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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03566355
Other study ID # NCC2018-0107
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 23, 2018
Est. completion date December 31, 2025

Study information

Verified date August 2019
Source National Cancer Center, Korea
Contact Dae Yong Kim, M.D.
Phone 82-31-920-1721
Email radiopia@ncc.re.kr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Proton alone therapy is performed

-> 5 times a week, 7200 cGy / 15 fractions for 3 weeks total


Description:

This clinical trial is a prospective, single-organ, phase II clinical trial to evaluate the efficacy of curative proton therapy for pulmonary metastasis of colon cancer diagnosed histologically as adenocarcinoma.

Patients who meet the selection criteria should be selected, signed for consent, and treated 5 times a week for 7200 cGy / 15 fractions alone for 3 weeks.


Recruitment information / eligibility

Status Recruiting
Enrollment 36
Est. completion date December 31, 2025
Est. primary completion date December 31, 2025
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

1. Histologically diagnosed colon adenocarcinoma in primary or metastatic lesions..

2. If there is no other remote metastasis other than lung, or if there is, control is possible

3. If there are less than 2 lung metastatic lesions

4. If they refuse lung surgery or surgery is inappropriate (medically unsuitable for surgery due to surgery refusal, diabetes mellitus, high blood pressure, pulmonary disease, heart disease, etc., repeated surgery, poor systematic function, short disease-free period, etc.)

Exclusion Criteria:

1. Other histologic cancer other than adenocarcinoma of the colorectal

2. Colorectal cancer without primary lesion resection

3. If there is another remote metastasis and is not completely resected or regulated

4. If the patient has experience of other invasive cancer diagnosis within 5 years of colorectal cancer diagnosis

5. Pregnancy and women under lactation

Study Design


Intervention

Radiation:
curative proton therapy
Patients who meet the selection criteria are selected, signed for consent, and treated with proton therapy alone at 7200 cGy / 15 fractions, 5 times a week for 3 weeks

Locations

Country Name City State
Korea, Republic of National Cancer Center Korea Goyang-si Gyeonggi-do

Sponsors (1)

Lead Sponsor Collaborator
National Cancer Center, Korea

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary 3-year local control ratio of the treated lung area The primary goal of this study is the 3-year local control rate of pulmonary lesions treated with proton therapy. It is judged that the local control rate is improved when the pulmonary metastases of colorectal cancer using conventional X-ray is assumed to have 3-year local control rate of 60% and the 3-year local control rate of proton therapy is set to 80% or more up to 3 years
Secondary 3-year survival rate of treated patients To evaluate whether high doses of proton therapy can replace conventional surgical resection. From date of initiation of proton therapy until the date of documented date of death from any cause, assessed up to 3 years documented data of death, up to 3 years
Secondary 3-year disease-free survival rate of treated patients To evaluate whether high doses of proton therapy can replace conventional surgical resection. From date of initiation of proton therapy until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 3 years. documented date of progression or death, up to 3 years
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