Metvix PDT in Participant With "High Risk" Basal Cell Carcinoma

NCT00473343 | Completed Phase 3 Results

• 1 other identifier: PC T310/00
• Study Type: interventional
• Target: 102
• Locations: 1 country
• Sites: 7

Brief Summary

Photodynamic therapy (PDT) is the selective destruction of abnormal cells through light activation of a photosensitiser in the presence of oxygen. These cells accumulate more photosensitiser than normal cells. The photosensitiser generates reactive oxygen species upon illumination. For skin diseases, there has been an increasing interest in using precursors of the endogenous photoactive porphyrins. The most commonly used precursors have been 5-aminolevulinic acid (ALA) and its derivatives. The present test drug, Metvix®, contains the methyl ester of ALA, which penetrates the lesions well and shows high lesion selectivity . BCC is a highly frequent skin malignancy, and accounts for approximately 75% of all non-melanoma skin cancers. It is the most common cancer in humans. Several non-pharmacological treatment modalities are used for BCC, including excision surgery, curettage and electrodesiccation, cryosurgery and more advanced modalities like radiation therapy, plastic surgery with reconstruction and Moh's surgery. The treatment used depends on the type, size, depth and localisation of the BCC lesion. Treatment options for BCC give good response rates in the majority of participants but are inadequate in a small group of participants defined as "high-risk" BCC. In this particular participant group, even a moderate complete response rate with good cosmetic results may be considered beneficial, since the number of participant who have to receive more advanced therapy with the possibility of high morbidity and poor cosmetic outcome was reduced. Even a partial response is of clinical interest since the remaining tumour was require less extensive surgery. In the case of treatment failure, Metvix PDT does not interfere with the use of other treatment modalities. The variable "complete response" after one or two Metvix treatment cycles was used as the basis for the justification of sample size.

Conditions

Basal Cell Carcinoma

Keywords

Photodynamic therapy (PDT); PDT with Metvix cream; "High risk" BCC; Basal Cell carcinoma; Histologically confirmed complete response

Outcome Measures

Primary Outcomes (1)

• Percentage of Participants With Histologically Confirmed Patient Complete Response (CR) 3 Months After Last Metvix PDT Cycle

  Patient Complete Response (CR) was defined as 100 percentage of the lesions within the participant having negative findings for nodular basal cell carcinoma (BCC) in the histological examination.

  3 months after last Metvix PDT cycle, up to 6 months

Secondary Outcomes (5)

• Number of Lesion With Complete Response 3 Months After Last Metvix PDT Cycle

  3 months after last Metvix PDT cycle, up to 6 months

• Overall Cosmetic Outcome Assessed by Investigator 3 Months After the Last Metvix PDT Cycle

  3 months after the last metvix PDT cycle, up to 6 months

• Overall Cosmetic Outcome Assessed by Participants 3 Months After the Last Metvix PDT Cycle

  3 months after the last metvix PDT cycle, up to 6 months

• Recurrence Rate in Complete Clearance Group

  12, 24, 36, 48 and 60 months after last Metvix PDT cycle, up to 5 years

• Overall Cosmetic Outcome Assessed by Investigator 24, 36, 48, and 60 Months After the Last Metvix PDT Cycle

  24, 36, and 60 Months After the Last Metvix PDT Cycle, up to 5 years

Study Arms (1)

Metvix® PDT

EXPERIMENTAL

Participants with basal cell carcinoma (BCC) lesions were administered to photodynamic therapy (PDT) with Metvix® cream 160 milligrams per gram (mg/g) applied for three hours, followed by illumination using non-coherent light with a fluency of 75 Joule per centimeter square (J/cm\*2) and fluency rate of 70-200 milliwatt per centimeter square (mW/cm\*2) up to 13 weeks.

Drug: Metvix® cream

Interventions

Metvix® cream DRUG

Also known as: Methyl 5-aminolevulinate hydrochloride

Metvix® PDT

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Clinical diagnosis of BCC lesions verified by histology (2-3 mm punch biopsy)
• Males or females above 18 years of age.
• Written informed consent. AND
• Participants with high risk of surgical complications due to:
• Anticoagulant medication or bleeding disorders
• Cardiac risk factors
• Anaesthetic contraindications
• Poor surgical compliance because of participant refusal, dementia, or inability to perform wound care.
• Participants with "high-risk BCC lesion(s). A "high-risk" BCC lesion is defined as:
• A large BCC lesion with the largest diameter:
• Equal to or greater than 15 mm on extremities, except below the knees, where largest diameter should be equal to or greater than 10 mm
• Equal to or greater than 20 mm on the trunk
• Equal to or greater than 15 mm in the face, or A lesion in the mid-face region (H-zone according to Swanson) or on the ear In participants with more then 6 eligible lesions, the 6 lesions to be treated was randomly chosen.

You may not qualify if:

• Prior treatment of the lesion within 4 weeks.
• A pure morpheaform and/or highly infiltrated lesion assessed clinically and/or by histology. A mixed nodular/morpheaform lesion which is not highly infiltrated (clinically) may be included.
• Participant with porphyria.
• Pigmented lesions.
• Known allergy to Metvix® or a similar compound.
• Participation in another clinical study either concurrently or within the last 30 days
• Participant with Gorlin's syndrome.
• Participant with Xeroderma pigmentosum
• Pregnant or breast-feeding (all women of child-bearing potential must document a negative pregnancy test and use contraception during the treatments and for at least one month thereafter).
• Conditions associated with a risk of poor protocol compliance.

Sponsors & Collaborators

• Galderma R&D: lead

Study Sites (7)

Department of Dermatology, St. George Hospital

Kogarah, New South Wales, NSW 2217, Australia

Location

South East Dermatology, The Belmont Specialist Clinic

Carnia, Queensland, 4152, Australia

Location

Department of Dermatology, Royal Adelaide Hospital

Adelaide, South Australia, SA 5000, Australia

Location

Dermatology Department, The Queen Elisabeth Hospital

Adelaide, South Australia, SA 5011, Australia

Location

Clinic B, Repatriation Campus, Austin & Repatriation Medical Centre

Heidelberg, Victoria, VIC 3081, Australia

Location

Fremantle Dermatology

Fremantle, Western Australia, WA 6106, Australia

Location

Dermatology Surgery & Laser Centre, The Perth Surgicentre

Perth, Western Australia, WA 6151, Australia

Location

MeSH Terms

Conditions

Carcinoma, Basal Cell

Condition Hierarchy (Ancestors)

Carcinoma; Neoplasms, Glandular and Epithelial; Neoplasms by Histologic Type; Neoplasms; Neoplasms, Basal Cell

Results Point of Contact

• Title: Clinical Operations
• Organization: Galderma

Clinical.Studies@galderma.com

817 961 5000

Study Officials

• Carl Vinciullo, MD

  Dermatology Surgery & Laser Centre, Perth

  PRINCIPAL INVESTIGATOR

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: Yes

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY

Study Record Dates

• First Submitted: May 14, 2007
• First Posted: May 15, 2007
• Study Start: September 1, 2000
• Primary Completion: June 1, 2006
• Study Completion: June 1, 2006
• Last Updated: January 5, 2023
• Results First Posted: January 5, 2023

Record last verified: 2021-06

Locations

AU (7)