- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07603856
A Study Evaluating The Combination of Immunotherapy With Radiotherapy in Non-Small Cell Lung Cancer (REVIVE)
12 juin 2026 mis à jour par: University of Chicago
A Randomized Phase II Study of Radiotherapy Plus Immune Checkpoint Inhibitor Therapy Versus Standard of Care Chemotherapy in Patients With Metastatic or Relapsed Non-Small Cell Lung Cancer Previously Treated With Immunotherapy
Current clinical trials testing the combination of immunotherapy with radiotherapy.
Aperçu de l'étude
Statut
Recrutement
Intervention / Traitement
- Médicament: Investigator Choice Immunotherapy (for example: pembrolizumab, cemiplimab, durvalumab, ipilimumab plus nivolumab)
- Radiation: Ablative Hypofractionated Radiotherapy
- Médicament: Investigator Choice Chemotherapy (for example docetaxel with or without ramucirumab, gemcitabine, or other National Comprehensive Cancer Network (NCCN)-recommended treatments)
Type d'étude
Interventionnel
Inscription (Estimé)
39
Phase
- Phase 2
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
-
-
Illinois
-
Chicago, Illinois, États-Unis, 60637
- Recrutement
- o University of Chicago Medicine Comprehensive Cancer Center
-
Contact:
- Clinical Trials Intake
- Numéro de téléphone: 1-855-702-8222
- E-mail: cancerclinicaltrials@bsd.uchicago.edu
-
Chercheur principal:
- Aditya Juloori
-
-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
La description
Inclusion Criteria:
Disease-Related Criteria
- Patients must have histologically or cytologically confirmed metastatic or recurrent non-small cell lung cancer (NSCLC) with progression on prior immunotherapy
- The patient's disease is eligible for SOC treatment with immunotherapy or chemotherapy.
- Patients must have measurable disease per RECIST v1.1, defined as at least one lesion that can be accurately measured in at least one dimension with longest diameter ≥10 mm (or ≥15 mm short axis for lymph nodes) by CT or MRI
- Patients must have at least one lesion that meets criteria for hypofractionated ablative RT treatment:
- Tumor volume 0.25 cc to 65 cc (approximately ≤5 cm maximal dimension)
- Located in sites amenable to ablative RT (see radiotherapy section for specific anatomic criteria)
- Note: Tumors >65 cc may be partially treated to 65 cc volume
- Prior/Concurrent Therapy Criteria
- Patients must have received exactly ONE prior line of anti-PD-1 or anti-PD-L1 therapy for non-small cell lung cancer. This therapy may have been given as:
- Monotherapy
- In combination with chemotherapy
- In combination with another immunotherapy such as CTLA-4 inhibition
- In combination with a targeted therapy, such as adagrasib
- Special Cases for Neoadjuvant/Adjuvant Immunotherapy:
- If patient received neoadjuvant, adjuvant, or consolidation anti-PD-1/PD-L1 therapy for Stage I-III disease and progressed ≤365 days from initiation (Cycle 1 Day 1), this counts as the single allowed therapy for advanced disease
- If patient progressed >365 days from neoadjuvant/adjuvant therapy initiation, this does NOT count as therapy for advanced disease, and patient must have received subsequent anti-PD-1/PD-L1 therapy for Stage IV or recurrent disease
- Patients with the following sensitizing mutations are ineligible, given known poor response to immunotherapy: EGFR, ALK, ROS1, RET, NTRK, HER2.
- Patients with the following sensitizing mutations must have previously received at least one of the appropriate targeted therapies, in addition to prior immunotherapy: BRAF, KRAS, MET. Prior targeted therapy for participants with targetable alterations is allowed if all other eligibility criteria is also met.
Clinical/Laboratory Criteria
- Age ≥18 years
- ECOG Performance Status 0-2 (see Appendix A)
- Participants must be able to safely receive the investigational drug combination and the investigator's choice of standard of care regimens described in Section 5.1 (Agent Administration), per the current FDA-approved package inserts, treating investigator's discretion, and institutional guidelines.
- Patients with new or progressive brain metastases (active brain metastases) or leptomeningeal disease are eligible if the treating physician determines that immediate CNS specific treatment is not required and is unlikely to be required during the first cycle of therapy.
- Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial.
- Because radiation and chemotherapy are known to be teratogenic, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately. Both men and women treated or enrolled on this protocol must also agree to use adequate contraception prior to the study, for the duration of study participation, and 3 months after completion of immunotherapy, radiation, and/or chemotherapy administration.
- Ability to understand and the willingness to sign a written informed consent document.
Exclusion Criteria:
- Patients with history of (non-infectious) pneumonitis requiring corticosteroids.
- Patients with evidence of interstitial lung disease.
- Patients with uncontrolled intercurrent illness.
- Pregnant women are excluded from this study. Radiation is considered Class X and chemotherapy such as docetaxel are considered Class D agents with the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with radiation, immunotherapy, and chemotherapy breastfeeding should be discontinued if the mother is participating in the study.
Radiation-Specific Exclusions
- Patients who have received prior radiation to any of the planned treatment sites (>10% dose overlap)
- Patients with lesions in locations not amenable to safe ablative RT delivery, including:
- Esophagus or stomach directly involved by tumor (unless dose constraints can be met)
- Small bowel or colon directly involved by tumor (unless dose constraints can be met)
- Spinal cord lesions with <3 mm clearance between epidural disease and spinal cord
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Radiotherapy (RT) + Immunotherapy
Participants will receive standard immunotherapy of investigator's choice in combination with radiation treatment.
|
Participant will receive an FDA approved immunotherapy according to usual routine practice.
Participant will receive radiotherapy according to usual routine practice.
|
|
Comparateur actif: Standard Chemotherapy (Investigator's Choice")
Participants will receive standard chemotherapy of investigator's choice.
|
Description something along the lines of Participant will receive an FDA approved chemotherapy according to usual routine practice.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Progression-free survival (PFS)
Délai: 48 months
|
To compare progression-free survival (PFS) in patients with metastatic or relapsed non-small cell lung cancer (mNSCLC) who have progressed after immunotherapy-based treatment, randomized to investigators choice standard of care immunotherapy plus hypofractionated ablative radiotherapy versus investigators' choice of standard of care chemotherapy.
|
48 months
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Overall survival (OS)
Délai: 48 months
|
To compare overall survival (OS) between treatment arms
|
48 months
|
|
Objective response rates (ORR)
Délai: 48 months
|
To compare objective response rates (ORR) between treatment arms.
|
48 months
|
|
Correlation between amount of L1RE1 (LINE1 retrotransposable element 1) and clinical response to treatment
Délai: 24 months
|
Dose amount of L1RE1 in blood correlate to clinical response (for example are higher levels of the protein in the blood a sign of response to treatment)?
|
24 months
|
|
Pharmacodynamic Properties
Délai: 24 months
|
Establishing the pharmacodynamic properties of L1RE1 clearance during treatment.
L1RE1 serum levels will be measured descriptively using NPX (normalized protein expression) .
|
24 months
|
|
Safety of Giving Ablative Radiation and Immunotherapy Together
Délai: 3 months
|
Number of Common Terminology Criteria for Adverse Events (CTCAE) version 5 Grade 3 adverse events
|
3 months
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Estimé)
12 décembre 2026
Achèvement primaire (Estimé)
25 juin 2030
Achèvement de l'étude (Estimé)
25 juin 2030
Dates d'inscription aux études
Première soumission
9 mars 2026
Première soumission répondant aux critères de contrôle qualité
21 mai 2026
Première publication (Réel)
22 mai 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
16 juin 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
12 juin 2026
Dernière vérification
1 mai 2026
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Tumeurs par site
- Tumeurs
- Maladies des voies respiratoires
- Maladies pulmonaires
- Tumeurs des voies respiratoires
- Tumeurs thoraciques
- Carcinome bronchique
- Tumeurs bronchiques
- Tumeurs pulmonaires
- Carcinome pulmonaire non à petites cellules
- Acides aminés, peptides et protéines
- Protéines
- Composés hétérocycliques, 1 anneau
- Composés hétérocycliques
- Anticorps, monoclonal, humanisé
- Anticorps, monoclonal
- Anticorps
- Immunoglobulines
- Immunoprotéines
- Protéines sanguines
- Globulines sériques
- Globulines
- Désoxycytidine
- Cytidine
- Nucléosides pyrimidine
- Pyrimidines
- Nivolumab
- Ipilimumab
- Gemcitabine
- Ramucirumab
- durvalumab
- cémiplimab
Autres numéros d'identification d'étude
- IRB25-1914
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Oui
Étudie un produit d'appareil réglementé par la FDA américaine
Non
produit fabriqué et exporté des États-Unis.
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .