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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02290574
Other study ID # 2014-10-019
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date November 2014
Est. completion date March 2016

Study information

Verified date October 2019
Source Samsung Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators start this prospective study to evaluate the efficacy of laparoscopic total mesorectal excision after concurrent chemo-radiation therapy with hyperthermia in locally advanced rectal cancer.


Description:

The current standard treatment of locally advanced rectal cancer is neoadjuvant concurrent chemo-radiation therapy (CCRT) followed by total mesorectal excision (TME). Recently, laparoscopic surgery is getting substitute open surgery based on the advantages of early recovery, short admission, less pain, less blood loss, and little scar without compromising oncologic outcomes.

It is reported that hyperthermia is effective in synthetic (S) phase, Low oxgen pressure, acidic, and low perfusion site which are known as radio-resistant. Because of these characteristics, it considered as the most valuable radiosensitizer in cancer treatment, theoretically. Furthermore, mild hyperthermia (41 to 41.5 ÂșC) can promote tumor reoxygenation.

Based on those background, the investigators start this prospective study to evaluate the efficacy of laparoscopic TME after CCRT with hyperthermia in locally advanced rectal cancer.


Recruitment information / eligibility

Status Terminated
Enrollment 14
Est. completion date March 2016
Est. primary completion date March 2016
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- 20 years or older

- pathologically confirmed rectal cancer

- Eastern Cooperative Oncology Group performance status 0 to 2

- Candidate of laparoscopic TME

- Optimal bone marrow function

- Locally advanced rectal cancer confirmed by magnetic resonance imaging

Exclusion Criteria:

- Extrapelvic metastasis

- Previous pelvic irradiation

- Current status of pregnant or breast feeding

- Confirmed other malignancy within two years except thyroid cancer

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
Hyperthermia with concurrent chemo-radiation therapy


Locations

Country Name City State
Korea, Republic of Samsung Medical Center Seoul

Sponsors (1)

Lead Sponsor Collaborator
Samsung Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Curative Resection Rate of Laparoscopic TME Curative resection rate of laparoscopic TME after CCRT and hyperthermia treament expected average of 6 weeks after neoadjuvant treatement
Primary Pathologic Response of Thermo-radio-chemotherapy The pathologic response was assessed according to the Dworak's system. The pathologic response grades were as follows: grade 0, no response; grade 1, dominant tumor mass with obvious fibrosis, vasculopathy, or both (minimal response); grade 2, dominant fibrotic changes with a few easy-to-find tumor cells or groups (moderate response); grade 3, few (difficult to find microscopically) tumor cells in fibrotic tissue with or without mucous substance (near complete response); and grade 4, no viable tumor (complete response) expected average of 6 weeks after neoadjuvant treatement
Primary Adverse Event of Laparoscopic TME and Hyperthermia With CCRT Adverse event according to CTCAE V 4.0 after laparoscopic TME and hyperthermia with CCRT expected average of 16 weeks after neoadjuvant treatement
Secondary Rate of Open TME Rate of open TME was measured as ten percent expected average of 6 weeks after neoadjuvant treatement
Secondary Pathologic Complete Response of Hyperthermia With CCRT Pathologic complete response of hyperthermia with CCRT was achieved in 20% of participants expected average of 6 weeks after neoadjuvant treatement
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