Resistance to Systemic Agents in Renal Cell Carcinoma Predict and Overcome Genomic Strategies Adopted by Tumor.

PD-1/PD-L1 VEGF VEGFR acquired resistance immune-checkpoint inhibitors mTOR predictive markers primary resistance renal cell carcinoma target therapy

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
14 Jun 2019
Historique:
received: 29 04 2019
revised: 25 05 2019
accepted: 11 06 2019
entrez: 19 6 2019
pubmed: 19 6 2019
medline: 19 6 2019
Statut: epublish

Résumé

The development of new systemic agents has led us into a "golden era" of management of metastatic renal cell carcinoma (RCC). Certainly, the approval of immune-checkpoint inhibitors and the combination of these with targeted compounds has irreversibly changed clinical scenarios. A deeper knowledge of the molecular mechanisms that correlate with tumor development and progression has made this revolution possible. In this amazing era, novel challenges are awaiting us in the clinical management of metastatic RCC. Of these, the development of reliable criteria which are able to predict tumor response to treatment or primary and acquired resistance to systemic treatments still remain an unmet clinical need. Thanks to the availability of data provided by studies evaluating genomic assessments of the disease, this goal may no longer be out of reach. In this review, we summarize current knowledge about genomic alterations related to primary and secondary resistance to target therapy and immune-checkpoint inhibitors in RCC.

Identifiants

pubmed: 31207938
pii: cancers11060830
doi: 10.3390/cancers11060830
pmc: PMC6627706
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Veronica Mollica (V)

Division of Oncology, S.Orsola-Malpighi Hospital, 40138 Bologna, Italy. veronica.mollica7@gmail.com.

Vincenzo Di Nunno (V)

Division of Oncology, S.Orsola-Malpighi Hospital, 40138 Bologna, Italy. dinunnovincenzo88@gmail.com.

Lidia Gatto (L)

Division of Oncology, S.Orsola-Malpighi Hospital, 40138 Bologna, Italy. lidia.gatto83@gmail.com.

Matteo Santoni (M)

Oncology Unit, Macerata Hospital, 62100 Macerata, Italy. mattymo@alice.it.

Marina Scarpelli (M)

Section of Pathological Anatomy, Polytechnic University of the Marche Region, School of Medicine, United Hospitals, Via Conca 71, I-60126 Ancona, Italy. m.scarpelli@univpm.it.

Alessia Cimadamore (A)

Section of Pathological Anatomy, Polytechnic University of the Marche Region, School of Medicine, United Hospitals, Via Conca 71, I-60126 Ancona, Italy. alessiacimadamore@gmail.com.

Antonio Lopez-Beltran (A)

Department of Pathology and Surgery, Faculty of Medicine, University of Córdoba, 14071 Cordoba, Spain. em1lobea@gmail.com.

Liang Cheng (L)

Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA. liang_cheng@yahoo.com.

Nicola Battelli (N)

Oncology Unit, Macerata Hospital, 62100 Macerata, Italy. nicola.battelli@sanita.marche.it.

Rodolfo Montironi (R)

Section of Pathological Anatomy, Polytechnic University of the Marche Region, School of Medicine, United Hospitals, Via Conca 71, I-60126 Ancona, Italy. r.montironi@univpm.it.

Francesco Massari (F)

Division of Oncology, S.Orsola-Malpighi Hospital, 40138 Bologna, Italy. fmassari79@gmail.com.

Classifications MeSH