Combination of Cetuximab With Afatinib for Patient With EGFR Mutated Lung Cancer (ACE-Lung)
Primary Purpose
Non Small Cell Lung Cancer
Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Afatinib
Cetuximab
Sponsored by

About this trial
This is an interventional treatment trial for Non Small Cell Lung Cancer focused on measuring EGFR, Lung Cancer
Eligibility Criteria
Principal Inclusion Criteria:
- Stage III or IV NSCLC, non irradiable non operable
- Non squamous NSCLC histologically or cytologically confirmed
- No previous treatment of NSCLC
- EGFR mutation (exon 19 deletion, L858R mutation, G719X , L861Q or S768I mutations or exon 19 insertion)
- Presence of at least one lesion that can be measured
- PS 0 or 1
Principal Exclusion Criteria:
- Symptomatic brain metastasis or requiring immediate radiotherapy
- T790M mutation or exon 20 insertion
- Radiotherapy less than 2 weeks prior randomization including symptomatic radiotherapy
- Interstitial pneumopathy
Sites / Locations
- Centre Hospitalier du Pays d'Aix
- Clinique de L'Europe
- Angers - CHU
- Annecy - CH
- Bordeaux - Institut Bergonié
- Bordeaux - Polyclinique Nord
- Boulogne - Ambroise Paré
- Clermont-Ferrand - CHU
- CH
- CHRU Grenoble
- Centre Hospitalier - Pneumologie
- CHRU de Lille
- Lille - Polyclinique de la Louvière
- Lyon - Hôpital Privé Jean Mermoz
- Institut Paoli Calmette
- Montpellier - GCS Centre de Cancérologie du Grand Montpellier
- CH de Mulhouse
- Nantes - ICO René Gauducheau
- Nevers - CH
- Centre Antoine Lacassagne
- Orléans - Hôpital de la Source
- AP-HP Hopital Tenon - Pneumologie
- Paris - APHP Bichat
- Paris - APHP Saint-Louis
- Pau - CH
- Pontoise - CH
- Centre Hospitalier
- Nouvel Hopital Civil - Pneumologie
- Centre Hospitalier Intercommunal
- HIA Saint Anne
- Tours - CHU
- CH de Villefranche - Pneumologie
- Villeneuve d'Ascq - Hôpital Privé
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Experimental
Arm Label
Afatinib
Afatinib + cetuximab
Arm Description
Afatinib 40 mg/d until progression
Afatinib 40 mg/d until progression + cetuximab 500 mg/m² every 2 weeks during 6 months (beginning at D15 at 250 mg/m²)
Outcomes
Primary Outcome Measures
Time to Treatment Failure
Secondary Outcome Measures
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Response Rate
Overall survival
Overall survival
Overall survival
Progression-Free Survival
Progression-Free Survival
Progression-Free Survival
Progression-Free Survival
Full Information
NCT ID
NCT02716311
First Posted
November 30, 2015
Last Updated
August 9, 2022
Sponsor
Intergroupe Francophone de Cancerologie Thoracique
1. Study Identification
Unique Protocol Identification Number
NCT02716311
Brief Title
Combination of Cetuximab With Afatinib for Patient With EGFR Mutated Lung Cancer
Acronym
ACE-Lung
Official Title
Phase II Study Evaluating the Combination of Cetuximab With Afatinib as First-line Treatment for Patients With EGFR Mutated Non Small Cell Lung Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
May 2016 (Actual)
Primary Completion Date
February 2019 (Actual)
Study Completion Date
April 7, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Intergroupe Francophone de Cancerologie Thoracique
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Until recently, the first line treatment of metastatic Non Small Cell Lung Cancer (NSCLC) was a platine-based chemotherapy. It has been changed by the discovery of EGFR (Epidermal Growth Factor Receptor) mutations and associated treatment with Tyrosine Kinase Inhibitor (TKI) of EGFR. The superiority of EGFR TKI over chemotherapy for EGFR mutated patients has been proved in several phase III trials with gefitinib, erlotinib or afatinib.
Nevertheless, all patients will progress after 9 to 12 months of treatment due to the appearance of a treatment resistance.
Afatinib is an irreversible EGFR TKI. It binds to its receptor permanently.Contrary to erlotinib and gefitinb which inhibits only EGFR, afatinib inhibits the kinase activity of all HER family (Human Epidermal growth factor Receptor). Nevertheless, there is no proof that afatinib delay the appearance of resistance.
Cetuximab is a monoclonal antibody which binds specifically with EGFR. The double inhibition of EGFR by afatinib and cetuximab has demonstrated its efficacy in pre-clinical models. The hypothesis of this study is that the combination between cetuximab and afatinib will permit to delay or decrease the appearance of resistances.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non Small Cell Lung Cancer
Keywords
EGFR, Lung Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
118 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Afatinib
Arm Type
Other
Arm Description
Afatinib 40 mg/d until progression
Arm Title
Afatinib + cetuximab
Arm Type
Experimental
Arm Description
Afatinib 40 mg/d until progression + cetuximab 500 mg/m² every 2 weeks during 6 months (beginning at D15 at 250 mg/m²)
Intervention Type
Drug
Intervention Name(s)
Afatinib
Intervention Type
Drug
Intervention Name(s)
Cetuximab
Primary Outcome Measure Information:
Title
Time to Treatment Failure
Time Frame
9 months
Secondary Outcome Measure Information:
Title
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Time Frame
1 month
Title
Response Rate
Time Frame
9 months
Title
Overall survival
Time Frame
6 months
Title
Overall survival
Time Frame
9 months
Title
Overall survival
Time Frame
12 months
Title
Progression-Free Survival
Time Frame
6 months
Title
Progression-Free Survival
Time Frame
9 months
Title
Progression-Free Survival
Time Frame
12 months
Title
Progression-Free Survival
Time Frame
18 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Principal Inclusion Criteria:
Stage III or IV NSCLC, non irradiable non operable
Non squamous NSCLC histologically or cytologically confirmed
No previous treatment of NSCLC
EGFR mutation (exon 19 deletion, L858R mutation, G719X , L861Q or S768I mutations or exon 19 insertion)
Presence of at least one lesion that can be measured
PS 0 or 1
Principal Exclusion Criteria:
Symptomatic brain metastasis or requiring immediate radiotherapy
T790M mutation or exon 20 insertion
Radiotherapy less than 2 weeks prior randomization including symptomatic radiotherapy
Interstitial pneumopathy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexis CORTOT, MD, PhD
Organizational Affiliation
CHRU, Lille
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jacques CADRANEL, MD, PhD
Organizational Affiliation
AP-HP Hôpital Tenon, Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Hospitalier du Pays d'Aix
City
Aix-en-Provence
Country
France
Facility Name
Clinique de L'Europe
City
Amiens
Country
France
Facility Name
Angers - CHU
City
Angers
Country
France
Facility Name
Annecy - CH
City
Annecy
ZIP/Postal Code
74374
Country
France
Facility Name
Bordeaux - Institut Bergonié
City
Bordeaux
Country
France
Facility Name
Bordeaux - Polyclinique Nord
City
Bordeaux
Country
France
Facility Name
Boulogne - Ambroise Paré
City
Boulogne-Billancourt
Country
France
Facility Name
Clermont-Ferrand - CHU
City
Clermont-Ferrand
Country
France
Facility Name
CH
City
Colmar
Country
France
Facility Name
CHRU Grenoble
City
Grenoble
Country
France
Facility Name
Centre Hospitalier - Pneumologie
City
Le Mans
ZIP/Postal Code
72000
Country
France
Facility Name
CHRU de Lille
City
Lille
Country
France
Facility Name
Lille - Polyclinique de la Louvière
City
Lille
Country
France
Facility Name
Lyon - Hôpital Privé Jean Mermoz
City
Lyon
Country
France
Facility Name
Institut Paoli Calmette
City
Marseille
Country
France
Facility Name
Montpellier - GCS Centre de Cancérologie du Grand Montpellier
City
Montpellier
Country
France
Facility Name
CH de Mulhouse
City
Mulhouse
Country
France
Facility Name
Nantes - ICO René Gauducheau
City
Nantes
Country
France
Facility Name
Nevers - CH
City
Nevers
ZIP/Postal Code
58033
Country
France
Facility Name
Centre Antoine Lacassagne
City
Nice
Country
France
Facility Name
Orléans - Hôpital de la Source
City
Orléans
Country
France
Facility Name
AP-HP Hopital Tenon - Pneumologie
City
Paris
ZIP/Postal Code
75020
Country
France
Facility Name
Paris - APHP Bichat
City
Paris
Country
France
Facility Name
Paris - APHP Saint-Louis
City
Paris
Country
France
Facility Name
Pau - CH
City
Pau
ZIP/Postal Code
64046
Country
France
Facility Name
Pontoise - CH
City
Pontoise
Country
France
Facility Name
Centre Hospitalier
City
Saint-Quentin
Country
France
Facility Name
Nouvel Hopital Civil - Pneumologie
City
Strasbourg
ZIP/Postal Code
63000
Country
France
Facility Name
Centre Hospitalier Intercommunal
City
Toulon
Country
France
Facility Name
HIA Saint Anne
City
Toulon
Country
France
Facility Name
Tours - CHU
City
Tours
ZIP/Postal Code
37000
Country
France
Facility Name
CH de Villefranche - Pneumologie
City
Villefranche
Country
France
Facility Name
Villeneuve d'Ascq - Hôpital Privé
City
Villeneuve-d'Ascq
Country
France
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
34031056
Citation
Cortot AB, Madroszyk A, Giroux-Leprieur E, Molinier O, Quoix E, Berard H, Otto J, Rault I, Moro-Sibilot D, Raimbourg J, Amour E, Morin F, Hureaux J, Moreau L, Debieuvre D, Morel H, Renault A, Pichon E, Huret B, Charpentier S, Denis MG, Cadranel J. First-Line Afatinib plus Cetuximab for EGFR-Mutant Non-Small Cell Lung Cancer: Results from the Randomized Phase II IFCT-1503 ACE-Lung Study. Clin Cancer Res. 2021 Aug 1;27(15):4168-4176. doi: 10.1158/1078-0432.CCR-20-4604. Epub 2021 May 24.
Results Reference
result
Links:
URL
http://www.ifct.fr/index.php/fr/la-recherche/item/2032-ifct-1503-ace
Description
IFCT website
Learn more about this trial
Combination of Cetuximab With Afatinib for Patient With EGFR Mutated Lung Cancer
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