UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000053550
Receipt number R000060604
Scientific Title A retrospective study using 18F-FDG-PET/CT for the prediction of immunotherapy-related interstitial lung disease in lung cancer.
Date of disclosure of the study information 2024/02/06
Last modified on 2024/02/13 09:14:48

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Basic information

Public title

A retrospective study using 18F-FDG-PET/CT for the prediction of immunotherapy-related interstitial lung disease in lung cancer.

Acronym

A retrospective study using 18F-FDG-PET/CT for the prediction of immunotherapy-related interstitial lung disease in lung cancer.

Scientific Title

A retrospective study using 18F-FDG-PET/CT for the prediction of immunotherapy-related interstitial lung disease in lung cancer.

Scientific Title:Acronym

A retrospective study using 18F-FDG-PET/CT for the prediction of immunotherapy-related interstitial lung disease in lung cancer.

Region

Japan


Condition

Condition

Advanced or recurrent lung cancer

Classification by specialty

Pneumology Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Immune checkpoint inhibitors (ICIs) have improved the lung cancer prognosis; however, ICI-related interstitial lung disease (ILD) is fatal and difficult to predict. Herein, we presumed that presence of inflammation on noncancerous lung (background lung) may be a risk factor for ILD onset. Under this hypothesis, the present study investigates the association between a high uptake of noncancerous lung on 18F fluorodeoxyglucose positron emission tomography/computed tomography, an indicator of inflammation, and ICI-ILD in lung cancer.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Interstitial lung disease after administration of immune checkpoint inhibitors

Key secondary outcomes

Prognosis after administration of immune checkpoint inhibitors


Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

18 years-old <=

Age-upper limit

100 years-old >=

Gender

Male and Female

Key inclusion criteria

(1) Patients with clinical stage II-IV or recurrent lung cancer who received ICIs in Niigata University Medical and Dental Hospital from August 2016 to August 2022
(2) FDG-PET/CT was taken within three months before ICI therapy.

Key exclusion criteria

(1) FDG uptake on lung region was difficult to evaluate owing to massive consolidation or pleural effusion
(2) Patients with bilateral multiple primary lung cancers.

Target sample size

200


Research contact person

Name of lead principal investigator

1st name Satoshi
Middle name
Last name Watanabe

Organization

Niigata University Medical and Dental Hospital

Division name

Department of Respiratory Medicine and Infectious Diseases

Zip code

9518510

Address

1-754 Asahimachi-dori, Chuo-ku, Niigata City, Niigata Prefecture

TEL

025-368-9325

Email

satoshi7@med.niigata-u.ac.jp


Public contact

Name of contact person

1st name Satoshi
Middle name
Last name Watanabe

Organization

Niigata University Medical and Dental Hospital

Division name

Department of Respiratory Medicine and Infectious Diseases

Zip code

9518510

Address

1-754 Asahimachi-dori, Chuo-ku, Niigata City, Niigata Prefecture

TEL

025-368-9325

Homepage URL


Email

satoshi7@med.niigata-u.ac.jp


Sponsor or person

Institute

Niigata University Medical and Dental Hospital

Institute

Department

Personal name



Funding Source

Organization

None

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

Institutional Review Board of Niigata University

Address

1-754 Asahimachi-dori, Chuo-ku, Niigata City, Niigata Prefecture

Tel

025-368-9325

Email

sanonao@adm.niigata-u.ac.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

Institutions



Other administrative information

Date of disclosure of the study information

2024 Year 02 Month 06 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled

165

Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

No longer recruiting

Date of protocol fixation

2023 Year 04 Month 01 Day

Date of IRB

2023 Year 06 Month 05 Day

Anticipated trial start date

2023 Year 04 Month 01 Day

Last follow-up date

2028 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

None


Management information

Registered date

2024 Year 02 Month 06 Day

Last modified on

2024 Year 02 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000060604


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name