Evidence map›Paper›PMID 37440421›Full record

ArticleThe British journal of surgery2023

Predictive value of baseline serum carbohydrate antigen 19-9 level on treatment effect of neoadjuvant chemoradiotherapy in patients with resectable and borderline resectable pancreatic cancer in two randomized trials.

Deesje Doppenberg, Jacob L van Dam, Youngmin Han, Bert A Bonsing, Olivier R Busch, Sebastiaan Festen, Erwin van der Harst, Ignace H de Hingh, Marjolein Y V Homs, Wooil Kwon and 18 more

Open access · hybridAbstract read
In one paragraph

Article in The British journal of surgery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 13 institutions in 2 countries.

Deesje DoppenbergDepartment of Surgery, Amsterdam UMC, Location University of Amsterdam, Amsterdam, the Netherlands.
Jacob L van DamDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.ORCID 0000-0002-6947-9035
Youngmin HanDepartment of Surgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Bert A BonsingDepartment of Surgery, Leiden University Medical Centre, Leiden, the Netherlands.
Olivier R BuschDepartment of Surgery, Amsterdam UMC, Location University of Amsterdam, Amsterdam, the Netherlands.ORCID 0000-0001-9605-6831
Sebastiaan FestenDepartment of Surgery, OLVG, Amsterdam, the Netherlands.
Erwin van der HarstDepartment of Surgery, Maasstad Hospital, Rotterdam, the Netherlands.
Ignace H de HinghDepartment of Surgery, Catherina Hospital, Eindhoven, the Netherlands.
Marjolein Y V HomsDepartment of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
Wooil KwonDepartment of Surgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Mirang LeeDepartment of Surgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Daan J LipsDepartment of Surgery, Medisch Spectrum Twente, Enschede, the Netherlands.
Vincent E de MeijerDepartment of Surgery, University of Groningen and University Medical Centre Groningen, Groningen, the Netherlands.ORCID 0000-0002-7900-5917
I Quintus MolenaarDepartment of Surgery, Regional Academic Cancer Centre Utrecht, University of Utrecht, Utrecht, the Netherlands.
Joost J NuyttensDepartment of Radiation Oncology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
Gijs A PatijnDepartment of Surgery, Isala Oncology Centre, Zwolle, the Netherlands.
Stijn van RoesselDepartment of Surgery, Amsterdam UMC, Location University of Amsterdam, Amsterdam, the Netherlands.ORCID 0000-0002-3041-0452
George P van der SchellingDepartment of Surgery, Amphia Hospital, Breda, the Netherlands.
Mustafa SukerDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
Eva VersteijneCancer Centre Amsterdam, Amsterdam, the Netherlands.
Judith de Vos-GeelenDepartment of Internal Medicine, Division of Medical Oncology, GROW, Maastricht University Medical Centre, Maastricht, the Netherlands.ORCID 0000-0003-2578-1766
Johanna W WilminkCancer Centre Amsterdam, Amsterdam, the Netherlands.
Casper H J van EijckDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
Geertjan van TienhovenCancer Centre Amsterdam, Amsterdam, the Netherlands.
Jin-Young JangDepartment of Surgery, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Korea.
Marc G BesselinkDepartment of Surgery, Amsterdam UMC, Location University of Amsterdam, Amsterdam, the Netherlands.ORCID 0000-0003-2650-9350
Bas Groot KoerkampDepartment of Surgery, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.ORCID 0000-0003-1917-6973
Dutch Pancreatic Cancer Group
Amsterdam University Medical Centers · NLErasmus MC Cancer Institute · NLSeoul National University Hospital · KRAmphia Ziekenhuis · NLIsala · NLLeiden University · NLMaasstad Ziekenhuis · NLMaastricht University Medical Centre · NLMedisch Spectrum Twente · NLOLVG · NLRadboud University Nijmegen · NLUniversity Medical Center Groningen · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGuidelines suggest that the serum carbohydrate antigen (CA19-9) level should be used when deciding on neoadjuvant treatment in patients with resectable and borderline resectable pancreatic ductal adenocarcinoma (hereafter referred to as pancreatic cancer). In patients with resectable pancreatic cancer, neoadjuvant therapy is advised when the CA19-9 level is 'markedly elevated'. This study investigated the impact of baseline CA19-9 concentration on the treatment effect of neoadjuvant chemoradiotherapy (CRT) in patients with resectable and borderline resectable pancreatic cancers.

methodsIn this post hoc analysis, data were obtained from two RCTs that compared neoadjuvant CRT with upfront surgery in patients with resectable and borderline resectable pancreatic cancers. The effect of neoadjuvant treatment on overall survival was compared between patients with a serum CA19-9 level above or below 500 units/ml using the interaction test.

resultsOf 296 patients, 179 were eligible for analysis, 90 in the neoadjuvant CRT group and 89 in the upfront surgery group. Neoadjuvant CRT was associated with superior overall survival (HR 0.67, 95 per cent c.i. 0.48 to 0.94; P = 0.019). Among 127 patients (70, 9 per cent) with a low CA19-9 level, median overall survival was 23.5 months with neoadjuvant CRT and 16.3 months with upfront surgery (HR 0.63, 0.42 to 0.93). For 52 patients (29 per cent) with a high CA19-9 level, median overall survival was 15.5 months with neoadjuvant CRT and 12.9 months with upfront surgery (HR 0.82, 0.45 to 1.49). The interaction test for CA19-9 level exceeding 500 units/ml on the treatment effect of neoadjuvant CRT was not significant (P = 0.501).

conclusionBaseline serum CA19-9 level defined as either high or low has prognostic value, but was not associated with the treatment effect of neoadjuvant CRT in patients with resectable and borderline resectable pancreatic cancers, in contrast with current guideline advice.

Indexed as

AdenocarcinomaPancreatic NeoplasmsCA-19-9 AntigenCarbohydratesChemoradiotherapyHumansNeoadjuvant TherapyRandomized Controlled Trials as TopicRetrospective StudiesCA-19-9 AntigenCarbohydrates

Identifiers

PMID37440421
PMCPMC10480034
OpenAlexW4384118646

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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.