RecruitingNCT04677205

Molecular Signature From Tumor to Lymph Nodes

Molecular Signature From Tumor to Lymph Nodes: How to Identify the Right Candidate for IIIA-N2 Lung Cancer Surgery?


Sponsor

Assistance Publique - Hôpitaux de Paris

Enrollment

200 participants

Start Date

Mar 30, 2021

Study Type

OBSERVATIONAL

Conditions

Summary

Mediastinal lymph node (LN) involvement (N2) in non-small cell lung cancer (NSCLC) concerns 15% of resectable tumors and is associated with a poor prognosis and an overall survival reaching 9 to 49%. Literature fails to provide any definitive consensus regarding the management of these patients, except for the platinum-based doublet chemotherapy. The N2 involvement remains a matter of debate because of its not yet well-classified heterogeneity. Regarding anatomy, the Mountain and Dresler's regional LN classification for lung cancer staging remains the reference. Different studies classified IIIA-N2 disease into 4 groups, in addition to the skip-N2 phenomenon: minimal-N2, N2 single station, N2 multiple stations, and bulky-N2. Other subgroups were recently proposed for the 8th edition of the TNM: N2a1 - single station skip, N2a2 - single station non-skip, N2b - multiple stations. The French National Cancer Institute (INCa) proposed guidelines, but in case of cN2 staging without mediastinal infiltration, guidelines remained imprecise ("resectability should be discussed for each case") and suggested surgery first, or induction chemotherapy, or concomitant chemoradiation. Thus, optimal management of cIIIA-N2 remains controversial but complete tumor resection can be related to long-term survival in some patients, including 10 years after surgery \[1\]. In this situation, the identification of markers that will help select IIIA-N2 patients who will benefit from surgical resection is mandatory.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Adult patient, men and women age \>18 years
  • Patients operated with a curative intent for an IIIA-cN2 NSCLC
  • Social security affiliation
  • Written informed consent for patient included in part 2 (prospective) or not opposing the use of this data for patient included in part 1 (retrospective)

Exclusion Criteria3

  • Patient with T4, R1 or R2 surgical resection, sublobar resection, no radical lymphadenectomy
  • Patient under protectives measures
  • Pregnancy or breast-feeding

Locations(12)

Hôpital Bichat

Paris, France

Hôpital Cochin

Paris, France

Hôpital du Haut-Lévêque, CHU de Bordeaux

Bordeaux, France

Hôpital Militaire Percy

Clamart, France

Hôpital Nord

Marseille, France

Hôpital Pasteur, CHU de Nice

Nice, France

Hegp-Aphp

Paris, France

Hôpital Européen Georges-Pompidou

Paris, France

Hôpital Pontchaillou, CHU de Rennes

Rennes, France

Hôpitaux universitaires de Strasbourg

Strasbourg, France

Hôpital Larrey, CHU de Toulouse

Toulouse, France

CHRU de Tours

Tours, France

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NCT04677205


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