Unique ID issued by UMIN | UMIN000019893 |
---|---|
Receipt number | R000022856 |
Scientific Title | Phase II study of biweekly cetuximab and irinotecan as third-line therapy in patients with pre-treated KRAS exon2 wild-type metastatic colorectal cancer |
Date of disclosure of the study information | 2015/11/24 |
Last modified on | 2015/11/14 15:30:45 |
Phase II study of biweekly cetuximab and irinotecan as third-line therapy in patients with pre-treated KRAS exon2 wild-type metastatic colorectal cancer
Phase II study of biweekly cetuximab and irinotecan as third-line therapy in patients with pre-treated KRAS exon2 wild-type metastatic colorectal cancer
Phase II study of biweekly cetuximab and irinotecan as third-line therapy in patients with pre-treated KRAS exon2 wild-type metastatic colorectal cancer
Phase II study of biweekly cetuximab and irinotecan as third-line therapy in patients with pre-treated KRAS exon2 wild-type metastatic colorectal cancer
Japan |
Metastatic colorectal cancer
Gastroenterology | Hematology and clinical oncology |
Malignancy
YES
To evaluate the efficacy and safety of Cetuximab and Irinotecan as third-line treatment in patients with pre-treated KRAS exon2 wild-type metastatic colorectal cancer
Safety,Efficacy
Exploratory
Phase II
Response rate
Progression free survival
Overall survival
Pharmacokinetic parameter
Safety profile
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Medicine |
Cetuximab 500 mg/M2/2week
Irinotecan 150 mg/M2/2week
20 | years-old | <= |
75 | years-old | >= |
Male and Female
Written IC.
Pathologically diagnosed colorectal adenocarcinoma.
Unresectable colorectal cancer.
No KRAS mutation (codon 12 or codon13).
Age over 20 years old and under 75 years.
ECOG PS0-2.
Target lesion(RECIST 1.0).
Previously treated within 2 regimens and
Wihtout cetuximab. at least 2 week rest.
2 months or longer expected survival.
Adequate organ function.
Receive blood infusion, G-CSF within 7days before primary registration.
UGT1A1*28 homo, *6 homo,*28*6
Severe heart disease.
Severe liver disease.
Severe lung disease.
Active gastrointestinal bleeding.
Severe mental disease.
Severe diabetes.
Ileus.
Active infectious disease.
Other active cancer.
Cerebral metastasis.
Icterus .
Severe diarrhea.
Severe allergic reaction for drugs (irinotecan anti-EGFR antibody).
Massive ascites, plerural effusion.
Under treatment with atazanavir.
Past history of treatment with EGFR antibody.
Alcoholic or drug Intoxication.
Hbs antibody positive.
HCV antibody positive.
HIV antibody positive.
A pregnant woman, a woman in breast-feeding, a man who expects his baby.
An inappropriate case judged by docter in charge.
35
1st name | |
Middle name | |
Last name | Nobuyuki Mizunuma |
The Cancer Institute Hospital, Japanese Foundation for Cancer Research
Department of Gastroenterology
3-8-31 Ariake, Koto-ku, Tokyo 135-8550, Japan
03-3520-0111
nobuyuki.mizunuma@jfcr.or.jp
1st name | |
Middle name | |
Last name | Eiji Shinozaki |
The Cancer Institute Hospital, Japanese Foundation for Cancer Research
Department of Gastroenterology
3-8-31 Ariake, Koto-ku, Tokyo 135-8550, Japan
03-3520-0111
eiji.shinozaki@jfcr.or.jp
The Cancer Institute Hospital, Japanese Foundation for Cancer Research
The Cancer Institute Hospital, Japanese Foundation for Cancer Research
Other
NO
がん研有明病院 (東京都)
2015 | Year | 11 | Month | 24 | Day |
Unpublished
Completed
2011 | Year | 06 | Month | 01 | Day |
2011 | Year | 10 | Month | 24 | Day |
2015 | Year | 11 | Month | 22 | Day |
2015 | Year | 11 | Month | 14 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022856