Hyperthermia Clinical Trial
Official title:
Effectiveness of the Combined Whole Liver Irradiation (WLI) and Hyperthermia for Unresectable Chemoresistant Multiple Liver Metastasis From Gastrointestinal Tract Cancer: Prospective Phase II Trial
Verified date | August 2014 |
Source | Samsung Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The standard treatment of unresectable liver metastasis in gastrointestinal tract cancer is
chemotherapy, but considerable portion of the patients progressed and most of the liver is
converted to metastatic tumor lesions. Significant quality of life decrement was detected in
those patients, especially in patients suffered severe symptoms Several studies reported that
whole liver RT (WLRT) can be used effectively to control severe symptoms from unresectable
liver metastasis in gastrointestinal tract cancer patients. However, it is well known fact
that the liver is a very sensitive to RT. Despite symptom palliation is obtained after 20 to
30 Gy RT but only in small subset of patients get local control. In this aspect, the combined
with radiosensitizer with WLRT is considered to enhance RT effect to palliate symptom and
control local tumor progression, and increase the quality of life ultimately.
It is reported that hyperthermia is considered as the most valuable radiosensitizer in cancer
treatment, theoretically. Based on those studies, we start this prospective study to
investigate the effect of combination treatment of WLRT and hyperthermia on quality of life
in the patients with unresectable chemoresistant liver metastasis from gastrointestinal tract
cancer.
Status | Terminated |
Enrollment | 11 |
Est. completion date | April 2015 |
Est. primary completion date | November 2014 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years and older |
Eligibility |
Inclusion Criteria: - 1 Patients must have a diagnosis of pathologic proven gastrointestinal tract cancer - 2 Unresectable and unsuitable to other local modalities - 3 Not responded and/or unsuitable to chemotherapy - 4 Eastern Cooperative Oncology Group ECOG) performance status 0 to 3 - 5 Assessment by colorectal tumor board (surgeon, radiation oncologist and medical oncologist participated) - 6 Age = 20 - 7 Agreement of study-specific informed consent - 8 Blood work requirements - Absolute neutrophil count (ANC) = 1,500 /mm3, Platelet = 50,000/mm3, Hgb = 8 g/dl - Liver function test(LFT): Total bilirubin<3.0 mg/dL, International normalized ratio(INR) < 1.7, Albumin = 2.8g/dL, Aspartate aminotransferase (AST)/Alanine aminotransferase (ALT)< 6 X normal - Serum creatinine < 1.5 X normal, or Creatinine clearance rate (CCr) = 60 mL/min - 9 Child-Pugh score 10 or less within 1 week before WLI - 10 Childbearing potential woman, consent contraception at least 6 months - 11 Stable breathing more than 5 minutes Exclusion Criteria: - 1 Life expectancy less than 8 weeks - 2 Pregnant and/or breastfeeding woman - 3 Previous upper abdominal RT history - 4 Uncontrolled ascites or hepatic encephalopathy - 5 Unstable respiration due to pleural effusion, chronic obstructive pulmonary disease COPD) etc |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Samsung Medical Center | Seoul |
Lead Sponsor | Collaborator |
---|---|
Samsung Medical Center |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time to Local Tumor Progression After Combined Hyperthermia and RT | Local progression will be defined as more than 20% size increase of metastatic lesions or new metastatic lesion in liver. Time to local tumor progression will be measured from the date of RT start to the date of local progression or last follow-up visit. | Patient will be evaluated after combined hyperthermia and RT until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 19 months. | |
Secondary | Objective Response Rate of Combined Hyperthermia and RT | Response will be evaluated at 3 month after combined hyperthermia and RT. Modified RECIST will be used to define resopnse. | ||
Secondary | Change in the Grade of Quality of Life at 3 Months From That Before the Combined Hyperthermia and RT | To measure the quality of life, European Organisation for Research and Treatment of Cancer (EORTC)- quality of life questionnaire (QLQ) 30 and Functional Assessment of Cancer Therapy-Hepatobiliary will be used. (grade 1 to 4, 1; not at all, 2; a little, 3; quite a bit, 4; very much) | Quality of life will be ssessed at baseline and 3 months after combined hyperthemica and RT, data reported 3 months after combined hyperthemica and RT with grade from 1 to 4. | |
Secondary | Local Tumor Progression Free Survival Rate After Combined Hyperthermia and RT | Local progression will be defined as more than 20% size increase of metastatic lesions or new metastatic lesion in liver. Local progression free survival will be measured from the date of RT start to the date of local progression or last follow-up visit. | Response will be evaluated at 3 month after combined hyperthermia and RT. Modified RECIST will be used to define resopnse. | |
Secondary | Adverse Event After Combined Hyperthermia and RT. | All grade III or higher toxicities (repeated measure) | Adverse event will be evaluated at 3 month. The common terminology criteria for adverse events (CTCAE) version 4.0 will be used. | |
Secondary | Overall Survival Rate After Combined Hyperthermia and RT | Overall survival will be measured from the date of RT start to the date of death or last follow-up visit. | Pathient will be evaluated at 3 month after combined hyperthermia and RT. |
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