Lung NeoplasmsSTALKLUNG01NCT02372448
Multicenter Validation of the Sensitivity of Theranostic ALK Rearrangement Detection by FISH Analysis and Prevalence of Escaping Mutations in Circulating Tumor Cells for the Non-invasive Management of Lung Cancer Patients
A study testing ALK analysis on CTCs detected by ISET in people with Lung Neoplasms, run by Centre Hospitalier Universitaire de Nice at 11 sites in France.
Trial summary
Patients eligibility to targeted therapies relies on a molecular test performed on a tumor sample collected by biopsy. This invasive procedure is associated with a relative high risk of morbidity and requires the intervention of a costly and important technical platform. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Lung Neoplasms
- What is being tested?
- ALK analysis on CTCs detected by ISET
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 206 participants
- Where
- 11 sitesFrance
- Study dates
- 23 Jan 2015to 21 Nov 2019
- 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
- Age 18 years old or older
- Histologically confirmed stage IIIb/IV non-squamous NSCLC undergoing biopsy or surgery
- Presence of ALK rearrangement result by FISH analysis (gold standard method) on tumor tissue
- Signed specific informed consent approved by the Institutional Review Board prior to patient entry
- Affiliation to the social security system
Who cannot join
- Vulnerable persons: adults under guardianship or persons deprived of their liberty, patients under 18 years old
- Medical and/or psychiatric problems of sufficient severity to limit full compliance with the study or expose patients to undue risk
Trial locations and contacts
11 sites in 1 country.
11 sites in 1 country
France11 sites
Centre François Baclesse
Caen, 14000
Grenoble university hospital
Grenoble, 38043
Marseille University Hospital
Marseille, 13915
Nancy university hospital
Nancy, 54511
Centre Antoine Lacassagne
Nice, 06100
CHU de Nice
Nice
Hôpital Tenon
Paris, 75020
Institut arnault tzanck
Saint-Laurent-du-Var, 06700
Toulouse University Hospital
Toulouse, 31059
Institut de Cancérologie de Lorraine
Vandœuvre-lès-Nancy, 54500
Institut Gustave Roussy
Villejuif, 94800
About this study
Patients eligibility to targeted therapies relies on a molecular test performed on a tumor sample collected by biopsy. This invasive procedure is associated with a relative high risk of morbidity and requires the intervention of a costly and important technical platform. Thus, inoperable patients can be deprived from potentially more efficient therapies. A "liquid biopsy" of Circulating Tumor Cells (CTCs) present in the blood and their molecular characterization is an appealing alternative to meet an urgent need for these patients. Moreover no CTC-based molecular test is currently routinely available.
The 5-year survival rate of patients with non-small cell lung carcinoma (NSCLC) is low. Recent reports demonstrated that the detection of an ALK rearrangement in the tumor tissue allows patients with late-stages NSCLC to benefit from crizotinib treatment.
Read more
However, 1) the detection of an ALK rearrangement is currently performed on small biopsies or fine-needle aspirates and can be hindered by the limited tissue quantities available. Tumor tissue is difficult to obtain in patients with advanced/metastatic lung cancer for whom surgery is rarely a component of treatment. Finding alternative and more effective means of diagnosing an ALK rearrangement are critical issues for identifying patients who may benefit from treatment with crizotinib; 2) some patients develop resistance to crizotinib due to de novo ALK mutations.
In this setting, circulating tumor cells (CTCs), which have been shown to be detectable by ISET (Isolation by Size of Epithelial Tumor Cells) method in 80% to 100 % of late stages lung cancer patients represent a non-invasive and easily accessible source of tumor material for assessing ALK rearrangement and escaping mutations in a kinetic manner. The ISET method was first published in 2000 and several independent teams have now established its high sensitivity and specificity of ISET for NSCLC. With ISET, specificity can be achieved using the same methods and criteria used by cytopathologists to diagnose solid tumors.
The high sensitivity and specificity of ISET are two essential starting points for the feasibility of this present project. Low-throughput molecular characterization of CTCs isolated by ISET has also been achieved. The remaining challenge consists in developing high-throughput ISET-based molecular tests for personalized medicine that are transferable to the clinics.
The Team 1 at the CHU de Nice and the Team 2 at the Gustave Roussy Institute have demonstrated that the detection of an ALK rearrangement in CTC isolated by ISET is feasible and consistent with results obtained in corresponding tumor tissues. In this context, the aim of this project is to obtain 1) a definitive prospective clinical validation of the use of CTC as an alternative to tumor tissue for ALK analysis-based patients stratification; 2) a proof that escaping mutations can be detected early by kinetic analysis of CTC in patients treated by crizotinib. ALK rearrangement will be prospectively investigated in CTCs isolated by ISET at diagnosis and during follow up from patients with stage IIIb/IV lung cancer and de novo mutations will be searched in patients with resistance to crizotinib. This study will provide both clinical and economic benefit to targeted treatment of patients with advanced lung cancer.
This project is strongly original as no CTC-based ALK rearrangement test has been independently validated up to now with clinical samples. The development of non-invasive theranostic test through the genetic analysis of CTCs is a clinically relevant goal for non-invasive stratification of cancer patients, avoiding morbidity related to lung biopsy and surgery. It would allow determining patient's eligibility to targeted therapies on a blood sample analysis. CTC-based ALK test could be useful to guide the choice of ALK targeted therapy in patients with lung cancer. Furthermore, developing biomarkers based on CTCs analysis would open the way to the non-invasive follow up of aggressive cancers, early detection of mutations associated with resistance to targeted therapies and tailoring treatment to a real time analysis of the evolving tumor cell populations. This test is expected to markedly improve patients' quality of life avoiding invasive diagnostic procedures.
- Conditions
- Lung Neoplasms
- Being tested
- ALK analysis on CTCs detected by ISET
- Medical subject headings
- Lung Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ALK analysis on CTCs detected by ISETOther
| Study group | Role | What they receive |
|---|---|---|
| ALK-positive | Other | ALK positive analysis on CTCs detected by ISET Receives: Other: ALK analysis on CTCs detected by ISET |
| ALK-negative | Other | ALK negative analysis on CTCs detected by ISET Receives: Other: ALK analysis on CTCs detected by ISET |
What is being measured
The primary outcome is the main question the study is designed to answer.
sensitivity and specificity of the FISH technique for the detection of the ALK rearrangement in CTCs Change from Baseline to 6 and 12 months
ALK rearrangement positivity by FISH analysis in CTC will be defined as the presence of an ALK rearrangement in four or more CTCs isolated per 1 ml blood. The proportion of ALK-rearranged CTCs (determined by FISH analysis) among the total numbers of CTCs determined by cytomorphological examination or by combining immunofluorescent staining and cytomorphological examination will be also determined and compared to that obtained in the tumor tissue.
Measured: at the inclusion, 6 months and 12 months
Secondary outcomes (2)
sensitivity and specificity of the ICC analysis on CTCs
The intensity of cytoplasmic staining as well as percentages of positive CTCs will be assessed as follows: 0 = no or faint staining in <10% CTCs; 1+ = faint staining in >10% CTCs; 2+ = moderate staining in >10% CTCs; 3+ = strong staining in >10% CTCs. Positive ALK expression is considered as between 2+ and 3+.
Measured: at the inclusion, 6 months and 12 months
association between the ALK-rearranged CTC levels evolution and tumor progression at 6 and 12 months
The ALK-rearranged CTC levels evolution will be defined as the difference, between baseline and respectively M6 and M12, of the CTC number per 1 ml blood as determined by the ISET method. The systemic progression under crizotinib or another ALK inibitor will be evaluated according to the Response Evaluation Criteria In Solid Tumors (RECIST) version 1.1 (http://www.recist.com/). Patients will be categorized into 3 groups with: stable disease, response (complete/partial) or with progressive disease. The association will be adjusted on covariates such as gender, age, smoking history, histology, T4 subtypes (in patients with stage IIIB), and M1 subtypes (in patients with stage IV disease), the initial treatment modality (i.e., surgery, radiotherapy, none, or both).
Measured: at the inclusion, 6 and 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Feb 2015 (estimated)
- Study start23 Jan 2015
- Primary completion21 Nov 2019
- Study completion21 Nov 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Lung NeoplasmsStudies of the same condition, open and under way.
- More trials run by Centre Hospitalier Universitaire de NiceThe sponsor's other registered studies.
- 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
- Diagnosis
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 206 participants (actual)
Sponsor and investigators
- Lead sponsor
- Centre Hospitalier Universitaire de Nice
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Paul HOFMAN, Pr, Principal investigator, Centre Hospitalier Universitaire de Nice
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02372448
- Sponsor's protocol ID
- 13-APN-01
- Acronym
- STALKLUNG01
- Status last verified
- Mar 2026
- First submitted
- 22 Sep 2014
- Last updated
- 27 Mar 2026
- Results posted
- No
- Data monitoring committee
- No
Publications
Heeke S, Benzaquen J, Vallee A, Allegra M, Mazieres J, Fayada J, Rajamani J, Lee M, Ordinario E, Tiotiu A, Cadranel J, Poudenx M, Moro-Sibilot D, Barlesi F, Gervais R, Thariat J, Tanga V, Boutros J, Ilie M, Hofman V, Marquette CH, Denis MG, Hofman P. Detection of ALK fusion transcripts in plasma of non-small cell lung cancer patients using a novel RT-PCR based assay. Ann Transl Med. 2021 Jun;9(11):922. doi: 10.21037/atm-20-7900.
PubMed 34350237
Study at a glance
From the registry record, last updated by the sponsor on 27 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Multicenter Validation of the Sensitivity of Theranostic ALK Rearrangement Detection by FISH Analysis and Prevalence of Escaping Mutations in Circulating Tumor Cells for the Non-invasive Management of Lung Cancer Patients
- ClinicalTrials.gov ID
- NCT02372448
- Acronym / sponsor ID
- STALKLUNG01 / 13-APN-01
- Conditions
- Lung Neoplasms
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 206 participants (actual)
- Lead sponsor
- Centre Hospitalier Universitaire de NiceUniversity, hospital or other
- Study start
- 23 Jan 2015 (actual)
- Primary completion
- 21 Nov 2019 (actual)
- Study completion
- 21 Nov 2019 (actual)
- First posted
- 26 Feb 2015 (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.
Patients eligibility to targeted therapies relies on a molecular test performed on a tumor sample collected by biopsy. This invasive procedure is associated with a relative high risk of morbidity and requires the intervention of a costly and important technical platform. Thus, inoperable patients can be deprived from potentially more efficient therapies. A "liquid biopsy" of Circulating Tumor Cells (CTCs) present in the blood and their molecular characterization is an appealing alternative to meet an urgent need for these patients. Moreover no CTC-based molecular test is currently routinely available.
The 5-year survival rate of patients with non-small cell lung carcinoma (NSCLC) is low. Recent reports demonstrated that the detection of an ALK rearrangement in the tumor tissue allows patients with late-stages NSCLC to benefit from crizotinib treatment.
However, 1) the detection of an ALK rearrangement is currently performed on small biopsies or fine-needle aspirates and can be hindered by the limited tissue quantities available. Tumor tissue is difficult to obtain in patients with advanced/metastatic lung cancer for whom surgery is rarely a component of treatment. Finding alternative and more effective means of diagnosing an ALK rearrangement are critical issues for identifying patients who may benefit from treatment with crizotinib; 2) some patients develop resistance to crizotinib due to de novo ALK mutations.
In this setting, circulating tumor cells (CTCs), which have been shown to be detectable by ISET (Isolation by Size of Epithelial Tumor Cells) method in 80% to 100 % of late stages lung cancer patients represent a non-invasive and easily accessible source of tumor material for assessing ALK rearrangement and escaping mutations in a kinetic manner. The ISET method was first published in 2000 and several independent teams have now established its high sensitivity and specificity of ISET for NSCLC. With ISET, specificity can be achieved using the same methods and criteria used by cytopathologists to diagnose solid tumors.
The high sensitivity and specificity of ISET are two essential starting points for the feasibility of this present project. Low-throughput molecular characterization of CTCs isolated by ISET has also been achieved. The remaining challenge consists in developing high-throughput ISET-based molecular tests for personalized medicine that are transferable to the clinics.
The Team 1 at the CHU de Nice and the Team 2 at the Gustave Roussy Institute have demonstrated that the detection of an ALK rearrangement in CTC isolated by ISET is feasible and consistent with results obtained in corresponding tumor tissues. In this context, the aim of this project is to obtain 1) a definitive prospective clinical validation of the use of CTC as an alternative to tumor tissue for ALK analysis-based patients stratification; 2) a proof that escaping mutations can be detected early by kinetic analysis of CTC in patients treated by crizotinib. ALK rearrangement will be prospectively investigated in CTCs isolated by ISET at diagnosis and during follow up from patients with stage IIIb/IV lung cancer and de novo mutations will be searched in patients with resistance to crizotinib. This study will provide both clinical and economic benefit to targeted treatment of patients with advanced lung cancer.
This project is strongly original as no CTC-based ALK rearrangement test has been independently validated up to now with clinical samples. The development of non-invasive theranostic test through the genetic analysis of CTCs is a clinically relevant goal for non-invasive stratification of cancer patients, avoiding morbidity related to lung biopsy and surgery. It would allow determining patient's eligibility to targeted therapies on a blood sample analysis. CTC-based ALK test could be useful to guide the choice of ALK targeted therapy in patients with lung cancer. Furthermore, developing biomarkers based on CTCs analysis would open the way to the non-invasive follow up of aggressive cancers, early detection of mutations associated with resistance to targeted therapies and tailoring treatment to a real time analysis of the evolving tumor cell populations. This test is expected to markedly improve patients' quality of life avoiding invasive diagnostic procedures.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| ALK-positive | Other | Other: ALK analysis on CTCs detected by ISETALK positive analysis on CTCs detected by ISET |
| ALK-negative | Other | Other: ALK analysis on CTCs detected by ISETALK negative analysis on CTCs detected by ISET |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Age 18 years old or older
- Histologically confirmed stage IIIb/IV non-squamous NSCLC undergoing biopsy or surgery
- Presence of ALK rearrangement result by FISH analysis (gold standard method) on tumor tissue
- Signed specific informed consent approved by the Institutional Review Board prior to patient entry
- Affiliation to the social security system
Key exclusion criteria (2 listed)
- Vulnerable persons: adults under guardianship or persons deprived of their liberty, patients under 18 years old
- Medical and/or psychiatric problems of sufficient severity to limit full compliance with the study or expose patients to undue risk
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 |
|---|---|---|
| ALK analysis on CTCs detected by ISET | Other | ALK-negative, ALK-positive |
Primary outcome
sensitivity and specificity of the FISH technique for the detection of the ALK rearrangement in CTCs Change from Baseline to 6 and 12 months
Time frame: at the inclusion, 6 months and 12 months
ALK rearrangement positivity by FISH analysis in CTC will be defined as the presence of an ALK rearrangement in four or more CTCs isolated per 1 ml blood. The proportion of ALK-rearranged CTCs (determined by FISH analysis) among the total numbers of CTCs determined by cytomorphological examination or by combining immunofluorescent staining and cytomorphological examination will be also determined and compared to that obtained in the tumor tissue.
2 secondary outcomes
sensitivity and specificity of the ICC analysis on CTCs
Time frame: at the inclusion, 6 months and 12 months
association between the ALK-rearranged CTC levels evolution and tumor progression at 6 and 12 months
Time frame: at the inclusion, 6 and 12 months
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 27 Mar 2026.
- Results publication: PubMed 34350237Heeke S, Benzaquen J, Vallee A, Allegra M, Mazieres J, Fayada J, Rajamani J, Lee M, Ordinario E, Tiotiu A, Cadranel J, Poudenx M, Moro-Sibilot D, Barlesi F, Gervais R, Thariat J, Tanga V, Boutros J, Ilie M, Hofman V, Marquette CH, Denis MG, Hofman P. Detection of ALK fusion transcripts in plasma of non-small cell lung cancer patients using a novel RT-PCR based assay. Ann Transl Med. 2021 Jun;9(11):922. doi: 10.21037/atm-20-7900.
Related trials for Lung Neoplasms
RecruitingPhase 1/2
Study of INBRX-106 and INBRX-106 in Combination With Pembrolizumab (Keytruda®) in Subjects With Locally Advanced or Metastatic Solid Tumors (Hexavalent OX40 Agonist)
Solid Tumor, Non-Small Cell Lung Cancer
RecruitingObservational study
A Prospective ,Multicenter ,Non-interventional ,Real-world Study Observing Changes in Molecular Markers Osimertinib Targeted Therapy in EGFRm NSCLC
Non Small Cell Lung Cancer
Active, not recruiting
Streamlined Geriatric and Oncological Evaluation Based On IC Technology
Breast Cancer, Comorbidities and Coexisting Conditions
RecruitingPhase 3
A Study Evaluating Sotorasib Platinum Doublet Combination Versus Pembrolizumab Platinum Doublet Combination as a Front-Line Therapy in Participants With Stage IV or Advanced Stage IIIB/C Nonsquamous Non-Small Cell Lung Cancers (CodeBreaK 202)
Non-Small Cell Lung Cancer (NSCLC)
Active, not recruitingPhase 2
Datopotamab Deruxtecan (Dato-DXd, DS-1062a) in Advanced and/or Unresectable Non-Small Cell Lung Cancer
Metastatic Lung Cancer, Advanced Non Small Cell Lung Cancer
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.
Paul HOFMAN, Pr principal investigator
Centre Hospitalier Universitaire de Nice
11 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing ALK analysis on CTCs detected by ISET in people with Lung Neoplasms, run by Centre Hospitalier Universitaire de Nice at 11 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 5 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 27 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 11 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?
sensitivity and specificity of the FISH technique for the detection of the ALK rearrangement in CTCs Change from Baseline to 6 and 12 months (time frame: at the inclusion, 6 months and 12 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02372448, which also lists 1 linked publication.
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 27 Mar 2026.