Lung CancerGFPC-REBIOPNCT02086071
Feasibility of re Biopsies at Progression
A study testing re biopsy in people with Lung Cancer, run by Groupe Francais De Pneumo-Cancerologie at 9 sites in France.
Trial summary
Feasibility of new biological and histological samples at progression in patients with advanced or metastatic Non Small Cell Lung Cancer (NSCLC). A recent paper from Professor Sequist and coll. has depicted the resistance mechanisms as Thréonine790Methionine (T890M) mutation oncogene cMet (CMet) amplification. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Lung Cancer
- What is being tested?
- re biopsy
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- 9 sitesFrance
- Study dates
- May 2012to May 2013
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- All the patient more than 18 years old with advanced or metastatic NSCLC in progression after one or more treatment by chemotherapy.
Who cannot join
- SCLC, neuroendocrine carcinoma,
- Patients with judicial protection or deprived of liberty
Trial locations and contacts
9 sites in 1 country.
9 sites in 1 country
France9 sites
Centre Hospitalier Universitaire
Angers, 49033
Centre Hospitalier du Morvan
Brest, 29200
Centre François Baclesse
Caen, 14000
Site 04
Gap, 05000
Hospital du Cluzeau
Limoges, 87042
Site 25
Mantes-la-Jolie, 78200
Site 06
Marseille, 13274
Hospital Saint Antoine
Paris, 75012
Site 20
Rennes, 35033
About this study
Official title: Feasibility of New Biological and Histological Samples at Progression for Patients With Advanced or Metastatic Non Small Cell Lung Cancer (NSCLC)
Feasibility of new biological and histological samples at progression in patients with advanced or metastatic Non Small Cell Lung Cancer (NSCLC).
A recent paper from Professor Sequist and coll. has depicted the resistance mechanisms as Thréonine790Methionine (T890M) mutation oncogene cMet (CMet) amplification. Re-biopsies showed in 14% of cases the transition between NSCLC to Small Cells Lung Cancer (SCLC). In 3 patients, resistance mechanisms have disappeared and they became again sensitive to Tyrosine Kinase Inhibitors (TKIs). It is mandatory to have a better description to natural history of the disease. This study will be conducted by the French Group of Pneumology-Oncology (Groupe Français de Pneumo Cancérologie (GFPC)) up to 100 patients during 18 Months. Each center will have to define if re-biopsies are possible or not and explain why not.
Read the detailed description
ABSTRACT PROMOTOR GFPC
MAIN INVESTIGATORS Pr Vergnenegre Alain, Dr Dujon Cécile, Pr Rosell Rafael TITLE Feasibility of new biological and histological samples at progression in patients with advanced or metastatic Non Small Cell Lung Cancer (NSCLC)
JUSTIFICATION / BACKGROUND In NSCLC, recent progresses have been reached, with better outcome in terms of survival without relapse, response rate, and improvement of Qualify of Life (QoL). In the detail, patients with mutations of Epidermal Growth Factor Receptor (EGF-R) are sensitive to tyrosine kinase inhibitors (TKIs).
- Patients with EGF-R mutation Response and disease control are frequently achieved on some long period of time but, in the majority of cases, resistances appear around a period of 12 months after the diagnosis. One of the major resistance mechanisms is the onset of T790M mutation, which induces a non sensitivity to TKIs. At the opposite, some recent papers have depicted that, after a free interval, resistant tumor can be responder in a second phase to TKIs]. The type of the mutation has different consequences on the disease evolution. A recent paper from Pr. Sequist and coll. has depicted the resistance mechanisms as mutation T790M or oncogene cMet (CMet) amplification. Re-biopsies showed in 14% of cases the transition between NSCLC to SCLC. In 3 patients, resistance mechanisms have disappeared and they became again sensitive to TKIs. It is mandatory to have a better description to natural history of the disease.
- Patients without EGF-R mutation The knowledge of genetic characteristics is currently needed to perform an inclusion in some research protocol.
TRIAL DESIGN Translational study with iterative biopsies.
OUTCOMES CRITERIA Principal outcome Feasibility of re-biopsies
Secondary outcomes
- analyses and types of resistances,
- time until metastasis disappearance
- correlations with disease management
- biological history of the disease.
INCLUSION CRITERIA All the patient more than 18 years old, with advanced or metastatic NSCLC.
NON INCLUSION CRITERIA
- SCLC, neuroendocrine carcinoma,
- Patients with judicial protection or deprived of liberty
PROCEDURES
A paper CRF will be recorded with data on :
- Patients's characteristics,
- Tumor Node Metastasis classification (TNM) and stage,
- Number of metastasis and location at the diagnosis,
- First line treatment: surgery, radiotherapy, chemotherapy,
- Date of EGF-R status response,
- Date of relapse,
- Type of procedures,
- Treatment for second and third line management
NUMBER OF PATIENTS 100 patients NUMBER OF CENTRES 20 centres DURATION 18 months
PRACTICAL ORGANIZATION IN EACH CENTER Each center will have to define if re-biopsies are possible or not (and explain why not). Some localisations are difficult to biopsy like bone metastasis or deep brain metastasis. A bronchial fiberscopy will be systematically performed to search an endoluminal lesion, which could allow 3 to 5 tissue samples. When possible, liver, adrenal gland, superficial brain metastases will be analysed after the relapse.
- For patients with EGF-R mutation The samples will be prepared with the usual technic of each center. The corresponding slides have to be send to spanish laboratory (Pr R Rosell, Badalona hospital) A comparison between patients with impossible re-biopsies and the final patients group will be performed.
- For patients without EGF-R mutation the usual practice will be used with biological platforms
BIOLOGICAL PROCEDURES
- Patients with EGF-R mutation Biological markers analysis will be coordinated by Catalan Institute of Oncology.
- Patients without EGF-R mutation: usual biological analysis will be performed in the local platform.
STATISTICAL ANALYSES A description of each items will be performed in terms of frequence, range, mean and median. Correlation between biological markers will be assessed by non parametric tests Wilcoxon or Mann-Whitney.
POSSIBLE APPLICATIONS
- a better knowledge of resistance mechanisms in EGF-R mutated patients
- a better knowledge of genetical and molecular history of these diseases
- a better management according to biological changes and evolution
- Conditions
- Lung Cancer
- Being tested
- re biopsy
- Keywords
- REBIOP re-biopsies advanced or metastatic NSCLC
- Medical subject headings
- Lung Neoplasms, Carcinoma, Non-Small-Cell Lung
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
re biopsyProcedure or surgery
re biopsy depending on the location of the pathology
| Study group | Role | What they receive |
|---|---|---|
| Re biopsies feasibility | Other | the Interest of the study is to evaluate the feasibility of the re biopsy; the re biopsy is done if the patient agrees to perform it. Receives: Procedure: re biopsy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Feasibility of re-biopsies
Feasibility of re-biopsies in patients with advanced or metastatic NSCLC after progression of disease under treatment. If the re-biopsy could not be performed : reason of no re-biopsy. If the biopsy could be performed : site and method of rebiopsy.
Measured: 18 months / 100 patients
Secondary outcomes (3)
Type of resistance
Comparison of types and numbers of resistances before treatment (on the first biopsy) and after treatment (on the re-biopsy). Appearance and/or disappearance of some resistances.
Measured: 18 months/100 patients
Disease management
Description of population: age, performance status, smoking status, sex (number, medium, maximum, minimum). Description of treatment: chemotherapy (type and products), radiotherapy (site), surgery (site)
Measured: 18 months / 100 patients
Biological history of the disease
Description and comparison of histology on the first biopsy and on the rebiopsy
Measured: 18 months / 100 patients
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Mar 2014 (estimated)
- Study startMay 2012
- Primary completionDec 2012
- Study completionMay 2013
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Lung CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 100 participants (actual)
Sponsor and investigators
- Lead sponsor
- Groupe Francais De Pneumo-Cancerologie
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- DUJON Cécile, MD, Principal investigator, CENTRE HOSPITALIER André MIGNOT VERSAILLES FRANCE
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02086071
- Sponsor's protocol ID
- GFPC-REBIOP
- Acronym
- GFPC-REBIOP
- Status last verified
- Mar 2014
- First submitted
- 6 Oct 2013
- Last updated
- 13 Mar 2020
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 13 Mar 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Feasibility of New Biological and Histological Samples at Progression for Patients With Advanced or Metastatic Non Small Cell Lung Cancer (NSCLC)
- ClinicalTrials.gov ID
- NCT02086071
- Acronym / sponsor ID
- GFPC-REBIOP / GFPC-REBIOP
- Conditions
- Lung Cancer
- Keywords
- REBIOP re-biopsies advanced or metastatic NSCLC
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 100 participants (actual)
- Lead sponsor
- Groupe Francais De Pneumo-CancerologieUniversity, hospital or other
- Study start
- May 2012
- Primary completion
- Dec 2012 (actual)
- Study completion
- May 2013 (actual)
- First posted
- 13 Mar 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Feasibility of new biological and histological samples at progression in patients with advanced or metastatic Non Small Cell Lung Cancer (NSCLC).
A recent paper from Professor Sequist and coll. has depicted the resistance mechanisms as Thréonine790Methionine (T890M) mutation oncogene cMet (CMet) amplification. Re-biopsies showed in 14% of cases the transition between NSCLC to Small Cells Lung Cancer (SCLC). In 3 patients, resistance mechanisms have disappeared and they became again sensitive to Tyrosine Kinase Inhibitors (TKIs). It is mandatory to have a better description to natural history of the disease. This study will be conducted by the French Group of Pneumology-Oncology (Groupe Français de Pneumo Cancérologie (GFPC)) up to 100 patients during 18 Months. Each center will have to define if re-biopsies are possible or not and explain why not.
Detailed description
ABSTRACT PROMOTOR GFPC
MAIN INVESTIGATORS Pr Vergnenegre Alain, Dr Dujon Cécile, Pr Rosell Rafael TITLE Feasibility of new biological and histological samples at progression in patients with advanced or metastatic Non Small Cell Lung Cancer (NSCLC)
JUSTIFICATION / BACKGROUND In NSCLC, recent progresses have been reached, with better outcome in terms of survival without relapse, response rate, and improvement of Qualify of Life (QoL). In the detail, patients with mutations of Epidermal Growth Factor Receptor (EGF-R) are sensitive to tyrosine kinase inhibitors (TKIs).
- Patients with EGF-R mutation Response and disease control are frequently achieved on some long period of time but, in the majority of cases, resistances appear around a period of 12 months after the diagnosis. One of the major resistance mechanisms is the onset of T790M mutation, which induces a non sensitivity to TKIs. At the opposite, some recent papers have depicted that, after a free interval, resistant tumor can be responder in a second phase to TKIs]. The type of the mutation has different consequences on the disease evolution. A recent paper from Pr. Sequist and coll. has depicted the resistance mechanisms as mutation T790M or oncogene cMet (CMet) amplification. Re-biopsies showed in 14% of cases the transition between NSCLC to SCLC. In 3 patients, resistance mechanisms have disappeared and they became again sensitive to TKIs. It is mandatory to have a better description to natural history of the disease.
- Patients without EGF-R mutation The knowledge of genetic characteristics is currently needed to perform an inclusion in some research protocol.
TRIAL DESIGN Translational study with iterative biopsies.
OUTCOMES CRITERIA Principal outcome Feasibility of re-biopsies
Secondary outcomes
- analyses and types of resistances,
- time until metastasis disappearance
- correlations with disease management
- biological history of the disease.
INCLUSION CRITERIA All the patient more than 18 years old, with advanced or metastatic NSCLC.
NON INCLUSION CRITERIA
- SCLC, neuroendocrine carcinoma,
- Patients with judicial protection or deprived of liberty
PROCEDURES
A paper CRF will be recorded with data on :
- Patients's characteristics,
- Tumor Node Metastasis classification (TNM) and stage,
- Number of metastasis and location at the diagnosis,
- First line treatment: surgery, radiotherapy, chemotherapy,
- Date of EGF-R status response,
- Date of relapse,
- Type of procedures,
- Treatment for second and third line management
NUMBER OF PATIENTS 100 patients NUMBER OF CENTRES 20 centres DURATION 18 months
PRACTICAL ORGANIZATION IN EACH CENTER Each center will have to define if re-biopsies are possible or not (and explain why not). Some localisations are difficult to biopsy like bone metastasis or deep brain metastasis. A bronchial fiberscopy will be systematically performed to search an endoluminal lesion, which could allow 3 to 5 tissue samples. When possible, liver, adrenal gland, superficial brain metastases will be analysed after the relapse.
- For patients with EGF-R mutation The samples will be prepared with the usual technic of each center. The corresponding slides have to be send to spanish laboratory (Pr R Rosell, Badalona hospital) A comparison between patients with impossible re-biopsies and the final patients group will be performed.
- For patients without EGF-R mutation the usual practice will be used with biological platforms
BIOLOGICAL PROCEDURES
- Patients with EGF-R mutation Biological markers analysis will be coordinated by Catalan Institute of Oncology.
- Patients without EGF-R mutation: usual biological analysis will be performed in the local platform.
STATISTICAL ANALYSES A description of each items will be performed in terms of frequence, range, mean and median. Correlation between biological markers will be assessed by non parametric tests Wilcoxon or Mann-Whitney.
POSSIBLE APPLICATIONS
- a better knowledge of resistance mechanisms in EGF-R mutated patients
- a better knowledge of genetical and molecular history of these diseases
- a better management according to biological changes and evolution
Study design
- Primary purpose
- Basic science
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Re biopsies feasibility | Other | Procedure: re biopsythe Interest of the study is to evaluate the feasibility of the re biopsy; the re biopsy is done if the patient agrees to perform it. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- All the patient more than 18 years old with advanced or metastatic NSCLC in progression after one or more treatment by chemotherapy.
Key exclusion criteria (2 listed)
- SCLC, neuroendocrine carcinoma,
- Patients with judicial protection or deprived of liberty
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| re biopsyre biopsy depending on the location of the pathology | Procedure or surgery | Re biopsies feasibility |
Primary outcome
Feasibility of re-biopsies
Time frame: 18 months / 100 patients
Feasibility of re-biopsies in patients with advanced or metastatic NSCLC after progression of disease under treatment. If the re-biopsy could not be performed : reason of no re-biopsy. If the biopsy could be performed : site and method of rebiopsy.
3 secondary outcomes
Type of resistance
Time frame: 18 months/100 patients
Disease management
Time frame: 18 months / 100 patients
Biological history of the disease
Time frame: 18 months / 100 patients
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Mar 2020.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
DUJON Cécile, MD principal investigator
CENTRE HOSPITALIER André MIGNOT VERSAILLES FRANCE
9 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing re biopsy in people with Lung Cancer, run by Groupe Francais De Pneumo-Cancerologie at 9 sites in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 13 Mar 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 9 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Feasibility of re-biopsies (time frame: 18 months / 100 patients). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Mar 2020.