Unique ID issued by UMIN | UMIN000027581 |
---|---|
Receipt number | R000031510 |
Scientific Title | Safety and efficacy of neoadjuvant hormone therapy with combination of Estramustine Phosphate Sodium Hydrate and LH-RH agonist for high-risk prostate cancer treated with intensity modulated radiotherapy |
Date of disclosure of the study information | 2017/05/31 |
Last modified on | 2020/01/06 10:42:33 |
Safety and efficacy of neoadjuvant hormone therapy with combination of Estramustine Phosphate Sodium Hydrate and LH-RH agonist for high-risk prostate cancer treated with intensity modulated radiotherapy
neoadjuvant hormone therapy with combination of Estramustine Phosphate Sodium Hydrate for high-risk prostate cancer
Safety and efficacy of neoadjuvant hormone therapy with combination of Estramustine Phosphate Sodium Hydrate and LH-RH agonist for high-risk prostate cancer treated with intensity modulated radiotherapy
neoadjuvant hormone therapy with combination of Estramustine Phosphate Sodium Hydrate for high-risk prostate cancer
Japan |
prostate cancer
Urology |
Malignancy
NO
We evaluate biochemical free survival for patients with high-risk prostate cancer who treated with neoadjuvant hormone therapy combined Estramustine Phosphate Sodium Hydrate and LH-RH agonist before intensity modulated radiotherapy
Efficacy
biochemical recurrence free survival
progression free survival, over all survival
Interventional
Single arm
Non-randomized
Open -no one is blinded
Self control
1
Treatment
Medicine |
A principal investigator or subinvestigators make a decision of an agent for neodjuvant hormone therapy. Participants are treated with neoadjuvant hormone therapy for 6 months before intensity modulated radiotherapy. After radiotherapy they are folled for maximum 36 months without any hormone or anticancer agents.
20 | years-old | <= |
Not applicable |
Male
1)PSA>20 or Gleason scores>=8 or Tumor stage T2c~T3(high risk prsotate cancer)
2)patients without history of hormone hterapies
3)ECOG Performance Status:0-1
4)patient's agreement to this study
5)men aged 20 years and older
1)patinets with another active cancers
2)patinets with severe cardiovascular diseases and diabetis militus
3)patients treated with 5a-reductase inhibitors for prostate hyperplasia
4)patientes treated with adrenocortical steroids
5)patinets with another anticancer agents
6)patients ineligible for this study judged by investigators
100
1st name | Yoshhide |
Middle name | |
Last name | Kawasaki |
Tohoku University Graduate School of Medicine
Department of Urology
9808574
Seiryo-Machi 1-1 Aoba-Ku Sendai
022-717-7278
kawasaki@uro.med.tohoku.ac.jp
1st name | Yoshhide |
Middle name | |
Last name | Kawasaki |
Tohoku University Graduate School of Medicine
Department of Urology
9808574
Seiryo-Machi 1-1 Aoba-Ku Sendai
022-717-7278
kawasaki@uro.med.tohoku.ac.jp
Tohoku University
Self funding
Self funding
Tohoku University Graduate School of Medicine
Seiryo-Machi 1-1 Aoba-Ku Sendai
022-717-7278
kawasaki@uro.med.tohoku.ac.jp
NO
2017 | Year | 05 | Month | 31 | Day |
This study was terminated because there were not any enrolled cases.
Unpublished
This study was terminated because there were not any enrolled cases.
0
This study was terminated because there were not any enrolled cases.
2020 | Year | 01 | Month | 06 | Day |
This study was terminated because there were not any enrolled cases.
This study was terminated because there were not any enrolled cases.
This study was terminated because there were not any enrolled cases.
This study was terminated because there were not any enrolled cases.
Terminated
2012 | Year | 12 | Month | 01 | Day |
2017 | Year | 06 | Month | 15 | Day |
2017 | Year | 11 | Month | 30 | Day |
2017 | Year | 11 | Month | 30 | Day |
2017 | Year | 11 | Month | 30 | Day |
2017 | Year | 11 | Month | 30 | Day |
2017 | Year | 11 | Month | 30 | Day |
2017 | Year | 05 | Month | 31 | Day |
2020 | Year | 01 | Month | 06 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031510