Post SBRT Pulmonary Metastasectomy (PSPM) Trial (PSPM)
Primary Purpose
Surgical Resection, Stereotactic Body Radiotherapy, Lung Cancer
Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Surgical resection and stereotactic body radiation therapy (SBRT)
Sponsored by
About this trial
This is an interventional treatment trial for Surgical Resection focused on measuring Surgical resection, Stereotactic body radiation therapy, Pulmonary metastasectomy, Lung Cancers
Eligibility Criteria
Inclusion Criteria:
- Patient age >18, resectable pulmonary metastases without a more effective systemic therapy option (regardless of type of primary malignancy, excluding hematologic malignancies) with the primary malignancy already having been treated without evidence of local recurrence
- Patient having single-organ metastasis to lung only (with the exception of colorectal CA (Cancer) with synchronous hepatic metastasis)
- Tumors <5cm
- Patient with no evidence of nodal disease on pre-treatment CT scan
- Patient having adequate pulmonary function to tolerate lung resection (post-operative predictive FEV1≥40%).
Exclusion Criteria:• Patient having comorbidities not amenable to surgery
- Patient with uncontrolled primary malignancy
- Patient with hematologic malignancies (leukemia or lymphoma)
- Patient having more than 5 tumors in one lung
- Patient with prior history of thoracic radiation
- Patient having history of lung cancer diagnosis within 5 years of assessment
Sites / Locations
- McMaster University/St. Joseph's Hospital HealthcareRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
SBRT followed by pulmonary metastasectomy
Arm Description
SBRT+Surgery
Outcomes
Primary Outcome Measures
Rates of complete pathologic response (pCR)
pCR in surgical specimens post SBRT as assessed using the Junker grading scale for lung malignancies: Grade I, no regression or only spontaneous tumor regression; Grade II, morphologic evidence of tumor regression with at least 10% (grade IIa) or <10% (grade IIb) viable tumor tissue; and Grade III, complete tumor regression with no viable tumor.
Secondary Outcome Measures
Overall survival (OS)
Followup over all survival (OS) at 3 years
Disease-free survival (DFS)
Followup over all survival (OS) at 3 years. Based on 1. clinical 2. CT scan results
local recurrence rates
CT scan at follow-up
Radiation related toxicity
Follow Radiation Therapy Oncology Group (RTOG) Common Toxicity Criteria (Cox, 1995)
Postoperative pulmonary complication rate (including prolonged air leak, need for invasive or noninvasive mechanical ventilation, postop pneumonia and empyema)
Using Society of Thoracic Surgery (STS) Database
The effect on time-to-resection and tumour histology on pCR
Time analysis
Identify mRNA tumor markers by Circulating Tumor Cell/CTC test
Identify mRNA tumor markers for circulating tumor cell/CTC detection from blood sample to get cancer specific tumor biomarkers correlate with SBRT effects including different targeted gene such MUC1, HER2, EPCAM, ER/PR for Breast Cancer, PSA, PSMA, EGFR, AR for Prostate Cancer, EPCAM, EGFR, CEA for Colon Cancer, EPCAM, MUC1, CA125, ERCC1 for Ovarian Cancer and Stemcell . The CTC test will be doing to get information about whether or not disease has disseminated from the primary site and mainly as a prognostic and/or predictive marker in the metastatic settings. This test will be done in baseline or Pre SBRT, Post SBRT and Post Surgery.
Full Information
NCT ID
NCT04160143
First Posted
October 29, 2019
Last Updated
February 23, 2021
Sponsor
McMaster University
1. Study Identification
Unique Protocol Identification Number
NCT04160143
Brief Title
Post SBRT Pulmonary Metastasectomy (PSPM) Trial
Acronym
PSPM
Official Title
Evaluating the Histologic Effects of Neoadjuvant Stereotactic Body Radiation Therapy (SBRT) Followed by Pulmonary Metastasectomy-Post SBRT Pulmonary Metastasectomy (PSPM) Trial
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Recruiting
Study Start Date
July 14, 2020 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The goal of this study is to determine the effectiveness of SBRT on reducing tumor viability at a pathologic level and also to evaluate the effects of combined modality treatment on low volume pulmonary metastases, in hopes of extrapolating this information to both primary and secondary lung cancer.
Detailed Description
The role of SBRT as a potentially non-invasive treatment for small-volume tumors in the lung is well established, but the effectiveness of tumor eradication has yet to be determined. This prospective Phase 2 trial will provide several novel contributions to the literature: 1) the assessment of SBRT effectiveness in metastatic tumor control (radiotherapeutic metastasectomy), 2) the evaluation of pathologic response to SBRT by surgical resection, 3) identification of histologic predictors of radiation effect and toxicity (i.e. what are the effects of SBRT on different type of metastatic disease), and 4) the effect of combined modality SBRT and surgery on survival and local recurrence as compared to either modality alone. This trial will uniquely assess whether surgery as an adjunct to radiotherapy offers better tumor control as compared to SBRT alone, and whether it decreases locoregional recurrence. The study is an open-label unblinded single-arm prospective trial evaluating induction SBRT followed by pulmonary metastasectomy. This is a collaborative effort between the divisions of Thoracic Surgery and Radiation Oncology to evaluate the effects of dual treatment of pulmonary metastasis amenable to curative resection with neoadjuvant SBRT followed by surgical resection. Study recruitment and analysis will be conducted at St. Joseph Healthcare Hamilton and the Juravinski Cancer Center. Institutional data suggests that the Division of Thoracic Surgery at McMaster University performs an average of 450 pulmonary resections per year with approximately 10-15% being pulmonary metastasectomies for a spectrum of malignancies (including colorectal carcinoma, renal cell carcinoma and soft tissue sarcoma).
Surgical resection and stereotactic body radiation therapy (SBRT) are generally regarded as mutually exclusive treatment options for the local management of pulmonary malignancies. The Primary Outcome will be measured as the Rates of complete pathologic response (pCR) in surgical specimens post SBRT as assessed using the Junker grading scale for lung malignancies: Grade I, no regression or only spontaneous tumor regression; Grade II, morphologic evidence of tumor regression with at least 10% (grade IIa) or <10% (grade IIb) viable tumor tissue; and Grade III, complete tumor regression with no viable tumor. The Secondary Outcomes: Overall survival (OS) at 3 years, Disease-free survival (DFS) at 3 years, local recurrence rates, radiation related toxicity, postoperative pulmonary complication rate (including prolonged air leak, need for invasive or noninvasive mechanical ventilation, postop pneumonia and empyema), the effect on time-to-resection and tumour histology on pCR. In addition, it will be explored whether cancer specific tumor biomarkers correlate with SBRT effects and related toxicity. Based on institutional data from other local prospective trials, the Thoracic Surgery division at McMaster averages a study accrual rate of 25-30% and retention rate of approximately 80%. The most pertinent metric in determining the necessary sample size is the effect size estimate of pCR. The MISSILE study preliminary data demonstrated a pCR of 60%. This serves as the only representative value in the literature, even though our study evaluates SBRT and surgery for metastatic disease and NOT primary lung cancer. In contrast, the SBRT literature (using post-treatment CT scan surveillance only) reports local control rates of nearly 90%. Using the Fleming procedure, in order to measure the true pCR with a 95% confidence interval ± 10% using an estimated true pCR of 70%, estimated dropout rate of 20%, and 80% power, the calculated sample size requirement is 39 patients. It is estimated being able to recruit approximately 1-2 patients per month.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Surgical Resection, Stereotactic Body Radiotherapy, Lung Cancer, Pulmonary Metastasectomy
Keywords
Surgical resection, Stereotactic body radiation therapy, Pulmonary metastasectomy, Lung Cancers
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
This innovative study is an open-label unblinded single-arm prospective trial evaluating induction SBRT followed by pulmonary metastasectomy. As a Phase 2 trial, the primary purpose is to assess the efficacy of SBRT on metastatic tumor viability and the safety of SBRT as induction treatment prior to surgery
Masking
None (Open Label)
Allocation
N/A
Enrollment
39 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
SBRT followed by pulmonary metastasectomy
Arm Type
Experimental
Arm Description
SBRT+Surgery
Intervention Type
Procedure
Intervention Name(s)
Surgical resection and stereotactic body radiation therapy (SBRT)
Intervention Description
Surgical resection and stereotactic body radiation therapy (SBRT) are generally regarded as mutually exclusive treatment options for the local management of pulmonary malignancies. This Phase 2 prospective trial is a collaborative effort between the divisions of Thoracic Surgery and Radiation Oncology to evaluate the effects of dual treatment of pulmonary metastasis amenable to curative resection with neoadjuvant SBRT followed by surgical resection.
Primary Outcome Measure Information:
Title
Rates of complete pathologic response (pCR)
Description
pCR in surgical specimens post SBRT as assessed using the Junker grading scale for lung malignancies: Grade I, no regression or only spontaneous tumor regression; Grade II, morphologic evidence of tumor regression with at least 10% (grade IIa) or <10% (grade IIb) viable tumor tissue; and Grade III, complete tumor regression with no viable tumor.
Time Frame
post-operative 3 weeks
Secondary Outcome Measure Information:
Title
Overall survival (OS)
Description
Followup over all survival (OS) at 3 years
Time Frame
Post operative 3 years
Title
Disease-free survival (DFS)
Description
Followup over all survival (OS) at 3 years. Based on 1. clinical 2. CT scan results
Time Frame
Disease-free survival (DFS) at 3 years
Title
local recurrence rates
Description
CT scan at follow-up
Time Frame
post operative 3 years
Title
Radiation related toxicity
Description
Follow Radiation Therapy Oncology Group (RTOG) Common Toxicity Criteria (Cox, 1995)
Time Frame
Post radiation 1 year
Title
Postoperative pulmonary complication rate (including prolonged air leak, need for invasive or noninvasive mechanical ventilation, postop pneumonia and empyema)
Description
Using Society of Thoracic Surgery (STS) Database
Time Frame
post operative 30 days
Title
The effect on time-to-resection and tumour histology on pCR
Description
Time analysis
Time Frame
8 to 12 weeks at different time post operative
Title
Identify mRNA tumor markers by Circulating Tumor Cell/CTC test
Description
Identify mRNA tumor markers for circulating tumor cell/CTC detection from blood sample to get cancer specific tumor biomarkers correlate with SBRT effects including different targeted gene such MUC1, HER2, EPCAM, ER/PR for Breast Cancer, PSA, PSMA, EGFR, AR for Prostate Cancer, EPCAM, EGFR, CEA for Colon Cancer, EPCAM, MUC1, CA125, ERCC1 for Ovarian Cancer and Stemcell . The CTC test will be doing to get information about whether or not disease has disseminated from the primary site and mainly as a prognostic and/or predictive marker in the metastatic settings. This test will be done in baseline or Pre SBRT, Post SBRT and Post Surgery.
Time Frame
Baseline/ pre-SBRT; 6 Weeks post SBRT/6 weeks post Radiation , 6 weeks post Surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient age >18, resectable pulmonary metastases without a more effective systemic therapy option (regardless of type of primary malignancy, excluding hematologic malignancies) with the primary malignancy already having been treated without evidence of local recurrence
Patient having single-organ metastasis to lung only (with the exception of colorectal CA (Cancer) with synchronous hepatic metastasis)
Tumors <5cm
Patient with no evidence of nodal disease on pre-treatment CT scan
Patient having adequate pulmonary function to tolerate lung resection (post-operative predictive FEV1≥40%).
Exclusion Criteria:• Patient having comorbidities not amenable to surgery
Patient with uncontrolled primary malignancy
Patient with hematologic malignancies (leukemia or lymphoma)
Patient having more than 5 tumors in one lung
Patient with prior history of thoracic radiation
Patient having history of lung cancer diagnosis within 5 years of assessment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dr. John Agzarian, MD, MPH
Phone
(905) 522-1155
Ext
32701
Email
agzarij@mcmaster.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Housne Begum, MSc, PhD
Phone
(905) 522-1155
Ext
35338
Email
begumh@mcmaster.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John Agzarian, MD, MPH
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
McMaster University/St. Joseph's Hospital Healthcare
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 4A6
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John Agzarian, MD, FRCSC
Phone
905-522-1155
Ext
32701
Email
agzarij@mcmaster.ca
First Name & Middle Initial & Last Name & Degree
Housne Begum, MSc, PhD
Phone
905-522-1155
Ext
35338
Email
begumh@mcmaster.ca
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
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25981812
Citation
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Results Reference
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Citation
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Results Reference
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Post SBRT Pulmonary Metastasectomy (PSPM) Trial
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