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Analysis of Biological Characteristics of Advanced ALK-rearranged NSCLC

Not Applicable
Recruiting
Conditions
Non-small Cell Lung Cancer
ALK Gene Rearrangement Positive
Interventions
Genetic: RNAseq
Registration Number
NCT05122806
Lead Sponsor
Groupe Francais De Pneumo-Cancerologie
Brief Summary

BioEXALK is a prospective study evaluating the biological characteristics of advanced ALK-rearranged NSCLC treated with next generation TKIs in first line, included in the national EXPLORE ALK cohort (GFPC 03-2019), a non-interventional, national, multi-center cohort of ALK-rearranged NSCLC patients.

BioExALK study will be proposed to every patient included in the Explore ALK GFPC 03-2019 study.

Biological analysis will be performed on tumor tissue at diagnosis and at the time of disease progression when available and on circulating tumor DNA (ctDNA).

For plasma testing, after obtained patient consent, blood samples will be taken and analyzed at the Léon Bérard Center (Lyon).

Biological analysis on tissue obtained at diagnosis and at disease progression will be collected and be sent for centralized analysis to the Rouen University Hospital.

Detailed Description

BioEXALK is a prospective study evaluating the biological characteristics of advanced ALK-rearranged NSCLC treated with new generation TKIs in first line, included in the national EXPLORE ALK cohort (GFPC 03-2019).

Explore ALK GFPC 03-2019 is a non-interventional, national, multi-center cohort of ALK-rearranged NSCLC patients, whose RCB reference is 2020-A00771-38 and which obtained an approval from the IDF II Ethic Committee on 25/05/2020. Biological analysis will be performed on tissue at diagnosis and at the time of disease progression when available and on circulating tumor DNA (ctDNA) on three timepoints (diagnosis, at first tumor evaluation and at the time of disease progression).

* Tissue : RNAseq will be performed on tumor biopsy (10 slides of 5 microns) to identify the ALK fusion partner and its variant and associated co-mutations..

* ctDNA : NGS panel on DNA including a large panel of fusions and mutations will be performed on blood samples (30mL on EDTA or STRECKs tubes) at diagnosis, at the time of the first evaluation and at the time of progression).

For plasma testing, after obtained patient consent, blood samples (35mL on EDTA or STRECKs tubes) at diagnosis, at the first evaluation and at disease progression will be taken.

The ALKis include alectinib and brigatinib as first-line therapy or other drugs with marketing authorizations (lorlatinib, entrectinib) or in early access programs (EAPs).

Liquid biopsies will be analyzed with a NGS panel allowing the identification of ALK fusion partners and resistance mechanisms (mutations, fusions, copy number variations). Samples will be sent for centralized analysis to the Léon Bérard Center (Lyon).

For biological analysis on tissue obtained at diagnosis, the ALK fusion partner and its variant will be identified by RNAseq. Whenever a tissue re-biopsy is performed at the time of disease progression as part of the standard of care management of the patient, the remaining tissue sample will be collected as part of the BioExALK study, so that RNAseq analysis will be performed to look for resistance mechanisms. Tissue samples (10 slides of 5 microns) will be sent for centralized analysis to the Rouen University Hospital.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Stage IIIB/IV NSCLC non eligible to locoregional treatment with curative intent
  • ALK rearrangement confirmed by IHC and/or FISH or NGS according to local methods
  • Patient included in the EXPLORE ALK study
  • Age > or = 18 years
  • Patient treated with first-line new generation ALKi
  • Patient agrees to sign an informed consent form and to collect blood samples at inclusion, first tumor evaluation and progression and for whom tumor biopsy at diagnosis is available
  • Patient enrolled in the french National Health Insurance program or with a third- party payer
Exclusion Criteria
  • Patients who do not wish to participate in Bioexalk
  • Patients under guardianship

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Bioexalk cohortRNAseqAll patients included in Explore ALK GFPC 03-2019 study who agree to participate in Bioexalk.
Primary Outcome Measures
NameTimeMethod
Progression Free Survival (PFS)From date of treatment initiation up to 72 months

PFS assessed by local review using RECIST v1.1, defined as time from treatment initiation to the first clinical or radiological progression or death from any cause

Secondary Outcome Measures
NameTimeMethod
Circulating tumoral DNA (ctDNA) clearance on Overall Survival (OS) of stage IV ALK-rearranged NSCLC patientsFrom date of treatment initiation up to 72 months

ctDNA clearance will be determine as clearance of the fusion when detectable and/or clearance of relevant mutations when fusion not detected

Circulating tumoral DNA (ctDNA) clearance on Duration of Response (DoR) of stage IV ALK-rearranged NSCLC patientsFrom date of treatment initiation up to 72 months

ctDNA clearance will be determine as clearance of the fusion when detectable and/or clearance of relevant mutations when fusion not detected

Description of mechanism of resistance associated with each ALK-fusion partnerFrom date of treatment initiation up to 72 months

The following mechanisms of resistance will be assessed: secondary mutations on ALK, mutations or translocations on other genes of interest, histological transformations

Overall Response Rate (ORR)From date of treatment initiation up to 72 months

ORR defined as objective response rate of complete response or partial response measured by local review RECIST v1.1.

Overall Survival (OS)From date of treatment initiation up to 72 months

OS defined as time from treatment initiation to death from any cause.

Impact of presence or absence of serum Anti-ALK antibodies at diagnosis on OSFrom date of treatment initiation up to 72 months
Circulating tumoral DNA (ctDNA) clearance on Progression Free Survival (PFS) of stage IV ALK-rearranged NSCLC patientsFrom date of treatment initiation up to 72 months

ctDNA clearance will be determine as clearance of the fusion when detectable and/or clearance of relevant mutations when fusion not detected

Duration of Response (DoR)From date of treatment initiation up to 72 months

DoR assessed by local review using RECIST v1.1, defined as time from treatment initiation to the first clinical or radiological progression, death, consent withdrawn, adverse event, protocol deviations, lost to follow-up, or initiation of a new line of anticancer therapy.

Description of mechanisms of resistance associated with first-line tyrosine kinase inhibitorsFrom date of treatment initiation up to 72 months

The following mechanisms of resistance will be assessed: secondary mutations on ALK, mutations or translocations on other genes of interest, histological transformations

Circulating tumoral DNA (ctDNA) clearance on Overall Response Rate (ORR) of stage IV ALK-rearranged NSCLC patientsFrom date of treatment initiation up to 72 months

ctDNA clearance will be determine as clearance of the fusion when detectable and/or clearance of relevant mutations when fusion not detected

Concordance between ALK fusion partner and co-mutationsFrom date of treatment initiation up to 72 months

ALK fusion partner and co-mutation identifications based on liquid and tissue biopsies at Baseline

Trial Locations

Locations (45)

Centre Léon Bérard

🇫🇷

Lyon, France

Oncologie CLCC Jean Perrin

🇫🇷

Clermont-Ferrand, France

Pneumologie Hôpital Mignot

🇫🇷

Le Chesnay, France

Pneumologie CHU Limoges

🇫🇷

Limoges, France

Centre Hospitalier d'Aix en Provence

🇫🇷

Aix En Provence, France

Centre Hospitalier d'Annecy

🇫🇷

Annecy, France

Oncologie Centre Oscar Lombret

🇫🇷

Lille, France

Centre Hospitalier du Morvan

🇫🇷

Brest, France

Centre François Baclesse

🇫🇷

Caen, France

Pneumologie Centre Hospitalier

🇫🇷

Pau, France

Oncologie Hôpital François Quesnay

🇫🇷

Mantes-la-Jolie, France

Oncologie Institut Paoli Calmette

🇫🇷

Marseille, France

Oncologie Institut du Cancer de Montpellier

🇫🇷

Montpellier, France

Pneumologie Hôpital Yves Le Foll

🇫🇷

Saint-Brieuc, France

Pneumologie Hôpital privé Jean Mermoz

🇫🇷

Lyon, France

Pneumologie Hôpital Européen

🇫🇷

Marseille, France

Hôpital Nord

🇫🇷

Marseille, France

Oncologie CH Morlaix

🇫🇷

Morlaix, France

CHU Pontchailloux

🇫🇷

Rennes, France

Pneumologie Hôpital Sainte Musse

🇫🇷

Toulon, France

Oncologie CH Bretagne-Atlantique

🇫🇷

Vannes, France

Hôpital Larrey

🇫🇷

Toulouse, France

Hôpital du Haut Leveque

🇫🇷

Pessac, France

Centre Hospitalier de Villefranche sur Saone

🇫🇷

Villefranche Sur Saone, France

Pneumologie CHI

🇫🇷

Villeneuve-Saint-Georges, France

Hôpital Charles Nicolle

🇫🇷

Rouen, France

Pneumologie Hôpital Foch

🇫🇷

Suresnes, France

Oncologie Institut Gustave Roussy

🇫🇷

Villejuif, France

Centre Hospitalier Universitaire

🇫🇷

Angers, France

Pneumologie CH

🇫🇷

Le Mans, France

Pneumologie CHU

🇫🇷

Amiens, France

Pneumologie CH Métropole Savoie

🇫🇷

Chambéry, France

Centre Hospitalier Intercommunal de Créteil

🇫🇷

Creteil, France

Pneumologie CHD Vendée

🇫🇷

La Roche-sur-Yon, France

Pneumologie Hôpital Calmette

🇫🇷

Lille, France

Hôpital du Scorff

🇫🇷

Lorient, France

Hôpital de Meaux

🇫🇷

Meaux, France

Pneumologie CHR

🇫🇷

Orléans, France

Oncologie Institut Curie

🇫🇷

Paris, France

Institut Lucien Neuwirth

🇫🇷

Saint-Priest-en-Jarez, France

Centre Paul Strauss

🇫🇷

Strasbourg, France

Pneumologie HIA

🇫🇷

Talence, France

Hôpital d'Instruction des Armées Ste Anne

🇫🇷

Toulon, France

Pneumologie CH Eure-Seine

🇫🇷

Évreux, France

Pneumologie CHU Félix Guyon

🇫🇷

Saint-Denis, La Réunion, France

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