UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000047960
Receipt number R000054652
Scientific Title Usefulness and Tolerability of Postoperative Adjuvant Chemotherapy for Colorectal Cancer in the Elderly
Date of disclosure of the study information 2022/06/06
Last modified on 2022/06/22 10:38:38

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Basic information

Public title

Usefulness and Tolerability of Postoperative Adjuvant Chemotherapy for Colorectal Cancer in the Elderly

Acronym

Usefulness and Tolerability of Postoperative Adjuvant Chemotherapy for Colorectal Cancer in the Elderly

Scientific Title

Usefulness and Tolerability of Postoperative Adjuvant Chemotherapy for Colorectal Cancer in the Elderly

Scientific Title:Acronym

Usefulness and Tolerability of Postoperative Adjuvant Chemotherapy for Colorectal Cancer in the Elderly

Region

Japan


Condition

Condition

Colorectal cancer

Classification by specialty

Gastrointestinal surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Stage II high risk and Stage III colorectal cancer patients are treated with adjuvant chemotherapy to prevent recurrence after radical surgery. Although the proportion of elderly patients with colorectal cancer continues to increase with the aging of society, the rationale for administering adjuvant chemotherapy to elderly patients with colorectal cancer is based on the results of large clinical trials, mainly in non-elderly patients.
In addition, because adjuvant chemotherapy is often not administered to elderly patients in daily practice, the tolerability, prognosis, additional effect of combination therapy to monotherapy of postoperative adjuvant chemotherapy in elderly patients with colorectal cancer have not been adequately investigated.
Therefore, in this study, we will conduct an integrated analysis using data from JFMC Study No.7, 15, 33, 35, 37, 38, 41 to examine tolerability, prognosis, correlation between tolerability and prognosis, and additional effect of combination therapy to monotherapy in elderly and nonelderly patients.
The purpose of this study is to obtain findings for optimizing treatment methods for elderly colorectal cancer patients, which is an important clinical question in clinical practice.

Basic objectives2

Others

Basic objectives -Others

We will conduct an integrated analysis using data from JFMC Study No.7, 15, 33, 35, 37, 38, 41 to examine tolerability, prognosis, correlation between tolerability and prognosis, and additional effect of combination therapy to monotherapy in elderly and nonelderly patients.
The purpose of this study is to obtain findings for optimizing treatment methods for elderly colorectal cancer patients, which is an important clinical question in clinical practice.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Relapse-free survival
Overall survival
Safety
Tolerability
Recurrence rate

Key secondary outcomes



Base

Study type

Others,meta-analysis etc


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

20 years-old <=

Age-upper limit

83 years-old >=

Gender

Male and Female

Key inclusion criteria

All colorectal cancer patients enrolled in clinical studies conducted by JFMC in the past (No 7, 15, 33, 35, 37, 38, 41) who received adjuvant chemotherapy will be included.
Any type of chemotherapy and duration of administration.

Key exclusion criteria

-

Target sample size

7405


Research contact person

Name of lead principal investigator

1st name Takaki
Middle name
Last name Yoshikawa

Organization

Japanese Foundation for Multidisciplinary Treatment of Cancer

Division name

Database Project Support Committee

Zip code

136-0071

Address

Tani Building 3F, 1-28-6 Kameido, Koto-ku, Tokyo

TEL

0356277594

Email

jfmc-dc@jfmc.or.jp


Public contact

Name of contact person

1st name Yukari/Masaru
Middle name
Last name Kawamura/Mutoh

Organization

Japanese Foundation for Multidisciplinary Treatment of Cancer

Division name

Data Management Section/Statistical Analysis Section

Zip code

136-0071

Address

Tani Building 3F, 1-28-6 Kameido, Koto-ku, Tokyo

TEL

0356277594

Homepage URL


Email

jfmc-dc@jfmc.or.jp


Sponsor or person

Institute

Tani Building 3F, 1-28-6 Kameido, Koto-ku, Tokyo

Institute

Department

Personal name



Funding Source

Organization

Japanese Foundation for Multidisciplinary Treatment of Cancer

Organization

Division

Category of Funding Organization

Non profit foundation

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Epidemiological and Clinical research Information Network (ECRIN)

Address

21-7 Shogoin Sannocho Sakyo-ku, Kyoto-shi, Kyoto-fu 606-8392

Tel

075-762-1200

Email

naomi.iwahori@ecrin.or.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

2022 Year 06 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


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

2022 Year 03 Month 25 Day

Date of IRB

2022 Year 03 Month 25 Day

Anticipated trial start date

2022 Year 09 Month 01 Day

Last follow-up date

2023 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Relapse-free survival
Overall survival
Safety
Tolerability
Recurrence rate


Management information

Registered date

2022 Year 06 Month 06 Day

Last modified on

2022 Year 06 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000054652