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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04242329
Other study ID # SUMMIST
Secondary ID
Status Withdrawn
Phase Phase 2
First received
Last updated
Start date March 11, 2021
Est. completion date September 13, 2023

Study information

Verified date January 2024
Source Vastra Gotaland Region
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date September 13, 2023
Est. primary completion date September 3, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Surgical metastasectomy
Surgical removal of metastases aimed at R0 resection.
Drug:
Immunotherapy
Continued PD1-inhibitor treatment according to current treatment standards.

Locations

Country Name City State
Sweden Sahlgrenska University Hospital Gothenburg

Sponsors (1)

Lead Sponsor Collaborator
Vastra Gotaland Region

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary DFS 12 months Disease free survival 12 months
Secondary SAE 12 months Serious adverse events 12 months
Secondary Complications Surgical complications according to the Clavien-Dindo classification 3 months post operatively
Secondary R0 resection Rate of R0 resections according to pathology report 3 months post operatively
Secondary PFS 12 months Progression free survival 12 months
Secondary MSS 12 months Melanoma specific survival 12 months
Secondary OS 12 months Overall survival 12 months
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