UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000056588
Receipt number R000064669
Scientific Title Phase II study of stereotactic MR-guided online adaptive radiosurgery for kidney cancer
Date of disclosure of the study information 2025/02/10
Last modified on 2024/12/27 10:00:38

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Basic information

Public title

Phase II study of stereotactic MR-guided online adaptive radiosurgery for kidney cancer

Acronym

Stereotactic adaptive radiosurgery for kidney cancer

Scientific Title

Phase II study of stereotactic MR-guided online adaptive radiosurgery for kidney cancer

Scientific Title:Acronym

Stereotactic adaptive radiosurgery for kidney cancer

Region

Japan


Condition

Condition

Kidney cancer(primary kidney cancer)

Classification by specialty

Urology Radiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To investigate the efficacy and safety of MR-Linac based online adaptive stereotactic radiosurgery for primary kidney cancer.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase

Phase II


Assessment

Primary outcomes

One-year local control rate.

Key secondary outcomes

One-year overall survival rate, 1-year progression free survival rate and incidences of serious adverse events


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Other

Interventions/Control_1

To perform stereotactic MR-guided online adaptive radiosurgery for kidney cancer.

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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

(1)Primary kidney cancer which has pathological diagnosis or clinical diagnosis
(2)T1N0M0, or T1NanyMany and all lymph nodes and distant metastases have been controlled
(3)Performance status is from 0 to 2
(4)Twenty or more years old
(5)Urologists and radiologists agree to perform stereotactic radiotherapy instead of surgery, cryotherapy or active surveillance, or patient refused surgery and cryotherapy.
(6)Written informed consent

Key exclusion criteria

(1)Radiation oncologists judge not to have a tolerance or not to be suitable for stereotacitc radiotherapy because of coexisting illness
(2)Double cancer or past history of double cancer within 3 years.
(3)Implanted metal in the body
(4)Mental disorder, especially claustrophobiady
(5)Infection
(6)Pregnant or lactating woman, likelihood of pregnancy
(7)Past-radiotherapy history for the same site
(8)Patients with psychiatric illness or symptoms making participation in the study difficult to assess

Target sample size

25


Research contact person

Name of lead principal investigator

1st name Takaya
Middle name
Last name Yamamoto

Organization

Tohoku University Hospital

Division name

Department of Radiation Oncology

Zip code

980-8574

Address

Seiryo-machi 1-1, Aoba-ku, Sendai

TEL

+81-22-717-7312

Email

takaya.yamamoto.c3@tohoku.ac.jp


Public contact

Name of contact person

1st name Takaya
Middle name
Last name Yamamoto

Organization

Tohoku University Hospital

Division name

Department of Radiation Oncology

Zip code

980-8574

Address

Seiryo-machi 1-1, Aoba-ku, Sendai

TEL

+81-22-717-7312

Homepage URL


Email

takaya.yamamoto.c3@tohoku.ac.jp


Sponsor or person

Institute

Tohoku University

Institute

Department

Personal name



Funding Source

Organization

Self funding

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 tohoku university

Address

1-1, seiryo-machi, aoba-ku, sendai city, Japan

Tel

+81-22-728-4105

Email

ec-med@grp.tohoku.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

2025 Year 02 Month 10 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

2024 Year 12 Month 05 Day

Date of IRB


Anticipated trial start date

2025 Year 02 Month 10 Day

Last follow-up date

2030 Year 01 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2024 Year 12 Month 27 Day

Last modified on

2024 Year 12 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064669