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Disease

Carcinoma, Renal Cell

Late-stage therapeutic developmentActively researchedCooling momentum
43
Publications
18
Clinical trials
10
Related conditions
8
Related treatments
12
Associated genes
12
Related proteins
2026
Latest publication
Latest activity
beta

Recent clinical, regulatory, research and industry developments relating to this disease.

Immune Checkpoint Inhibitors in Clear Cell Renal Cell Carcinoma (ccRCC).

Research2025-06-11International journal of molecular sciences

Renal Cell Carcinoma: A Review.

Research2024-09-01JAMA

What's happening now

An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.

Major developments
Research Highlights2View
Clinical Milestones6View
Activity timeline8

Therapeutic landscape

Therapies with a regulatory footing for this condition, alongside the wider set of agents co-studied with it in the literature.

Approved & established therapies
Belzutifanapproved

Approval — Renal cell carcinoma (RCC) Welireg is indicated as monotherapy for the treatment of adul… (2025)

Axitinibapproved

Approval — Axitinib Accord is indicated for the treatment of adult patients with advanced renal cell… (2024)

Sorafenibapproved

Approval — Hepatocellular carcinomaSorafenib Accord is indicated for the treatment of hepatocellular… (2022)

Sunitinibapproved

Approval — Gastrointestinal stromal tumour (GIST) Sunitinib Accord is indicated for the treatment of… (2021)

Bevacizumabapproved

Approval — Aybintio in combination with fluoropyrimidine-based chemotherapy is indicated for treatme… (2020)

Avelumabapproved

Approval — Bavencio is indicated as monotherapy for the treatment of adult patients with metastatic… (2017)

Tivozanibapproved

Approval — Fotivda is indicated for the first line treatment of adult patients with advanced renal c… (2017)

Cabozantinibapproved

Accelerated approval — Renal Cell Carcinoma (RCC) Cabometyx is indicated as monotherapy for advanced renal cell… (2016)

Clinical trials

12 sponsors · 1 new · 0 completed in the last 12 months (net +1)

The current development programme across all trial phases.

Clinical programme
18
All trials
6
Active
13
Late-stage
6
Completed
Late-stage studies
Recently completed

Regulatory timeline

Drug regulatory events matched to this condition by indication — EMA.

First approvals
2025emaApprovalBelzutifan· Renal cell carcinoma (RCC) Welireg is indicated as monotherapy for the treatment of adult patients with advanced clear cell renal cell carcinoma that progressed following two or more lines of therapy that included a PD-(L)1 inhibitor and at least two VEGF-targeted therapies. von Hippel-Lindau (VHL) disease-associated tumours Welireg is indicated as monotherapy for the treatment of adult patients with von Hippel-Lindau disease who require therapy for associated, localised renal cell carcinoma (RCC), central nervous system (CNS) haemangioblastomas, or pancreatic neuroendocrine tumours (pNET), and for whom localised procedures are unsuitable. source ↗
2024emaApprovalAxitinib· Axitinib Accord is indicated for the treatment of adult patients with advanced renal cell carcinoma (RCC) after failure of prior treatment with sunitinib or a cytokine. source ↗
2022emaApprovalSorafenib· Hepatocellular carcinomaSorafenib Accord is indicated for the treatment of hepatocellular carcinoma (see section 5.1). Renal cell carcinomaSorafenib Accord is indicated for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy. source ↗
2021emaApprovalSunitinib· Gastrointestinal stromal tumour (GIST) Sunitinib Accord is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (GIST) in adults after failure of imatinib treatment due to resistance or intolerance. Metastatic renal cell carcinoma (MRCC) Sunitinib Accord is indicated for the treatment of advanced/metastatic renal cell carcinoma (MRCC) in adults. Pancreatic neuroendocrine tumours (pNET) Sunitinib Accord is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours (pNET) with disease progression in adults. source ↗
2020emaApprovalBevacizumab· Aybintio in combination with fluoropyrimidine-based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. Aybintio in combination with paclitaxel is indicated for first-line treatment of adult patients with metastatic breast cancer. For further information as to human epidermal growth factor receptor 2 (HER2) status, please refer to section 5.1 of the SmPC. Aybintio in combination with capecitabine is indicated for first-line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. Patients who have received taxane and anthracyclinecontaining regimens in the adjuvant setting within the last 12 months should be excluded from treatment with Aybintio in combination with capecitabine. For further information as to HER2 status, please refer to section 5.1 of the SmPC. Aybintio, in addition to platinum-based chemotherapy, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-small cell lung cancer other than predominantly squamous cell histology. Aybintio, in combination with erlotinib, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-squamous non-small cell lung cancer with Epidermal Growth Factor Receptor (EGFR) activating mutations (see section 5.1 of the SmPC). Aybintio in combination with interferon alfa-2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. Aybintio, in combination with carboplatin and paclitaxel is indicated for the front-line treatment of adult patients with advanced (International Federation of Gynecology and Obstetrics (FIGO) stages III B, III C and IV) epithelial ovarian, fallopian tube, or primary peritoneal cancer (see section 5.1 of the SmPC). Aybintio, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum-sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other VEGF inhibitors or VEGF receptor targeted agents. Aybintio, in combination with topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum-resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other VEGF inhibitors or VEGF receptor targeted agents (see section 5.1 of the SmPC). Aybintio, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix (see section 5.1 of the SmPC). source ↗
2017emaApprovalAvelumab· Bavencio is indicated as monotherapy for the treatment of adult patients with metastatic Merkel cell carcinoma (MCC). Bavencio in combination with axitinib is indicated for the first-line treatment of adult patients with advanced renal cell carcinoma (RCC). Bavencio is indicated as monotherapy for the first?line maintenance treatment of adult patients with locally advanced or metastatic urothelial carcinoma (UC) who are progression-free following platinum?based chemotherapy. source ↗
2017emaApprovalTivozanib· Fotivda is indicated for the first line treatment of adult patients with advanced renal cell carcinoma (RCC) and for adult patients who are VEGFR and mTOR pathway inhibitor-naïve following disease progression after one prior treatment with cytokine therapy for advanced RCC. Treatment of advanced renal cell carcinoma. source ↗
2016emaAccelerated approvalCabozantinib· Renal Cell Carcinoma (RCC) Cabometyx is indicated as monotherapy for advanced renal cell carcinoma as first-line treatment of adult patients with intermediate or poor risk, in adults following prior vascular endothelial growth factor (VEGF)-targeted therapy. Cabometyx, in combination with nivolumab, is indicated for the first-line treatment of advanced renal cell carcinoma in adults. Hepatocellular carcinoma (HCC)Cabometyx is indicated as monotherapy for the treatment of hepatocellular carcinoma (HCC) in adults who have previously been treated with sorafenib.Differentiated thyroid carcinoma (DTC)Cabometyx is indicated as monotherapy for the treatment of adult patients with locally advanced or metastatic differentiated thyroid carcinoma (DTC), refractory or not eligible to radioactive iodine (RAI) who have progressed during or after prior systemic therapy.Neuroendocrine Tumours (NET)Cabometyx is indicated for the treatment of adult patients with unresectable or metastatic, well differentiated extra-pancreatic (epNET) and pancreatic (pNET) neuroendocrine tumours who have progressed following at least one prior systemic therapy other than somatostatin analogues. source ↗
Safety updates
2021emaMarket withdrawalBevacizumab· Treatment of carcinoma of the colon or rectum, breast cancer, non-small cell lung cancer, renal cell cancer, epithelial ovarian, fallopian tube or primary peritoneal cancer, and carcinoma of the cervix. source ↗

European Medicines Agency (CC BY 4.0). Events are matched to this condition by drug indication text — approvals/updates for drugs indicated for it, not disease-specific acts.

Research activity

43 papers

Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.

Publications over time
20132026
Most influential

Safety, activity, and immune correlates of anti-PD-1 antibody in cancer.

The New England journal of medicine · 2012 · 9,851 cites

Intratumor heterogeneity and branched evolution revealed by multiregion sequencing.

The New England journal of medicine · 2012 · 5,974 cites

Nivolumab versus Everolimus in Advanced Renal-Cell Carcinoma.

The New England journal of medicine · 2015 · 4,442 cites

Nivolumab plus Ipilimumab versus Sunitinib in Advanced Renal-Cell Carcinoma.

The New England journal of medicine · 2018 · 3,404 cites

Pembrolizumab plus Axitinib versus Sunitinib for Advanced Renal-Cell Carcinoma.

The New England journal of medicine · 2019 · 2,427 cites
Recent publications
Major themes8
  • Carcinoma, Renal Cell25
  • Kidney Neoplasms25
  • Antineoplastic Combined Chemotherapy Protocols3
  • Lung Neoplasms3
  • Melanoma3
  • Carcinoma, Non-Small-Cell Lung2
  • Fecal Microbiota Transplantation2
  • Immunotherapy2
Leading journals6
  • The New England journal of medicine11
  • Journal for immunotherapy of cancer3
  • Nature medicine3
  • Cancer treatment reviews2
  • International journal of molecular sciences2
  • Journal of clinical oncology : official journal of the American Society of Clinical Oncology2
Leading researchers8
  • Choueiri TK13
  • Motzer RJ11
  • Powles T7
  • Rini BI7
  • Tannir NM7
  • Donskov F6
  • Escudier B6
  • Gurney H6
Affiliations (unnormalised)6
  • Dana-Farber Cancer Institute7
  • Memorial Sloan Kettering Cancer Center6
  • The University of Texas MD Anderson Cancer Center5
  • Beth Israel Deaconess Medical Center4
  • Lank Center for Genitourinary Oncology3
  • Memorial Sloan-Kettering Cancer Center3

Associated genes

12 matches

Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.

Disease biology

12 matches

Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.

Related conditions

10 matches

Diseases frequently studied alongside this one. Number shows shared papers.

Disease profile

A grounded synthesis of the condition — overview, causes, mechanism, risk factors and current standard of care.

Overview

Renal cell carcinoma is a heterogeneous group of kidney cancers that can arise sporadically or in hereditary settings. It includes several histologic subtypes, such as clear cell, papillary, chromophobe, collecting duct, sarcomatoid, and mixed cell-type carcinoma.

Causes

The grounding supports a hereditary component in some cases and a sporadic origin in others. Clear cell renal cell carcinoma is commonly associated with inactivation of the von Hippel-Lindau tumor suppressor gene.

Pathophysiology

The disease is biologically heterogeneous, with subtype-specific mechanisms. In clear cell renal cell carcinoma, VHL inactivation is linked to angiogenesis and immune escape, and the tumor microenvironment contributes to immune suppression. Reported resistance and progression mechanisms include disruption of hypoxia pathways, activation of PI3K/AKT/mTOR signaling, and increased expression of alternative proangiogenic factors.

Risk factors

The supplied grounding does not support specific patient-level risk factors for renal cell carcinoma beyond hereditary predisposition in some cases. Tumor histology and risk stratification are used to guide treatment selection, but these are not presented as causes of disease risk.

Current standard of care

Localized disease is generally treated with surgical resection. Relapsed or stage IV renal cell carcinoma is typically managed with surgery and/or systemic therapy, with treatment selection guided by histology and risk group. Systemic therapy classes described in the grounding include tyrosine kinase inhibitors, mTOR inhibitors, and immune checkpoint inhibitors, including combinations of anti-angiogenic agents with immunotherapy.

AI-generated summary grounded in MeSH and 6 peer-reviewed sources. Informational only — not medical advice. Generated 2026-07-07.

Reference

Authoritative identity, definition & identifiers.

Defined in MeSH

A heterogeneous group of sporadic or hereditary carcinoma derived from cells of the KIDNEYS. There are several subtypes including the clear cells, the papillary, the chromophobe, the collecting duct, the spindle cells (sarcomatoid), or mixed cell-type carcinoma.

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
  • Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.