Unique ID issued by UMIN | UMIN000039048 |
---|---|
Receipt number | R000044525 |
Scientific Title | Phase II study of VAC1.2(vincristine, actinomycin-D, cyclophosphamide) therapy for patients with newly diagnosed low-risk subset A rhabdomyosarcoma. |
Date of disclosure of the study information | 2020/01/10 |
Last modified on | 2020/01/03 10:50:35 |
Phase II study of VAC1.2(vincristine, actinomycin-D, cyclophosphamide) therapy for patients with newly diagnosed low-risk subset A rhabdomyosarcoma.
Phase II study of VAC1.2 therapy for patients with newly diagnosed low-risk subset A rhabdomyosarcoma.
Phase II study of VAC1.2(vincristine, actinomycin-D, cyclophosphamide) therapy for patients with newly diagnosed low-risk subset A rhabdomyosarcoma.
Phase II study of VAC1.2 therapy for patients with newly diagnosed low-risk subset A rhabdomyosarcoma.
Japan |
rhabdomyosarcoma
Hematology and clinical oncology | Surgery in general | Obstetrics and Gynecology |
Pediatrics | Ophthalmology | Dermatology |
Oto-rhino-laryngology | Orthopedics | Urology |
Radiology | Oral surgery | Neurosurgery |
Plastic surgery | Child |
Malignancy
NO
Determine the safety and efficacy of VAC1.2 (vincristine, actinomycin-D, cyclophosphamide) therapy and/or radiation therapy for patients with low-risk subset A rhabdomyosarcoma stratified by IRS-V risk classification.
Safety,Efficacy
Exploratory
Phase II
event free survival
overall survival
time to treatment failure
response rate of chemotherapy (for group III orbit patients)
frequency of adverse event
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Medicine |
chemotherapy 24 weeks
VAC1.2 therapy 8 cycles
vincristine 1.5mg/m2 day 1
dactinomycin 0.045mg/kg day 1
cyclophosphamide 1.2g/m2 day1
surgery
radiotherapy
Not applicable |
18 | years-old | >= |
Male and Female
1) Histologically confirmed newly diagnosed embryonal rhabdomyosarcoma (RMS), meeting criteria for low-risk subset A by IRS-V classification.
2) Age younger than 19 years old.
3) Initiation of chemotherapy within 42 days after first surgery.
4) No prior history of malignancy.
5) ECOG 0-3
6) Patients must have sufficient organ function.
7) All patients and/or their parents or legal guardians must sign a written informed consent.
1) patients with synchronous or metachronous concomitant malignancies
2) patients with prior history of chemotherapy
3) patients with prior history of radiation therapy
4) Female patients who are pregnant or breastfeeding mother
5) patients with contraindication of drugs used in this study
6) patients with Charcot-Marie-Tooth disease, varicella or pentostatin medication
7) Patients with any other inappropriate condition judged by physician
32
1st name | Hajime |
Middle name | |
Last name | Hosoi |
Kyoto Prefectural University of Medicine
Department of Pediatrics, Graduate School of Medical Science
602-8566
465 Kajii-cho, Kwaramachi-Hirokoji, Kyoto
075-251-5571
hhosoi@koto.kpu-m.ac.jp
1st name | Mitsuru |
Middle name | |
Last name | Miyachi |
Kyoto Prefectural University of Medicine
Department of Pediatrics, Graduate School of Medical Science
602-8566
465 Kajii-cho, Kwaramachi-Hirokoji, Kyoto
075-251-5571
mmiyachi@koto.kpu-m.ac.jp
Japan Rhabdomyosarcoma Study Group
Ministry of Health, Labour, and Welfare
Japanese Governmental office
Kyoto Prefectural University of Medicine
465 Kajii-cho, Kwaramachi-Hirokoji, Kyoto
075-251-5111
rinri@koto.kpu-m.ac.jp
NO
2020 | Year | 01 | Month | 10 | Day |
Unpublished
12
Completed
2004 | Year | 04 | Month | 01 | Day |
2004 | Year | 04 | Month | 23 | Day |
2004 | Year | 05 | Month | 01 | Day |
2020 | Year | 12 | Month | 28 | Day |
2020 | Year | 01 | Month | 03 | Day |
2020 | Year | 01 | Month | 03 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000044525