Evidence map›Paper›PMID 36842942›Full record

ArticleEuropean urology oncology2023

A Matching-adjusted Indirect Comparison of Nivolumab Plus Cabozantinib Versus Pembrolizumab Plus Axitinib in Patients with Advanced Renal Cell Carcinoma.

Bradley McGregor, Daniel M Geynisman, Mauricio Burotto, Cristina Suárez, Maria T Bourlon, Pedro C Barata, Shuchi Gulati, Stephen Huo, Flavia Ejzykowicz, Steven I Blum and 13 more

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in European urology oncology, 2023. 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
2.3field-weighted citation impact, top 11% 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, 9 citations in OpenAlex.

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

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 13 institutions in 5 countries.

Bradley McGregorThe Lank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Daniel M GeynismanDepartment of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA, USA.
Mauricio BurottoBradford Hill Clinical Research Center, Santiago, Chile.
Cristina SuárezDepartment of Medical Oncology, Vall d'Hebron Institute of Oncology (VHIO), Hospital Universitari Vall d'Hebron, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
Maria T BourlonHematology-Oncology Department, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
Pedro C BarataDeming Department of Medicine, Tulane Medical School, New Orleans, LA, USA.
Shuchi GulatiDivision of Hematology and Oncology, Department of Medicine, University of Cincinnati Cancer Center, Cincinnati, OH, USA.
Stephen HuoWorldwide Health Economics and Outcomes Research US Market, Bristol Myers Squibb, Princeton, NJ, USA.
Flavia EjzykowiczWorldwide Health Economics and Outcomes Research US Market, Bristol Myers Squibb, Princeton, NJ, USA.
Steven I BlumWorldwide Health Economics and Outcomes Research US Market, Bristol Myers Squibb, Princeton, NJ, USA.
Viviana Del TejoUS Medical Oncology, Bristol Myers Squibb, Princeton, NJ, USA.
Melissa HamiltonWorldwide Health Economics and Outcomes Research US Market, Bristol Myers Squibb, Princeton, NJ, USA.
Jessica R MayWorldwide Health Economics and Outcomes Research Markets, Bristol Myers Squibb, Uxbridge, UK.
Ella X DuAnalysis Group, Inc., Los Angeles, CA, USA.
Aozhou WuAnalysis Group, Inc., Los Angeles, CA, USA.
Pavol KralPatient Centered Solutions, IQVIA, Bratislava, Slovakia.
Cristina IvanescuPatient Centered Solutions, IQVIA, Amsterdam, The Netherlands.
Andi ChinAnalysis Group, Inc., Los Angeles, CA, USA.
Keith A BettsAnalysis Group, Inc., Los Angeles, CA, USA.
Chung-Han LeeDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Toni K ChoueiriThe Lank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Brigham and Women's Hospital, Boston, MA, USA; Harvard Medical School, Boston, MA, USA.
David CellaDepartment of Medical Social Sciences, Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL, USA. Electronic address: d-cella@northwestern.edu.
Camillo PortaInterdisciplinary Department of Medicine, University of Bari "A. Moro", Bari, Italy. Electronic address: camillo.porta@gmail.com.
Bristol-Myers Squibb (United States) · USAnalysis Group (United States) · USDana-Farber Cancer Institute · USFox Chase Cancer Center · USHealth Economics and Outcomes Research (United Kingdom) · GBInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MXIQVIA (United Kingdom) · GBMemorial Sloan Kettering Cancer Center · USNorthwestern University · USTulane Medical Center · USUniversity of Bari Aldo Moro · ITUniversity of Cincinnati · USVall d'Hebron Hospital Universitari · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe comparative efficacy and health-related quality of life (HRQoL) outcomes of nivolumab plus cabozantinib versus pembrolizumab plus axitinib as first-line treatments for advanced renal cell carcinoma (aRCC) have not been assessed in head-to-head trials.

objectiveTo assess the efficacy and HRQoL outcomes of nivolumab plus cabozantinib versus pembrolizumab plus axitinib. DESIGN, SETTING, AND

participantsPatient-level data for nivolumab plus cabozantinib from the CheckMate 9ER trial and published data for pembrolizumab plus axitinib from the KEYNOTE-426 trial were used. CheckMate 9ER data were reweighted to match the key baseline characteristics as reported in KEYNOTE-426.

interventionNivolumab (240 mg every 2 wk) plus cabozantinib (40 mg once daily) and pembrolizumab (200 mg every 3 wk) plus axitinib (5 mg twice daily, initially). OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Hazard ratios (HRs) for progression-free survival (PFS), duration of response, overall survival (OS), and deterioration in HRQoL were assessed using weighted Cox proportional-hazard models, with sunitinib as a common anchor. Objective response rates (ORRs) and changes in HRQoL scores from baseline were assessed as difference-in-differences for the two treatments relative to sunitinib. RESULTS AND LIMITATIONS: After balancing patient characteristics between the trials, nivolumab plus cabozantinib was associated with significantly improved PFS (HR [95% confidence interval {CI}] 0.70 [0.53-0.93]; p = 0.01) and a significantly decreased risk of confirmed deterioration in HRQoL (Functional Assessment of Cancer Therapy-Kidney Symptom Index-Disease-related Symptoms: HR [95% CI] 0.48 [0.34-0.69]) versus pembrolizumab plus axitinib. OS was similar between treatments (HR [95% CI] 0.99 [0.67-1.44]; p = 0.94). Nivolumab plus cabozantinib was associated with numerically greater ORRs (difference-in-difference [95% CI] 8.4% [-1.7 to 18.4]; p = 0.10) and longer duration of response (HR [95% CI] 0.79 [0.47-1.31]; p = 0.36) than pembrolizumab plus axitinib. Comparative studies using data with a longer duration of follow-up are warranted.

conclusionsNivolumab plus cabozantinib significantly improved PFS and HRQoL compared with pembrolizumab plus axitinib as first-line treatment for aRCC. PATIENT SUMMARY: This study was conducted to indirectly compare the results of two immunotherapy-based combinations-nivolumab plus cabozantinib versus pembrolizumab plus axitinib-for patients who have not received any treatment for advanced renal cell carcinoma. Patients who received nivolumab plus cabozantinib had a significant improvement in the length of time without worsening of their disease and in their perceived physical and mental health compared with pembrolizumab plus axitinib; patients remained alive for a similar length of time from the start of either treatment. This analysis further adds to our current knowledge of the relative benefits of these two treatment regimens and will help with physician and patient treatment decisions.

Indexed as

Antineoplastic AgentsCarcinoma, Renal CellKidney NeoplasmsAnilidesAntibodies, Monoclonal, HumanizedAxitinibHumansNivolumabPyridinesQuality of LifeSunitinibAnilidesAntibodies, Monoclonal, HumanizedAntineoplastic AgentsAxitinibcabozantinibNivolumabpembrolizumabPyridinesSunitinibAdvanced renal cell carcinomaAxitinibCabozantinibHealth-related quality of lifeMatching-adjusted indirect comparisonNivolumabOverall survivalPembrolizumabProgression-free survival

Identifiers

PMID36842942
OpenAlexW4321769237

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.