Final Analysis of DeCOG-SLT Trial: No Survival Benefit for Complete Lymph Node Dissection in Patients With Melanoma With Positive Sentinel Node

Author:

Leiter Ulrike1,Stadler Rudolf2,Mauch Cornelia3,Hohenberger Werner4,Brockmeyer Norbert H.2,Berking Carola5,Sunderkötter Cord67,Kaatz Martin89,Schatton Kerstin10,Lehmann Percy11,Vogt Thomas12,Ulrich Jens13,Herbst Rudolf14,Gehring Wolfgang15,Simon Jan-Christoph16,Keim Ulrike1,Verver Danielle17,Martus Peter1,Garbe Claus1,

Affiliation:

1. Eberhard Karls University of Tübingen, Tübingen, Germany

2. Ruhr University Bochum, Bochum, Germany

3. University of Köln/Bonn, Cologne, Germany

4. University of Erlangen, Erlangen, Germany

5. Ludwig-Maximilians University, Munich, Germany

6. University of Munster, Munster, Germany

7. University Hospital Halle, Halle, Germany

8. SRH Wald-Klinikum Gera, Gera, Germany

9. University of Jena, Jena, Germany

10. University of Düsseldorf, Dusseldorf, Germany

11. HELIOS-Klinikum Wuppertal, Wuppertal, Germany

12. University of Homburg, Homburg, Germany

13. University of Magdeburg, Quedlinburg, Germany

14. HELIOS-Klinikum Erfurt, Erfurt, Germany

15. Carl Von Ossietzky University, Oldenburg, Germany

16. University of Leipzig, Leipzig, Germany

17. Erasmus MC Cancer Institute, Rotterdam, the Netherlands

Abstract

PURPOSE We have previously reported on the 3-year results of the phase III German Dermatologic Cooperative Oncology Group trial (DeCOG; ClinicalTrials.gov identifier: NCT02434107 ) comparing distant metastasis-free survival (DMFS), recurrence-free survival (RFS), and overall survival (OS) in patients with positive sentinel lymph-node biopsy who were randomly assigned to complete lymph node dissection (CLND) or observation. Here, we report the final analysis with 72 months of median follow up. PATIENTS AND METHODS The multicenter randomized phase III trial included patients with cutaneous melanoma of the trunk and extremities who were randomly assigned (1:1) to undergo CLND or observation. DMFS was analyzed as the primary end point, and RFS, OS, and recurrences in the regional lymph node basin were secondary end points. The analysis was by intention to treat. Disease and survival information were collected quarterly. RESULTS From January 2006 to December 2014, 5,547 patients were screened to identify 1,256 with metastases in the sentinel lymph node (SLN). Of these, 483 (39%) were included: 241 in the observation arm and 242 in the CLND arm. In the final analysis, median follow up was 72 months (interquartile range, 67-77 months). No significant treatment-related difference was seen in the 5-year DMFS between the observation and CLND arms (67.6% v 64.9%, respectively; hazard ratio [HR], 1.08; P = .87). The 5-year RFS and OS also showed no difference (HR, 1.01 and 0.99, respectively). Grade 3 and 4 adverse effects occurred in 32 patients (13%) in the CLND arm; lymphedema (n = 20) and delayed wound healing (n = 5) were most common and no serious adverse events were reported. CONCLUSION The final results of the German Dermatologic Cooperative Oncology Group trial with a median follow up of 72 months showed higher event rates, but similar HRs compared with those at the 3-year analysis. These results confirm that immediate CLND in SLN-positive patients is not superior to observation in terms of DMFS, RFS, or OS and support not recommending CLND in patients with SLN metastasis.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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