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Conservative Nodal Surgery (Node-picking) of Patients With Stage III Melanoma With Low-burden of Nodal Disease (MELCONSURG MULTICENTRE COHORT)

Conservative Nodal Surgery (Node-picking) of Patients With Stage III Melanoma With Low-burden of Nodal Disease (MELCONSURG MULTICENTRE COHORT)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05445752
Enrollment
68
Registered
2022-07-06
Start date
2022-07-01
Completion date
2024-12-31
Last updated
2022-07-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Melanoma Stage III

Keywords

Surgery, Lymph node dissection, Conservative nodal surgery, Lymph node metastasis, Melanoma, Stage III melanoma

Brief summary

Background: Standard treatment for stage III melanoma with lymph node metastases involves complete lymph node dissection, which is a radical surgical procedure aimed at the removal of the entire regional lymph node basin. Conservative surgery for low-burden nodal metastasis involves removal of the metastatic lymph node or nodes (node-picking), leaving uninvolved nodes within the regional basin. This is expected to provide adequate regional control of the disease with no negative impact on patient survival and a lower rate of surgical complications. Aims: The MelConSurg Cohort will provide the first data on conservative surgery for patients with stage III melanoma with nodal metastases detected clinically or by imaging. Methods: A multicentre, single-arm prospective cohort study. Inclusion criteria: Patients with melanoma aged between 18 and 90 years, Eastern Cooperative Oncology Group performance status 0-1, non-matted regional lymph node metastasis (N1b or N2b) in a single regional basin detected clinically or by imaging (ultrasound, CT scan, PET scan). Study period: A 3-year recruitment period and a 3-year follow-up phase. Intervention: Patients will undergo conservative nodal surgery using conventional surgery, radio-guided surgery, or imaging guided surgery. Outcome measures: 3-year nodal relapse-free survival, 3-year disease-free survival, 3-year melanoma-specific survival, rate of surgical complications, and quality of life (SF-36 questionnaire). Sample size & Statistics: the estimated sample size to be recruited is 68 patients. Survival outcomes will be analysed through the Kaplan-Meier method, with the log-rank test. Conclusions: This Project is expected to provide unique evidence regarding a less radical nodal surgery for patients with melanoma. If favourable results are obtained, controlled studies could be conducted and changes in current clinical practice could be considered.

Interventions

None listed

Sponsors

Hospital Universitario Virgen Macarena
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years

Inclusion criteria

* Patients with melanoma aged between 18 and 90 years. * Eastern Cooperative Oncology Group (ECOG) performance status 0-1. * Nodal stage N1b or N2b (American Joint Committee on Cancer 8th edition) in a single regional basin detected clinically or by imaging (ultrasound, CT scan, PET scan).

Exclusion criteria

* Single lymph node metastasis in more than one regional basin. * Multiple primary melanoma (except for limb melanoma). * Primary occult melanoma. * Previous nodal, locoregional, or distant metastasis. * Previous lymph node surgery, except for SLNB. * Distant metastases detected at the screening evaluations or first postoperative PET-CT scan.

Design outcomes

Primary

MeasureTime frameDescription
Nodal relapse-free survival3-yearThe primary outcome measure is the frequency and time to develop recurrence in the same nodal basin.

Secondary

MeasureTime frameDescription
Disease-free survival3-yearFrequency and time to develop recurrence at any site, both regional or at distance.
Melanoma-specific survival3-yearFrequency and time to death directly related to melanoma progression.
Surgical complication rate3-yearFrequency of long-term complications (seroma, lymphedema, nerve injury, others). health-related quality of life questionnaire.
Quality of life3-yearQuality of life as tested by the SF-36 health-related quality of life questionnaire.

Countries

Spain

Contacts

Primary ContactDavid Moreno-Ramírez, PhD, Prof.
david.moreno.ramirez.sspa@juntadeandalucia.es0034697959068

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026