Evidence map›Paper›PMID 29967214›Full record

ReviewMolecular cancer therapeutics2018

Resistance to Systemic Therapies in Clear Cell Renal Cell Carcinoma: Mechanisms and Management Strategies.

Peter Makhov, Shreyas Joshi, Pooja Ghatalia, Alexander Kutikov, Robert G Uzzo, Vladimir M Kolenko

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular cancer therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 323 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
323citing papers in PubMed, 1 pooled it
20.3field-weighted citation impact, top 1% of its field
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

323 citing papers in PubMed, 1 synthesis or guideline pooled it, 550 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Allogeneic CD70-Targeted Chimeric Antigen Receptor T-Cell Therapy for Advanced Renal Cell Carcinoma: Results From the Phase I TRAVERSE Trial.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
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263 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Peter MakhovCancer Biology Program, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Shreyas JoshiDivision of Urologic Oncology, Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Pooja GhataliaDivision of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Alexander KutikovDivision of Urologic Oncology, Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Robert G UzzoDivision of Urologic Oncology, Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
Vladimir M KolenkoCancer Biology Program, Fox Chase Cancer Center, Philadelphia, Pennsylvania. vladimir.kolenko@fccc.edu.
Fox Chase Cancer Center · US

Funding

LDL cholesterol and TKI resistance in renal cell carcinomaR03CA212949 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI KOLENKO, VLADIMIR M · 2017 to 2018
$183k
Disrupting lysosomal sequestration of sunitinib by farnesyl-transferase inhibitors as a next generation therapeutic approach for TKI resistant RCCR03CA216173 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI MAKHOV, PETR B. · 2018 to 2019
$183k
NCI NIH HHS R03 CA212949NCI NIH HHS R03 CA216173
6 · The paper itself

Abstract

Renal cell carcinoma (RCC) is the most common form of kidney cancer. It is categorized into various subtypes, with clear cell RCC (ccRCC) representing about 85% of all RCC tumors. The lack of sensitivity to chemotherapy and radiation therapy prompted research efforts into novel treatment options. The development of targeted therapeutics, including multi-targeted tyrosine kinase inhibitors (TKI) and mTOR inhibitors, has been a major breakthrough in ccRCC therapy. More recently, other therapeutic strategies, including immune checkpoint inhibitors, have emerged as effective treatment options against advanced ccRCC. Furthermore, recent advances in disease biology, tumor microenvironment, and mechanisms of resistance formed the basis for attempts to combine targeted therapies with newer generation immunotherapies to take advantage of possible synergy. This review focuses on the current status of basic, translational, and clinical studies on mechanisms of resistance to systemic therapies in ccRCC.

Indexed as

AnimalsCarcinoma, Renal CellCombined Modality TherapyDisease ManagementDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansImmunotherapyKidney NeoplasmsLysosomesMolecular Targeted TherapyMutationNeoplasm MetastasisNeovascularization, PathologicProtein Kinase InhibitorsRadiation ToleranceProtein Kinase Inhibitors

Identifiers

PMID29967214
PMCPMC6034114
OpenAlexW2810166643

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.