Literature DB >> 34009481

Treatment Following Progression in Metastatic Melanoma: the State of the Art from Scientific Literature to Clinical Need.

F Serra1, S Barruscotti2, T Dominioni3, A Zuccarini1, P Pedrazzoli1, S Chiellino4.   

Abstract

INTRODUCTION: In the last few years, the advent of targeted therapy and immunotherapy has improved the management and the prognosis of metastatic melanoma, but the spread of resistance mechanisms can lead to disease progression. The clinical management in this setting can be challenging because the oncologist has to decide what is the best treatment strategy among therapy beyond progression (TBP), therapy change, and the rechallenge approach. This review of the relevant scientific literature is intended to clarify which patients with progressing metastatic melanoma will benefit from continuation of ongoing therapy and which ones will not. The data are based on a total of about 4300 patients coming from the main retrospective studies in the chosen field. The article body is divided into four sections which analyze respectively the targeted therapy beyond progression, the immunotherapy beyond progression, the possible treatment sequences, and finally the rechallenge strategy. RECENT
FINDINGS: Despite the possible approaches of TBP or rechallenge, the patient may not have an optimal response and may need new therapy, which is currently missing. To broaden the pharmacological offer in the fight against melanoma, cancer research is studying new disease targets, like the NRAS, PI3K, and cKIT pathways or combination treatment of targeted therapy plus immunotherapy. Despite the limitations of this work, mainly due to the limited number of studies, their retrospective nature and the lack of comparative studies, the analysis performed allows us to draw some important conclusions: therapy beyond progression, both targeted therapy and immunotherapy, represents a valid treatment option with positive effects on disease control and survival outcomes for patients with low clinical risk, expressed as low disease burden, normal LDH levels, and good performance status; moreover, the prognosis and quality of life of these patients improve when TBP is associated with locoregional treatments. In patients with progressive metastatic melanoma and high clinical risk (high disease burden, high LDH levels, and poor performance status), it is recommended to change therapy, without ever forgetting the possibility of enrolling the patient in a clinical trial. Finally, an efficacious treatment alternative is the rechallenge strategy; this approach consists in a re-treatment with the same drug after a variable interval of discontinuation. Preliminary studies seem to have demonstrated that patients retreated with targeted therapy achieved a greater benefit if they had a low clinical risk and if the drug doublet (BRAF + MEK inhibitors) was used. On the side of immunotherapy, the rechallenge strategy produced a major benefit in patients who prior experienced a severe toxic episode.

Entities:  

Keywords:  Immunotherapy; Rechallenge; Targeted therapy; Therapy change; Treatment beyond progression

Mesh:

Substances:

Year:  2021        PMID: 34009481     DOI: 10.1007/s11912-021-01065-3

Source DB:  PubMed          Journal:  Curr Oncol Rep        ISSN: 1523-3790            Impact factor:   5.075


  23 in total

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Authors:  Darrell S Rigel
Journal:  Semin Cutan Med Surg       Date:  2010-12

Review 2.  Combination therapy with BRAF and MEK inhibitors for melanoma: latest evidence and place in therapy.

Authors:  Zeynep Eroglu; Antoni Ribas
Journal:  Ther Adv Med Oncol       Date:  2016-01       Impact factor: 8.168

Review 3.  Meta-analysis of risk factors for cutaneous melanoma: II. Sun exposure.

Authors:  Sara Gandini; Francesco Sera; Maria Sofia Cattaruzza; Paolo Pasquini; Orietta Picconi; Peter Boyle; Carmelo Francesco Melchi
Journal:  Eur J Cancer       Date:  2005-01       Impact factor: 9.162

4.  The nature and management of metastatic melanoma after progression on BRAF inhibitors: effects of extended BRAF inhibition.

Authors:  Matthew M K Chan; Lauren E Haydu; Alexander M Menzies; Mary W F Azer; Oliver Klein; Megan Lyle; Arthur Clements; Alexander Guminski; Richard F Kefford; Georgina V Long
Journal:  Cancer       Date:  2014-07-01       Impact factor: 6.860

5.  Anti-PD-1 and PD-L1 antibodies in metastatic melanoma.

Authors:  Ester Simeone; Paolo A Ascierto
Journal:  Melanoma Manag       Date:  2017-11-21

6.  Novel patterns of response under immunotherapy.

Authors:  E Borcoman; Y Kanjanapan; S Champiat; S Kato; V Servois; R Kurzrock; S Goel; P Bedard; C Le Tourneau
Journal:  Ann Oncol       Date:  2019-03-01       Impact factor: 32.976

7.  The genetic landscape of clinical resistance to RAF inhibition in metastatic melanoma.

Authors:  Eliezer M Van Allen; Nikhil Wagle; Antje Sucker; Daniel J Treacy; Cory M Johannessen; Eva M Goetz; Chelsea S Place; Amaro Taylor-Weiner; Steven Whittaker; Gregory V Kryukov; Eran Hodis; Mara Rosenberg; Aaron McKenna; Kristian Cibulskis; Deborah Farlow; Lisa Zimmer; Uwe Hillen; Ralf Gutzmer; Simone M Goldinger; Selma Ugurel; Helen J Gogas; Friederike Egberts; Carola Berking; Uwe Trefzer; Carmen Loquai; Benjamin Weide; Jessica C Hassel; Stacey B Gabriel; Scott L Carter; Gad Getz; Levi A Garraway; Dirk Schadendorf
Journal:  Cancer Discov       Date:  2013-11-21       Impact factor: 39.397

8.  Survival rates of patients with metastatic malignant melanoma.

Authors:  A Sandru; S Voinea; E Panaitescu; A Blidaru
Journal:  J Med Life       Date:  2014 Oct-Dec

9.  Progression patterns under BRAF inhibitor treatment and treatment beyond progression in patients with metastatic melanoma.

Authors:  Jessica C Hassel; Kristina Buder-Bakhaya; Carolin Bender; Lisa Zimmer; Benjamin Weide; Carmen Loquai; Selma Ugurel; Alla Slynko; Ralf Gutzmer
Journal:  Cancer Med       Date:  2017-12-20       Impact factor: 4.452

10.  Combined vemurafenib and fotemustine in patients with BRAF V600 melanoma progressing on vemurafenib.

Authors:  Paola Queirolo; Francesco Spagnolo; Virginia Picasso; Laura Spano; Enrica Tanda; Valeria Fontana; Laura Giorello; Domenico Franco Merlo; Ester Simeone; Antonio Maria Grimaldi; Marcello Curvietto; Michele Del Vecchio; Paolo Bruzzi; Paolo Antonio Ascierto
Journal:  Oncotarget       Date:  2016-07-13
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  1 in total

1.  Neratinib and Capecitabine for the Treatment of Leptomeningeal Metastases from HER2-Positive Breast Cancer: A Series in the Setting of a Compassionate Program.

Authors:  Alessia Pellerino; Riccardo Soffietti; Francesco Bruno; Roberta Manna; Erminia Muscolino; Pierangela Botta; Rosa Palmiero; Roberta Rudà
Journal:  Cancers (Basel)       Date:  2022-02-25       Impact factor: 6.639

  1 in total

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