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Multicenter Study of Hypofractionated Postoperative Radiotherapy in Patients Diagnosed With Prostate Carcinoma

Primary Purpose

Prostate Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
hypofractionated postoperative radiation therapy
Sponsored by
Grupo de Investigación Clínica en Oncología Radioterapia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring Radiotherapy, prostate cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 years.
  • ECOG 0-1 status.
  • Previous radical prostatectomy (any modality will be allowed) with or without lymphadenectomy.
  • Histological confirmation of prostate adenocarcinoma in the prostatectomy specimen.
  • pT2-T3 Version 2.0, March 27, 2019
  • pN0-Nx
  • Indication of postoperative RT:

    • Adjuvant RT: pT3 and / or positive margins with PSA <0.2 ng / ml. Delayed RT is considered (> 6 months from the date of surgery but PSA <0.2 ng / ml).
    • Rescue RT: exclusive biochemical recurrence, without evidence of macroscopic local, regional or distant disease, after surgery. Biochemical recurrence is considered PSA ≥ 0.2 ng / ml after undetectable levels, confirmed with a subsequent determination.
  • PSA levels ≤ 2 ng / ml after, at least 45 days after surgery and 30 days before inclusion in the study.
  • No clinical evidence of lymph node disease. The presence will be admitted by imaging tests of pelvic nodes ≤ 1 cm in its shortest axis.
  • No evidence of disease in the prostatic fossa. If you doubt by digital rectal examination or CT, an MRI will be performed.
  • No evidence of distant disease after performing a thoraco-abdominal-pelvic CT scan and bone scan.
  • Reasonable follow-up possibilities.
  • Ability to complete the EPIC-26 questionnaire.
  • Written informed consent prior to inclusion in the study.

Exclusion Criteria:

  • - Previous pelvic radiation therapy.
  • Distant metastasis.
  • Macroscopic residual tumor.
  • PSA> 2 ng / ml.
  • Pathological stage T4.
  • Lymph node involvement.
  • Pelvic or para-aortic nodules in the reevaluation images after surgery, except pelvic nodes ≤ 1 cm in their shortest axis.
  • Indication of pelvic nodal RT. Version 2.0, March 27, 2019
  • Severe urinary incontinence at the time of indication for radiotherapy.
  • Uni / bilateral hip prosthesis
  • Previous tumors, except non-melanoma skin carcinoma, and which are not free of disease for at least 3 years from the end of the treatment of said neoplasms. Bladder tumors are excluded in all cases.
  • Genetic hyper-radio-sensitivity syndromes.
  • Chronic inflammatory bowel disease or partial or radical cystectomy for any reason.
  • Previously treated with androgen deprivation therapy for a period greater than 3 months.
  • Previously treated with chemotherapy for prostate cancer.
  • Life expectancy <5 years or severe comorbidity: unstable angina, congestive heart failure, transmural myocardial infarction requiring admission in the last 6 months, active infectious process, respiratory disease requiring hospitalization, liver failure (Child-Pugh Class B or C), HIV with a CD4 count <200 cells / ml, kidney failure requiring dialysis and immunosuppressed by other causes.

Sites / Locations

  • Hospital General Gregorio MarañónRecruiting
  • Hospital Universitario de San JuanRecruiting
  • ICO BadalonaRecruiting
  • Hospital Dr. NegrinRecruiting
  • Hospital Universitario de SantiagoRecruiting
  • Hospital de FuenlabradaRecruiting
  • Hospital Universitario TorrecárdenasRecruiting
  • Hospital Universitario de BadajozRecruiting
  • H. Sta. Cruz y San PabloRecruiting
  • Instituto Oncológico IMQRecruiting
  • Hospital Universitario San CecilioRecruiting
  • Hospital Universitario Ramón Y CajalRecruiting
  • Fundación Jimenez Díaz 1Recruiting
  • Fundación Jiménez Díaz 2Recruiting
  • Hospital de La PrincesaRecruiting
  • Hospital La LuzRecruiting
  • Hospital QuirónRecruiting
  • Hospital Ruber InternacionalRecruiting
  • Complejo Hospitalario de NavarraRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

IMRT, any mode

Arm Description

External radiation therapy with 6-18 MV photons on the 62.5 Gy prostate bed in 25 2.5 Gy fractions (EQD2 71 Gy). Serving per fraction: 2.5 Gy Total fractions: 25 No. fractions / week: 5 Total treatment time: 5 weeks Total nominal dose: 62.5 Gy EQD3 (TRT): 68.75 Gy EQD1.5 (CaP): 71.43 Gy EQD2 (CaP): 68.75 Gy EQD10 (TRA): 65.10 Gy

Outcomes

Primary Outcome Measures

Incidence of treatment-related gastrointestinal and genitourinary acute adverse events
using the Common Terminology Criteria for Adverse Events (CTCAE) v5.0 scale. The grades of severity from I (minimum) to V (maximum).
Incidence of late gastrointestinal and genitourinary adverse events
using the Radiation Therapy Oncology Group (RTOG) scale. The grades of severity from 1 (minimum) to 4 (maximum).

Secondary Outcome Measures

Biochemical failure-free survival
Time elapsed between the date of inclusion in the study and biochemical failure
Disease-free survival (locoregional and / or remote)
Time elapsed between the date of inclusion in the study and the detection of the disease locally, regionally and / or remotely
Overall survival
Time elapsed between the date of inclusion in the study and the patient's death from any cause
Cause-specific survival
Time elapsed between the date of inclusion in the study and the patient's death due to prostate cancer or toxicity derived from treatment
Assessment of quality of life for cancer Prostate patients
Use of Expanded Prostate Cancer Index questionnaire (EPIC) 26

Full Information

First Posted
July 15, 2020
Last Updated
July 21, 2020
Sponsor
Grupo de Investigación Clínica en Oncología Radioterapia
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1. Study Identification

Unique Protocol Identification Number
NCT04484038
Brief Title
Multicenter Study of Hypofractionated Postoperative Radiotherapy in Patients Diagnosed With Prostate Carcinoma
Official Title
Multicenter Study of Hypofractionated Postoperative Radiotherapy in Patients Diagnosed With Prostate Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Recruiting
Study Start Date
March 9, 2019 (Actual)
Primary Completion Date
March 2022 (Anticipated)
Study Completion Date
March 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Grupo de Investigación Clínica en Oncología Radioterapia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of this study is to evaluate, in patients diagnosed with prostate cancer who undergo radical prostatectomy and who require postoperative radiotherapy, tolerance in terms of acute and chronic GU and GI toxicity and efficacy in terms of biochemical control and survival, as well as of quality of life, from a hypofractional external radiotherapy scheme, increasing the dose per fraction in a shorter period of time.
Detailed Description
What the investigators present in this study is a hypofractionation scheme of 62.5 Gy in 25 daily fractions of 2.5 Gy / day, which was chosen to provide a biological equivalent dose (BED) of 166.67 Gy, comparable to the 163 Gy administered with a scheme Normally divided up to 70 Gy in daily fractions of 2 Gy / day Version 2.0, March 27, 2019 (assuming an α / β ratio of 1.5 Gy for prostate cancer). The BED in risk organs (mainly rectum and bladder) will be governed by the ratio used and will differ depending on whether acute or late toxicity is calculated. If selected an acute α / β of 10 Gy and a conservative α / β for late toxicity of 3 Gy, the standard fractionation will result in an acute BED of 84 Gy versus 78 Gy in the hypofractionation scheme and a BED of 116.67 vs. 114.5 Gy for late toxicity. Therefore, what the investigators expect is a toxicity profile that is at least similar, if not slightly better, compared to the norm-fractionated scheme of 70 Gy in 35 fractions and similar rates of biochemical control and survival. To all this is added the use of intensity modulated radiotherapy and image-guided radiotherapy techniques (IGRT) that will allow the investigators to significantly reduce the dose administered to risk organs.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Radiotherapy, prostate cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
This is a non-randomized prospective multicenter study of hypofractionated postoperative radiotherapy in patients diagnosed with prostate carcinoma.
Masking
None (Open Label)
Allocation
N/A
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
IMRT, any mode
Arm Type
Other
Arm Description
External radiation therapy with 6-18 MV photons on the 62.5 Gy prostate bed in 25 2.5 Gy fractions (EQD2 71 Gy). Serving per fraction: 2.5 Gy Total fractions: 25 No. fractions / week: 5 Total treatment time: 5 weeks Total nominal dose: 62.5 Gy EQD3 (TRT): 68.75 Gy EQD1.5 (CaP): 71.43 Gy EQD2 (CaP): 68.75 Gy EQD10 (TRA): 65.10 Gy
Intervention Type
Radiation
Intervention Name(s)
hypofractionated postoperative radiation therapy
Intervention Description
The patients included in the study will undergo intensity-modulated radiotherapy, of any modality, and image-guided (IGRT) with an emphasis on tissue preservation and administration precision through the use of devices that guarantee the stability and reproducibility of the same.
Primary Outcome Measure Information:
Title
Incidence of treatment-related gastrointestinal and genitourinary acute adverse events
Description
using the Common Terminology Criteria for Adverse Events (CTCAE) v5.0 scale. The grades of severity from I (minimum) to V (maximum).
Time Frame
≤90 days
Title
Incidence of late gastrointestinal and genitourinary adverse events
Description
using the Radiation Therapy Oncology Group (RTOG) scale. The grades of severity from 1 (minimum) to 4 (maximum).
Time Frame
up to 3 years
Secondary Outcome Measure Information:
Title
Biochemical failure-free survival
Description
Time elapsed between the date of inclusion in the study and biochemical failure
Time Frame
up to 3 years
Title
Disease-free survival (locoregional and / or remote)
Description
Time elapsed between the date of inclusion in the study and the detection of the disease locally, regionally and / or remotely
Time Frame
up to 3 years
Title
Overall survival
Description
Time elapsed between the date of inclusion in the study and the patient's death from any cause
Time Frame
up to 3 years
Title
Cause-specific survival
Description
Time elapsed between the date of inclusion in the study and the patient's death due to prostate cancer or toxicity derived from treatment
Time Frame
up to 3 years
Title
Assessment of quality of life for cancer Prostate patients
Description
Use of Expanded Prostate Cancer Index questionnaire (EPIC) 26
Time Frame
at the start of treatment at 3, 12, 24 and 36 months from the end of treatment

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years. ECOG 0-1 status. Previous radical prostatectomy (any modality will be allowed) with or without lymphadenectomy. Histological confirmation of prostate adenocarcinoma in the prostatectomy specimen. pT2-T3 Version 2.0, March 27, 2019 pN0-Nx Indication of postoperative RT: Adjuvant RT: pT3 and / or positive margins with PSA <0.2 ng / ml. Delayed RT is considered (> 6 months from the date of surgery but PSA <0.2 ng / ml). Rescue RT: exclusive biochemical recurrence, without evidence of macroscopic local, regional or distant disease, after surgery. Biochemical recurrence is considered PSA ≥ 0.2 ng / ml after undetectable levels, confirmed with a subsequent determination. PSA levels ≤ 2 ng / ml after, at least 45 days after surgery and 30 days before inclusion in the study. No clinical evidence of lymph node disease. The presence will be admitted by imaging tests of pelvic nodes ≤ 1 cm in its shortest axis. No evidence of disease in the prostatic fossa. If you doubt by digital rectal examination or CT, an MRI will be performed. No evidence of distant disease after performing a thoraco-abdominal-pelvic CT scan and bone scan. Reasonable follow-up possibilities. Ability to complete the EPIC-26 questionnaire. Written informed consent prior to inclusion in the study. Exclusion Criteria: - Previous pelvic radiation therapy. Distant metastasis. Macroscopic residual tumor. PSA> 2 ng / ml. Pathological stage T4. Lymph node involvement. Pelvic or para-aortic nodules in the reevaluation images after surgery, except pelvic nodes ≤ 1 cm in their shortest axis. Indication of pelvic nodal RT. Version 2.0, March 27, 2019 Severe urinary incontinence at the time of indication for radiotherapy. Uni / bilateral hip prosthesis Previous tumors, except non-melanoma skin carcinoma, and which are not free of disease for at least 3 years from the end of the treatment of said neoplasms. Bladder tumors are excluded in all cases. Genetic hyper-radio-sensitivity syndromes. Chronic inflammatory bowel disease or partial or radical cystectomy for any reason. Previously treated with androgen deprivation therapy for a period greater than 3 months. Previously treated with chemotherapy for prostate cancer. Life expectancy <5 years or severe comorbidity: unstable angina, congestive heart failure, transmural myocardial infarction requiring admission in the last 6 months, active infectious process, respiratory disease requiring hospitalization, liver failure (Child-Pugh Class B or C), HIV with a CD4 count <200 cells / ml, kidney failure requiring dialysis and immunosuppressed by other causes.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
ASUNCION R HERVAS, Investigator
Phone
0034649039866
Email
ahervas.hrc@salud.madrid.org
First Name & Middle Initial & Last Name or Official Title & Degree
ADELA MARIA López, Data Manager
Phone
0034656303686
Email
adelamaria.lopez@salud.madrid.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
ASUNCION R HERVAS, I
Organizational Affiliation
Ramon y Cajal University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital General Gregorio Marañón
City
Madrid
State/Province
Adrid
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
CARMEN GONZALEZ SANSEGUNDO, INVESTIGATOR
Phone
+34915868000
Ext
+34915868000
Email
cglezss@gmail.com
First Name & Middle Initial & Last Name & Degree
ANA ALVAREZ, INVESTIGATOR
Phone
+34915868000
Ext
+34915868000
Email
analvagonza@gmail.com
Facility Name
Hospital Universitario de San Juan
City
San Juan
State/Province
Alicante
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sandra González Montiel, Investigator
Phone
+34965169400
Email
Sandra.19792@gmail.com
Facility Name
ICO Badalona
City
Badalona
State/Province
Barcelona
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ana Álvarez García, Investigator
Phone
+34932607733
Email
ana.alvarez@iconcologia.net
Facility Name
Hospital Dr. Negrin
City
Las Palmas de Gran Canaria
State/Province
Gran Canaria
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juan Ignacio Rodriguez Melcón, Investigator
Phone
+34928450284
Email
nachorodriguezmelcon@gmail.com
Facility Name
Hospital Universitario de Santiago
City
Santiago de Compostela
State/Province
La Coruña
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ana María Carballo Castro, Investigator
Phone
+34981950000
Email
ana.maria.carballo.castro@sergas.es
Facility Name
Hospital de Fuenlabrada
City
Fuenlabrada
State/Province
Madrid
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Begoña Caballero
Phone
+34916006581
Email
begocaba@gmail.com
Facility Name
Hospital Universitario Torrecárdenas
City
Almería
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carmen Cano Soler, Investigator
Phone
+34950016000
Email
canosolercar@gmail.com
Facility Name
Hospital Universitario de Badajoz
City
Badajoz
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julia Muñoz García, Investigator
Phone
+34924218100
Email
jlmunozgarcia@gmail.com
Facility Name
H. Sta. Cruz y San Pablo
City
Barcelona
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gemma Sancho Pardo, Investigator
Phone
+34932919000
Email
gsancho@santpau.cat
Facility Name
Instituto Oncológico IMQ
City
Bilbao
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Clara Eito Valdovinos, Investigator
Phone
+34944755000
Email
c.eito@imq.es
Facility Name
Hospital Universitario San Cecilio
City
Granada
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Antonio Lazo Prados, Investigator
Phone
0034958023000
Email
anlaparados@gmail.com
Facility Name
Hospital Universitario Ramón Y Cajal
City
Madrid
ZIP/Postal Code
2834
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
ASUNCIÓN R HERVAS, Investigator
Email
ahervas.hrc@salud.madrid.org
First Name & Middle Initial & Last Name & Degree
ADELA MARIA López, Data Manager
Phone
0034656303686
Email
adelamaria.lopez@salud.madrid.org
Facility Name
Fundación Jimenez Díaz 1
City
Madrid
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jesús Olivera, Investigator
Phone
+34915504800
Email
jolivera@fjd.es
Facility Name
Fundación Jiménez Díaz 2
City
Madrid
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Walter Vasquez Rivas, Investigator
Phone
+34915494058
Email
walter.vasquez@quironsalud.es
Facility Name
Hospital de La Princesa
City
Madrid
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Almudena Zapatero, Investigator
Phone
+34915202315
Email
almudena.zapatero@salud.madrid.org
Facility Name
Hospital La Luz
City
Madrid
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luis L Guerrero Gómez, Investigator
Phone
+34914521900
Email
leoguerrero01@gmail.com
Facility Name
Hospital Quirón
City
Madrid
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Felipe Couñago Lorenzo, Investigator
Phone
+34914521900
Email
fcounago@gmail.com
Facility Name
Hospital Ruber Internacional
City
Madrid
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aurora Rodríguez Pérez, INVESTIGATOR
Phone
0034913875288
Email
aurora.rodriguezp@ruberinternacional.es
Facility Name
Complejo Hospitalario de Navarra
City
Pamplona
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marta Barrado Los Arcos, Investigator
Phone
+34848428482
Email
marta.barrado.losarcos@navarra.es
First Name & Middle Initial & Last Name & Degree
Margarita Illas Pérez-Mosso, Investigator
Phone
+34848428482
Email
margarita.illas.perezmosso@navarra.es

12. IPD Sharing Statement

Plan to Share IPD
No

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Multicenter Study of Hypofractionated Postoperative Radiotherapy in Patients Diagnosed With Prostate Carcinoma

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