Evidence map›Paper›PMID 42770041›Full record

ArticleCancer management and research2026

Cabozantinib After Immunotherapy in Advanced Renal Cell Carcinoma. The CARE Study by the Hellenic Gu Cancer Group.

Aristotelis Bamias, Michael Liontos, Ioannis Binas, Dimitra Stefanou, Kimon Tzannis, Roubini Zakopoulou, Nikolaos Dedes, Dimitrios Deligiannis, Ioanna Katsiana, Areti Mamali and 10 more

Abstract read
In one paragraph

Article in Cancer management and research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

20 authors.

Aristotelis Bamias2nd Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Chaidari, Greece.ORCID 0000-0002-5996-7262
Michael LiontosDepartment of Clinical Therapeutics, National and Kapodistrian University of Athens, Alexandra Hospital, Athens, Greece.ORCID 0000-0001-7192-4575
Ioannis BinasDepartment of Medical Oncology, Metropolitan Hospital, Piraeus, Greece.
Dimitra Stefanou1st Department of Internal Medicine, National and Kapodistrian University of Athens, Laikon Hospital, Athens, Greece.
Kimon Tzannis2nd Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Chaidari, Greece.
Roubini Zakopoulou2nd Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Chaidari, Greece.ORCID 0000-0001-8301-8879
Nikolaos DedesDepartment of Clinical Therapeutics, National and Kapodistrian University of Athens, Alexandra Hospital, Athens, Greece.
Dimitrios Deligiannis3rd Urology Department, National and Kapodistrian University of Athens, Attikon University Hospital, Chaidari, Greece.
Ioanna KatsianaDepartment of Clinical Therapeutics, National and Kapodistrian University of Athens, Alexandra Hospital, Athens, Greece.
Areti Mamali2nd Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Chaidari, Greece.
Meropi Galari2nd Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Chaidari, Greece.
Konstantina Kakogianni2nd Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Chaidari, Greece.
Vasiliki Nikolaidou2nd Propaedeutic Department of Internal Medicine, National and Kapodistrian University of Athens, Attikon University Hospital, Chaidari, Greece.
Dimitrios C Ziogas1st Department of Internal Medicine, National and Kapodistrian University of Athens, Laikon Hospital, Athens, Greece.
Napoleon Moulavasilis1st Urology Department, National and Kapodistrian University of Athens, Laikon Hospital, Athens, Greece.ORCID 0000-0002-1820-9027
Vasiliki MagoulaHellenic GenitoUrinary Cancer Group, Athens, Greece.
Efstathia GiannopoulouHellenic GenitoUrinary Cancer Group, Athens, Greece.
Christos ChristodoulouDepartment of Medical Oncology, Metropolitan Hospital, Piraeus, Greece.
Meletios Athanasios DimopoulosDepartment of Clinical Therapeutics, National and Kapodistrian University of Athens, Alexandra Hospital, Athens, Greece.
Michael Chrisofos3rd Urology Department, National and Kapodistrian University of Athens, Attikon University Hospital, Chaidari, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The widespread use of immune checkpoint inhibitor (ICI)-based combinations as first-line therapy for metastatic renal cell carcinoma (mRCC) has created an unmet need for effective treatment options at disease progression. Cabozantinib is recommended after ICI failure; however, real-world evidence regarding its efficacy and safety in this setting remains limited, particularly following contemporary ICI-containing regimens. Methods: CARE was a retrospective, multicenter, non-interventional study conducted in Greece. Patients with locally advanced or metastatic RCC who received cabozantinib monotherapy after progression on at least one prior ICI-containing regimen were included. The primary endpoint was objective response rate (ORR). Secondary endpoints included progression-free survival (PFS), overall survival (OS), and safety. Exploratory analyses evaluated outcomes according to prior therapies and timing of cabozantinib administration. Results: Thirty patients were included. Prior immunotherapy consisted mainly of nivolumab monotherapy or nivolumab plus ipilimumab, while cabozantinib was administered predominantly as second-line treatment. No complete responses were observed; twelve patients achieved partial response, resulting in an ORR of 40% (95% CI: 22.7-59.4). Stable disease was observed in 56.7% of patients. Median follow-up was 20 months (95% CI 15.2-24.6). Median PFS was 21 months (95% CI: 12.5-NR), and median OS was 29.7 months (95% CI: 25.5-NR). Prior exposure to tyrosine kinase inhibitors was associated with shorter PFS, while ORR and OS were not significantly affected. Cabozantinib demonstrated a manageable safety profile, with fatigue and diarrhea being the most common adverse events. Grade III-IV toxicities occurred in 26.7% of patients. Conclusion: In this real-world Greek cohort, cabozantinib demonstrated meaningful clinical activity and an acceptable safety profile in mRCC patients progressing after ICI-based therapy. These findings support cabozantinib as an effective treatment option in the post-immunotherapy setting and contribute valuable real-world evidence to inform therapeutic sequencing in mRCC.

Indexed as

cabozantinibimmunotherapymetastatic renal cancer

Identifiers

PMID42770041
PMCPMC13592345

What OpenQuestion holds

Textmetadata
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.