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Trial record 48 of 60 for:    PD-1 and breast cancer | Recruiting, Not yet recruiting, Available Studies

Trial to Evaluate Safety and Efficacy of Vinorelbine With Metronomic Administration in Combination With Atezolizumab as Second-line Treatment for Patients With Stage IV Non-small Cell Lung Cancer (VinMetAtezo)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT03801304
Recruitment Status : Recruiting
First Posted : January 11, 2019
Last Update Posted : March 11, 2019
Groupe Français de Pneumo-Cancérologie
Roche Farma, S.A
Pierre Fabre Medicament
Information provided by (Responsible Party):
University Hospital, Brest

Brief Summary:

The majority of patients diagnosed with advanced NSCLC are treated with platinum-doublet chemotherapy regimens, except those harboring specific oncogenic drivers such as epidermal growth-factor-receptor (EGFR) mutations or anaplastic lymphoma kinase (ALK) rearrangements. In the second-line setting, response rates remain low and median survival rarely exceeds 10 months.

Over the past few years, several checkpoint inhibitors targeting programmed cell death protein-1 (PD1) or its ligand (PDL1) used as second-line therapies generated evidence of improving survival and, more recently, as first-line NSCLC treatment.

Although pembrolizumab (anti-PD1) was recently approved as first-line treatment for patients with at least 50% of their NSCLC cells expressing PDL1, many patients are still not benefiting from this first-line agent.

For patients with relapsed NSCLC, atezolizumab (anti-PDL1) prolonged survival compared to docetaxel in the phase II POPLAR and phase III OAK trials. Novel concepts of synergic action between immunotherapy and chemotherapy have emerged recently. However, those types of treatments are given for different durations: chemotherapy is allowed for only a short period (rarely exceeding 6 cycles), while anti-PDL1 can be continued for several months until loss of its clinical benefit.

Metronomic chemotherapy is defined as low-dose and frequent chemotherapy administration, without prolonged drug-free breaks. Metronomic administration of oral vinorelbine has been tested against breast cancer and advanced refractory NSCLC. The combination could have immunostimulatory effects: induction of immunogenic cancer-cell death, enhancement of antigen presentation through dendritic cell modulation, increased cancer-cell immunogenicity, preferential depletion of regulatory T cells, modulation of myeloid-derived suppressor cells, enhancement of the cytotoxic activity of immune-effector cells.

Condition or disease Intervention/treatment Phase
Non-small Cell Lung Cancer Drug: Atezolizumab Drug: Vinorelbine Phase 2

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 71 participants
Intervention Model: Single Group Assignment
Intervention Model Description:
  • Atezolizumab will be administered of 1200 mg on day 1 of each 21-day cycle with IV infusions .
  • Vinorelbine at the dose of 40 mg per days will be administered on days 1, 3 and 5 of each week of the 21-day cycle.
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Open Label Phase II Trial to Evaluate Safety and Efficacy of Vinorelbine With Metronomic Administration in Combination With Atezolizumab as Second-line Treatment for Patients With Stage IV Non-small Cell Lung Cancer
Actual Study Start Date : January 24, 2019
Estimated Primary Completion Date : July 24, 2020
Estimated Study Completion Date : July 24, 2022

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Lung Cancer

Arm Intervention/treatment
Experimental: Atezolizumab associated with vinorelbine
  • Atezolizumab will be administered with IV infusions. The first one will be a 60-min IV infusion; the subsequent infusions will last 30 minutes when well-tolerated at the dose of 1200 mg on day 1 of each 21-day cycle.
  • Vinorelbine capsules are taken orally on days 1, 3 and 5 of each week of the 21-day cycle. Vinorelbine will be administered at the dose of 40 mg per day on days 1, 3 and 5 of each week of the 21-day cycle. In case of toxicity, the dose will be decreased to 30 mg.
Drug: Atezolizumab
Atezolizumab in IV infusions

Drug: Vinorelbine
Vinorelbine capsules

Primary Outcome Measures :
  1. Occurrence of death or progression of the disease [ Time Frame: 4 months ]
    To evaluate the occurrence of death or progression of the disease

Secondary Outcome Measures :
  1. Emergence of adverse events (Safety and tolerability) [ Time Frame: 12 months ]
    To evaluate the safety outcomes, tolerability, adverse events frequency

  2. Occurrence of death [ Time Frame: 12 months ]
    To evaluate the occurrence of death over 12 months of follow-up

  3. Objective Response Rate [ Time Frame: 4 months ]
    To evaluate the objective Response Rate and Disease Control Rate

  4. Following of the quality of life [ Time Frame: 12 months ]
    The scale EuroQol 5 dimensions (EDQ5) is used to evaluate the quality of life. The EQ-5D scale is a standardised measure of health status to provide a simple, generic measure of health for clinical and economic appraisal, whih is divided by the EQ-5D descriptive system (mobility, self care, usual activities, pain/discomfort, anxiety/depression) and the EQ Visual Analogue scale (EQ VAS). Each dimension has 5 levels (no problems, slight problems, moderate problems, severe problems, and extreme problems).

  5. Following of the quality of life [ Time Frame: 12 months ]
    The EORTC QLQ-C30 is a questionnaire with 30 questions developed to assess the quality of life of cancer patients. An essential aspect of the "modular" approach to QOL assessment adopted by the EORTC Quality of Life Group is the development of modules specific to tumour site, treatment modality, or a QOL dimension, to be administered in addition to the core questionnaire (EORTC QLQ-C30).

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Histologically confirmed NSCLC;
  • Locally advanced and/or metastatic stage IV NSCLC (according to American Joint Committee on Cancers) or recurrent NSCLC);
  • Patients without activating EGFR mutation or ALK rearrangement and ROS1 fusions.
  • Subject has provided a formalin-fixed tumor-tissue sample of a tumor-lesion biopsy, either at the time of or after metastatic disease was diagnosed AND from a site not previously irradiated to assess for PDL1 status. Archived tissue may be acceptable;
  • Patients must have a measurable lesion (RECIST V1.1);
  • Progressive disease after first-line platinum-doublet-based chemotherapy according to RECIST V.1.1;
  • Age ≥18 years, either sex;
  • Eastern Collaborative Oncology Group Performance status (ECOG PS) 0, 1 or 2;
  • Life expectancy exceeds 12 weeks;
  • No history of other malignancy within the last 5 years, except for adequately treated carcinoma in situ of the cervix or basal cell or spinocellular carcinoma of the skin;
  • Adequate organ function, demonstrated by the following laboratory results within 3 weeks prior to randomization: Normal hepatic function: bilirubin <1.5 × normal (N), Alanine aminotransferase and Aspartate aminotransferase <2.5 × N or <5 × N if liver metastasis is present;
  • Normal renal function (calculated creatinine clearance ≥45 mL/min);
  • Normal calcemia;
  • Normal hematological function (polynuclear neutrophils >1.5 G/L, platelets >100 G/L);
  • Women of child-bearing potential must use effective contraception;
  • Men might be surgically sterile or accept to use an effective contraceptive procedure during and until 6 months after the treatment;
  • Written informed consent to participate in the study
  • Patient with social insurance

Exclusion Criteria:

  • ECOG PS >2;
  • Known hypersensitivity to immunotherapy;
  • Small-cell lung cancer, bronchioloalveolar cancer, neuroendocrine cancer;
  • Tumor harbors EGFR-sensitizing (activating) mutations or ALK translocations or ROS1 fusions and that justify treatment with targeted therapy ;
  • Chemotherapy, hormonotherapy, immunotherapy or tyrosine-kinase inhibitors within the past 4 weeks prior to treatment with the trial drug;
  • Radiotherapy (except bone or brain) within the past 3 months prior to baseline imaging;
  • Medical contraindication to oral vinorelbine;
  • Persistence of clinical adverse events related to prior treatment;
  • Active brain metastases (e.g. stable for <4 weeks, no adequate previous radiotherapy, symptomatic, requiring anticonvulsants; dexamethasone will be allowed if administered at a stable dose <10 mg/day for at least 1 month before randomization);
  • Concurrent radiotherapy, except for palliative bone irradiation.
  • Other concurrent severe illnesses (congestive heart failure, unstable angina, significant arrhythmia or myocardial infarction <12 months before study entry);
  • Active or prior documented autoimmune or inflammatory disorders;
  • Active B hepatitis, HIV infection …;
  • Psychiatric or neurological disorders preventing the patient from understanding the nature of the trial;
  • Grade-3 peripheral neuropathy;
  • Uncontrolled infection;
  • Interstitial lung disease or pneumonitis requiring steroid management;
  • Corticosteroid therapy exceeding 10 mg/day;
  • Other severe organic disorders not allowing inclusion in the trial;
  • Malabsorption syndrome;
  • Pregnancy or breast-feeding;
  • Follow-up not possible; and incarcerated or institutionalized patients.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03801304

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Contact: Alain VERGNENEGRE, PUPH 555056629 ext +33
Contact: Sophie LECANUET 617987516 ext +33

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CH Aix en Provence Not yet recruiting
Aix-en-Provence, France
Contact: Marie BENARDI         
CH Beauvais Not yet recruiting
Beauvais, France
Contact: Jacky Crequit         
CHRU de Brest - Hôpital Morvan Recruiting
Brest, France, 29609
Contact: Gilles ROBINET   
CLCC Caen Not yet recruiting
Caen, France
Contact: Radj GERVAIS         
CH de Créteil Recruiting
Créteil, France, 94010
Contact: Isabelle MONNET   
Ch La Roche Sur Yon Recruiting
La Roche Sur Yon, France, 85000
Contact: Acya Bizieux   
CHU de Limoges - Hôpital DUPUYTREN Recruiting
Limoges, France, 87042
Contact: Alain VERGNENEGRE   
CH Lorient Not yet recruiting
Lorient, France
Contact: Régine LAMY         
CH MEAUX Not yet recruiting
Meaux, France
Contact: Chrystèle LOCHER         
CH Pringy Not yet recruiting
Pringy, France
Contact: Stéphane HOMINAL         
CH Quimper Not yet recruiting
Quimper, France
Contact: Anne-Marie CHIAPPA         
CHU de Rennes Active, not recruiting
Rennes, France, 35033
CHU Rouen Not yet recruiting
Rouen, France
Contact: Suzanna BOTA         
CH Saint-Brieuc Not yet recruiting
Saint-Brieuc, France
Contact: Gwénaëlle LE GARFF         
CH Villefranche sur Saône Not yet recruiting
Villefranche-sur-Saône, France
Contact: Lionel FALCHERO         
Sponsors and Collaborators
University Hospital, Brest
Groupe Français de Pneumo-Cancérologie
Roche Farma, S.A
Pierre Fabre Medicament

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Responsible Party: University Hospital, Brest Identifier: NCT03801304     History of Changes
Other Study ID Numbers: 29BRC18-0005 (VinMetAtezo)
First Posted: January 11, 2019    Key Record Dates
Last Update Posted: March 11, 2019
Last Verified: March 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: All collected data that underlie results in a publication
Supporting Materials: Study Protocol
Time Frame: Data will be available beginning five years and ending fifteen years following the final study report completion
Access Criteria: Data access requests will be reviewed by the internal committee of Brest UH. Requestors will be required to sign and complete a data access agreement.

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
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Lung Neoplasms
Respiratory Tract Neoplasms
Thoracic Neoplasms
Neoplasms by Site
Bronchial Neoplasms
Carcinoma, Non-Small-Cell Lung
Lung Diseases
Respiratory Tract Diseases
Carcinoma, Bronchogenic
Antibodies, Monoclonal
Antineoplastic Agents
Immunologic Factors
Physiological Effects of Drugs
Antineoplastic Agents, Phytogenic
Tubulin Modulators
Antimitotic Agents
Mitosis Modulators
Molecular Mechanisms of Pharmacological Action