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Phase II Trial of Carboplatin, Etoposide and Atezolizumab for Previously Untreated Elderly Patients with Advanced Small cell lung cancer

Phase 2
Recruiting
Conditions
Performance status 0-2
Small-cell lung cancer, elderly
Registration Number
JPRN-jRCT1061200024
Lead Sponsor
Kato Yuka
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
32
Inclusion Criteria

1) A definitive diagnosis of small cell lung cancer has been obtained by histology or cytology.
2) Diagnosed as advanced type (ED) by chest CT, head CT or MRI, PET-CT, etc.
3) No serious tumor-related complications.
4) The age of the registration date is 71 years or older.
5) Performance status (PS) is 0-2 according to the ECOG standard.
6) Has measurable lesions.
7) No history of surgery, radiation therapy, or chemotherapy for small cell lung cancer.
8) No surgery, chest radiation therapy, or chemotherapy within 1 year for other cancers.
9) The general condition is good, and the functions of blood, kidney, liver, etc. can be maintained.
10) Patient consent is obtained in writing from the patient.

Exclusion Criteria

1) Patients with positive HIV antibody.
2) Patients who are HCV antibody positive and HCV-RNA positive.
3) Patients positive for HBs antigen, HBc antibody or HBs antibody.
4) Patients with autoimmune diseases including past medical history.
5) Patients with complications such as active interstitial lung disease and active radiation pneumoni
tis.
6) Patients with tuberculosis.
7) Patients undergoing dialysis.
8) Patients with severe liver dysfunction.
9) Patients with severe impairment of cardiovascular system and respiratory function.
10) Patients with a history of Grade 3 or higher hypersensitivity to immune checkpoint inhibitors, ca
rboplatin or etoposide.
11) Patients with endocrine disorders that are difficult to control.
12) Patients with active inflammatory bowel disease.
13) Patients who receive continuous systemic administration of steroids over 5 mg/day in terms of predonin.
14) Patients with uncontrolled diabetes (HbA1c 8.0% or more).
15) Patients in need of double cancer treatment.
16) Patients who cannot consent to contraception by contraception methods such as condoms for 6 months after the consent is obtained and the therapeutic drug administration is completed.
17) Patients with severe infections.
18) Patients with mental disorders or dementia who have trouble obtaining proper consent.
19) Patients who have undergone transplantation therapy such as hematopoietic stem cell transpla ntation.
20) Patients who are judged to be unsuitable by the investigator or investigator.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1-year survival rate
Secondary Outcome Measures
NameTimeMethod
Overall survival, progression-free survival, response rate, safety, etc.
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