Evidence map›Paper›PMID 39563716›Full record

ArticleTherapeutic advances in medical oncology2024

SUNLAND: a randomized, double-blinded phase II GERCOR trial of sunitinib versus placebo and lanreotide in patients with advanced progressive midgut neuroendocrine tumors.

Pascal Hammel, Denis Smith, Pauline Afchain, Sophie Dominguez-Tinajero, Jean-François Seitz, Astrid Lievre, Eric Van Cutsem, Eric Assenat, Frédéric Di Fiore, Marc Peeters and 6 more

Abstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2024. 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
–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

2 citing papers in PubMed.

  1. Article
  2. 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

16 authors.

Pascal HammelDigestive and Medical Oncology Department, Hôpital Paul Brousse, University of Paris-Saclay, 12 Avenue Paul Vaillant-Couturier, 94800 Villejuif, France.ORCID https://orcid.org/0000-0002-4630-4996
Denis SmithCHU Haut-Lévêque, Pessac, France.
Pauline AfchainHôpital Saint-Antoine (AP-HP), University of Paris, Paris, France.
Sophie Dominguez-TinajeroHôpital Saint-Vincent de Paul, Lille, France.
Jean-François SeitzHôpital de la Timone, Marseille, France.
Astrid LievreHôpital Pontchaillou, Rennes, France.
Eric Van CutsemUZ Leuven, Campus Gasthuisberg, Leuven, Belgium.
Eric AssenatHôpital Saint Eloi, Montpellier, France.
Frédéric Di FioreHôpital Charles Nicolle, Rouen, France.
Marc PeetersULB, Bruxelles, Belgium.
Iradj SobhaniHôpital Henri Mondor (AP-HP), Créteil, France.
Eric RaymondHôpital Saint-Joseph, Paris, France.
Emilie ChartonMethodology and Quality of Life Unit in Oncology, University Hospital of Besançon, Besançon, France.
Dewi VernereyMethodology and Quality of Life Unit in Oncology, University Hospital of Besançon, Besançon, France.
Louis De MestierHôpital Beaujon (AP-HP), Clichy, France.
Catherine Lombard-BohasHôpital Edouard Herriot, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sunitinib, a multitarget tyrosine kinase inhibitor, showed encouraging antitumor activity and manageable toxicity in patients with advanced midgut neuroendocrine tumors (NETs) in earlier results from phase I and II trials. Patients and methods: In this phase II trial, patients with a nonresectable grade 1 or 2 midgut progressive NET and Eastern Cooperative Oncology Group performance status 0-1 were randomly assigned 1:1 to receive 37.5 mg sunitinib or a placebo, combined with 120 mg lanreotide autogel every 28 days. The planned sample size was 104 patients. The primary outcome was investigator-assessed progression-free survival (PFS). Results: The study was stopped early because of insufficient patient recruitment. Between January 2013 and December 2016, 44 patients were enrolled and received sunitinib ( Conclusion: Our study does not provide enough evidence to conclude the role of sunitinib in advanced midgut NETs, primarily due to a lower-than-expected number of enrolled patients. While we cannot entirely rule out the efficacy of sunitinib, lanreotide alone may play a significant role. Trial registration: EudraCT: 2012-001098-94.

Indexed as

lanreotidemidgutneuroendocrine tumorquality of lifesunitinib

Identifiers

PMID39563716
PMCPMC11574894

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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.