UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000039539
Receipt number R000045088
Scientific Title Retrospective study for optimal regimen of neoadjuvant chemotherapy for advanced epithelial ovarian cancers.
Date of disclosure of the study information 2020/02/21
Last modified on 2022/02/21 15:32:12

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Basic information

Public title

Retrospective study for optimal regimen of neoadjuvant chemotherapy for advanced epithelial ovarian cancers.

Acronym

SGSG-017

Scientific Title

Retrospective study for optimal regimen of neoadjuvant chemotherapy for advanced epithelial ovarian cancers.

Scientific Title:Acronym

SGSG-017

Region

Japan


Condition

Condition

Advanced epithelial ovarian, fallopian tube, and peritoneal cancers.

Classification by specialty

Obstetrics and Gynecology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to determine the optimal regimen of neoadjuvant chemotherapy (NAC) for advanced epithelial ovarian, fallopian tube, and peritoneal cancers.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Progression free survival

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

Female

Key inclusion criteria

Patients with advanced epithelial ovarian, fallopian tube, or peritoneal cancer treated in Japan between January 2007 and December 2016 who underwent NAC (TC, dose-dense TC, weekly-TC, TC+BEV) at least 3 cycles or more.

Key exclusion criteria

1) Patients with sarcomatous components (including carcinosarcoma).
2) Patients with borderline malignancy.
3) Patient who underwent primary debulking surgery for epithelial ovarian cancer without NAC.

Target sample size

300


Research contact person

Name of lead principal investigator

1st name Takashi
Middle name
Last name Shibutani

Organization

Hyogo Cancer Center

Division name

Gynecologic Oncology

Zip code

673-8558

Address

13-70, Kitaoji-town, Akashi-city, Hyogo, Japan

TEL

0789291151

Email

t-shibu@hp.pref.hyogo.jp


Public contact

Name of contact person

1st name Takashi
Middle name
Last name Shibutani

Organization

Hyogo Cancer Center

Division name

Gynecologic Oncology

Zip code

673-8558

Address

13-70, Kitaoji-town, Akashi-city, Hyogo, Japan

TEL

0789291151

Homepage URL


Email

t-shibu@hp.pref.hyogo.jp


Sponsor or person

Institute

Sankai Gynecology Study Group (SGSG)

Institute

Department

Personal name



Funding Source

Organization

Nothing

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Hyogo Cancer Center

Address

13-70, Kitaoji-town, Akashi-city, Hyogo, Japan

Tel

0789291151

Email

t-shibu@hp.pref.hyogo.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

2020 Year 02 Month 21 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

497

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

2020 Year 02 Month 12 Day

Date of IRB

2020 Year 02 Month 28 Day

Anticipated trial start date

2020 Year 03 Month 01 Day

Last follow-up date

2021 Year 02 Month 28 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Multicenter retrospective cohort study


Management information

Registered date

2020 Year 02 Month 19 Day

Last modified on

2022 Year 02 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000045088


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name