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Toxicity and outcomes in prostate cancer patient with gleason grade 5 treated with radiotherapy

Toxicity and outcomes in Gleason grade group 5 prostate cancer treated with radical radiotherapy: An Indian multi-institutional retrospective study - GG5

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/10/037611
Enrollment
500
Registered
2021-10-27
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Health Condition 1: D- Radiation Therapy

Interventions

None listed

Sponsors

Vedang Murthy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i. Histopathological diagnosis of adenocarcinoma of prostate ii. Gleason score 9 or 10 (Gleason grade group 5) iii. Disease stage at presentation: a. Absence of distant metastasis b. Any T and N Stage iv. Treated with radical intent radiotherapy to the prostate with any fractionation v. Androgen deprivation therapy received as per standard recommended surgical or medical means vi. Completion of recommended treatment radical intent radiotherapy vii. Minimum one follow-up available from the completion of radical therapy

Exclusion criteria

Exclusion criteria: i. Treatment given with palliative intent ii. Non-completion of recommended radical radiotherapy course iii. Treatment and follow up details not available after the completion of radical therapy

Design outcomes

Primary

MeasureTime frame
Biochemical failure free survivalTimepoint: 3 monthly for 2 years and 6 monthly for 5 years

Secondary

MeasureTime frame
Distant metastasis free survivalTimepoint: 3 monthly for 2 years and 6 monthly for 5 years;Overall survivalTimepoint: 3 monthly for 2 years and 6 monthly for 5 years;Patterns of failure and recurrenceTimepoint: 3 monthly for 2 years and 6 monthly for 5 years;Prostate cancer specific survivalTimepoint: 3 monthly for 2 years and 6 monthly for 5 years;Treatment related adverse effects- acute and lateTimepoint: 3 monthly for 2 years and 6 monthly for 5 years

Countries

India

Contacts

Public ContactVedang Murthy

ACTREC, Tata Memorial Centre

vedangmurthy@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026