Evidence map›Paper›PMID 22872705›Full record

ArticleJournal of clinical pathology2012

Sanger sequencing in routine KRAS testing: a review of 1720 cases from a pathologist's perspective.

Umberto Malapelle, Claudio Bellevicine, Maria Salatiello, Caterina de Luca, Elisabetta Rispo, Palmira Riccio, Lucianna Sparano, Alfonso De Stefano, Chiara Carlomagno, Francesco Maria Maiello and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of clinical pathology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
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  6. The ideal reporting ofPathologica · 2023
    Review
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  8. Diagnostics (Basel, Switzerland) · 2023
    Article
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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

13 authors at 5 institutions in 1 country.

Umberto MalapelleScienze Biomorfologiche e Funzionali, Universitá degli Studi di Napoli Federico II, Napoli, Italy.
Claudio Bellevicine
Maria Salatiello
Caterina de Luca
Elisabetta Rispo
Palmira Riccio
Lucianna Sparano
Alfonso De Stefano
Chiara Carlomagno
Francesco Maria Maiello
Giulia Vita
Oscar Nappi
Giancarlo Troncone
University of Naples Federico II · ITAzienda Ospedaliera S.Maria · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITOspedale Antonio Cardarelli · ITOspedale dei Pellegrini · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSanger sequencing (SS) of PCR products is still the most frequent method to test colorectal cancer for KRAS mutations in routine practice.

methodsAn audit of SS on 1720 routine cases was carried out, taking into account age, gender, specimen type (resection vs biopsies), tumour site (primary vs metastasis), tumour stage, neoplastic cells abundance (>30% vs <30%) and fixation type (buffered formalin vs simple formalin). In a subset of 50 wild-type (WT) patients correlations between SS findings and response rate (RR), progression-free survival (PFS) and overall survival (OS) were also evaluated.

resultsThe tests were informative in 1691 cases (98.3%). Mutations were detected in 671 cases (39.6%). No significant differences in mutation rates were observed with respect to age (p=0.2), gender (p=0.2), specimen type (p=0.3) and formalin fixation (p=0.08). Conversely, KRAS mutant rate was higher in metastatic tissue (50% vs 39%, p=0.02), in samples with over 30% of neoplastic cells (43.4% vs 26.6%, p=0.02) and in tumours tested in stage IV (p=0.05). The RR of SS KRAS WT patients was 26% (one complete and 12 partial responses). The disease control rate (objective responses plus stable disease) was 56%. Median PFS was 4.4 months and median OS was 10.4 months.

conclusionsPathological criteria that make SS a more robust method for KRAS testing and treatment response prediction are neoplastic cell abundance, metastatic tissue sample and stage IV primary tumour.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsColorectal NeoplasmsDisease-Free SurvivalDNA Mutational AnalysisFemaleGenes, rasHumansMaleMiddle AgedMutation

Identifiers

PMID22872705
PMCPMC3461636
OpenAlexW2126901447

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.