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Carbon Ion Followed by Proton Radiotherapy for Prostate Cancer With Pelvic Lymph Nodes Metastases

Primary Purpose

Prostate Cancer

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
proton plus carbon ion radiation
Sponsored by
Shanghai Proton and Heavy Ion Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring Carbon ion, Proton, prostate cancer, pelvic lymph nodes metastases

Eligibility Criteria

45 Years - 85 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologically proven initial diagnosis of adenocarcinoma of the prostate;
  • Clinical stage T1-4 N0 M0;
  • Prostatic assessment by multiparametric (mp) MRI;
  • Pelvic lymph node was assessed by PSMA PET/CT and mpMRI;
  • No distant metastasis was proven by PSMA PET/CT;
  • Patients may received neoadjuvant hormonal therapy;
  • 45≤ Age ≤85;
  • Adequate performance status (ECOG 0-1);
  • No previous pelvic radiation therapy (RT);
  • No previous prostatectomy;
  • No previous invasive cancer (within 5 years before the prostate cancer diagnosis);
  • Ability to understand character and individual consequences of the clinical trial;
  • Written informed consent;

Exclusion Criteria:

  • No pathologically confirmed adenocarcinoma of the prostate;
  • Distant metastasis (M1);
  • Previous pelvic radiotherapy;
  • Previous prostatectomy;

Sites / Locations

  • Shanghai Proton and Heavy Ion CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Carbon ion followed by Proton radiotherapy

Arm Description

All patients received whole pelvis and prostate region radiotherapy. The dose to metastatic LN was escalated using simultaneous integrated boost (SIB) technique.

Outcomes

Primary Outcome Measures

Biochemical relapse free survival
The prostate specific antigen less than nadir plus 2ng/ml (Phoenix definition)

Secondary Outcome Measures

Progression free survival
The time from start of systemic therapy to tumor progression or death
Overall survival
The time from diagnosis to death from any cause
Metastasis free survival
The time from start of systemic therapy to tumor metastatsis.
Acute toxicities
Treatment related acute toxicity assessed by Common Terminology Criteria for Adverse Events (CTCAE) version 4.03
Late toxicities
Treatment related late toxicity assessed by Radiation Therapy Oncology Group (RTOG) scale

Full Information

First Posted
October 24, 2021
Last Updated
October 24, 2021
Sponsor
Shanghai Proton and Heavy Ion Center
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1. Study Identification

Unique Protocol Identification Number
NCT05106699
Brief Title
Carbon Ion Followed by Proton Radiotherapy for Prostate Cancer With Pelvic Lymph Nodes Metastases
Official Title
Carbon Ion Boost Followed by Pelvic Proton Radiotherapy for Prostate Cancer With Pelvic Lymph Nodes Metastases: Prospective Phase II Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Recruiting
Study Start Date
June 8, 2021 (Actual)
Primary Completion Date
May 31, 2025 (Anticipated)
Study Completion Date
May 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Proton and Heavy Ion Center

4. Oversight

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

5. Study Description

Brief Summary
The present of clinically pelvic lymph node positive (cN1) represent one of the most important prognostic factors for recurrence and cancer-specific mortality of prostate cancer patients. Approximately 12% of prostate cancer patients present with cN1 disease at the time of diagnosis. Furthermore, with the advent of more sensitive advance diagnostic imaging techniques, such as PSMA PET/CT, the likelihood that pelvic nodes will be found earlier and more frequently. Unfortunately, The optimal treatment for patients with cN1 still remains unclear. Androgen deprivation therapy (ADT) is the cornerstone of prostate cancer with pelvic lymph node metastasis. Some retrospective and database studies have shown that addition of local radiotherapy (RT) to ADT improve the treatment outcome. The 2022 NCCN guideline recommend RT combined with 2 to 3 years ADT in patients with initially diagnosed cN1 prostate cancer who have a life expectancy greater than 5 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Carbon ion, Proton, prostate cancer, pelvic lymph nodes metastases

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
54 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Carbon ion followed by Proton radiotherapy
Arm Type
Experimental
Arm Description
All patients received whole pelvis and prostate region radiotherapy. The dose to metastatic LN was escalated using simultaneous integrated boost (SIB) technique.
Intervention Type
Radiation
Intervention Name(s)
proton plus carbon ion radiation
Intervention Description
All patients received whole pelvis and prostate region proton irradiation of 46 GyE in 23 fractionsfollowed by localized carbon ion irradiation of 32GyE in 8 fractions to the prostate region. The dose to metastatic LN was escalated using simultaneous integrated boost (SIB) technique. The dose was 60-62.1GyE in 23 fractions as much as dose constraints. All patients will be recommened receive 2-3 years endocrine therapy.
Primary Outcome Measure Information:
Title
Biochemical relapse free survival
Description
The prostate specific antigen less than nadir plus 2ng/ml (Phoenix definition)
Time Frame
From the start of systemic therapy, a median of 3 years
Secondary Outcome Measure Information:
Title
Progression free survival
Description
The time from start of systemic therapy to tumor progression or death
Time Frame
From the start of systemic therapy, a median of 3 years
Title
Overall survival
Description
The time from diagnosis to death from any cause
Time Frame
From the start of systemic therapy, a median of 3 years
Title
Metastasis free survival
Description
The time from start of systemic therapy to tumor metastatsis.
Time Frame
From the start of systemic therapy, a median of 3 years
Title
Acute toxicities
Description
Treatment related acute toxicity assessed by Common Terminology Criteria for Adverse Events (CTCAE) version 4.03
Time Frame
Within 3 months of the start of particle therapy
Title
Late toxicities
Description
Treatment related late toxicity assessed by Radiation Therapy Oncology Group (RTOG) scale
Time Frame
3 months after the completion of particle therapy

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically proven initial diagnosis of adenocarcinoma of the prostate; Clinical stage T1-4 N0 M0; Prostatic assessment by multiparametric (mp) MRI; Pelvic lymph node was assessed by PSMA PET/CT and mpMRI; No distant metastasis was proven by PSMA PET/CT; Patients may received neoadjuvant hormonal therapy; 45≤ Age ≤85; Adequate performance status (ECOG 0-1); No previous pelvic radiation therapy (RT); No previous prostatectomy; No previous invasive cancer (within 5 years before the prostate cancer diagnosis); Ability to understand character and individual consequences of the clinical trial; Written informed consent; Exclusion Criteria: No pathologically confirmed adenocarcinoma of the prostate; Distant metastasis (M1); Previous pelvic radiotherapy; Previous prostatectomy;
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ping Li, M.D.
Phone
+86-021-38296666
Email
ping.li@sphic.org.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Qing Zhang, M.D.
Organizational Affiliation
Shanghai Proton and Heavy Ion Center
Official's Role
Study Director
Facility Information:
Facility Name
Shanghai Proton and Heavy Ion Center
City
Shanghai
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ping Li
Phone
+86-021-38296666
Email
ping.li@sphic.org.cn
First Name & Middle Initial & Last Name & Degree
Qing Zhang
Email
qing.zhang@sphic.org.cn

12. IPD Sharing Statement

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Carbon Ion Followed by Proton Radiotherapy for Prostate Cancer With Pelvic Lymph Nodes Metastases

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