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Consolidation Sintilimab After Concurrent Chemoradiation in Patients With Unresectable Stage III NSCLC (CONSIST)

19 mars 2019 mis à jour par: Jinming Yu, Shandong Cancer Hospital and Institute

CONSIST: A Phase III Randomized Control Study of Consolidation Sintilimab (IBI308) After Concurrent Chemoradiation Versus Chemoradiation Alone in Patients With Unresectable Local Advanced Stage III NSCLC

This is an open label, multi-center, randomized, control phase III trial, to compare the efficacy and safety of consolidation therapy with sintilimab (IBI308) versus best supported care (BSC), in unresectable stage III NSCLC patients who do not experience disease progression after initial concurrent chemoradiation.

Aperçu de l'étude

Statut

Inconnue

Intervention / Traitement

Description détaillée

This is an open label, multi-center, randomized, control study of sintilimab versus BSC in unresectable local advanced stage III NSCLC patients without disease progression after concurrent chemoradiation.

Type d'étude

Interventionnel

Inscription (Anticipé)

162

Phase

  • Phase 3

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

    • Shandong
      • Jinan, Shandong, Chine
        • Recrutement
        • Shandong Cancer Hospital
        • Contact:

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

18 ans à 75 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  1. Signed written informed consent before initiation of any study procedures
  2. Age ≥ 18 years and ≤ 75 years
  3. Histologically or cytologically confirmed NSCLC, with unresectable local advanced disease (stage III according to NSCLC staging version 8)
  4. Expected survival over 3 months
  5. Eastern Cooperative Oncology Group (ECOG) performance status 0-1
  6. At least 1 measurable disease according to RECIST 1.1
  7. Pulmonary function: forced expiratory volume at one second (FEV1) > 1 liter(L)
  8. Patient must not have received any anti-cancer therapy for the purpose of treating lung cancer. However, exploratory thoracotomy, mediastinoscopy, excision biopsy, and other kinds of surgery for diagnosis and staging purpose is acceptable. Patients with local or regional recurrent disease after pneumonectomy is allowed to participate if they meet other inclusion criteria (e.g. stage III, inappropriate for re-operation).
  9. For all female patients of childbearing potential, a negative pregnancy test (either urine or serum) must be obtained within 3 days before the first dose (Cycle 1, Day 1) of study treatment. If a urine pregnancy test shows an unconfirmed result, a serum pregnancy test must be performed.
  10. Adequate hematopoietic function, defined as: absolute neutrophil count (ANC) ≥ 1.5 x 10*9/L; platelet count ≥100 x 10*9/L; hemoglobin ≥90 g/L [no blood transfusion within 7 days or not erythropoietin (EPO) dependent]
  11. Adequate liver function, defined as: total serum bilirubin ≤ 1.5 x upper limit of normal (ULN); serum alanine transaminase (ALT) and aspartic transaminase (AST) ≤ 2.5 x ULN, with no liver transplantation
  12. Adequate renal function, defined as: serum creatinine ≤ 1.5 x ULN or calculated creatinine-clearance ≥ 60 ml/min (Cockcroft-Gault). Urine protein less than 2+ by urinalysis or 24-hour urinary protein quantity < 1g
  13. Adequate coagulation function, defined as: international normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN. For patients receiving anticoagulant therapy can be enrolled if PT is within the range defined by anticoagulant therapy.
  14. Myocardial enzymes are within normal range
  15. All subjects of childbearing potential must agree to use efficient contraceptive methods that result in a failure rate of < 1% per year during the study treatment period and for at least 180 days after discontinuation from study treatment.

Exclusion Criteria:

  1. Being treated by other investigational drugs within an interventional study, or have received any investigational drugs or instruments within 4 weeks prior to the first dose of study treatment
  2. Being enrolled in other interventional studies, unless they are observational studies or during the follow-up stage of an interventional study
  3. NSCLC histology with small cell lung cancer (SCLC) components
  4. Active or autoimmune disease history (within the past 2 years), or history of immune deficiency
  5. Previous immune therapy including: anti PD-1, anti PD-L1, anti PD-L2 or treatment targeting other co-stimulatory or co-inhibitory T-cell receptors [e.g. cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), OX-40, and CD137]

    a) Systemic therapy with Chinese patent medicine or drugs of immunoregulation effect (including thymosin, interferon, interleukin, unless local delivery for controlling pleural effusion) within 2 weeks prior to the first dose of study treatment, or major surgery within 4 weeks prior to the first dose of study treatment

  6. Clinical evidence of active diverticulitis, abdominal abscess, or gastrointestinal obstruction
  7. Previous organ or blood system transplantation
  8. Known allergic to pemetrexed, paclitaxel, etoposide, cisplatin, carboplatin, sintilimab component and/or any excipients
  9. A history of active autoimmune disease requiring systemic treatment (e.g. using drugs for disease remission, corticosteroids or immunosuppressor) within 2 years prior to the first dose of study treatment. Substitution therapy (e.g. thyroxine, insulin or physiological corticosteroids for treating adrenal or pituitary dysfunction) is not considered as a systemic treatment.

    a) Diagnosis as immunodeficiency, or being treated with systemic glucocorticoid or other kinds of immunosuppressor within 7 days prior to the first dose of study treatment. A physiological dose of glucocorticoid (≤10 mg/day prednisone or equivalent dose of other steroids) is permitted.

  10. Previously diagnosis as other malignant tumors within 5 years prior to the first dose of study treatment, with the exception of: skin basal cell carcinoma or squamous cell carcinoma with radical treatment, and/or carcinoma in situ underwent radical resection
  11. History of non-infectious pneumonitis requiring treatment with glucocorticoid within 1 year prior to the first dose of study treatment, or currently existed interstitial lung disease
  12. Active infectious that required systemic therapy
  13. Know psychiatric illness or drug abuse that would limit compliance with study requirements
  14. Know human immunodeficiency virus (HIV) infection (HIV 1/2 antibody positive)
  15. Untreated active viral hepatitis B (HBV)

    Patients with HBV who meet the following criteria are also eligible:

    1. HBV virus load (VL) <1000 copy/ml (200 IU/ml), and patients must continuously receive anti-HBV therapy during all through study treatment phase to prevent virus activation
    2. Patients with a result of anti-HBc(+)、HBsAg (-)、anti-HBs (-) 和 HBV VL (-) are not required to receive prophylactic anti-HBV therapy, but must be closely monitored for virus re-activation
  16. Patients with active HCV infection (HCV antibody positive and HCV-RNA > the lower detection limit)
  17. History or evidence of disease, treatment or laboratory abnormalities that would interfere the study outcome, prevent patients from participating entirely, or ineligible to enroll per the investigators' judgement
  18. Pregnant or lactating women

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: Sintilimab Arm
Sintilimab consolidation therapy
Sintilimab consolidation therapy after concurrent chemoradiation, 200mg IV, every 3 weeks, until progressive disease (PD, unless patients can continuously benefit from study treatment per investigators' judgement), start new anti-cancer therapy, intolerable toxicity, withdraw informed consent or other conditions that require study treatment discontinuation. Sintilimab will be given at a maximum of 12 months.
Aucune intervention: Observation Arm
Observation

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Progression Free Survival (PFS)
Délai: up to 24 months after enrollment or study close
PFS (per RECIST 1.1 as assessed by the investigator) will be defined as the time from the date of randomisation until the date of objective disease progression or death (by any cause in the absence of progression).
up to 24 months after enrollment or study close

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Taux de contrôle de la maladie (DCR)
Délai: jusqu'à 24 mois après l'inscription ou la fin des études
La DCR (selon RECIST 1.1 telle qu'évaluée par l'investigateur) est définie comme la proportion (%) de patients avec au moins une réponse de visite de réponse complète (CR) ou de réponse partielle (PR) ou de maladie stable (SD).
jusqu'à 24 mois après l'inscription ou la fin des études
Durée de la réponse (DoR)
Délai: jusqu'à 24 mois après l'inscription ou la fin des études
La DoR (selon RECIST 1.1 telle qu'évaluée par l'investigateur) est définie comme le temps écoulé entre la date de la première réponse documentée de réponse complète (CR) ou de réponse partielle (PR) et la date de la première réponse documentée de maladie évolutive (MP) ou mort en l'absence de progression.
jusqu'à 24 mois après l'inscription ou la fin des études
Overall survival (OS)
Délai: up to 24 months after enrollment or study close
OS (per RECIST 1.1 as assessed by the investigator) is defined as the time from the date of randomisation until death due to any cause.
up to 24 months after enrollment or study close
Objective Response Rate (ORR)
Délai: up to 24 months after enrollment or study close
ORR (per RECIST 1.1 as assessed by the investigator) is defined as the proportion (%) of patients with at least one visit response of complete response (CR) or partial response (PR).
up to 24 months after enrollment or study close
Progression Free Survival (PFS) Rate at 12/18 months
Délai: From the date of randomization until the Kaplan-Meier estimate of PFS at 12/18months
PFS rate at 12/18 months is defined as the proportion (%) of patients who are alive and progression free at 12 and 18months from the date of randomisation.
From the date of randomization until the Kaplan-Meier estimate of PFS at 12/18months
Treatment-related Adverse Events (AEs)
Délai: From the date of randomization to 90 days after last dose of study treatment
The grade of AEs and the number of patients with AEs are assessed by the investigator based on CTCAE v4.03 from the date of randomization to 90 days after last dose of study treatment.
From the date of randomization to 90 days after last dose of study treatment

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

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 (Réel)

12 décembre 2018

Achèvement primaire (Anticipé)

30 décembre 2020

Achèvement de l'étude (Anticipé)

30 décembre 2021

Dates d'inscription aux études

Première soumission

11 janvier 2019

Première soumission répondant aux critères de contrôle qualité

19 mars 2019

Première publication (Réel)

21 mars 2019

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

21 mars 2019

Dernière mise à jour soumise répondant aux critères de contrôle qualité

19 mars 2019

Dernière vérification

1 mars 2019

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

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NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

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