| Recruitment status | Terminated |
| Unique ID issued by UMIN | UMIN000032585 |
| Receipt No. | R000037039 |
| Scientific Title | Phase II study of atezolizumab for advanced non-small-cell lung cancer patients not indicative of cytotoxic chemotherapy |
| Date of disclosure of the study information | 2018/07/01 |
| Last modified on | 2022/05/18 (Ver. 5) |
| Basic information | ||
| Public title | Phase II study of atezolizumab for advanced non-small-cell lung cancer patients not indicative of cytotoxic chemotherapy | |
| Acronym | atezolizuamab for NSCLC with poor PS | |
| Scientific Title | Phase II study of atezolizumab for advanced non-small-cell lung cancer patients not indicative of cytotoxic chemotherapy | |
| Scientific Title:Acronym | atezolizuamab for NSCLC with poor PS | |
| Region |
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| Condition | ||
| Condition | advanced NSCLC | |
| Classification by specialty |
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| Classification by malignancy | Malignancy | |
| Genomic information | NO | |
| Objectives | |
| Narrative objectives1 | To explore the efficacy and safety of atezolizumab for previously treated advanced lung cancer patients who have no indication for standard chemotherapy, including cytotoxic chemotherapy and molecular targeted therapy |
| Basic objectives2 | Efficacy |
| Basic objectives -Others | |
| Trial characteristics_1 | Exploratory |
| Trial characteristics_2 | Explanatory |
| Developmental phase | Phase II |
| Assessment | |
| Primary outcomes | Response rate |
| Key secondary outcomes | Progression-free survival, Overall survival, and Toxicity. AND, we will explore serum or blood-based biomarker analysis and immune state as the accompanying research with the informed consent |
| Base | |
| Study type | Interventional |
| Study design | |
| Basic design | Single arm |
| Randomization | Non-randomized |
| Randomization unit | |
| Blinding | Open -no one is blinded |
| Control | Uncontrolled |
| Stratification | NO |
| Dynamic allocation | NO |
| Institution consideration | |
| Blocking | |
| Concealment | |
| Intervention | ||
| No. of arms | 1 | |
| Purpose of intervention | Treatment | |
| Type of intervention |
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| Interventions/Control_1 | Nivolumab 1200mg (day 1, q3 weeks) until clinical progression or unacceptable toxicities | |
| Interventions/Control_2 | ||
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| Interventions/Control_7 | ||
| Interventions/Control_8 | ||
| Interventions/Control_9 | ||
| Interventions/Control_10 | ||
| Eligibility | ||||
| Age-lower limit |
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| Age-upper limit |
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| Gender | Male and Female | |||
| Key inclusion criteria | 1) Definitively diagnosed with having previously treated advanced non-small cell lung cancer by the specimens histologically or cytologically who have no indication for standard treatment of chemotherapy including cytotoxic chemotherapy and molecular targeted agents for driver mutation.
2) Age of 20 years and older 3) With adequate organ function of bone marrow reserve, liver, and kidney. (1) PS 2-4 (2) neutrophil count => 500/mm^3 (3) platelet => 50,000/mm^3 (4) hemoglobin => 8.0g/dL (5) AST/ALT < 5 times less than ULN (6) T.Bil <= 3.0mg/dL (7) serum creatinine <= 3.0mg/dL (8) ECG: without clinically problematic abnormalities (9) SpO2 more than 92% 4) With the status of below previous treatment at the time of beginning of chemotherapy. (1) Radiotherapy: irradiated extrathoracic lesion: more than two weeks from the date of last irradiation (2) Surgical procedure, including pleurodesis or pleural drainage * more than 8 weeks with lobectomy * more than 4 weeks without lobectomy, including exploratory thoracotomy * more than 2 weeks after completing procedure (pleurodesis or pleural drainage) 5) With written informed consent |
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| Key exclusion criteria | 1) The age of less than 20
2) Indicative for cytotoxic chemotherapy or molecular targeted agents 3) Uncontrolled brain metastasis treated by palliative radiotherapy 4) Clinically active infection 5) Severe complication (cardiac diseases, interstitial pneumonia, uncontrolled hypertension or diabetes) 6) Uncontrolled pleural effusion 7) Active other organ cancers 8) History of severe drug allergy 9) Uncontrolled digestive ulcer 10) Any patients judged by the investigator to be unfit to participate in the study |
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| Target sample size | 64 | |||
| Research contact person | |||||||
| Name of lead principal investigator |
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| Organization | Tokyo Metropolitan Cancer and Infectious disease Center Komagome Hospital | ||||||
| Division name | Department of Respiratory Medicine and Thoracic Oncology | ||||||
| Zip code | 113-8677 | ||||||
| Address | 3-18-22, Honkomagome, Bunkyo, Tokyo | ||||||
| TEL | 03-3823-2101 | ||||||
| yhosomi@cick.jp | |||||||
| Public contact | |||||||
| Name of contact person |
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| Organization | Tokyo Metropolitan Cancer and Infectious disease Center Komagome Hospital | ||||||
| Division name | Department of Respiratory Medicine and Thoracic Oncology | ||||||
| Zip code | 113-8677 | ||||||
| Address | 3-18-22, Honkomagome, Bunkyo, Tokyo | ||||||
| TEL | 03-3823-2101 | ||||||
| Homepage URL | |||||||
| y-okuma@cick.jp | |||||||
| Sponsor | |
| Institute | Tokyo Metropolitan Cancer and Infectious disease Center Komagome Hospital |
| Institute | |
| Department | |
| Funding Source | |
| Organization | Tokyo Metropolitan Cancer and Infectious disease Center Komagome Hospital |
| Organization | |
| Division | |
| Category of Funding Organization | Self funding |
| Nationality of Funding Organization | |
| Other related organizations | |
| Co-sponsor | |
| Name of secondary funder(s) | |
| IRB Contact (For public release) | |
| Organization | Ethics committee of Tokyo Metropolitan Komagome Hospital |
| Address | 3-28-22, Honkomagome, Bunkyo, Tokyo |
| Tel | 03-3823-2101 |
| rinri@cick.jp | |
| Secondary IDs | |
| Secondary IDs | NO |
| Study ID_1 | |
| Org. issuing International ID_1 | |
| Study ID_2 | |
| Org. issuing International ID_2 | |
| IND to MHLW | |
| Institutions | |
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| Date of disclosure of the study information |
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| Related information | |
| URL releasing protocol | |
| Publication of results | Unpublished |
| Result | |
| URL related to results and publications | |
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| Date of the first journal publication of results | |
| Baseline Characteristics | |
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| Plan to share IPD | |
| IPD sharing Plan description | |
| Progress | |||||||
| Recruitment status | Terminated | ||||||
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| Link to view the page | |
| URL(English) | https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000037039 |