Skip to main content
Clinical Trials/JPRN-jRCTs031190066
JPRN-jRCTs031190066
Completed
Phase 2

A Phase 2 Study of atezolizumab + carboplatin + paclitaxel + bevacizumab for previously-treated patients with NSCLC harboring EGFR mutations. - NEJ043

Kikuchi Toshiaki0 sites60 target enrollmentAugust 1, 2019

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
on-sequamous non-small cell lung cancer
Sponsor
Kikuchi Toshiaki
Enrollment
60
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 1, 2019
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Kikuchi Toshiaki

Eligibility Criteria

Inclusion Criteria

  • 1\) Stage III or IV Non\-Squamous, non\-small cell lung cancer proven by histology and/or cytology without indication of curative surgery or curative radiotherapy, 2\) Sensitizing EGFR mutations (19 deletion, L858R, G719X, S768I, L861Q, T790M), 3\) Prior therapy with EGFR\-TKIs, 4\) Measurable disease, as defined by RECIST ver 1\.1, 5\) No prior cytotoxic chemotherapy or immunotherapy, 6\) 20 years or older, 7\) ECOG PS 0 or 1, 8\) adequate hematologic and end organ function, 9\) Written informed consent form.

Exclusion Criteria

  • 1\) History of interstitial lung disease or radiation pneumonitis, 2\) Symptomatic CNS metastases, CNS metastases treated with corticosteroids, leptomeningeal disease, 3\) Irradiation for primary tumor or target lesion defined by RECIST ver 1\.1, 4\) Uncontrolled heart, lung, liver, renal diseases, 5\) History of autoimmune diseases, 6\) Known hypersensitivity or allergy to paclitaxel or polyoxyethylene castor oil containing formulations, 7\) History of hemoptysis, 8\)Invasion to major vessels or heart, 9\) Treatment with systemic corticosteroid or immunosuppressant, 10\) Patients with active hepatitis B or hepatitis C or positive for HIV test, 11\) Women who are pregnant, lactating, or intending to become pregnant during the study, 12\) Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures, 13\) Malignancies other than NSCLC within 5 years, 14\) History of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins, 15\) Plan for major surgical procedure during the course of the study.

Outcomes

Primary Outcomes

Not specified

Similar Trials