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Study of Cetuximab in Squamous Cell Carcinoma of the Skin Expressing EGFR (CTXSCC)

Primary Purpose

Skin Diseases, Carcinoma, Squamous Cell

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
cetuximab
Sponsored by
Centre Hospitalier of Chartres
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Skin Diseases focused on measuring Carcinoma, Squamous Cell, Skin, cetuximab, epidermal growth factor receptor

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Histological SCC of the skin expressing (IHC) moderately or highly the EGFR (++ and +++, on a semi-quantitative scale). Locally advanced or metastatic SCC of the skin not suitable for local surgery with documented progression. Presence of at least one measurable target lesion by RECIST criteria. At least one lesion accessible to biopsies. ECOG Performance status < 2. Life expectancy > 3 months. Age > 18 years. Normal hematological (Neutrophils > 1.5x109 cells/l, platelets > 100x109 cells/l), hepatic (bilirubin < 1.5 times the upper limit of the normal range (ULN); alkaline phosphatase and transaminases < 5 x UNL in case of hepatic metastases or < 2.5 x UNL in absence of hepatic metastases) and renal (serum creatinine < 150 micromol/L) functions. Written informed consent. In case of second tumor,excepted carcinoma of the cervix and adequately treated basal or squamous cell skin carcinoma, the possibility for including a patient may be discussed with the principal investigator. Exclusion Criteria: Prior chemotherapy Prior radiotherapy < 1 month. Prior therapy with agent targeting EGFR Unstable systemic diseases or active uncontrolled infections. Patients (male and female) not using effective contraception if of reproductive potential. Females pregnant or lactating. Women of child bearing potential must have a negative serum or urine pregnancy test prior to start each cycle of treatment.

Sites / Locations

  • Hospital of Caen
  • Hospital of Chartres
  • Hospital Hôtel Dieu
  • Beaujon's Hospital
  • CHR of Colmar
  • Hospital Henri Mondor
  • Hospital Tarnier-Cochin
  • Hospital Saint Louis, Department of P. Morel
  • Hospital Saint-Louis, department of L. Dubertret
  • Hospital Bichat
  • Hospital of Reims
  • Hospital Pontchaillou
  • Eugène Marquis Center
  • Hospital Charles Nicolle

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

cetuximab

Arm Description

cetuximab

Outcomes

Primary Outcome Measures

Disease control rate assessed by CT or MRI

Secondary Outcome Measures

Safety profile.
Time to disease progression.
Overall survival.
Duration of response in responder patients at 6 weeks.

Full Information

First Posted
October 17, 2005
Last Updated
February 18, 2012
Sponsor
Centre Hospitalier of Chartres
Collaborators
Hospital of Chartres- France
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1. Study Identification

Unique Protocol Identification Number
NCT00240682
Brief Title
Study of Cetuximab in Squamous Cell Carcinoma of the Skin Expressing EGFR
Acronym
CTXSCC
Official Title
Phase II Study of Cetuximab as Monotherapy and First Line Treatment in Patients With Locally Advanced or Metastatic Squamous Cell Carcinoma of the Skin Expressing EGFR.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2009
Overall Recruitment Status
Completed
Study Start Date
October 2005 (undefined)
Primary Completion Date
April 2009 (Actual)
Study Completion Date
June 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier of Chartres
Collaborators
Hospital of Chartres- France

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether cetuximab is effective in the treatment of locally advanced or metastatic squamous cell carcinoma of the skin expressing EGFR.
Detailed Description
Patients with locally advanced or metastatic squamous cell carcinoma (SCC) of the skin are often bad responders to conventional chemotherapy included cisplatin. The investigation of the EGFR expression may allow identifying new molecular targets for novel therapeutic strategies in patients with locally advanced or metastatic SCC of the skin. Several publications in the literature for primary lesions and one publication for metastatic lesions showed that EGFR was expressed in 80-90% of SCC of the skin. Immunohistochemistry studies performed at the Gustave Roussy Institute confirm these data: they found an over-expression of EGFR in 90% of patients with metastatic disease. These results are in favor of the investigation of cetuximab in patients with locally advanced or metastatic SCC of the skin expressing EGFR. Cetuximab is a monoclonal antibody targeted against EGFR administered weekly by intravenous route; it may be prescribed as out hospital to patients with locally advanced or metastatic SCC of the skin expressing EGFR. Due to the low occurrence of locally advanced or metastatic SCC of the skin, a multicenter trial will be required.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Skin Diseases, Carcinoma, Squamous Cell
Keywords
Carcinoma, Squamous Cell, Skin, cetuximab, epidermal growth factor receptor

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
37 (Actual)

8. Arms, Groups, and Interventions

Arm Title
cetuximab
Arm Type
Experimental
Arm Description
cetuximab
Intervention Type
Drug
Intervention Name(s)
cetuximab
Other Intervention Name(s)
Erbitux
Intervention Description
Dosage form: bottles of 50 ml, 2 mg/ml; Dosage:400 mg/m2 initial dose followed by 250 mg/m2 by infusion every week; Number of Cycles : until progression or unacceptable toxicity develops.
Primary Outcome Measure Information:
Title
Disease control rate assessed by CT or MRI
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Safety profile.
Time Frame
during treatment or within 30 days after the final administration with a cut-off date at week 48.
Title
Time to disease progression.
Time Frame
number of days from the start of treatment to the earliest day of progressive disease
Title
Overall survival.
Time Frame
from the first infusion until week 48 or death
Title
Duration of response in responder patients at 6 weeks.
Time Frame
time to disease progression

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histological SCC of the skin expressing (IHC) moderately or highly the EGFR (++ and +++, on a semi-quantitative scale). Locally advanced or metastatic SCC of the skin not suitable for local surgery with documented progression. Presence of at least one measurable target lesion by RECIST criteria. At least one lesion accessible to biopsies. ECOG Performance status < 2. Life expectancy > 3 months. Age > 18 years. Normal hematological (Neutrophils > 1.5x109 cells/l, platelets > 100x109 cells/l), hepatic (bilirubin < 1.5 times the upper limit of the normal range (ULN); alkaline phosphatase and transaminases < 5 x UNL in case of hepatic metastases or < 2.5 x UNL in absence of hepatic metastases) and renal (serum creatinine < 150 micromol/L) functions. Written informed consent. In case of second tumor,excepted carcinoma of the cervix and adequately treated basal or squamous cell skin carcinoma, the possibility for including a patient may be discussed with the principal investigator. Exclusion Criteria: Prior chemotherapy Prior radiotherapy < 1 month. Prior therapy with agent targeting EGFR Unstable systemic diseases or active uncontrolled infections. Patients (male and female) not using effective contraception if of reproductive potential. Females pregnant or lactating. Women of child bearing potential must have a negative serum or urine pregnancy test prior to start each cycle of treatment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eve Maubec, MD
Organizational Affiliation
Dermatology Department, Hospital Bichat, Paris, France
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital of Caen
City
Caen
ZIP/Postal Code
14000
Country
France
Facility Name
Hospital of Chartres
City
Chartres
ZIP/Postal Code
28018
Country
France
Facility Name
Hospital Hôtel Dieu
City
Clermont-Ferrand
ZIP/Postal Code
63058
Country
France
Facility Name
Beaujon's Hospital
City
Clichy
ZIP/Postal Code
92110
Country
France
Facility Name
CHR of Colmar
City
Colmar
ZIP/Postal Code
68000
Country
France
Facility Name
Hospital Henri Mondor
City
Créteil
ZIP/Postal Code
94000
Country
France
Facility Name
Hospital Tarnier-Cochin
City
Paris
ZIP/Postal Code
75006
Country
France
Facility Name
Hospital Saint Louis, Department of P. Morel
City
Paris
ZIP/Postal Code
75010
Country
France
Facility Name
Hospital Saint-Louis, department of L. Dubertret
City
Paris
ZIP/Postal Code
75010
Country
France
Facility Name
Hospital Bichat
City
Paris
ZIP/Postal Code
75018
Country
France
Facility Name
Hospital of Reims
City
Reims
ZIP/Postal Code
51100
Country
France
Facility Name
Hospital Pontchaillou
City
Rennes
ZIP/Postal Code
35000
Country
France
Facility Name
Eugène Marquis Center
City
Rennes
ZIP/Postal Code
35042
Country
France
Facility Name
Hospital Charles Nicolle
City
Rouen
ZIP/Postal Code
76000
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
15865067
Citation
Maubec E, Duvillard P, Velasco V, Crickx B, Avril MF. Immunohistochemical analysis of EGFR and HER-2 in patients with metastatic squamous cell carcinoma of the skin. Anticancer Res. 2005 Mar-Apr;25(2B):1205-10.
Results Reference
background
PubMed Identifier
11274625
Citation
Alam M, Ratner D. Cutaneous squamous-cell carcinoma. N Engl J Med. 2001 Mar 29;344(13):975-83. doi: 10.1056/NEJM200103293441306. No abstract available.
Results Reference
background
PubMed Identifier
11385224
Citation
Shimizu T, Izumi H, Oga A, Furumoto H, Murakami T, Ofuji R, Muto M, Sasaki K. Epidermal growth factor receptor overexpression and genetic aberrations in metastatic squamous-cell carcinoma of the skin. Dermatology. 2001;202(3):203-6. doi: 10.1159/000051637.
Results Reference
background
PubMed Identifier
10213503
Citation
Huang SM, Bock JM, Harari PM. Epidermal growth factor receptor blockade with C225 modulates proliferation, apoptosis, and radiosensitivity in squamous cell carcinomas of the head and neck. Cancer Res. 1999 Apr 15;59(8):1935-40.
Results Reference
background
Citation
Barbara A Burtness, Yi Li, William Flood, Bassam I Mattar, Arlene A Forastiere. Phase III trial comparing cisplatin (C) + placebo (P) to C + anti-epidermal growth factor antibody (EGF-R) C225 in patients (pts) with metastatic/recurrent head & neck cancer (HNC). Journal of Clinical Oncology,2002 ASCO Annual Meeting Proceedings. Abstract 901.
Results Reference
background
Citation
Nemunaitis JJ, Eiseman I, Cunningham C et al. A phase I trial of CI-1033, a pan-erbB tyrosine kinase inhibitor, given daily for 14 days every 3 weeks, in patients with advanced solid tumors. Proc Am Soc Clin Oncol 22: page 243, 2003 (abstr 974).
Results Reference
background
PubMed Identifier
21810686
Citation
Maubec E, Petrow P, Scheer-Senyarich I, Duvillard P, Lacroix L, Gelly J, Certain A, Duval X, Crickx B, Buffard V, Basset-Seguin N, Saez P, Duval-Modeste AB, Adamski H, Mansard S, Grange F, Dompmartin A, Faivre S, Mentre F, Avril MF. Phase II study of cetuximab as first-line single-drug therapy in patients with unresectable squamous cell carcinoma of the skin. J Clin Oncol. 2011 Sep 1;29(25):3419-26. doi: 10.1200/JCO.2010.34.1735. Epub 2011 Aug 1.
Results Reference
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Study of Cetuximab in Squamous Cell Carcinoma of the Skin Expressing EGFR

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