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Surgery of Melanoma Metastases After Systemic Therapy (SUMMIST)

Primary Purpose

Melanoma, Melanoma Stage IV, Metastatic Melanoma

Status
Withdrawn
Phase
Phase 2
Locations
Sweden
Study Type
Interventional
Intervention
Surgical metastasectomy
Immunotherapy
Sponsored by
Sahlgrenska University Hospital, Sweden
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Melanoma focused on measuring Immunotherapy, Metastatic surgery, Surgical oncology

Eligibility Criteria

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

Inclusion Criteria:

  • Age above 18 years
  • Signed and dated written informed consent before the start of specific protocol procedures
  • Biopsy or cytology proven metastatic melanoma stage M1a, M1b or M1c
  • Have received a minimum of 9 months of immunotherapy (PD1-inhibitor alone or in combination) resulting in stable disease or partial response according to RECIST 1.1
  • Metastases judged to be radically resectable by surgery at a multidisciplinary conference
  • ECOG performance status 0-2

Exclusion Criteria:

  • Brain metastasis (M1d)
  • Previous treatment with BRAF/MEK inhibitors
  • Inability to understand given information or undergo study procedures according to protocol

Sites / Locations

  • Sahlgrenska University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

PD1-inhibitor + surgery

PD1-inhibitor

Arm Description

Patients randomised to the interventional study arm, receiving both surgical metastasectomy and continued immunotherapy. Each patient case will be individually planned for surgery. Procedures will include, but will not be limited to, lung resections, liver resections, bowel resection, skin excisions and lymph node clearances. Patients in both study arms will continue with PD-1 inhibitor 12 months after randomization, and will then be treated according to their medical oncologist.

Patients randomized to control study arm, receiving continued immunotherapy only. Patients in both study arms will continue with PD-1 inhibitor 12 months after randomization, and will then be treated according to their medical oncologist.

Outcomes

Primary Outcome Measures

DFS 12 months
Disease free survival

Secondary Outcome Measures

SAE 12 months
Serious adverse events
Complications
Surgical complications according to the Clavien-Dindo classification
R0 resection
Rate of R0 resections according to pathology report
PFS 12 months
Progression free survival
MSS 12 months
Melanoma specific survival
OS 12 months
Overall survival

Full Information

First Posted
January 23, 2020
Last Updated
September 19, 2023
Sponsor
Sahlgrenska University Hospital, Sweden
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1. Study Identification

Unique Protocol Identification Number
NCT04242329
Brief Title
Surgery of Melanoma Metastases After Systemic Therapy
Acronym
SUMMIST
Official Title
Surgery of Melanoma Metastases After Systemic Therapy - the SUMMIST Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Withdrawn
Why Stopped
Not possible to recruit patients during COVID, and not possible to start enrolling after the pandemic.
Study Start Date
March 11, 2021 (Actual)
Primary Completion Date
September 3, 2023 (Actual)
Study Completion Date
September 13, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sahlgrenska University Hospital, Sweden

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
To evaluate if surgical removal of residual disease adds benefit in stage IV melanoma patients with partial response or stable disease after a minimum 9 months of first-line PD-1 inhibition. Primary endpoint: Disease-free survival (DFS) at 12 months.
Detailed Description
A Phase II Randomized Controlled Open-Label Parallel Group Interventional Multicenter Trial. Patients with metastatic melanoma, stratified for stage M1a or M1b/M1c, that have received first-line treatment with PD-1 inhibitors for a minimum of 9 months resulting in either partial response or stable disease according to RECIST 1.1 will be eligible. Patients will be screened for operability based on CT-scans examined by a multidisciplinary team, with the criteria that complete (R0) resection of all metastases should be possible. If the multidisciplinary team find that this would be possible, patients will be included and randomized 1:1 to either surgery with continued PD1-inhibition or current standard of care with continued PD1-inhibition only. At progression, treatment will be according to the treating medical oncologist. Active follow-up will be performed for 12 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma, Melanoma Stage IV, Metastatic Melanoma, Surgery
Keywords
Immunotherapy, Metastatic surgery, Surgical oncology

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
A Phase II Randomized Controlled Open-Label Parallel Group Interventional Multicenter Trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
PD1-inhibitor + surgery
Arm Type
Experimental
Arm Description
Patients randomised to the interventional study arm, receiving both surgical metastasectomy and continued immunotherapy. Each patient case will be individually planned for surgery. Procedures will include, but will not be limited to, lung resections, liver resections, bowel resection, skin excisions and lymph node clearances. Patients in both study arms will continue with PD-1 inhibitor 12 months after randomization, and will then be treated according to their medical oncologist.
Arm Title
PD1-inhibitor
Arm Type
Active Comparator
Arm Description
Patients randomized to control study arm, receiving continued immunotherapy only. Patients in both study arms will continue with PD-1 inhibitor 12 months after randomization, and will then be treated according to their medical oncologist.
Intervention Type
Procedure
Intervention Name(s)
Surgical metastasectomy
Intervention Description
Surgical removal of metastases aimed at R0 resection.
Intervention Type
Drug
Intervention Name(s)
Immunotherapy
Intervention Description
Continued PD1-inhibitor treatment according to current treatment standards.
Primary Outcome Measure Information:
Title
DFS 12 months
Description
Disease free survival
Time Frame
12 months
Secondary Outcome Measure Information:
Title
SAE 12 months
Description
Serious adverse events
Time Frame
12 months
Title
Complications
Description
Surgical complications according to the Clavien-Dindo classification
Time Frame
3 months post operatively
Title
R0 resection
Description
Rate of R0 resections according to pathology report
Time Frame
3 months post operatively
Title
PFS 12 months
Description
Progression free survival
Time Frame
12 months
Title
MSS 12 months
Description
Melanoma specific survival
Time Frame
12 months
Title
OS 12 months
Description
Overall survival
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age above 18 years Signed and dated written informed consent before the start of specific protocol procedures Biopsy or cytology proven metastatic melanoma stage M1a, M1b or M1c Have received a minimum of 9 months of immunotherapy (PD1-inhibitor alone or in combination) resulting in stable disease or partial response according to RECIST 1.1 Metastases judged to be radically resectable by surgery at a multidisciplinary conference ECOG performance status 0-2 Exclusion Criteria: Brain metastasis (M1d) Previous treatment with BRAF/MEK inhibitors Inability to understand given information or undergo study procedures according to protocol
Facility Information:
Facility Name
Sahlgrenska University Hospital
City
Gothenburg
ZIP/Postal Code
413 45
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Surgery of Melanoma Metastases After Systemic Therapy

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