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SHIP36B

Study of Seed and Hormone for IntermediateRisk Prostate Cancer Clinical Significance of 36month Prostatic Biopsy - SHIP36B

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs031180274
Enrollment
309
Registered
2019-03-14
Start date
2011-07-11
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer Prostate Cancer Biopsy Pathological diagnosis

Interventions

Prostate needle biopsy is performed at 36-39 months after insertion of the small radiation source. Biopsy method is basically transrectal ultrasound guided systematic biopsy. Six systematic biopsies a
Prostate Cancer Biopsy 36-months

Sponsors

Egawa Shin
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. be enrolled to SHIP0804 study. 2. be treated with trans-perineal prostate brachytherapy. 3. have the documented informed consent before SHIP0804. 4. have the documented informed consent before the protocol biopsy at 36 months after brachytherapy.

Exclusion criteria

Exclusion criteria: 1. have been diagnosed as any PSA recurrence or clinical recurrence before the protocol biopsy at 36 months after brachytherapy. 2. be inappropriate for participation in the present study for any other reason considered by a principal investigator or clinical investigator of this study.

Design outcomes

Primary

MeasureTime frame
The group of patients who had been diagnosed prostate cancer by prostatic biopsy 36 months after seed implantation is defined as "radiation ineffective group", and the group that had not been diagnosed prostate cancer is defined as "radiation effective group", and these are abbreviated as "radiation group". Undeterminable cases are included in the radiation ineffective group. Further, the AHT group and the non-AHT group are referred to as the treatment group. As a primary outcome, biochemical recurrent free survival by the following definition is compared between radiation groups. Comparison between radiation groups is performed for each treatment group (stratified analysis). However, when the number of patients in the radiation ineffective group is 10 or less, this stratified analysis is not performed, and only comparisons between the radiation groups are performed. Definition: The period up to the earliest from either one from following cases. The period between PSA examination date recognized as PSA recurrence and seed implantation date, the date of death due to any cause, or salvage therapy starting date when some treatment is applied before the PSA recurrence. In the survival case which has not been judged to be a recurrence, it is terminated by the last PSA examination date.

Secondary

MeasureTime frame
1)Overall survival Overall survival as defined below is compared between radiation groups. The comparison between the radiation groups will be performed stratified by the treatment group. However, if the number of patients in the radiation-ineffective group is 10 or less, stratified analysis will not be performed. Definition: The period from the start date of protocol treatment to the date of death due to any cause. In addition, in the case of surviving cases, the term will be terminated halfway on the final survival confirmation date. In untraceable cases, the final survival confirmation date before the follow-up becomes untraceable will be discontinued. 2)Clinical non-recurrence survival time The clinical non-recurrence survival time as defined below is compared between radiation groups. The comparison between the radiation groups will be performed stratified by the treatment group. However, if the number of patients in the radiation-ineffective group is 10 or less, stratified analysis will not be performed. In addition, the definition of clinical recurrence follows the description in the SHIP0804 study protocol. Definition: The period from the start date of protocol treatment to the date of examination recognized as clinical recurrence or the date of death due to any cause, whichever comes earlier. Survival cases and untraceable cases with no clinical recurrence shall be the period until the final survival confirmation date. 3)Disease-specific survival time Disease-specific survival times as defined below are compared between radiation groups. The comparison between the radiation groups will be performed stratified by the treatment group. However, if the number of patients in the radiation-ineffective group is 10 or less, stratified analysis will not be performed. Definition: The period from the start date of protocol treatment to the date of death from prostate cancer. In addition, for surviving cases and untraceable cases, the term will be terminated

Contacts

Public ContactErika Umemoto

Jikei University School of Medical

ship@jikei.ac.jp+81-3-3437-2370

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026