Radical Hypofractionated Radiotherapy for Localized Prostate Cancer
The aim of this trial is to study the safety outcomes of hypofractionated radiotherapy in treating patients with localized prostate cancer. Hypofractionated radiotherapy delivers higher doses of radiotherapy in a shorter time period, may enabling the killing of more tumor cells with fewer side effects. Accumulating evi
| Condition(s) | Localized Prostate Cancer |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | The aim of this trial is to study the safety outcomes of hypofractionated radiotherapy in treating patients with localized prostate cancer. Hypofractionated radiotherapy delivers higher doses of radiotherapy in a shorter time period, may enabling the killing of more tumor cells with fewer side effects. Accumulating evidence has proven the safety and feasibility of hypofractionated radiotherapy for localized prostate cancer.But for localized prostate cancer,the optimal dose per fraction of hypofractionated radiotherapy is still on its way. |
| Who can participate | Inclusion Criteria: * Age: ≥18 years old; * European Cooperative Oncology Group score(ECOG):≤ 2; * Patients with pathologically diagnosed prostate cancer; * Clinical stage was cTanyN0M0 any Gleason / ISUP group; * Expected survival time \>5 years; * The patient has no contraindications to radiotherapy and is suitable and willing to undergo radiotherapy; * Patients who voluntarily accept the experimental study protocol after being informed about the existing treatment options; Exclusion Criteria: * Patients who have received any other early treatment for prostate cancer, including radiotherapy, chemotherapy, focal therapy, etc; * a previous history of pelvic and abdominal radiotherapy; * Prior hormonal therapy (castration or antiandrogen); * Patients with other malignancies and acute or chr |
| Ages | 18 Years |
| Sex | Male |
| Lead sponsor | Changhai Hospital |
| Locations | Shanghai, Shanghai Municipality, China |
| Start date | 2024-09-01 |
| NCT ID | NCT06325774 |
| Official listing | https://clinicaltrials.gov/study/NCT06325774 |