Evidence map›Paper›PMID 25072303›Full record

ArticleBritish journal of cancer2014

A proposed new method for assessing the pathological response to chemotherapy in resected colorectal liver metastases.

M Sebagh, M-A Allard, A S Cunha, A Ruiz, R Araujo, A Lemoine, B Paule, V Delvart, D Cherqui, E Vibert and 1 more

Abstract read
In one paragraph

Article in British journal of cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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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

11 authors.

M Sebagh1] AP-HP Hôpital Paul Brousse, Laboratoire d'Anatomie Pathologique, Villejuif, France [2] Inserm U785, Université Paris-Sud, Villejuif, France.
M-A AllardAP-HP Hôpital Paul Brousse, Centre Hépatobiliaire, Villejuif, France.
A S Cunha1] Inserm U785, Université Paris-Sud, Villejuif, France [2] AP-HP Hôpital Paul Brousse, Centre Hépatobiliaire, Villejuif, France.
A Ruiz1] AP-HP Hôpital Paul Brousse, Centre Hépatobiliaire, Villejuif, France [2] University Medical Center Utrecht, Utrecht, The Netherlands.
R AraujoAP-HP Hôpital Paul Brousse, Centre Hépatobiliaire, Villejuif, France.
A LemoineAP-HP Hôpital Paul Brousse, Laboratoire de Biochimie, Villejuif, France.
B PauleAP-HP Hôpital Paul Brousse, Centre Hépatobiliaire, Villejuif, France.
V DelvartAP-HP Hôpital Paul Brousse, Centre Hépatobiliaire, Villejuif, France.
D CherquiAP-HP Hôpital Paul Brousse, Centre Hépatobiliaire, Villejuif, France.
E Vibert1] Inserm U785, Université Paris-Sud, Villejuif, France [2] AP-HP Hôpital Paul Brousse, Centre Hépatobiliaire, Villejuif, France.
R Adam1] AP-HP Hôpital Paul Brousse, Centre Hépatobiliaire, Villejuif, France [2] Inserm UMRS 776, Université Paris-Sud, Villejuif, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPathological response (PR) to preoperative chemotherapy for colorectal liver metastases (CLM) is recognised as a prognostic factor of outcome. However, the optimal system to assess this parameter is still debated. This study focuses on current methods and proposes a possibly better method for assessing PR.

methodsAmong 223 patients resected for CLM between 2004 and 2011, after more than three cycles of chemotherapy, the percentage of tumour cells, necrosis and fibrosis, and the tumour regression grade were assessed for each of 802 nodules. Pathological response was evaluated according to validated methods and their combinations. A new method combined the percentage of tumour cells and the size of all nodules as follows: , where n is each separate nodule, % is the percentage of remaining tumour cells within nodule n (%) and s is the size of nodule n (cm).The prognostic value of each method was calculated.

resultsAfter a median follow-up of 47 months (3-106), the cumulative 5-year overall survival rate after liver resection was 59%. The proposed method categorised as follows: 0 residual tumour; 0.1-6-cm residual tumour; >6-cm residual tumour, and necrosis rate >50% stratified prognosis (P=0.0027; P=0.02), while the other methods did not. At multivariate analysis, our method remained an independent predictor of outcome (P=0.001).

conclusionsCombining the percentage of tumour cells multiplied by the size of each separate tumour seems to be a better method for assessing PR. External validation is required.

Indexed as

AdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedAntineoplastic AgentsBevacizumabCetuximabCohort StudiesColorectal NeoplasmsCombined Modality TherapyFemaleHumansKaplan-Meier EstimateLiver NeoplasmsMaleMiddle AgedAntibodies, Monoclonal, HumanizedAntineoplastic AgentsBevacizumabCetuximab

Identifiers

PMID25072303
PMCPMC4119974

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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.