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| Name | Class |
|---|---|
| Ludwig-Maximilians - University of Munich | OTHER |
| University Hospital, Zürich | OTHER |
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As the most common carcinoma in men, prostate cancer is a significant tumor entity in oncology. In addition to the surgical approach, definitive radiotherapy is an equivalent therapy alternative in the non-metastatic primary situation. However, radiotherapy usually stretches over a period of several weeks (7 to 8 weeks) during which the patient receives irradiation on a daily basis. For this reason and for radiobiological considerations the total treatment time is increasingly shortened. It has been shown in several randomized phase III studies that shorting radiotherapy to about 4 weeks by increasing the single dose (so-called hypofractionation) is possible. Meanwhile there is also more data on extreme hypofractionation (max. 10 radiation sessions) available, however often times, extensive preparations are necessary (such as the invasive introduction of markers into the prostate). The current, prospective, non-randomized, multicentric, Phase II SMILE study is now testing whether the MRI-guided radiotherapy with a greatly shortened radiotherapy of the prostate over 5 radiation sessions is possible and safe.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| MR-guided Radiotherapy (5 x 7,5 Gy) | Experimental | 5 x 7,5 Gy prescribed on the PTV |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MR-guided Radiotherapy | Radiation | Total Dose 37,5 Gy, Single Dose 7,5 Gy, 5 Fractions applied in 1-2 weeks |
|
| Measure | Description | Time Frame |
|---|---|---|
| Toxicity or Discontinuation of Therapy | One of the the following events are counted as an Event (Number of Participants affected):
| Within 1 Year |
| Measure | Description | Time Frame |
|---|---|---|
| Mortality | Mortality due to study treatment or due to prostate Cancer (Number of Participants deceased) | Within 1 year and within 5 years |
| Number of Toxicities | Number and severity of urogenital or gastrointestinal toxicity |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospital of Heidelberg, Radiation Oncology | Heidelberg | 69120 | Germany |
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| ID | Term |
|---|---|
| D011471 | Prostatic Neoplasms |
| ID | Term |
|---|---|
| D005834 | Genital Neoplasms, Male |
| D014565 | Urogenital Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
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| Within 1 year and within 5 years after start of radiotherapy |
| bPFS | biochemical progression free survival | from start of radiotherapy (day 1) until PSA-relapse according to Phoenix-Criteria (Prostate-specific antigen (PSA) nadir + 2 ng/mL after radiotherapy), assessed up to 5 years |
| Hormone therapy-free Survival | Hormone therapy-free Survival | from start of radiotherapy until start of hormon treatment; maximum 3 months neoadjuvant |
| OS | overall survival | from start of radiotherapy (day 1) until death or censoring assessed up to 5 years |
| Quality of life according to EORTC QLQ-C30 | Quality of life according to EORTC QLQ-C30 | from start of radiotherapy (day 1) until end of follow-up (up to 5 years) |
| Quality of life according to EORTC QLQ-PR25 | Quality of life according to EORTC QLQ-PR25 | from start of radiotherapy (day 1) until end of follow-up (up to 5 years) |
| Symptoms and Toxicity | Symptoms and Toxicity according to NCI CTCAE (Rate) | from start of radiotherapy (day 1) until end of follow-up (up to 5 years) |
| D005832 |
| Genital Diseases, Male |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
| D011469 | Prostatic Diseases |
| D052801 | Male Urogenital Diseases |