UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000060836
Receipt number R000069587
Scientific Title Biomarker Study with FDG-PET/CT Analysis in Induction Chemo-radiation Therapy Followed by Surgery with Perioperative Immunotherapy for Resectable Stage Discreate N2 IIIA-B Non-small Cell Lung Cancer (SQUAT-TR2 Study) ( WJOG12119LTR2)
Date of disclosure of the study information 2026/03/05
Last modified on 2026/03/04 10:55:20

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Basic information

Public title

Biomarker Study with FDG-PET/CT Analysis in Induction Chemo-radiation Therapy Followed by Surgery with Perioperative Immunotherapy for Resectable Stage Discreate N2 IIIA-B Non-small Cell Lung Cancer (SQUAT-TR2 Study) (
WJOG12119LTR2)

Acronym

WJOG12119LTR2:SQUAT-TR2 study

Scientific Title

Biomarker Study with FDG-PET/CT Analysis in Induction Chemo-radiation Therapy Followed by Surgery with Perioperative Immunotherapy for Resectable Stage Discreate N2 IIIA-B Non-small Cell Lung Cancer (SQUAT-TR2 Study) (
WJOG12119LTR2)

Scientific Title:Acronym

WJOG12119LTR2:SQUAT-TR2 study

Region

Japan


Condition

Condition

Non-small cell lung cancer

Classification by specialty

Pneumology Chest surgery Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

This study aims to explore the clinical significance of FDG-PET/CT derived parameters as biomarkers for predicting preoperative pathological response and recurrence in patients enrolled in the Phase 2 trial entitled "A Phase 2 Study of Quadruple-Modality Therapy Incorporating Induction Chemoradiotherapy Plus Perioperative Immunotherapy for Resectable Discrete N2 Stage 3A-B Non-Small Cell Lung Cancer" (WJOG12119L).
FDG-PET/CT imaging data obtained as part of the WJOG12119L trial will be analyzed to evaluate their potential utility as predictive biomarkers of pathological response prior to surgery to the study treatment regimen, which consists of induction chemoradiotherapy combined with preoperative and postoperative immunotherapy.

Basic objectives2

Others

Basic objectives -Others

Association between pathological response (pCR/MPR) and FDG-PET/CT parameters

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Association between pathological response (pCR/MPR) and FDG-PET/CT parameters

Key secondary outcomes



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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients who were enrolled in WJOG12119L and, at the time of enrollment in the present study, had not withdrawn their informed consent for that trial.

Key exclusion criteria

Patients deemed inappropriate for inclusion by the attending physician.

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Tetsuya
Middle name
Last name Mitsudomi

Organization

Kindai University Faculty of Medicine

Division name

Division of Thoracic Surgery, Department of Surgery

Zip code

590-0197

Address

1-14-1 Mihara-dai, Minami-ku, Sakai, Osaka, Japan

TEL

072-288-7222

Email

mitsudom@gmail.com


Public contact

Name of contact person

1st name Naoki
Middle name
Last name Ishizuka

Organization

West Japan Oncology Group

Division name

WJOG datacenter

Zip code

556-0016

Address

Namba Plaza Bldg. 304-1-5-7, Motomachi Naniwa-ku, Osaka 556-0016 JAPAN

TEL

06-6633-7400

Homepage URL

https://www.wjog.jp/

Email

datacenter@wjog.jp


Sponsor or person

Institute

West Japan Oncology Group

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

Ethics Committee, Faculty of Medicine, Kinki University

Address

1-14-1 Mihara-dai, Minami-ku, Sakai, Osaka, Japan

Tel

072-288-7222

Email

zizen@med.kindai.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

2026 Year 03 Month 05 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


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

Preinitiation

Date of protocol fixation

2026 Year 02 Month 28 Day

Date of IRB


Anticipated trial start date

2026 Year 04 Month 20 Day

Last follow-up date

2028 Year 04 Month 19 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

None


Management information

Registered date

2026 Year 03 Month 05 Day

Last modified on

2026 Year 03 Month 04 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000069587