Evidence map›Paper›PMID 37875466›Full record

ArticleNature communications2023

Integrated radiogenomics models predict response to neoadjuvant chemotherapy in high grade serous ovarian cancer.

Mireia Crispin-Ortuzar, Ramona Woitek, Marika A V Reinius, Elizabeth Moore, Lucian Beer, Vlad Bura, Leonardo Rundo, Cathal McCague, Stephan Ursprung, Lorena Escudero Sanchez and 16 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
15.9field-weighted citation impact, top 1% 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

45 citing papers in PubMed, 58 citations in OpenAlex.

  1. Integrating multi-omics data for next-generation cancer research and precision medicine.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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  8. Special Issue "Resistance to Therapy in Ovarian Cancers".International journal of molecular sciences · 2026
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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

26 authors at 7 institutions in 5 countries.

Mireia Crispin-Ortuzar *Department of Oncology, University of Cambridge, Cambridge, UK. mc973@cam.ac.uk.ORCID http://orcid.org/0000-0002-4351-3709
Ramona Woitek *Cancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-9146-9159
Marika A V ReiniusCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-9778-3317
Elizabeth MooreCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Lucian BeerCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-4388-7580
Vlad BuraCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.
Leonardo RundoCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.
Cathal McCagueCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-9588-267X
Stephan UrsprungCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-2476-178X
Lorena Escudero SanchezCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-3464-9206
Paula Martin-GonzalezCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.
Florent MouliereCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0001-7043-0514
Dineika ChandranandaCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-8834-9500
James MorrisCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Teodora GoranovaCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Anna M PiskorzCancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.
Naveena SinghDepartment of Cellular Pathology, Barts Health NHS Trust, London, UK.
Anju SahdevDepartment of Radiology, Barts Health NHS Trust, London, UK.ORCID http://orcid.org/0000-0001-8520-3031
Roxana Pintican"Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Marta ZerunianDepartment of Surgical and Medical Sciences and Translational Medicine, Sapienza University of Rome-Sant'Andrea University Hospital, Rome, Italy.
Nitzan RosenfeldCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-2825-4788
Helen AddleyCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.
Mercedes Jimenez-LinanCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.
Florian MarkowetzCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-2784-5308
Evis SalaCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.
James D BrentonCancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-5738-6683
University of Cambridge · GBBarts Health NHS Trust · GBDanube Private University · ATIuliu Hațieganu University of Medicine and Pharmacy · ROSapienza University of Rome · ITUniversità Cattolica del Sacro Cuore · ITUniversity of Salerno · IT

Funding

Cancer Research UK 28292Cancer Research UK A17197Cancer Research UK A19274Cancer Research UK A20240Cancer Research UK A22905Cancer Research UK A25117Cancer Research UK A27066Cancer Research UK C9545/A29580Department of Health BRC-1215-20014Department of Health RC-1215-20014Medical Research CouncilWellcome TrustWellcome Trust RG98755
6 · The paper itself

Abstract

High grade serous ovarian carcinoma (HGSOC) is a highly heterogeneous disease that typically presents at an advanced, metastatic state. The multi-scale complexity of HGSOC is a major obstacle to predicting response to neoadjuvant chemotherapy (NACT) and understanding critical determinants of response. Here we present a framework to predict the response of HGSOC patients to NACT integrating baseline clinical, blood-based, and radiomic biomarkers extracted from all primary and metastatic lesions. We use an ensemble machine learning model trained to predict the change in total disease volume using data obtained at diagnosis (n = 72). The model is validated in an internal hold-out cohort (n = 20) and an independent external patient cohort (n = 42). In the external cohort the integrated radiomics model reduces the prediction error by 8% with respect to the clinical model, achieving an AUC of 0.78 for RECIST 1.1 classification compared to 0.47 for the clinical model. Our results emphasize the value of including radiomics data in integrative models of treatment response and provide methods for developing new biomarker-based clinical trials of NACT in HGSOC.

Indexed as

Ovarian NeoplasmsBiomarkers, TumorFemaleHumansNeoadjuvant TherapyBiomarkers, Tumor

Identifiers

PMID37875466
PMCPMC10598212
OpenAlexW4387903981

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.