Evidence map›Paper›PMID 37533955›Full record

ArticleEcancermedicalscience2023

Treatment outcomes and prognostic factors of esthesioneuroblastoma-a retrospective study from South India.

Lekha Madhavan Nair, John Mohan Mathew, Malu Rafi, Kainickal Cessal Thommachan, Jagathnath Krishna Km, Bipin T Varghese, Rejnish Ravikumar

Open access · goldAbstract readCase Reports
In one paragraph

Article in Ecancermedicalscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 78% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 1 institution in 1 country.

Lekha Madhavan NairDepartment of Radiation Oncology, Regional Cancer Centre, Thiruvananthapuram 695011, India.
John Mohan MathewDepartment of Radiation Oncology, Regional Cancer Centre, Thiruvananthapuram 695011, India.
Malu RafiDepartment of Radiation Oncology, Regional Cancer Centre, Thiruvananthapuram 695011, India.
Kainickal Cessal ThommachanDepartment of Radiation Oncology, Regional Cancer Centre, Thiruvananthapuram 695011, India.
Jagathnath Krishna KmDepartment of Epidemiology and Biostatistics, Regional Cancer Centre, Thiruvananthapuram 695011, India.
Bipin T VargheseDepartment of Surgical Oncology, Regional Cancer Centre, Thiruvananthapuram 695011, India.
Rejnish RavikumarDepartment of Radiation Oncology, Regional Cancer Centre, Thiruvananthapuram 695011, India.
Regional Cancer Center, Thiruvananthapuram · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Esthesioneuroblastoma (ENB) or olfactory neuroblastoma is a rare malignant neoplasm arising from the neural crest cells of the olfactory epithelium. The optimum treatment for this rare disease is still unclear. Most of the available literature on this rare head and neck tumour is limited to small retrospective series and single institutional reports. We conducted a retrospective study to investigate the clinical profile, treatment outcomes and prognostic factors of patients with ENB treated at a tertiary cancer centre in south India. Patients with a histopathological diagnosis of ENB treated from 2000 to 2019 were included. Patient demographics, tumour characteristics, stage, treatment details and outcome data were identified from medical records. Overall survival (OS) and disease-free survival (DFS) were estimated using the Kaplan-Meier method and the log-rank test was used for comparison. The prognostic factors were identified using Cox regression analysis. Forty-two patients underwent treatment for ENB from 2000 to 2019. Twenty-six patients underwent surgery. Twelve patients received radical radiotherapy (RT) while 24 patients underwent adjuvant radiation. After a median follow-up of 71 months, the estimated OS and DFS at 4 years were 64.4% and 54%, respectively. The estimated 4-year OS for modified Kadish A, B, C and D stages was 75.0%, 90.9%, 56.4% and 0%, respectively. Modified Kadish stage, nodal involvement, orbital invasion, intracranial extension, surgery, RT treatment and use of chemotherapy were significant predictors of OS and DFS in univariate Cox regression analysis. Orbital invasion and RT treatment were significant predictors of DFS in the multivariate analysis as well. However, only RT treatment came out to be a significant predictor for OS in multivariate Cox regression analysis. Surgery is the mainstay of treatment. Adjuvant RT may improve local control and survival in advanced cases. Advanced modified Kadish stage, lymph node involvement and orbital invasion are associated with poor outcomes.

Indexed as

esthesioneuroblastomaradiotherapysurgerysurvival

Identifiers

PMID37533955
PMCPMC10393312
OpenAlexW4385306241

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LicenceCC BY
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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.