UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000025209
Receipt number R000028999
Scientific Title Efficacy of presurgical targeting therapy on tumor shrinkage in patients with advanced renal cell carcinoma
Date of disclosure of the study information 2016/12/10
Last modified on 2022/12/05 21:57:43

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Basic information

Public title

Efficacy of presurgical targeting therapy on tumor shrinkage in patients with advanced renal cell carcinoma

Acronym

Efficacy of presurgical targeting therapy in patients with advanced renal cell carcinoma

Scientific Title

Efficacy of presurgical targeting therapy on tumor shrinkage in patients with advanced renal cell carcinoma

Scientific Title:Acronym

Efficacy of presurgical targeting therapy in patients with advanced renal cell carcinoma

Region

Japan


Condition

Condition

Renal cell carcinoma

Classification by specialty

Urology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluating efficacy of presurgical targeting therapy on tumor shrinkage in patients with advanced renal cell carcinoma

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

adiologic tumor response comparison among Response Evaluation Criteria in Solid Tumors (RECIST), Choi, and contrast medium enhancement reduction (CMER)

Key secondary outcomes

Pathological downstaging, theatment related adverse events (AE), postoperative complications, Ki67/MIB1 status, and tumor necrosis, pathological and molecular analysis to predict poor prognosis, progression free, cancer specific and overall survival


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Historical

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Medicine Maneuver

Interventions/Control_1

targeting therapy (TKI or mTORi) for aboout 3 months, and then, undergo radical nephrectomy

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

100 years-old >

Gender

Male and Female

Key inclusion criteria

Males, 20 years or older, in patients with advanced renal cell carcinoma without prior targeting therapy.
Clinically T3-4, or oligometastatic disease (not multiple, small, or resectable) who underwent tumor biopsy prier to targeting therapy
Agree to use TKI or mTORi prior to radical nephrectomy.

Key exclusion criteria

Sarcomatous renal cell carcinoma, not indicated for tyrosine kinase inhibitors(TKI) or mammalian target of rapamycin inhibitors(mTORi), untreated brain metastasis, active gastrointestinal hemorrhage, poor general health (ECOG PS > 2), major concomitant disease, other medical condition likely to result in death within 6 months after the treatment initiation.
Clinical evidence of any of unstable diseases including cardiovascular, infectious, immune, nervous system disease, and other active malignancies that influenced on therapy for renal cell carcinoma.
History of drug, alcohol, or substance abuse.
Have any condition, limitation, or disease that could, in the judgment of the investigator, preclude evaluation of response to targeting therapy

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Shingo
Middle name
Last name Hatakeyama

Organization

Hirosaki University Hospital

Division name

Urology

Zip code

036-8562

Address

53 Honchou, Hirosaki

TEL

0172395091

Email

shingoh@hirosaki-u.ac.jp


Public contact

Name of contact person

1st name Shingo
Middle name
Last name Hatakeyama

Organization

Hirosaki University Hospital

Division name

Urology

Zip code

036-8562

Address

53 Honchou, Hirosaki

TEL

0172395091

Homepage URL


Email

shingoh@hirosaki-u.ac.jp


Sponsor or person

Institute

Hirosaki University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Hirosaki University Graduate School of Medicine

Organization

Division

Category of Funding Organization

Government offices of other countries

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Hirosaki Universicy IRB

Address

5 Zaifu-chou, Hirosaki

Tel

0172395091

Email

rinri@hirosaki-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

弘前大学 医学部附属病院 


Other administrative information

Date of disclosure of the study information

2016 Year 12 Month 10 Day


Related information

URL releasing protocol


Publication of results

Partially published


Result

URL related to results and publications


Number of participants that the trial has enrolled

34

Results

The median radiologic tumor response by RECIST, Choi, and CMER was -19%, -24%, and -49%, respectively. Among the radiologic tumor response tests, CMER showed a higher association with tumor necrosis in surgical specimens than others. Ki67/MIB1 status was significantly decreased in surgical specimens than in biopsy specimens. The magnitude of the slope of the regression line associated with the tumor necrosis percentage was greater in CMER than in Choi and RECIST.

Results date posted

2022 Year 12 Month 05 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

A quantitative tumor response evaluation to molecular-targeting agents in advanced renal cell carcinoma (RCC) is debatable. We aimed to evaluate the relationship between radiologic tumor response and pathological response in patients with advanced RCC who underwent presurgical therapy.

Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2012 Year 03 Month 11 Day

Date of IRB

2012 Year 03 Month 11 Day

Anticipated trial start date

2012 Year 03 Month 11 Day

Last follow-up date

2022 Year 12 Month 05 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2016 Year 12 Month 09 Day

Last modified on

2022 Year 12 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000028999


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name