A Study Comparing Immunotherapy With Chemotherapy in the Treatment of Elderly Patients With Advanced NSCLC (MILES-5) (MILES-5)

  • STATUS
    Recruiting
  • End date
    Jun 30, 2023
  • participants needed
    460
  • sponsor
    National Cancer Institute, Naples
Updated on 9 February 2022
platelet count
measurable disease
carcinoma
serum bilirubin level
neutrophil count
durvalumab
cancer chemotherapy
lung carcinoma

Summary

This is a randomized phase 2 trial aiming to assess the early efficacy of two experimental treatment sequences.

Three arms are planned; (i) standard chemotherapy followed at progression by single agent immunotherapy with durvalumab (CT), (ii) experimental single agent immunotherapy with durvalumab followed at progression by chemotherapy, (iii) experimental combination immunotherapy with durvalumab+tremelimumab followed at progression by chemotherapy.

The the two experimental strategies will be compared with the standard strategy in terms of 12-month overall survival, time considered informative for the type of treatment and disease

Details
Condition Carcinoma, Non-Small-Cell Lung
Treatment tremelimumab, durvalumab, Chemotherapy
Clinical Study IdentifierNCT03975114
SponsorNational Cancer Institute, Naples
Last Modified on9 February 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Male or female >= 70 years of age
Histological documentation of primary squamous or non squamous non-small cell lung carcinoma
Availability of archived tumor tissue block or newly cut unstained slides for PD-L1 determination
Stage IV or IIIB disease with supraclavear metastatic nodes (according to TNM 7th edition)
Clinical or radiologic evidence of disease (at least one measurable or non measurable lesion)
ECOG performance status 0 to 1
Life expectancy > 3 months
Adequate renal and hepatic function, defined as
Total serum bilirubin 1.5 institutional ULN
AST and/or ALT 2.5 x ULN for the institution (or 5 x ULN if liver metastases are present)
Serum creatinine 1.5 x ULN for the institution (or calculated creatinine clearance 40 mL/min/1.73 m2)
Adequate bone marrow function, defined as
Haemoglobin <= 9.0 g/dL
Absolute neutrophils count (ANC) >= 1.5 x 109/L (> 1500 per mm3)
Platelet count <= 100 x 109/L(>100,000 per mm3)
Written informed consent obtained from the subject prior to performing any protocol-related procedures, including screening evaluations

Exclusion Criteria

Cancer related
Activating epidermal growth factor receptor mutation (exon19 deletion or exon 21 L858R mutation or other activating/sensitizing mutations)
ALK or ROS1 positive (immunohistochemistry or FISH)
Mixed small-cell lung cancer and NSCLC histology
Prior, current or planned treatment related
\. Prior chemotherapy or any other medical treatment for advanced NSCLC
(previous neoadjuvant or adjuvant chemotherapy is allowed if > 6 months
previously)
\. Prior exposure to immunomodulatory therapy, including, but not limited to
other anti-cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), anti-
programmed cell death1 (PD-1), anti-programmed cell death ligand 1 (PD-L1), or
anti PD-L2 antibodies
\. Current or prior use of immunosuppressive medication within 14 days before
the first dose of study treatment (intranasal and inhaled corticosteroids at
physiological doses not exceeding 10 mg/day of prednisone or an equivalent
corticosteroid are allowed)
\. Any concurrent investigational product or other anticancer treatment
Prior or concomitant conditions or procedures related
\. Active or prior documented autoimmune disease within the past 2 years
(subjects with vitiligo, Grave's disease, or psoriasis not requiring systemic
treatment within the past 2 years, are not excluded)
\. Active or prior documented inflammatory bowel disease (e.g., Crohn's
disease, ulcerative colitis)
\. History of allogeneic organ transplant
\. History of active primary immunodeficiency
\. Active infection, including tuberculosis (clinical evaluation that
includes clinical history, physical examination and radiographic findings, and
TB testing in line with local practice), hepatitis B (known positive HBV
surface antigen (HBsAg) result), hepatitis C, or human immunodeficiency virus
(positive HIV 1/2 antibodies). Patients with a past or resolved HBV infection
(defined as the presence of hepatitis B core antibody [anti-HBc] and absence
of HBsAg) are eligible. Patients positive for hepatitis C (HCV) antibody are
eligible only if polymerase chain reaction is negative for HCV RNA
\. Receipt of live attenuated vaccine within 30 days prior to the first dose
of study drugs
\. Patients with previous malignancies (except for adequately treated
carcinoma in situ of the cervix or basal or squamous cell skin cancer or
surgically resected prostate cancer with normal PSA) are excluded only if the
histological diagnosis of the current disease does not definitely support the
pulmonary origin
\. Brain metastases or spinal cord compression, unless asymptomatic
previously treated, and stable off steroids and anti-convulsants for at least
one month prior to study entry
\. Leptomeningeal carcinomatosis
\. Clinically significant cardiovascular disease, including
Myocardial infarction or unstable angina pectoris within < 6 months prior to the first study treatment
New York Heart Association (NYHA) grade II or greater congestive heart failure (CHF)
Uncontrolled hypertension
Serious cardiac arrhythmia requiring medication (with the exception of atrial fibrillation or paroxysmal supraventricular tachycardia)
Peripheral vascular disease > grade 3 (i.e. symptomatic and interfering with activities of daily living requiring repair or revision)
Mean QT interval corrected for heart rate (QTc) 470 ms calculated from 3 electrocardiograms (ECGs) using Fredericia's Correction
Serious active infection requiring i.v. antibiotics at enrollment
Known hypersensitivity to any of the study drugs or excipients
Evidence of any other concomitant pathologies, physical examination or laboratory findings (including but not limited to active peptic ulcer disease or gastritis, active bleeding diatheses or psychiatric illness) or social situation that may interfere with the planned treatment, affect patient compliance or place the patient at high risk from treatment related complications
Radiotherapy treatment to the chest or to more than 30% of the bone marrow or with a wide field of radiation within 4 weeks of the first dose of study treatment (patients who have had radiotherapy 4 weeks prior to the first dose of study treatment, but who are still experiencing acute toxic effects of radiotherapy are also excluded)
Major surgical procedure within 28 days prior to the first dose of study drugs
Male patients of reproductive potential who are not willing to employ effective birth control from screening to 180 days after the last dose of study treatment
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