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      Combined immunotherapy with nivolumab and ipilimumab with and without local therapy in patients with melanoma brain metastasis: a DeCOG* study in 380 patients

      research-article
      1 , , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 , 25 , 4 , 3 , 14 , 16 , 26 ,   1 , 1 , 27 , *German Dermatological Cooperative Oncology Group
      Journal for Immunotherapy of Cancer
      BMJ Publishing Group
      immunology, oncology, radiotherapy, surgery

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          Abstract

          Background

          Nivolumab combined with ipilimumab have shown activity in melanoma brain metastasis (MBM). However, in most of the clinical trials investigating immunotherapy in this subgroup, patients with symptomatic MBM and/or prior local brain radiotherapy were excluded. We studied the efficacy of nivolumab plus ipilimumab alone or in combination with local therapies regardless of treatment line in patients with asymptomatic and symptomatic MBM.

          Methods

          Patients with MBM treated with nivolumab plus ipilimumab in 23 German Skin Cancer Centers between April 2015 and October 2018 were investigated. Overall survival (OS) was evaluated by Kaplan-Meier estimator and univariate and multivariate Cox proportional hazard analyses were performed to determine prognostic factors associated with OS.

          Results

          Three hundred and eighty patients were included in this study and 31% had symptomatic MBM (60/193 with data available) at the time of start nivolumab plus ipilimumab. The median follow-up was 18 months and the 2 years and 3 years OS rates were 41% and 30%, respectively. We identified the following independently significant prognostic factors for OS: elevated serum lactate dehydrogenase and protein S100B levels, number of MBM and Eastern Cooperative Oncology Group performance status. In these patients treated with checkpoint inhibition first-line or later, in the subgroup of patients with BRAFV600-mutated melanoma we found no differences in terms of OS when receiving first-line either BRAF and MEK inhibitors or nivolumab plus ipilimumab (p=0.085). In BRAF wild-type patients treated with nivolumab plus ipilimumab in first-line or later there was also no difference in OS (p=0.996). Local therapy with stereotactic radiosurgery or surgery led to an improvement in OS compared with not receiving local therapy (p=0.009), regardless of the timepoint of the local therapy. Receiving combined immunotherapy for MBM in first-line or at a later time point made no difference in terms of OS in this study population (p=0.119).

          Conclusion

          Immunotherapy with nivolumab plus ipilimumab, particularly in combination with stereotactic radiosurgery or surgery improves OS in asymptomatic and symptomatic MBM.

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          Most cited references34

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          Melanoma staging: Evidence-based changes in the American Joint Committee on Cancer eighth edition cancer staging manual

          Answer questions and earn CME/CNE To update the melanoma staging system of the American Joint Committee on Cancer (AJCC) a large database was assembled comprising >46,000 patients from 10 centers worldwide with stages I, II, and III melanoma diagnosed since 1998. Based on analyses of this new database, the existing seventh edition AJCC stage IV database, and contemporary clinical trial data, the AJCC Melanoma Expert Panel introduced several important changes to the Tumor, Nodes, Metastasis (TNM) classification and stage grouping criteria. Key changes in the eighth edition AJCC Cancer Staging Manual include: 1) tumor thickness measurements to be recorded to the nearest 0.1 mm, not 0.01 mm; 2) definitions of T1a and T1b are revised (T1a, <0.8 mm without ulceration; T1b, 0.8-1.0 mm with or without ulceration or <0.8 mm with ulceration), with mitotic rate no longer a T category criterion; 3) pathological (but not clinical) stage IA is revised to include T1b N0 M0 (formerly pathologic stage IB); 4) the N category descriptors "microscopic" and "macroscopic" for regional node metastasis are redefined as "clinically occult" and "clinically apparent"; 5) prognostic stage III groupings are based on N category criteria and T category criteria (ie, primary tumor thickness and ulceration) and increased from 3 to 4 subgroups (stages IIIA-IIID); 6) definitions of N subcategories are revised, with the presence of microsatellites, satellites, or in-transit metastases now categorized as N1c, N2c, or N3c based on the number of tumor-involved regional lymph nodes, if any; 7) descriptors are added to each M1 subcategory designation for lactate dehydrogenase (LDH) level (LDH elevation no longer upstages to M1c); and 8) a new M1d designation is added for central nervous system metastases. This evidence-based revision of the AJCC melanoma staging system will guide patient treatment, provide better prognostic estimates, and refine stratification of patients entering clinical trials. CA Cancer J Clin 2017;67:472-492. © 2017 American Cancer Society.
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            Five-Year Outcomes with Dabrafenib plus Trametinib in Metastatic Melanoma

            Patients who have unresectable or metastatic melanoma with a BRAF V600E or V600K mutation have prolonged progression-free survival and overall survival when receiving treatment with BRAF inhibitors plus MEK inhibitors. However, long-term clinical outcomes in these patients remain undefined. To determine 5-year survival rates and clinical characteristics of the patients with durable benefit, we sought to review long-term data from randomized trials of combination therapy with BRAF and MEK inhibitors.
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              Combination nivolumab and ipilimumab or nivolumab alone in melanoma brain metastases: a multicentre randomised phase 2 study

              Nivolumab monotherapy and combination nivolumab plus ipilimumab increase proportions of patients achieving a response and survival versus ipilimumab in patients with metastatic melanoma; however, efficacy in active brain metastases is unknown. We aimed to establish the efficacy and safety of nivolumab alone or in combination with ipilimumab in patients with active melanoma brain metastases.
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                Author and article information

                Journal
                J Immunother Cancer
                J Immunother Cancer
                jitc
                jitc
                Journal for Immunotherapy of Cancer
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                2051-1426
                2020
                26 March 2020
                : 8
                : 1
                : e000333
                Affiliations
                [1 ] departmentCenter for Dermatooncology, Department of Dermatology, Eberhard Karls University of Tuebingen , Eberhard Karls University of Tuebingen , Tubingen, Germany
                [2 ] departmentSkin Cancer Center, Department of Dermatology , Charité Universitätsmedizin Berlin , Berlin, Germany
                [3 ] departmentSkin Cancer Center, Department of Dermatology and National Center for Tumor Diseases (NCT) , University Hospital Heidelberg , Heidelberg, Germany
                [4 ] departmentDepartment of Dermatology , University Medical Center Mainz , Mainz, Germany
                [5 ] departmentSkin Cancer Center, Department of Dermatology , University Hospital Kiel , Kiel, Germany
                [6 ] departmentSkin Cancer Center, Department of Dermatology , University of Lübeck , Lübeck, Germany
                [7 ] departmentDepartment of Dermatology , University Hospital Wuerzburg , Wuerzburg, Germany
                [8 ] departmentSkin Cancer Center Hannover, Department of Dermatology , Hannover Medical School , Hannover, Germany
                [9 ] departmentDepartment of Dermatology , University of Regensburg , Regensburg, Germany
                [10 ] departmentSkin Cancer Unit , German Cancer Research Center (DKFZ) , Heidelberg, Germany
                [11 ] departmentDepartment of Dermatology, Venereology and Allergology , University Medical Center Mannheim, Ruprecht-Karl University of Heidelberg , Mannheim, Germany
                [12 ] departmentDepartment of Dermatology , Universitätsklinikum Erlangen, Friedrich-Alexander-Universität (FAU) , Erlangen-Nürnberg, Germany
                [13 ] departmentDepartment of Dermatology and Allergy , University Hospital Munich, Ludwig Maximilian University , Munich, Germany
                [14 ] departmentSkin Cancer Center, Department of Dermatology and Venerology , Medical Centre University of Freiburg, Faculty of Medicine, University of Freiburg , Freiburg, Germany
                [15 ] departmentSkin Cancer Center at the University Cancer Center and National Center for Tumor Diseases Dresden, Department of Dermatology , University Hospital Carl Gustav Carus at the TU Dresden , Dresden, Germany
                [16 ] departmentDepartment of Dermatology , University Hospital Magdeburg , Magdeburg, Germany
                [17 ] departmentDepartment of Dermatology and Allergy , Technical University of Munich, School of Medicine , Munich, Germany
                [18 ] Sigmund Freud Universität Wien, Faculty of Medicine , Wien, Austria
                [19 ] departmentSkin Cancer Center, Department of Dermatology , Ruhr-University Bochum , Bochum, Germany
                [20 ] departmentDepartment of Dermatology , Saarland University Medical School , Homburg/Saar, Germany
                [21 ] departmentDepartment of Dermatology, Venereology and Allergology , University Medical Center Göttingen , Göttingen, Germany
                [22 ] departmentDepartment of Dermatology and Allergology , Augsburg Medical Center , Augsburg, Germany
                [23 ] departmentSkin Cancer Center, Department of Dermatology , Paracelsus Medical University, General Hospital Nuremberg , Nuremberg, Germany
                [24 ] HELIOS Klinikum Erfurt , Erfurt, Germany
                [25 ] departmentClinic for Dermatology and Venereology , University Medical Center , Rostock, Germany
                [26 ] departmentClinic of Radiation Oncology , Eberhard Karls University of Tuebingen , Tuebingen, Germany
                [27 ] departmentDepartment of Dermatology , University Hospital Essen , Essen, Germany
                Author notes
                [Correspondence to ] Dr Teresa Amaral; teresa.amaral@ 123456med.uni-tuebingen.de
                Author information
                http://orcid.org/0000-0002-2516-5181
                http://orcid.org/0000-0002-7850-3199
                Article
                jitc-2019-000333
                10.1136/jitc-2019-000333
                7206917
                32221017
                c6b670d9-93e4-4a7f-97e3-5ccab1a7b61b
                © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 11 March 2020
                Categories
                Clinical/Translational Cancer Immunotherapy
                1506
                2435
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                immunology,oncology,radiotherapy,surgery
                immunology, oncology, radiotherapy, surgery

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