search
Back to results

Lung Cancer in Women Treated With Anti-oestrogens anD Inhibitors of EGFR (LADIE)

Primary Purpose

Stage IV Lung Cancer

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Gefitinib
Fulvestrant
Erlotinib
Sponsored by
Intergroupe Francophone de Cancerologie Thoracique
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stage IV Lung Cancer focused on measuring lung cancer, women

Eligibility Criteria

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

Inclusion Criteria:

  • Histologically confirmed predominant non-squamous, non-small cell lung cancer
  • The presence of analysable tissue for the research of EGFR activating mutation. Analysis must be performed in INCa-labelled laboratories or platforms according to a validated technique
  • Not suitable for radiation, inoperable stage III or stage IV
  • Patients with an EGFR mutation must never have taken chemotherapy or must be in progression after only one previous line of chemotherapy (including maintenance). Patients without an EGFR mutation must have received one or two lines of chemotherapy beforehand. Maintenance chemotherapy is not considered to be a treatment line. Adjuvant chemotherapy is not considered to be a first line of treatment if it dates back to over a year
  • Female
  • Menopausal: older than 60 years of age or history of ovariectomy or younger than 60 years old with amenorrhoea for more than 12 months or an FSH rate that corresponds to a post-menopausal rate (according to the laboratory)

Exclusion Criteria:

  • History of cancer except for skin cancer or cancer dating from over five years ago and considered to be cured
  • Known or suspected Cerebral metastases or spinal cord compression unless they are asymptomatic without treatment or stable after being treated by surgery and/or radiation therapy. Corticosteroid treatments for symptoms must have discontinued for more than four weeks
  • Pregnancy and breast-feeding
  • Patient taking hormone replacement therapy for menopause that has not been stopped two weeks before the start of the trial treatment
  • A change in bone marrow, kidney and liver functions inconsistent with treatment

Sites / Locations

  • Annemasse - CH
  • Clinique de l'Europe
  • Angers - CHU
  • CH de la Côte Basque
  • CHU Besancon - Pneumologie
  • Bobigny - Hôpital Avicenne
  • Hôpital Ambroise Paré - Pneumologie
  • HCL Hôpital Louis Pradel
  • Béziers - CH
  • Caen - Centre François Baclesse
  • Caen - CHU Côte de Nacre
  • Cahors - CH
  • Chambéry - CH
  • Centre Hospitalier
  • Hôpital de Cholet - Pneumologie
  • Clamart - Hôpital Percy
  • CHU
  • CH
  • Clinique des Cèdres
  • Créteil - CHI
  • CH de Dax
  • Dijon - CAC
  • Grenoble - CHU
  • Chartres - CH
  • Centre Hospitalier - Pneumologie
  • CHU (Hôpital Calmette) - Pneumologie
  • CH
  • Hôpital Nord - Oncologie Multidisciplinaire & Innovations Thérapeutiques
  • Institut Paoli Calmette
  • Polyclinique du Val de Sambre
  • Mont de Marsan - CH
  • Mulhouse - CH
  • CHU Nancy
  • Nantes - Centre René Gauducheau
  • Nevers - CH
  • Centre Antoine Lacassagne
  • Hopital Tenon - Pneumologie
  • HIA Val-de-Grâce
  • Hôpital Bichat - Claude - Bernard
  • Hôpital Européen Georges Pompidou
  • Hôpital Saint-Joseph
  • Paris - Curie
  • Pau - CH
  • Perpignan - Ch
  • HCL - Lyon Sud (Pneumologie)
  • Centre Hospitalier
  • CHU de Reims
  • Institut Jean Godinot
  • Rouen - CHU
  • Saint Quentin - CH
  • Strasbourg - NHC
  • Suresnes - Hopital Foch
  • Centre Hospitalier Intercommunal
  • Clinique Pasteur
  • Toulouse - CHU Larrey
  • Tourcoing - CH
  • CHU Tours - Pneumologie
  • Versailles - CH
  • CHI de la Haute-Saône - Pneumologie
  • CH de Villefranche - Pneumologie
  • Institut Gustave Roussy

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Experimental

Active Comparator

Arm Label

Gefinitib + Fulvestrant (patient with EGFR mutations)

Erlotinib (wild type patients)

Erlotinib + Fulvestrant (wild type patients)

Gefinib (patient with EGFR mutations)

Arm Description

Outcomes

Primary Outcome Measures

progression-free survival
From date of randomization until the date of first progression for EGFR mutated patient
Progression free survival
From date of randomization until the date of first progression for EGFR wild type patients

Secondary Outcome Measures

toxicity of EGFR-TKI and fulvestrant
The number of patients for whom at least an adverse event will have been reported, the number of events, according to the relation to the treatment, the intensity, and the cycle of appearance for EGFR WT patients
Response rate
For EGFR WT patients
Overall survival
For all patients
toxicity of EGFR-TKI and fulvestrant
The number of patients for whom at least an adverse event will have been reported, the number of events, according to the relation to the treatment, the intensity, and the cycle of appearance for EGFR mutated patients
Response rate
For EGFR-Mutated patients

Full Information

First Posted
March 8, 2012
Last Updated
January 6, 2021
Sponsor
Intergroupe Francophone de Cancerologie Thoracique
search

1. Study Identification

Unique Protocol Identification Number
NCT01556191
Brief Title
Lung Cancer in Women Treated With Anti-oestrogens anD Inhibitors of EGFR
Acronym
LADIE
Official Title
Phase II Randomised Clinical Trial Evaluating an EGFR Tyrosine Kinase Inhibitor (EGFR-TKI) Versus an EGFR-TKI Combined With an Anti-oestrogen Treatment (Fulvestrant) in Women With Advanced Stage Non-squamous Lung Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
May 15, 2012 (Actual)
Primary Completion Date
May 15, 2018 (Actual)
Study Completion Date
June 17, 2020 (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
Lung Cancer is to become the first cause of death related to cancer in France as it's already the case in United States. At Present, Lung Cancer in women and in men is treated similarly. Nevertheless, numerous studies shows that lung cancer in women has specificities : at the time of the diagnosis female patients are younger, there are less clinical signs, clinical stages are earlier, histology is often adenocarcinoma. The link with tabagism is weaker . Sensitivity to tabagism is higher (more cancer in women with the same tabagism). Response rate to chemotherapy is better. Prognosis is better Numerous hypotheses have been put forward to account for the specific characteristics of female lung cancer described above. One hypothesis is that there are different genetic anomalies in women. Some studies show an increase of EGFR mutation and HER2 expression and a decrease of expression of repair enzymes (ERCC1, RRM1, BRCA) which can explain the increase sensitivity to tabagism and to chemotherapy. Another hypothesis is that hormones play a role in oncogenesis. Indeed, lung cancer presents hormonal risk factors : pre-menopause, less than 3 kids, short menstrual cycle, hormone replacement therapy. Estrogens would have a deleterious effect on cancer incidence and on survival of lung cancer in women. Cellular and animal models show that ER pathway is activated in lung cancer and participates in oncogenesis. Moreover an interaction between RE and EGFR pathway has been demonstrated on lung cancer cell lines and mouse models. EGFR-TKI have shown benefit in women with wild type EGFR or unknown status (with erlotinib) and in women with EGFR mutations (with gefitinib). In this study, the use of these two treatment will be in accordance with their market authorisations. The objective of this study is to test the addition of an anti-estrogen (fulvestrant) to EGFR-TKI. Fulvestrant is a pure anti-oestrogen that binds to ER, blocks it and accelerates its breakdown. It has a market authorisation in breast cancer. Furthermore the association between EGFR-TKI and anti-estrogen could have a synergetic effect due to interaction between RE and EGFR pathways .

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stage IV Lung Cancer
Keywords
lung cancer, women

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
379 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Gefinitib + Fulvestrant (patient with EGFR mutations)
Arm Type
Experimental
Arm Title
Erlotinib (wild type patients)
Arm Type
Active Comparator
Arm Title
Erlotinib + Fulvestrant (wild type patients)
Arm Type
Experimental
Arm Title
Gefinib (patient with EGFR mutations)
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Gefitinib
Intervention Description
250 mg per day (oral)
Intervention Type
Drug
Intervention Name(s)
Fulvestrant
Intervention Description
500 mg (2 x 250 mg), IV by month with an additional 500 mg dose two weeks after the initial dose
Intervention Type
Drug
Intervention Name(s)
Erlotinib
Intervention Description
150 mg per day (oral)
Primary Outcome Measure Information:
Title
progression-free survival
Description
From date of randomization until the date of first progression for EGFR mutated patient
Time Frame
Around nine months
Title
Progression free survival
Description
From date of randomization until the date of first progression for EGFR wild type patients
Time Frame
Around three months
Secondary Outcome Measure Information:
Title
toxicity of EGFR-TKI and fulvestrant
Description
The number of patients for whom at least an adverse event will have been reported, the number of events, according to the relation to the treatment, the intensity, and the cycle of appearance for EGFR WT patients
Time Frame
Around three months
Title
Response rate
Description
For EGFR WT patients
Time Frame
Around three months
Title
Overall survival
Description
For all patients
Time Frame
Up to 18 months
Title
toxicity of EGFR-TKI and fulvestrant
Description
The number of patients for whom at least an adverse event will have been reported, the number of events, according to the relation to the treatment, the intensity, and the cycle of appearance for EGFR mutated patients
Time Frame
Around Nine months
Title
Response rate
Description
For EGFR-Mutated patients
Time Frame
Around nine months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically confirmed predominant non-squamous, non-small cell lung cancer The presence of analysable tissue for the research of EGFR activating mutation. Analysis must be performed in INCa-labelled laboratories or platforms according to a validated technique Not suitable for radiation, inoperable stage III or stage IV Patients with an EGFR mutation must never have taken chemotherapy or must be in progression after only one previous line of chemotherapy (including maintenance). Patients without an EGFR mutation must have received one or two lines of chemotherapy beforehand. Maintenance chemotherapy is not considered to be a treatment line. Adjuvant chemotherapy is not considered to be a first line of treatment if it dates back to over a year Female Menopausal: older than 60 years of age or history of ovariectomy or younger than 60 years old with amenorrhoea for more than 12 months or an FSH rate that corresponds to a post-menopausal rate (according to the laboratory) Exclusion Criteria: History of cancer except for skin cancer or cancer dating from over five years ago and considered to be cured Known or suspected Cerebral metastases or spinal cord compression unless they are asymptomatic without treatment or stable after being treated by surgery and/or radiation therapy. Corticosteroid treatments for symptoms must have discontinued for more than four weeks Pregnancy and breast-feeding Patient taking hormone replacement therapy for menopause that has not been stopped two weeks before the start of the trial treatment A change in bone marrow, kidney and liver functions inconsistent with treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julien MAZIERES, MD, phD
Organizational Affiliation
University Hospital, Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
Annemasse - CH
City
Ambilly
ZIP/Postal Code
74100
Country
France
Facility Name
Clinique de l'Europe
City
Amiens
Country
France
Facility Name
Angers - CHU
City
Angers
ZIP/Postal Code
49000
Country
France
Facility Name
CH de la Côte Basque
City
Bayonne
Country
France
Facility Name
CHU Besancon - Pneumologie
City
Besancon
ZIP/Postal Code
25000
Country
France
Facility Name
Bobigny - Hôpital Avicenne
City
Bobigny
ZIP/Postal Code
93000
Country
France
Facility Name
Hôpital Ambroise Paré - Pneumologie
City
Boulogne
Country
France
Facility Name
HCL Hôpital Louis Pradel
City
Bron
Country
France
Facility Name
Béziers - CH
City
Béziers
ZIP/Postal Code
34525
Country
France
Facility Name
Caen - Centre François Baclesse
City
Caen
ZIP/Postal Code
14000
Country
France
Facility Name
Caen - CHU Côte de Nacre
City
Caen
ZIP/Postal Code
14000
Country
France
Facility Name
Cahors - CH
City
Cahors
ZIP/Postal Code
46000
Country
France
Facility Name
Chambéry - CH
City
Chambéry
Country
France
Facility Name
Centre Hospitalier
City
Chauny
Country
France
Facility Name
Hôpital de Cholet - Pneumologie
City
Cholet
Country
France
Facility Name
Clamart - Hôpital Percy
City
Clamart
ZIP/Postal Code
92140
Country
France
Facility Name
CHU
City
Clermont-Ferrand
Country
France
Facility Name
CH
City
Colmar
Country
France
Facility Name
Clinique des Cèdres
City
Cornebarrieu
Country
France
Facility Name
Créteil - CHI
City
Créteil
ZIP/Postal Code
94000
Country
France
Facility Name
CH de Dax
City
Dax
Country
France
Facility Name
Dijon - CAC
City
Dijon
ZIP/Postal Code
21000
Country
France
Facility Name
Grenoble - CHU
City
Grenoble
ZIP/Postal Code
38000
Country
France
Facility Name
Chartres - CH
City
Le Coudray
ZIP/Postal Code
28630
Country
France
Facility Name
Centre Hospitalier - Pneumologie
City
Le Mans
ZIP/Postal Code
72000
Country
France
Facility Name
CHU (Hôpital Calmette) - Pneumologie
City
Lille
ZIP/Postal Code
59000
Country
France
Facility Name
CH
City
Longjumeau
Country
France
Facility Name
Hôpital Nord - Oncologie Multidisciplinaire & Innovations Thérapeutiques
City
Marseille
Country
France
Facility Name
Institut Paoli Calmette
City
Marseille
Country
France
Facility Name
Polyclinique du Val de Sambre
City
Maubeuge
Country
France
Facility Name
Mont de Marsan - CH
City
Mont de Marsan
ZIP/Postal Code
40000
Country
France
Facility Name
Mulhouse - CH
City
Mulhouse
ZIP/Postal Code
68000
Country
France
Facility Name
CHU Nancy
City
Nancy
Country
France
Facility Name
Nantes - Centre René Gauducheau
City
Nantes
ZIP/Postal Code
44805
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
Hopital Tenon - Pneumologie
City
Paris
ZIP/Postal Code
75020
Country
France
Facility Name
HIA Val-de-Grâce
City
Paris
Country
France
Facility Name
Hôpital Bichat - Claude - Bernard
City
Paris
Country
France
Facility Name
Hôpital Européen Georges Pompidou
City
Paris
Country
France
Facility Name
Hôpital Saint-Joseph
City
Paris
Country
France
Facility Name
Paris - Curie
City
Paris
Country
France
Facility Name
Pau - CH
City
Pau
ZIP/Postal Code
64046
Country
France
Facility Name
Perpignan - Ch
City
Perpignan
ZIP/Postal Code
66046
Country
France
Facility Name
HCL - Lyon Sud (Pneumologie)
City
Pierre Bénite
ZIP/Postal Code
69495
Country
France
Facility Name
Centre Hospitalier
City
Rambouillet
Country
France
Facility Name
CHU de Reims
City
Reims
Country
France
Facility Name
Institut Jean Godinot
City
Reims
Country
France
Facility Name
Rouen - CHU
City
Rouen
ZIP/Postal Code
76000
Country
France
Facility Name
Saint Quentin - CH
City
Saint Quentin
ZIP/Postal Code
02100
Country
France
Facility Name
Strasbourg - NHC
City
Strasbourg
ZIP/Postal Code
63000
Country
France
Facility Name
Suresnes - Hopital Foch
City
Suresnes
ZIP/Postal Code
92151
Country
France
Facility Name
Centre Hospitalier Intercommunal
City
Toulon
Country
France
Facility Name
Clinique Pasteur
City
Toulouse
Country
France
Facility Name
Toulouse - CHU Larrey
City
Toulouse
Country
France
Facility Name
Tourcoing - CH
City
Tourcoing
ZIP/Postal Code
59208
Country
France
Facility Name
CHU Tours - Pneumologie
City
Tours
Country
France
Facility Name
Versailles - CH
City
Versailles
ZIP/Postal Code
78157
Country
France
Facility Name
CHI de la Haute-Saône - Pneumologie
City
Vesoul
Country
France
Facility Name
CH de Villefranche - Pneumologie
City
Villefranche
Country
France
Facility Name
Institut Gustave Roussy
City
Villejuif
ZIP/Postal Code
94800
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
32144133
Citation
Mazieres J, Barlesi F, Rouquette I, Molinier O, Besse B, Monnet I, Audigier-Valette C, Toffart AC, Renault PA, Fraboulet S, Hiret S, Mennecier B, Debieuvre D, Westeel V, Masson P, Madroszyk-Flandin A, Pichon E, Cortot AB, Amour E, Morin F, Zalcman G, Moro-Sibilot D, Souquet PJ. Randomized Phase II Trial Evaluating Treatment with EGFR-TKI Associated with Antiestrogen in Women with Nonsquamous Advanced-Stage NSCLC: IFCT-1003 LADIE Trial. Clin Cancer Res. 2020 Jul 1;26(13):3172-3181. doi: 10.1158/1078-0432.CCR-19-3056. Epub 2020 Mar 6.
Results Reference
derived
Links:
URL
http://www.ifct.fr
Description
IFCT official website

Learn more about this trial

Lung Cancer in Women Treated With Anti-oestrogens anD Inhibitors of EGFR

We'll reach out to this number within 24 hrs