Evidence map›Paper›PMID 35687336›Full record

ArticleJAMA network open2022

Imaging Response to Contemporary Immuno-oncology Combination Therapies in Patients With Metastatic Renal Cell Carcinoma.

Vishal Navani, Matthew Ernst, J Connor Wells, Takeshi Yuasa, Kosuke Takemura, Frede Donskov, Naveen S Basappa, Andrew Schmidt, Sumanta K Pal, Luis Meza and 11 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in JAMA network open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
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

21 authors at 15 institutions in 8 countries.

Vishal NavaniTom Baker Cancer Centre, Department of Medical Oncology, University of Calgary, Calgary, Canada.
Matthew ErnstTom Baker Cancer Centre, Department of Medical Oncology, University of Calgary, Calgary, Canada.
J Connor WellsBC Cancer Agency, Vancouver, Canada.
Takeshi YuasaCancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Kosuke TakemuraCancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Frede DonskovDepartment of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Naveen S BasappaCross Cancer Institute, Department of Medical Oncology, University of Alberta, Edmonton, Canada.
Andrew SchmidtDana Farber Cancer Institute, Boston, Massachusetts.
Sumanta K PalCity of Hope Comprehensive Cancer Center, Duarte, California.
Luis MezaCity of Hope Comprehensive Cancer Center, Duarte, California.
Lori A WoodQueen Elizabeth II Health Sciences Centre, Halifax, Canada.
D Scott ErnstLondon Regional Cancer Centre, London, Canada.
Bernadett SzabadosBarts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Thomas PowlesBarts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Rana R McKayMoores Cancer Center, University of California, San Diego, La Jolla.
Andrew WeickhardtOlivia Newton-John Cancer and Wellness Centre, Melbourne, Australia.
Cristina SuarezVall d'Hebron Institute of Oncology, Universitat Autònoma de Barcelona, Barcelona, Spain.
Anil KapoorJuravinski Cancer Centre, McMaster University, Hamilton, Canada.
Jae Lyun LeeUniversity of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.
Toni K ChoueiriDana Farber Cancer Institute, Boston, Massachusetts.
Daniel Y C HengTom Baker Cancer Centre, Department of Medical Oncology, University of Calgary, Calgary, Canada.
University of Calgary · CACity of Hope · USDana-Farber Cancer Institute · USJapanese Foundation For Cancer Research · JPQueen Mary University of London · GBAarhus University Hospital · DKAsan Medical Center · KRBC Cancer Agency · CAJuravinski Cancer Centre · CAOlivia Newton-John Cancer Wellness & Research Centre · AUOttawa Regional Cancer Foundation · CAQueen Elizabeth II Health Sciences Centre · CAUniversitat Autònoma de Barcelona · ESUniversity of Alberta · CAUniversity of California, San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: The association between treatment with first-line immuno-oncology (IO) combination therapies and physician-assessed objective imaging response among patients with metastatic renal cell carcinoma (mRCC) remains uncharacterized. Objective: To compare the likelihood of objective imaging response (ie, complete or partial response) to first-line IO combination ipilimumab-nivolumab (IOIO) therapy vs approved IO with vascular endothelial growth factor inhibitor (IOVE) combination therapies among patients with mRCC. Design, Setting, and Participants: This multicenter international cohort study was nested in routine clinical practice. A data set from the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) was used to identify consecutive patients with mRCC who received treatment with IO combination therapies between May 30, 2013, and September 9, 2021. A total of 899 patients with a histologically confirmed diagnosis of mRCC who received treatment with a first-line IOVE or IOIO regimen and had evaluable responses were included. Exposures: Best overall response to first-line IO combination therapy based on Response Evaluation Criteria in Solid Tumors, version 1.1. Main Outcomes and Measures: The primary outcome was the difference in treating physician-assessed objective imaging response based on the type of first-line IO combination therapy received. Secondary outcomes included the identification of baseline characteristics positively associated with objective imaging response and the association of objective imaging response with overall survival. Results: Among 1085 patients with mRCC who received first-line IO combination therapies, 899 patients (median age, 62.8 years [IQR, 55.9-69.2 years]; 666 male [74.2%]) had evaluable responses. A total of 794 patients had information available on IMDC risk classification; of those, 127 patients (16.0%) had favorable risk, 442 (55.7%) had intermediate risk, and 225 (28.3%) had poor risk. With regard to best overall response among all participants, 37 patients (4.1%) had complete response, 344 (38.3%) had partial response, 315 (35.0%) had stable disease, and 203 (22.6%) had progressive disease. Corresponding median overall survival was not estimable (95% CI, 53.3 months to not estimable) among patients with complete response, 55.9 months (95% CI, 44.1 months to not estimable) among patients with partial response, 48.1 months (95% CI, 33.4 months to not estimable) among patients with stable disease, and 13.0 months (95% CI, 8.4-18.1 months) among patients with progressive disease (log rank P < .001). Treatment with IOVE therapy was found to be independently associated with an increased likelihood of obtaining response (OR, 1.89; 95% CI, 1.26-2.81; P = .002) compared with IOIO therapy. The presence of lung metastases (odds ratio [OR], 1.49; 95% CI, 1.01-2.20), receipt of cytoreductive nephrectomy (OR, 1.59; 95% CI, 1.04-2.43), and favorable IMDC risk (OR, 1.93; 95% CI, 1.10-3.39) were independently associated with an increased likelihood of response. Conclusions and Relevance: In this study, treatment with IOVE therapy was associated with significantly increased odds of objective imaging response compared with IOIO therapy. The presence of lung metastases, receipt of cytoreductive nephrectomy, and favorable IMDC risk were associated with increased odds of experiencing objective imaging response. These findings may help inform treatment selection, especially in clinical contexts associated with high-volume multisite metastatic disease, in which obtaining objective imaging response is important.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsLung NeoplasmsCohort StudiesHumansMaleMiddle AgedVascular Endothelial Growth Factor AVascular Endothelial Growth Factor A

Identifiers

PMID35687336
PMCPMC9187954
OpenAlexW4281957023

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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.