Actively Recruiting

Phase 2
Age: 18Years +
All Genders
NCT06078384

Pembrolizumab and Chemotherapy Treatment or no Treatment Guided by the Level of TILs in Resected Early-stage TNBC

Led by UNICANCER · Updated on 2025-11-17

354

Participants Needed

44

Research Sites

365 weeks

Total Duration

On this page

Sponsors

U

UNICANCER

Lead Sponsor

M

MSD France

Collaborating Sponsor

AI-Summary

What this Trial Is About

Triple-negative breast cancer (TNBC) is a group of tumors that occurs mainly in young, premenopausal women and accounts for 10-20% of breast cancers. Over the past decade, the incidence of women diagnosed with early-stage TNBC has significantly increased due to the widespread use of screening mammography. Treatment of patients with localized TNBC mainly involves surgery and (neo)adjuvant chemotherapy with or without radiotherapy. However, the benefit of chemotherapy may be controversial in patients with early-stage TNBC defined by small size and absence of lymph node involvement, and with significant tumor lymphocyte infiltration. The ETNA study is a phase II trial designed to evaluate a chemotherapy de-escalation strategy in patients with TNBC T1b/c N0M0 and stromal TILs (sTILs) ≥ 30%. ETNA comprises two cohorts defined according to the level of TILs and the age of patients. Patients aged \> 40 years with 30% ≤ sTILs \< 50% and those aged ≤ 40 years with 30% ≤ sTILs \< 75% will be included in the cohort 1 and will receive adjuvant pembrolizumab 200 mg every three weeks for 9 cycles and Paclitaxel 80 mg/m² weekly for 12 cycles. Patients aged \> 40 years with sTILs ≥ 50% and those aged ≤ 40 years with sTILs ≥ 75% will be included in cohort 2 and will not receive adjuvant treatment, they will undergo standard surveillance every six months.

CONDITIONS

Official Title

Pembrolizumab and Chemotherapy Treatment or no Treatment Guided by the Level of TILs in Resected Early-stage TNBC

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Men and women with confirmed triple-negative breast cancer (TNBC) of stage pT1b/c N0M0
  • ECOG performance status 0 or 1
  • Tumor must be histologically confirmed as TNBC with negative HER2, ER, and PgR status
  • Tumor surgically removed with clear margins and adequate lymph node evaluation
  • Sentinel lymph node biopsy and/or axillary lymph node dissection performed with at least six nodes evaluated
  • Treatment must start within 4 to 12 weeks after surgery depending on cohort
  • Tumor stromal tumor-infiltrating lymphocytes (sTILs) centrally assessed and meet cohort-specific thresholds
  • Negative pregnancy test for women of childbearing potential before treatment
  • Agreement to use contraception during and after trial as specified
  • Affiliated with social security system in France
  • Willing and able to comply with study procedures and visits
  • For cohort 1 only: left ventricular ejection fraction 50% or higher and adequate organ function as defined by blood tests and cardiac assessments
Not Eligible

You will not qualify if you...

  • History of invasive malignancy within 3 years except certain skin cancers
  • Received chemotherapy or targeted therapy within past 12 months
  • Prior systemic or radiotherapy for DCIS or LCIS in the same breast except surgery alone or contralateral radiotherapy
  • Prior treatment with anti-PD-1, anti-PD-L1, anti-PD-L2, or other immune checkpoint inhibitors
  • Use of systemic immunostimulatory agents within 4 weeks prior to inclusion
  • Immunodeficiency or chronic systemic steroid or immunosuppressive therapy within 7 days before inclusion
  • Active autoimmune disease requiring systemic treatment in past 2 years except controlled dermatologic conditions
  • Known HIV infection
  • Prior allogeneic stem cell or solid organ transplant
  • Active tuberculosis infection
  • Any illness requiring hospitalization or incompatible with trial treatments
  • Pregnant or breastfeeding women or those planning pregnancy during study and follow-up
  • Inability to comply with trial requirements or understand study purpose
  • Legal restrictions such as protective custody or guardianship
  • Psychiatric or substance abuse disorders affecting cooperation
  • For cohort 1 only: significant cardiac dysfunction or certain cardiac conditions
  • Known hypersensitivity to study drugs
  • Recent live or live-attenuated vaccine within 30 days prior to treatment
  • Active hepatitis B or C infection
  • Severe infections or recent therapeutic antibiotic use before treatment
  • Major surgery within 4 weeks before treatment or planned during study
  • History of pneumonitis or interstitial lung disease requiring steroids or current active disease
  • Participation in another interventional clinical trial within 4 weeks prior to study treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 44 locations

1

CHU Amiens Picardie_Site Sud

Amiens, France, 80054

Actively Recruiting

2

Institut Sainte Catherine

Avignon, France, 84918

Actively Recruiting

3

Centre Hospitalier de la Côte Basque

Bayonne, France, 64109

Actively Recruiting

4

Institut Bergonié

Bordeaux, France, 33000

Not Yet Recruiting

5

Polyclinique Bordeaux Nord Aquitaine

Bordeaux, France, 33077

Actively Recruiting

6

Centre François Baclesse

Caen, France, 14000

Actively Recruiting

7

Pôle Santé Republique

Clermont-Ferrand, France, 63000

Actively Recruiting

8

Centre Jean Perrin

Clermont-Ferrand, France, 63011

Actively Recruiting

9

Centre Georges-François Leclerc

Dijon, France, 21000

Not Yet Recruiting

10

Hôpital Franco-Britannique-Fondation Cognacq-Jay

Levallois-Perret, France, 92300

Not Yet Recruiting

11

CHU de Limoges

Limoges, France, 87042

Actively Recruiting

12

Centre Léon Bérard

Lyon, France, 69008

Actively Recruiting

13

Hopital Privé Jean Mermoz

Lyon, France, 69008

Actively Recruiting

14

Institut Paoli-Calmettes

Marseille, France, 13009

Actively Recruiting

15

Institut régional du Cancer de Montpellier

Montpellier, France, 34298

Not Yet Recruiting

16

Hôpital privé du confluent

Nantes, France, 44200

Actively Recruiting

17

Centre Antoine Lacassagne

Nice, France, 61000

Actively Recruiting

18

CHU de Nîmes

Nîmes, France, 30029

Actively Recruiting

19

Centre Hospitalier de Pau

Pau, France, 64046

Actively Recruiting

20

Hôpital Privé des côtes d'Armor

Plérin, France, 22190

Not Yet Recruiting

21

Hôpital NOVO

Pontoise, France, 95300

Actively Recruiting

22

Centre Hospitalier de Cornouaille

Quimper, France, 29107

Actively Recruiting

23

Clinique La Croix du Sud

Quint-Fonsegrives, France, 31130

Withdrawn

24

Institut Godinot

Reims, France, 51100

Actively Recruiting

25

Centre Eugène Marquis

Rennes, France, 35000

Actively Recruiting

26

CHU de Saint Etienne

Saint-Etienne, France, 42055

Actively Recruiting

27

Institut Claudius Regaud

Toulouse, France, 31059

Actively Recruiting

28

CHU Bretonneau

Tours, France, 37000

Actively Recruiting

29

Centre Alexis Vautrin

Vandœuvre-lès-Nancy, France, 54519

Actively Recruiting

30

Gustave Roussy

Villejuif, France, 94805

Actively Recruiting

31

Hospital General Universitario Dr.Balmis

Alicante, Spain

Not Yet Recruiting

32

Ico Badalona

Badalona, Spain, 08916

Not Yet Recruiting

33

Hospital Vall D'Hebrón

Barcelona, Spain, 08035

Not Yet Recruiting

34

Hospital Clinico Universitario Virgen de La Arrixaca

El Palmar, Spain, 30120

Not Yet Recruiting

35

Hospital Universitario Clinico San Cecilio

Granada, Spain, 18016

Not Yet Recruiting

36

Ico Hospitalet

L'Hospitalet de Llobregat, Spain, 08908

Actively Recruiting

37

Complejo Asistencial Universitario de Leon

León, Spain, 24071

Not Yet Recruiting

38

Hu Arnau de Vilanova Lleida

Lleida, Spain, 25198

Not Yet Recruiting

39

Hospital Ramon Y Cajal

Madrid, Spain, 28034

Not Yet Recruiting

40

Hospital 12 de Octubre

Madrid, Spain, 28041

Not Yet Recruiting

41

Hospital Universitari Son Espases

Palma de Mallorca, Spain, 07120

Not Yet Recruiting

42

Hospital Sant Joan de Reus

Reus, Spain, 43204

Not Yet Recruiting

43

Hospital Universitario Virgen Del Rocio

Seville, Spain, 41013

Not Yet Recruiting

44

Hospital Clínico Valencia

Valencia, Spain, 46010

Not Yet Recruiting

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Research Team

T

Telma ROQUE, PhD

CONTACT

S

Sylvie Mijonnet

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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