Evidence map›Paper›PMID 39887919›Full record

ArticleANZ journal of surgery2025

Vascular encasement image defined risk factors independently predict surgical complications in neuroblastoma.

Rachael Stokes, Aidan Bannon, Bonnie Leung, Jasmin Alloo, David Davies-Payne, Mark Winstanley, Andrew Wood, Stephen Evans, James Hamill

Abstract read
In one paragraph

Article in ANZ journal of surgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Surgical Treatment of Adrenal Neuroblastoma in Children - A Narrative Review.International braz j urol : official journal of the Brazilian Society of Urology
    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

9 authors.

Rachael StokesDepartment of Paediatric Surgery, Starship Children's Hospital, Auckland, New Zealand.ORCID 0000-0002-3796-874X
Aidan BannonDepartment of Paediatric Surgery, Starship Children's Hospital, Auckland, New Zealand.
Bonnie LeungDepartment of Radiology, Starship Children's Hospital, Auckland, New Zealand.
Jasmin AllooDepartment of Oncology, Starship Children's Hospital, Auckland, New Zealand.
David Davies-PayneDepartment of Radiology, Starship Children's Hospital, Auckland, New Zealand.
Mark WinstanleyDepartment of Oncology, Starship Children's Hospital, Auckland, New Zealand.
Andrew WoodDepartment of Oncology, Starship Children's Hospital, Auckland, New Zealand.
Stephen EvansDepartment of Paediatric Surgery, Starship Children's Hospital, Auckland, New Zealand.
James HamillDepartment of Paediatric Surgery, Starship Children's Hospital, Auckland, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpecific image defined risk factors (IDRF) immediately prior to surgery may be more relevant to paediatric oncology surgeons than pre-neoadjuvant IDRFs at diagnosis. The aim of this study was to determine IDRF subtypes that independently predict postoperative complications.

methodsWe searched the New Zealand Children's Cancer Registry for all cases of neuroblastoma treated at a single paediatric oncology centre between January 2007 and February 2021 and determined the IDRF status on pre-operative imaging at diagnosis and after neoadjuvant therapy. Surgical complications (Clavien-Dindo grade) were correlated with total number of IDRFs (pre- and post-chemotherapy) and three subsets: vascular encasement (VE), invasive (I), and extensive (E).

resultsOf 101 patients, 73 underwent surgical resection, and 32 (44%) had a surgical complication. Of the 54 IDRF-positive tumours, all were treated by neoadjuvant therapy and in 17, all IDRFs resolved. Complications correlated with the number of post-neoadjuvant therapy VE-IDRFs at OR 1.2 (95% CI 1.0-1.4, P = 0.02) and extensive IDRFs at OR 1.7 (95% CI 1.1-1.9, P = 0.02). Pre-neoadjuvant IDRF status was not independently associated with complications when controlling for post-neoadjuvant IDRF status. The total number of VE-IDRF reduced from 181 pre-neoadjuvant therapy to 86 post, with tumour encasing the aorta and/or vena cava being the most common.

conclusionsThe vascular encasement and extensive subtypes of IDRF may be more useful prognostic indicators of surgical complications than the total number of IDRFs. This may have implications for reporting IDRF status on preoperative imaging and surgical planning but needs validation in larger cohort studies.

Indexed as

NeuroblastomaPostoperative ComplicationsChildChild, PreschoolFemaleHumansInfantMaleNeoadjuvant TherapyNew ZealandRegistriesRetrospective StudiesRisk Factorsimage defined risk factorsneuroblastomapostoperative complicationssurgical oncology

Identifiers

PMID39887919
PMCPMC12227851

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