Adjuvant therapy versus watch-and-wait post surgery for stage III melanoma: a multicountry retrospective chart review.

adjuvant therapy interferon melanoma metastatic melanoma nodal disease stage III melanoma

Journal

Melanoma management
ISSN: 2045-0885
Titre abrégé: Melanoma Manag
Pays: England
ID NLM: 101649842

Informations de publication

Date de publication:
04 Oct 2019
Historique:
entrez: 25 12 2019
pubmed: 25 12 2019
medline: 25 12 2019
Statut: epublish

Résumé

To describe treatment patterns among patients with stage III melanoma who underwent surgical excision in years 2011-2016, and assess outcomes among patients who subsequently received systemic adjuvant therapy versus watch-and-wait. Chart review of 380 patients from 17 melanoma centers in North America, South America and Europe. Of 129 (34%) patients treated with adjuvant therapy, 85% received interferon α-2b and 56% discontinued treatment (mostly due to adverse events). Relapse-free survival was significantly longer for patients treated with adjuvant therapy versus watch-and-wait (hazard ratio = 0.63; p < 0.05). There was considerable heterogeneity in adjuvant treatment schedules and doses. Similar results were found in patients who received interferon-based adjuvant therapy. Adjuvant therapies with better safety/efficacy profiles will improve clinical outcomes in patients with stage III melanoma.

Identifiants

pubmed: 31871622
doi: 10.2217/mmt-2019-0015
pmc: PMC6923782
doi:

Types de publication

Journal Article

Langues

eng

Pagination

MMT33

Informations de copyright

© 2019 The authors.

Déclaration de conflit d'intérêts

Financial & competing interests disclosure This study was funded by Novartis Pharmaceuticals Corporation. P Mohr: honoraria: Amgen, Bristol-Myers Squibb, Merck, Merck Sharp & Dohme, Pierre Fabre, Novartis, Sanofi and Roche. F Kiecker: advisory boards: Amgen, Bristol-Myers Squibb, Merck Sharp & Dohme, Novartis, Pierre Fabre, Sanofi and Roche; honoraria: Amgen, Bristol-Myers Squibb, Merck Sharp & Dohme, Novartis, Pierre Fabre and Roche; clinical trial participation (principal investigator): Amgen, Bristol-Myers Squibb, Merck Sharp & Dohme, Novartis, Pierre Fabre, Sanofi and Roche. R Koneru: research funding from Novartis; advisory boards: Novartis, Bristol-Myers Squibb, Merck. O Dereure: advisory board or honoraria and travel support: Bristol-Myers Squibb, Merck Sharp and Dohme, Roche, Novartis, Pierre Fabre, Sanofi. P Saiag: personal fees: Amgen, Bristol-Myers Squibb, Merck Sharp & Dohme, Merck-Serono, Pfizer, Roche-Genentech, Pierre Fabre and Novartis; nonfinancial support from Bristol-Myers Squibb, Merck Sharp & Dohme, Roche-Genentech and Novartis. J Utikal: advisory board or honoraria and travel support: Amgen, Bristol-Myers Squibb, GlaxoSmithKline, LeoPharma, Merck Sharp & Dohme, Novartis, Pierre Fabre and Roche. C Robert: honoraria: Amgen, Bristol-Myers Squibb, Merck, Merck Sharp & Dohme, Pierre Fabre, Novartis, Sanofi and Roche. F Cuadros received research funding from Novartis; advisory boards: Novartis, Bristol-Myers Squibb, Merck Sharp & Dohme; speakers bureau: Novartis, Bristol-Myers Squibb, Merck Sharp & Dohme. RU Villarroel: Advisory Board: Novartis, Merck Sharp & Dohme, Bristol-Myers Squibb; honoraria: Novartis, Merck Sharp & Dohme, Bristol-Myers Squibb; clinical trial participation principal investigator: Novartis, Merck Sharp & Dohme. YG Najjar: research funding: Merck; advisory board: Array Biopharma; clinical trial participation: Novartis, Genentech, Merck and Array Biopharma. L Kottschade: advisory board: Array BioPharma; research funding: Bristol-Myers Squibb. EM Couselo: advisory board: Amgen, Bristol-Myers Squibb, Merck, Sharp & Dohme, Novartis, Pierre Fabre, Sanofi and Roche; honoraria: Amgen, Bristol-Myers Squibb, Merck, Sharp & Dohme, Novartis, Pierre Fabre and Roche; clinical trial participation (principal investigator): Amgen, Bristol-Myers Squibb, GlaxoSmithKline, Merck, Sharp & Dohme, Novartis, Pierre Fabre, Sanofi and Roche. R Koruth is an employee of Novartis Pharmaceutical Corporation. A Guérin, R Burne and R Ionescu-Ittu are employees of Analysis Group, Inc., which has received consulting fees from Novartis. M Perrinjaquet is an employee of Navigant Germany GmbH, whose parent company has received consulting fees from Novartis. JS Zager: research funding: Novartis, Amgen, Philogen, Provectus, Delcath Systems, Castle Biosciences; advisory boards: Merck and Array Biopharma; medical advisory board: Delcath Systems; consulting: Philogen; speakers bureau: Sun Pharma and Array Biopharma. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed. Medical writing assistance was provided by S Rochette and G DeWalt, employees of Analysis Group, Inc.; support for this assistance was provided by Novartis Pharmaceuticals Corporation. Data collection was coordinated by M Perrinjaquet and E Chater, employees of Navigant, while support for this assistance was provided by Novartis Pharmaceuticals Corporation.

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Auteurs

Peter Mohr (P)

Department of Dermatology, Elbe Kliniken, Stade, Germany.

Felix Kiecker (F)

Department of Dermatology and Allergy, Skin Cancer Center, Charité Universitätsmedizin Berlin, Berlin, Germany.

Virtudes Soriano (V)

Department of Medical Oncology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.

Olivier Dereure (O)

Department of Dermatology and INSERM U1058 'pathogenesis and control of chronic infections', University of Montpellier, Montpellier, France.

Karmele Mujika (K)

Department of Medical Oncology, Onkologikoa-Oncology Institute Gipuzkoa, Gipuzkoa, Spain.

Philippe Saiag (P)

Department of General and Oncologic Dermatology Ambroise Paré Hospital, APHP; EA 4340 'Biomarkers in cancerology and hemato-oncology', UVSQ, Université Paris-Saclay, Boulogne-Billancourt, France.

Jochen Utikal (J)

Skin Cancer Unit, German Cancer Research Center (DKFZ), Heidelberg, Germany and Department of Dermatology, Venereology and Allergology; University Medical Center, Ruprecht-Karl University of Heidelberg, Mannheim, Germany.

Rama Koneru (R)

RS McLaughlin Durham Regional Cancer Centre, Lakeridge Health, Oshawa, Oshawa, Ontario, Canada.

Caroline Robert (C)

Dermatology Unit, Gustave Roussy and Paris-Saclay University, Villejuif, France.

Florencia Cuadros (F)

Medical Oncology, Instituto de Oncologia de Rosario, Rosario, Santa Fe, Argentina.

Matias Chacón (M)

Departments of Medical and Surgical Oncology, Instituto Alexander Fleming, Buenos Aires, Argentina.

Rodrigo U Villarroel (RU)

Cancer Institute São Vicente de Paulo, Passo Fundo, RS, Brazil.

Yana G Najjar (YG)

UPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA 15213, USA.

Lisa Kottschade (L)

Department of Medical Oncology, Mayo Clinic, Rochester, MN 55905, USA.

Eva M Couselo (EM)

Department of Medical Oncology, Vall d'Hebron Hospital and VHIO (Vall d'Hebron Institute of Oncology), Barcelona, Spain.

Roy Koruth (R)

Novartis Pharmaceuticals Corporation, East Hanover, NJ 07936, USA.

Annie Guérin (A)

Analysis Group, Inc. Montreal, Quebec, Canada.

Rebecca Burne (R)

Analysis Group, Inc. Montreal, Quebec, Canada.

Raluca Ionescu-Ittu (R)

Analysis Group, Inc. Montreal, Quebec, Canada.

Maurice Perrinjaquet (M)

Navigant Germany GmbH, Berlin, Germany.

Jonathan S Zager (JS)

Departments of Cutaneous Oncology and Sarcoma, Moffitt Cancer Center, Tampa, FL 33612, USA.

Classifications MeSH