde County Hospital; 🇩🇰 Roskilde, Denmark

Hilleroed Hospital; 🇩🇰 Hilleroed, Denmark

Viborg Hospital; 🇩🇰 Viborg, Denmark