Evidence map›Paper›PMID 29492762›Full record

SynthesisTargeted oncology2018

Cabozantinib Versus Standard-of-Care Comparators in the Treatment of Advanced/Metastatic Renal Cell Carcinoma in Treatment-naïve Patients: a Systematic Review and Network Meta-Analysis.

Elvira Schmidt, Johanna Lister, Monika Neumann, Witold Wiecek, Shuai Fu, Anne-Lise Vataire, Jelena Sostar, Shengnan Huang, Florence Marteau

Abstract readNetwork Meta-AnalysisSystematic Review
In one paragraph

Synthesis in Targeted oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Review
  7. Cabozantinib as first-line treatment in advanced renal cell carcinoma: a profile of its use.Drugs & therapy perspectives : for rational drug selection and use · 2018
    Article
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

9 authors.

Elvira SchmidtAnalytica LA-SER Intl. Inc, Chester Platz 1, 79539, Lörrach, Germany. e.schmidt@analytica-laser.com.ORCID 0000-0001-6159-4787
Johanna ListerAnalytica LA-SER Intl. Inc, Chester Platz 1, 79539, Lörrach, Germany.
Monika NeumannAnalytica LA-SER Intl. Inc, Chester Platz 1, 79539, Lörrach, Germany.
Witold WiecekAnalytica LA-SER Intl. Inc, Chester Platz 1, 79539, Lörrach, Germany.
Shuai FuAnalytica LA-SER Intl. Inc, Chester Platz 1, 79539, Lörrach, Germany.
Anne-Lise VataireIPSEN Pharma SAS, Boulogne-Billancourt Cedex, France.
Jelena SostarAnalytica LA-SER Intl. Inc, Chester Platz 1, 79539, Lörrach, Germany.
Shengnan HuangAnalytica LA-SER Intl. Inc, Chester Platz 1, 79539, Lörrach, Germany.
Florence MarteauIPSEN Pharma SAS, Boulogne-Billancourt Cedex, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCabozantinib has recently been evaluated as a first-line treatment in advanced renal cell carcinoma (aRCC).

objectiveTo indirectly assess efficacy of cabozantinib versus standard-of-care (SoC) comparators in the first-line treatment of aRCC.

methodsWe conducted a systematic literature review (SLR) to identify randomized controlled studies in the first-line setting for aRCC. The outcomes analyzed were overall survival (OS) and progression-free survival (PFS). A network meta-analysis (NMA) was conducted comparing OS and PFS hazard ratios (HRs).

resultsThirteen studies were identified in the SLR to be eligible for inclusion in the NMA. The overall study populations were heterogeneous in terms of risk groups; some studies included favorable risk patients. In intermediate-risk patients, HRs (95% confidence interval) for PFS were 0.52 (0.33, 0.82), 0.46 (0.26, 0.80), 0.20 (0.12, 0.36), and 0.37 (0.20, 0.68) when cabozantinib was compared with sunitinib, sorafenib, interferon (IFN), or bevacizumab plus IFN, respectively. In poor-risk patients, the NMA also demonstrated significant superiority in terms of PFS for cabozantinib; HRs were 0.31 (0.11, 0.90), 0.22 (0.06, 0.87), 0.16 (0.04, 0.64), and 0.20 (0.05, 0.88), when cabozantinib was compared with sunitinib, temsirolimus, IFN, or bevacizumab plus IFN, respectively. When the overall study populations were compared, the results were similar to the subgroup analyses. OS HRs in all analyses favored cabozantinib, but were not statistically significant.

conclusionsThe results suggest that cabozantinib significantly increases PFS in intermediate-, and poor-risk subgroups when compared to standard-of-care comparators. Although overall populations included favorable risk patients in some studies, the results seen were consistent with the subgroup analyses.

Indexed as

AnilidesCarcinoma, Renal CellPyridinesHumansAnilidescabozantinibPyridines

Identifiers

PMID29492762
PMCPMC5887000

What OpenQuestion holds

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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.