Unique ID issued by UMIN | UMIN000013882 |
---|---|
Receipt number | R000016196 |
Scientific Title | A Randomized, phase 2 study comparing irinotecan versus amrubicin as maintenance therapy after first-line induction therapy for extensive disease small-cell lung cancer HOT1401/NJCLG1401 |
Date of disclosure of the study information | 2014/06/10 |
Last modified on | 2019/05/07 11:35:38 |
A Randomized, phase 2 study comparing irinotecan versus amrubicin as maintenance therapy after first-line induction therapy for extensive disease small-cell lung cancer HOT1401/NJCLG1401
Randomized P2 ED SCLC maintenance CPT vs AMR
A Randomized, phase 2 study comparing irinotecan versus amrubicin as maintenance therapy after first-line induction therapy for extensive disease small-cell lung cancer HOT1401/NJCLG1401
Randomized P2 ED SCLC maintenance CPT vs AMR
Japan |
chemotherapy-naive extensive disease small-cell lung cancer
Pneumology |
Malignancy
NO
To evaluate the efficacy and safety of amrubicin versus irinotecan as maintenance therapy to be performed subsequent to initial chemotherapy with cisplatin and irinotecan for extensive disease small cell lung cancer.
Safety,Efficacy
Exploratory
Pragmatic
Phase II
progression free survival rate at 6 months
progression free survival, overall survival,progression free survival of maintenance therapy, adverse events, 1 year survival rate, transition rate to maintenance therapy
Interventional
Parallel
Randomized
Individual
Open -but assessor(s) are blinded
Active
YES
YES
Institution is not considered as adjustment factor.
NO
Central registration
2
Treatment
Medicine |
Patients receive induction therapy of cisplatin plus irinotecan followed by irinotecan maintenance therapy (60mg/m2, day1,8, every 3 weeks).
Patients receive induction therapy of cisplatin plus irinotecan followed by amrubicin maintenance therapy (35mg/m2, day1-3, every 3 weeks).
20 | years-old | <= |
75 | years-old | > |
Male and Female
1) non-small-cell lung cancer
2) Chemotherapy-naive
3) Radiotherapy-naive
4) IIIB to IV or postoperative recurrent without indication of resection or radiation.
5) ECOG-PS 0 or 1 or 2
6) Measurable lesion by RECIST ver.1.1 criteria
7) Adequate organ function
8) Life expectancy more than 3 months
9) Written informed consent
1) Clinically active interstitial pneumonia or pulmonary fibrosis, detectable on CT scan
2) History of heart disorder.
3) Severe co-morbidities (ex. uncontrolled heart or lung or hepatic or renal disease or diabetes)
4) Regular use of corticosteroid (less than 2 weeks interval after cessation)
5) Pregnancy or lactation, or those who decline contraception
6) Contraindication with chemotherapy
7) Active concomitant malignancy. Except carcinoma in situ or those who did not relapse 5-years or more
8) Those judged to be not suitable by the attending physician
80
1st name | |
Middle name | |
Last name | Naoto Morikawa |
Iwate Medical University School of Medicine
Division of Pulmonary Medicine, Allergy, and Rheumatology, Department of Internal Medicine
19-1, Uchimaru, Morioka,Iwate, 020-8505, JAPAN
+81-19-651-5111(2334)
carcinoma@nifty.com
1st name | |
Middle name | |
Last name | Hisashi Tanaka |
Hirosaki University Graduate School of Medicine
Cardiology, Respiratory medicine and Nephrology
5 Zaifu-cho Hirosaki city, Aomori Prefecture, JAPAN
0172-39-5057
xyghx335@gmail.com
North Japan Lung Cancer Study Group and Hokkaido Lung Cancer Clinical Study Group
Iwate Medical University School of Medicine
Self funding
YES
NJLCG1401
North Japan Lung Cancer Study Group
HOT1401
Hokkaido Lung Cancer Clinical Study Group
2014 | Year | 06 | Month | 10 | Day |
Unpublished
Terminated
2014 | Year | 05 | Month | 02 | Day |
2014 | Year | 07 | Month | 14 | Day |
2014 | Year | 07 | Month | 20 | Day |
2018 | Year | 07 | Month | 20 | Day |
2018 | Year | 10 | Month | 20 | Day |
2018 | Year | 10 | Month | 20 | Day |
2019 | Year | 03 | Month | 31 | Day |
2014 | Year | 05 | Month | 03 | Day |
2019 | Year | 05 | Month | 07 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000016196