Evidence map›Paper›PMID 33850792›Full record

ReviewTranslational andrology and urology2021

Adjuvant therapy in renal cell carcinoma: is it the right strategy to inhibit VEGF?

Veronica Mollica, Alessandro Rizzo, Vincenzo Di Nunno, Matteo Santoni, Liang Cheng, Antonio Lopez-Beltran, Marina Scarpelli, Alessia Cimadamore, Rodolfo Montironi, Francesco Massari

Open access · diamondAbstract readReview
In one paragraph

Review in Translational andrology and urology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. 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

10 authors at 6 institutions in 3 countries.

Veronica MollicaOncologia Medica, Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italia.
Alessandro RizzoOncologia Medica, Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italia.
Vincenzo Di NunnoDepartment of Medical Oncology, Azienda USL of Bologna, Bologna, Italy.
Matteo SantoniMacerata Hospital, Macerata, Italy.
Liang ChengDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Antonio Lopez-BeltranDepartment of Surgery, Cordoba University Medical School, Cordoba, Spain.
Marina ScarpelliSection of Pathological Anatomy, Polytechnic University of the Marche Region, School of Medicine, United Hospitals, Ancona, Italy.
Alessia CimadamoreSection of Pathological Anatomy, Polytechnic University of the Marche Region, School of Medicine, United Hospitals, Ancona, Italy.
Rodolfo MontironiSection of Pathological Anatomy, Polytechnic University of the Marche Region, School of Medicine, United Hospitals, Ancona, Italy.
Francesco MassariOncologia Medica, Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italia.
Marche Polytechnic University · ITMedica (Italy) · ITAzienda USL di Bologna · ITIndiana University School of MedicineOspedale di MacerataUniversity of Córdoba · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite several clinical trials have assessed different agents in the adjuvant setting, renal cell carcinoma (RCC) still remains a disease orphan of an effective adjuvant treatment. In fact, systemic therapies targeting angiogenesis that have been observed to be effective in metastatic setting failed to show an improvement in terms of clinical outcomes when used ad adjuvant treatments. In this study, we performed a meta-analysis of 5 randomized clinical trials to assess the impact of tyrosine kinase inhibitors (TKIs) targeting angiogenesis after surgery: ASSURE, S-TRAC, PROTECT, ATLAS, SORCE. Among the 6,531 patients assessed, we confirmed the lack of efficacy of adjuvant treatments in terms of disease-free survival (DFS) (pooled-HR 0.93, 95% CI, 0.84-1.02, P=0.16) and overall survival (OS) (pooled-HR 0.98, 95% CI, 0.88-1.09, P=0.54). To the best of our knowledge, we still ignore why some treatments active in the metastatic setting do not show similar efficacy as adjuvant treatment. Exploring possible reasons of this apparently conflicting results is important as it may offer new insights that should be evaluated in next generation adjuvant trials. Immune checkpoint inhibitors (ICIs) have reported significant results-as monotherapy or in combinations with other anticancer agents-in metastatic setting, and the results of trials evaluating these agents in the adjuvant setting are awaited.

Indexed as

Adjuvant therapydisease-free survival (DFS)renal cell carcinoma (RCC)tyrosine kinase inhibitor (TKI)

Identifiers

PMID33850792
PMCPMC8039625
OpenAlexW3112480029

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.