Fact CheckerSign in

NCT03774732Active, not recruitingPhase 3

PD-1 Inhibitor and Chemotherapy With Concurrent Irradiation at Varied Tumour Sites in Advanced Non-small Cell Lung Cancer

Source: ClinicalTrials.gov · Last updated 25 Feb 2026

Brief summary (registry, in English)

Overall survival (OS) of patients with advanced (stage IIIB/IV) non-small-cell lung cancer (NSCLC) remains short after the first line of treatment with a median OS of 12.2 months in non squamous NSCLC and 9.2 months in squamous NSCLC . In this setting the programmed death 1/ligand 1 (PD-1/-L1) were targeted with nivolumab (IgG4) in advanced squamous and nonsquamous NSCLC leading to an increase of the 1-year OS rate of approximately 10-15% in both histologies. Nivolumab, pembrolizumab and atezolizumab are now considered a standard of care in 2nd line advanced NSCLC and in 1st line for pembrolizumab but but prognosis still remains poor in advanced NSCLC. Overall survival (OS) of patients with advanced (stage III/IV) NSCLC remains limited with a median OS of 12.2 months in non-squamous NSCLC and 9.2 months in squamous NSCLC if anti-PD1 alone. It is of around 16 months if pembrolizumab is combined with chemotherapy. Preclinical data indicates that anti-tumor efficacy is increased when anti-PD-1/-L1 are combined with irradiation (IR). Radiotherapy alone can elicit tumor cell death which can increase tumor antigen in the blood stream, favoring recognition by the immune system and its activation against tumor cells outside of the radiation field (="abscopal effect"). IR may also reverse acquired resistance to PD-1 blockade immunotherapy by limiting T-cell exhaustion. Because of these preclinical and clinical data several studies analysing the combination of IR and anti-PD1 in NSCLC are ongoing. Among them, two studies are testing the administration of IR and nivolumab in stage III NSCLC: the NCT02768558 phase III trial (RTOG), and the NCT02434081 phase II trial (ETOP). Antonia et al \[2017\] tested the use of anti-PD-L1 after chemoradiotherapy in unresectable stage III NSCLC. Median time to distant metastasis was increased (23.2 months vs. 14.6 months, p\<0.001). An increase of OS is consequently expected. However, no study involving concurrent RT and pembrolizumab combined with chemotherapy in advanced NSCLC is ongoing, which is the purpose of the present study, NIRVANA-Lung.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
327 (estimated)
First submitted
26 Sept 2018
Start date
24 Jan 2018
Primary completion date
22 Dec 2026
Lead sponsor
UNICANCER
Diseases
Lung cancer
NCT number
NCT03774732

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 327
  • From 24 Jan 2018 to the primary completion date, 22 Dec 2026
  • 58 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • Patient must have signed a written informed consent form prior to any study specific procedures
  • Histologically or cytologically confirmed advanced (stage IIIB/IIIC/IV), squamous or non-squamous NSCLC
  • NSCLC patients eligible for treatment with pembrolizumab and chemotherapy according to the European Marketing Authorization:
    • squamous: in combination with carboplatin and either paclitaxel or nab-paclitaxel
    • non squamous with no EGFR or ALK positive mutations: in combination with pemetrexed and a platinum based chemotherapy
  • Patient ≥18 of age
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 - 1
  • Life expectancy \>3 months
  • Measurable lesion as assessed by RECIST version 1.1
  • Metastases and/or primary tumour eligible for 3 dimensional conventional radiotherapy (3D-CRT) or stereotactic ablative radiotherapy (SABR) in terms of dose constraints at organ at risk (according to QUANTEC review)
  • Patients must have adequate organ function defined by the following laboratory results obtained within 14 days prior to the first study treatment:
    • absolute neutrophil count of ≥1 500 /mm³
    • platelets ≥ 100 000/mm³
    • haemoglobin \>9 g/dL (transfusions allowed)
    • creatinine clearance \>60 mL/min
    • bilirubin ≤1.5 X upper limit of normal (ULN) (unless Gilbert's syndrome where 3 X ULN is permitted)
    • serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5 X ULN (unless documented liver metastasis where ≤5 X ULN is permitted)
    • Alkaline phosphatase (ALP) ≤2.5 X ULN (unless documented bone or liver metastasis where ≤5 X ULN is permitted)
    • International normalized ratio (INR), prothrombin (PT), and prothrombin time (PTT) ≤1.5 X ULN (unless the subject is receiving anticoagulant therapy)
  • Woman of childbearing potential and male patients must agree to use adequate contraception for the duration of study participation and up to 6 months after completing treatment/therapy
  • Patients affiliated to the social security system (or equivalent)
  • Patient is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits, and examinations including follow-up
    • NON-INCLUSION CRITERIA:
  • Non-squamous NSCLC with targetable tumor mutations, activating EGFR mutations or ALK translocation Note: documentation of these mutation for non-squamous histology is mandatory as standard of care
  • Stage IIIB/IIIC NSCLC patient eligible to curative (thoracic radiotherapy or surgery) treatments in first line treatment
  • Prior therapy with T-cell costimulation or checkpoint-targeted agents Note: Stage I-III NSCLC who previously received single-agent anti-PD(L)1 immunotherapy and ultimately develop metastases remain eligible (minimal immunotherapy washout period of 3 months)
  • Clinical need of radiotherapy (e.g.: whole brain irradiation, painful metastasis, bleeding, compressive metastases)
  • Irradiation within 2 months before inclusion
  • Leptomeningeal carcinomatosis, or metastases with indistinct borders making targeting not feasible
  • Patient with evidence of active (presence of symptoms or requiring steroid treatment) central nervous system (CNS) metastases and/or carcinomatous meningitis. Patient with brain metastasis can be included if asymptomatic and not requiring steroids
  • Metastases located within 3 cm of the previously irradiated structures (EQD2doses):
    • Spinal cord previously irradiated to \>40 Gy;
    • Brachial plexus previously irradiated to \>50 Gy;
    • Small intestine, large intestine, or stomach previously irradiated to \>45 Gy;
    • Brainstem previously irradiated to \>50 Gy;
    • Lung previously irradiated with prior V20Gy \>30%
  • Active autoimmune disease except vitiligo, type-1 diabetes, hypothyroid stabilized with hormonal substitution, psoriasis
  • Symptomatic interstitial lung disease
  • Systemic immunosuppression or systemic immunosuppressive medicinal products within 2 weeks prior to study entry
  • Concomitant treatment with steroids \> 10 mg Note1: higher dose of steroids can be prescribed in case of occurrence of toxicities during radiotherapy; prophylactic dose of maximum 1 mg per kg during 2 weeks are authorized during the delivery of more than 6 Gy per fraction Note2: temporary use of steroid (less than 4 weeks) at a dose of 1 mg/kg is accepted
  • Prior invasive malignancy within the past 2 years (except non-melanomatous skin cancer non-invasive carcinoma in-situ of the breast, oral cavity, bladder or cervix)
  • Known Acquired Immune Deficiency Syndrome (AIDS) or severe uncontrolled co-morbidity
  • Known currently active infection including hepatitis B and hepatitis C
  • Patient who was administered a live, attenuated vaccine within 28 days prior to enrolment
  • Patient with any other disease or illness that requires hospitalisation or is incompatible with the study treatment are not eligible. Patient unable to comply with study obligations for geographic, social, or physical reasons, or who is unable to understand the purpose and procedures of the study
  • Patient who have taken any investigational medicinal product or have used an investigational device within 30 days of inclusion
  • Pregnant or breast feeding woman
  • Person deprived of their liberty or under protective custody or guardianship
  • If pemetrexed: patient is unable or unwilling to take folic acid or vitamin B12 supplementation
  • Pre-existing peripheral neuropathy of a severity of grade ≥ 2 by NCI CTCAE v5.0
  • Known hypersensitivity to one of the compounds or substances used in this protocol
  • Major surgery within the 28 days before initiating study treatment

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (58)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Institut de Cancérologie de l'Ouest - Site Paul Papin
Coordinator of this site? Confirm its status
AngersFranceUnknown status
Hôpital Privé Arras Les Bonnettes
Coordinator of this site? Confirm its status
ArrasFranceUnknown status
Centre Marie Curie
Coordinator of this site? Confirm its status
ArrasFranceUnknown status
Institut Sainte-Catherine
Coordinator of this site? Confirm its status
AvignonFranceUnknown status
Centre Pierre Curie
Coordinator of this site? Confirm its status
BeuvryFranceUnknown status
Clinique Ambroise Pare
Coordinator of this site? Confirm its status
BeuvryFranceUnknown status
Hôpital Simone Veil Blois
Coordinator of this site? Confirm its status
BloisFranceUnknown status
Institut Bergonie
Coordinator of this site? Confirm its status
BordeauxFranceUnknown status
CHRU de Brest
Coordinator of this site? Confirm its status
BrestFranceUnknown status
Centre Hospitalier Universitaire de Caen - Hôpital Côte de Nacre
Coordinator of this site? Confirm its status
CaenFranceUnknown status
Centre François Baclesse
Coordinator of this site? Confirm its status
CaenFranceUnknown status
Centre Hospitalier Dr Jean-Eric TECHER
Coordinator of this site? Confirm its status
CalaisFranceUnknown status
Centre hospitalier de Cannes Simone Veil
Coordinator of this site? Confirm its status
CannesFranceUnknown status
Centre Hospitalier William Morey
Coordinator of this site? Confirm its status
Chalon-sur-SaôneFranceUnknown status
Institut de Cancérologie de Bourgogne
Coordinator of this site? Confirm its status
Chalon-sur-SaôneFranceUnknown status
Pôle départemental de Cancérologie Libérale 37
Coordinator of this site? Confirm its status
Chambray-lès-ToursFranceUnknown status
Centre Jean Perrin
Coordinator of this site? Confirm its status
Clermont-FerrandFranceUnknown status
Centre Hospitalier Intercommunal de Créteil
Coordinator of this site? Confirm its status
CréteilFranceUnknown status
Polyclinique du Parc Drevon
Coordinator of this site? Confirm its status
DijonFranceUnknown status
Centre Georges François Leclerc
Coordinator of this site? Confirm its status
DijonFranceUnknown status
Institut de Cancérologie de Bourgogne
Coordinator of this site? Confirm its status
DijonFranceUnknown status
Centre Hospitalier de Dunkerque
Coordinator of this site? Confirm its status
DunkirkFranceUnknown status
Centre André DUTREIX
Coordinator of this site? Confirm its status
DunkirkFranceUnknown status
Centre de radiothérapie et de cancérologie de Blois
Coordinator of this site? Confirm its status
La Chaussée-Saint-VictorFranceUnknown status
CHU Sud de la Réunion
Coordinator of this site? Confirm its status
La RéunionFranceUnknown status
Hôpital de Bicêtre
Coordinator of this site? Confirm its status
Le Kremlin-BicêtreFranceUnknown status
Centre Oscar Lambret
Coordinator of this site? Confirm its status
LilleFranceUnknown status
Clinique Chenieux
Coordinator of this site? Confirm its status
LimogesFranceUnknown status
Hopital Europeen Marseille
Coordinator of this site? Confirm its status
MarseilleFranceUnknown status
Hôpital Privé Clairval
Coordinator of this site? Confirm its status
MarseilleFranceUnknown status
Centre Hospitalier de Montelimar
Coordinator of this site? Confirm its status
MontélimarFranceUnknown status
Centre de cancérologie du grand Montpellier-Clinique Clementville
Coordinator of this site? Confirm its status
MontpellierFranceUnknown status
Centre Hospitalier des Pays de Morlaix
Coordinator of this site? Confirm its status
MorlaixFranceUnknown status
Hôpital Privé Arnault Tzanck
Coordinator of this site? Confirm its status
MouginsFranceUnknown status
Centre Azuréen de Cancérologie
Coordinator of this site? Confirm its status
MouginsFranceUnknown status
Centre Antoine Lacassagne
Coordinator of this site? Confirm its status
NiceFranceUnknown status
CHU de Nîmes
Coordinator of this site? Confirm its status
NîmesFranceUnknown status
Hopital Pitie-Salpetriere
Coordinator of this site? Confirm its status
ParisFranceUnknown status
Hôpital Tenon
Coordinator of this site? Confirm its status
ParisFranceUnknown status
Fondation Hôpital Saint-Joseph
Coordinator of this site? Confirm its status
ParisFranceUnknown status
Centre Catalan d'Oncologie
Coordinator of this site? Confirm its status
PerpignanFranceUnknown status
Institut Jean Godinot
Coordinator of this site? Confirm its status
ReimsFranceUnknown status
Centre Frédéric JOLIOT
Coordinator of this site? Confirm its status
RouenFranceUnknown status
Centre Henri Becquerel
Coordinator of this site? Confirm its status
RouenFranceUnknown status
Clinique Saint-Hilaire
Coordinator of this site? Confirm its status
RouenFranceUnknown status
Hôpital Charles Nicolle
Coordinator of this site? Confirm its status
RouenFranceUnknown status
Institut Curie - Hôpital René Huguenin
Coordinator of this site? Confirm its status
Saint-CloudFranceUnknown status
Chu St-Etienne
Coordinator of this site? Confirm its status
Saint-EtienneFranceUnknown status
Centre Joliot Curie
Coordinator of this site? Confirm its status
Saint-Martin-BoulogneFranceUnknown status
Centre Paul Strauss
Coordinator of this site? Confirm its status
StrasbourgFranceUnknown status
Polyclinique de l'Ormeau
Coordinator of this site? Confirm its status
TarbesFranceUnknown status
CHU de Toulouse - Hopital Larrey
Coordinator of this site? Confirm its status
ToulouseFranceUnknown status
Institut Claudius Regaud
Coordinator of this site? Confirm its status
ToulouseFranceUnknown status
Centre Marie Curie
Coordinator of this site? Confirm its status
ValenceFranceUnknown status
Hôpital Privé Drôme Ardèche
Coordinator of this site? Confirm its status
ValenceFranceUnknown status
Institut de Cancérologie de Lorraine
Coordinator of this site? Confirm its status
Vandœuvre-lès-NancyFranceUnknown status
Gustave Roussy
Coordinator of this site? Confirm its status
VillejuifFranceUnknown status
Centre Hospitalier Princesse Grace
Coordinator of this site? Confirm its status
MonacoMonacoUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.