Actively Recruiting
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
Eligibility Criteria
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
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
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
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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