Evidence map›Paper›PMID 31207938›Full record

ReviewCancers2019

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

Veronica Mollica, Vincenzo Di Nunno, Lidia Gatto, Matteo Santoni, Marina Scarpelli, Alessia Cimadamore, Antonio Lopez-Beltran, Liang Cheng, Nicola Battelli, Rodolfo Montironi and 1 more

Abstract readReview
In one paragraph

Review in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Veronica MollicaDivision of Oncology, S.Orsola-Malpighi Hospital, 40138 Bologna, Italy. veronica.mollica7@gmail.com.
Vincenzo Di NunnoDivision of Oncology, S.Orsola-Malpighi Hospital, 40138 Bologna, Italy. dinunnovincenzo88@gmail.com.ORCID 0000-0003-4441-9834
Lidia GattoDivision of Oncology, S.Orsola-Malpighi Hospital, 40138 Bologna, Italy. lidia.gatto83@gmail.com.
Matteo SantoniOncology Unit, Macerata Hospital, 62100 Macerata, Italy. mattymo@alice.it.
Marina ScarpelliSection 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 CimadamoreSection of Pathological Anatomy, Polytechnic University of the Marche Region, School of Medicine, United Hospitals, Via Conca 71, I-60126 Ancona, Italy. alessiacimadamore@gmail.com.ORCID 0000-0001-5981-3514
Antonio Lopez-BeltranDepartment of Pathology and Surgery, Faculty of Medicine, University of Córdoba, 14071 Cordoba, Spain. em1lobea@gmail.com.
Liang ChengDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA. liang_cheng@yahoo.com.ORCID 0000-0001-6049-5293
Nicola BattelliOncology Unit, Macerata Hospital, 62100 Macerata, Italy. nicola.battelli@sanita.marche.it.
Rodolfo MontironiSection 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 MassariDivision of Oncology, S.Orsola-Malpighi Hospital, 40138 Bologna, Italy. fmassari79@gmail.com.ORCID 0000-0001-6476-6871

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

acquired resistanceimmune-checkpoint inhibitorsmTORPD-1/PD-L1predictive markersprimary resistancerenal cell carcinomatarget therapyVEGFVEGFR

Identifiers

PMID31207938
PMCPMC6627706

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.