Evidence map›Paper›PMID 32975815›Full record

Trial reportCancer2020

Everolimus plus bevacizumab is an effective first-line treatment for patients with advanced papillary variant renal cell carcinoma: Final results from a phase II trial.

Darren R Feldman, Yasser Ged, Chung-Han Lee, Andrea Knezevic, Ana M Molina, Ying-Bei Chen, Joshua Chaim, Devyn T Coskey, Samuel Murray, Satish K Tickoo and 8 more

Open access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Phase II Trial of Cabozantinib Plus Nivolumab in Patients With Non-Clear-Cell Renal Cell Carcinoma and Genomic Correlates.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    Trial
  5. Integrative Clinical and Molecular Evaluation of Renal Cell Carcinoma with Merlin Protein Deficiency and Biallelic Loss of NF2.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  6. Review
  7. Review
  8. Review
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  10. Hypoxia-targeting bacteria in cancer therapy.Seminars in cancer biology · 2024
    Review
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  12. Article
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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

18 authors at 2 institutions in 1 country.

Darren R FeldmanDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-2424-4635
Yasser GedDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-6671-7002
Chung-Han LeeDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Andrea KnezevicDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Ana M MolinaDepartment of Medicine, Weill Cornell Medical College, New York, New York.
Ying-Bei ChenDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Joshua ChaimDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
Devyn T CoskeyDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Samuel MurrayDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Satish K TickooDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Victor E ReuterDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Sujata PatilDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
Han XiaoDepartment of Medicine, Memorial Sloan Kettering Cancer Center, Basking Ridge, New Jersey.
Jahan AghalarDepartment of Medicine, Memorial Sloan Kettering Cancer Center, Commack, New York.
Arlyn J ApolloDepartment of Medicine, Memorial Sloan Kettering Cancer Center, Center at Rockville Center, Woodmere, New York.
Maria I CarloDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
Robert J MotzerDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-6925-2327
Martin H VossDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-0551-5807
Memorial Sloan Kettering Cancer Center · USCornell University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748Novartis PharmaUnited States National Institute of Health NIH P30 Cancer Center Support Grant (P30 CA008748)
6 · The paper itself

Abstract

backgroundWe previously reported on a phase 2 study of everolimus plus bevacizumab across various nonclear cell renal cell carcinoma (nccRCC) histologies and observed encouraging activity among patients with papillary RCC (pRCC) and unclassified RCC (uRCC) with a major papillary component. We subsequently expanded the study to enroll additional patients with pRCC variants.

methodsEverolimus plus bevacizumab was administered at standard doses until disease progression or intolerance to therapy. The primary endpoint was the 6-month progression-free survival (PFS) rate; secondary endpoints included objective response rate (ORR), progression-free survival (PFS), overall survival (OS), and safety. Correlative analyses included next-generation sequencing (NGS) from tumor and germline across >341 genes of interest.

resultsIn addition to 19 patients with pRCC variants in the original cohort, 20 patients with similar features were enrolled on the expansion cohort (uRCC with papillary features [n = 24], pRCC [n = 14], and translocation-associated RCC with papillary features [n = 1]). Among 37 evaluable patients, the 6-month PFS rate was 78%, the median PFS was 13.7 months (95% CI, 10.8-16.4 months), and the ORR was 35%. With a median follow-up of 17.6 months, the median OS was 33.9 months (95% CI, 23.3-71.9). Tolerance was consistent with prior reports for everolimus plus bevacizumab. NGS results (n = 33) identified responses in patients with a wide spectrum of genomic alterations, including ARID1A, FH, and MET mutations.

conclusionThe expansion cohort results confirm robust activity of everolimus plus bevacizumab in metastatic pRCC variants, supporting this regimen as a standard option for this patient population.

Indexed as

AdultAgedAntineoplastic Combined Chemotherapy ProtocolsBevacizumabCarcinoma, Renal CellDNA-Binding ProteinsEverolimusFemaleFumarate HydrataseHigh-Throughput Nucleotide SequencingHumansKidney NeoplasmsMaleMiddle AgedMutationProto-Oncogene Proteins c-metARID1A protein, humanBevacizumabDNA-Binding ProteinsEverolimusFumarate HydrataseMET protein, humanProto-Oncogene Proteins c-metTranscription Factorsbevacizumabeverolimusgenomicspapillary RCCRCC

Identifiers

PMID32975815
PMCPMC8366407
OpenAlexW3089329253

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.