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- Ensaio Clínico NCT01744860
Comparison of In-House Methods and Cobas BRAF V600 Mutation Assay in Melanoma Tumor Samples
25 de fevereiro de 2016 atualizado por: Hoffmann-La Roche
Evaluation of Concordance Between the Methods Used in INCa Platforms and the Cobas® 4800 BRAF V600 Mutation Test for Detection of BRAF V600 Mutations in Melanoma in Real Life Setting
This non-interventional study will compare the Cobas BRAF V600 mutation assay with in-house methods used in molecular laboratories for the assessment of the BRAF mutation status in melanoma tumor samples.
No patients will be enrolled in this study.
Data will be collected for approximately 6 months.
Visão geral do estudo
Status
Concluído
Condições
Tipo de estudo
Observacional
Inscrição (Real)
420
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Locais de estudo
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Boulogne Billancourt, França, 92104
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Colmar, França, 68024
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Lille, França, 59037
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Lyon, França, 69437
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Marseille, França, 13015
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Montpellier, França, 34295
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Nantes, França, 44093
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Paris, França, 75010
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Pessac, França, 33604
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Rouen, França, 76031
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Vandoeuvre Les Nancy, França, 54511
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Villejuif, França, 94505
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Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
- Filho
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Não
Gêneros Elegíveis para o Estudo
Tudo
Método de amostragem
Amostra de Probabilidade
População do estudo
No patients are enrolled in this study.
Use of melanoma tumor samples.
Descrição
Inclusion Criteria:
No patients are enrolled. Use of tumor samples only.
- Histologically proven melanoma tumor sample
- Any type of tumor sample: biopsy or surgical specimen of primary tumor or metastasis
- Tumor samples must be fixed and paraffin-embedded.
Exclusion Criteria:
No patients are enrolled. Use of tumor samples only.
- Fixative unknown
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
Coortes e Intervenções
Grupo / Coorte |
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INCa molecular genetics laboratory "in-house" methods
BRAF V600 mutations were analysed using INCa (Institut National du Cancer [French National Cancer Institute]) molecular genetics laboratories using "in-house" methods
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Cobas 4800 Mutation Test
BRAF V600 mutations were analysed using Cobas 4800 mutation test
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
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BRAF Mutation Status According to Cobas 4800 BRAF V600 Mutation Test vs. INCa Laboratories Molecular Genetics Laboratories
Prazo: Up to 6 months
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BRAF V600 mutation status was determined by INCa molecular laboratories "in-house" methods and Cobas 4800 BRAF V600 mutation test.
Samples were analysed as V600 mutation, No V600 mutation and Non evaluable.
Additionally, the type of V600 mutation (E, K, R, D, E2, other V600 mutation, not specified) was also evaluated only by INCa molecular laboratory "in-house" method.
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Up to 6 months
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
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Tumor Sample Characteristics-Type of Tumor Sample
Prazo: Up to 6 months
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The type of tumor sample used for evaluation of BRAF V600 mutation whether it was a biopsy or surgical specimen were reported
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Up to 6 months
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Tumor Sample Characteristics - Source of Tumor Sample
Prazo: Up to 6 months
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The source of tumor sample for BRAF V600 mutation detection whether taken from internal or external pathology laboratory were reported
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Up to 6 months
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Type of Pathology Laboratory Performing the Fixation or Embedding-Pre-analytical Method
Prazo: Up to 6 months
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The external or internal pathology laboratories involved in the process of fixation or embedding of the tumor sample was evaluated.
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Up to 6 months
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Time From Sampling to Fixation- Pre-analytical Method
Prazo: Up to 6 months
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Time taken from the sampling to the fixation of the tumor sample was reported in range of 0-2 hours, 2-6 hours, >6 hours and unknown.
Number of samples falling in each of the class were reported.
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Up to 6 months
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Type of Fixative Used- Pre-analytical Method
Prazo: Up to 6 months
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The different types of fixative Excell, formol, alcohol formol acetic acid and other, used to fix the tumor samples were reported.
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Up to 6 months
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Fixation Duration by Pre-analytical Method
Prazo: Up to 6 months
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Fixation duration is defined as the amount of time required in hours for the fixation of a samples.
The fixation duration was categorized as <6 hours, 6-24 hours and >24 hours and unknown.
Number of samples falling in each category were reported
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Up to 6 months
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Slice Thickness by Pre-analytical Method
Prazo: Up to 6 months
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Slice thickness of all the tumour samples was measured.
The slice thickness was measured in micrometer.
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Up to 6 months
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Dewaxing by Pre-analytical Method
Prazo: Up to 6 Months
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Dewaxing is a method to recover the DNA from samples.
Dewaxing information was collected as "Yes, No or Missing"
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Up to 6 Months
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Necrosis Percentage Determination by Pre-analytical Method
Prazo: Up to 6 months
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The percentage of necrosis defined as the death of one or more cells in the analysed zone was reported.
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Up to 6 months
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Percentage of Tumor Cells by Pre-analytical Method
Prazo: Up to 6 months
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The percentage of tumor cells in the given tumor sample were reported.
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Up to 6 months
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Tumor Samples With Presence of Melanin by Pre-analytical Method
Prazo: Up to 6 months
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The tumor samples with presence of melanin were categorized as Important, Few, Medium and Absent.
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Up to 6 months
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DNA Extraction - Extraction Method by Pre-analytical Method
Prazo: Up to 6 months
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This method assessed DNA from the tumor samples was extracted by Automated method or Manual method.
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Up to 6 months
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Median DNA Elution Volume by Pre-analytical Method
Prazo: Up to 6 months
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Median DNA elution volume microliters [mcl] was reported.
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Up to 6 months
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Mean DNA Concentration by Pre-analytical Method
Prazo: Up to 6 months
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The DNA concentration in the tissue elute was measured in nanogram per microliter (ng/mcL).
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Up to 6 months
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Amount of DNA by Pre-analytical Method
Prazo: Up to 6 months
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The total DNA concentration extracted from the tissue was measured in nanogram (ng).
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Up to 6 months
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Size of Amplicons Used by "In-house" Analytical Method
Prazo: Up to 6 months
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The method described the size of amplicon used.
It was measured in base pairs (bp).
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Up to 6 months
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Method of Mutation Detection by "In-house" Analytical Method
Prazo: Up to 6 months
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Allele-specific PCR, High Resolution Melting (HRM) + Sanger sequencing, Pyrosequencing, Sanger sequencing, Real time PCR, SNaPshot were used for BRAF V600 mutation detection.
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Up to 6 months
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Number of Samples Punched in In-house Analytical Method
Prazo: Up to 6 months
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Total number of samples for whom punch was used in 'in-house analytical' method are reported.
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Up to 6 months
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Mean Number of Slices Per Sample Used for "In-house"- Analytical Method
Prazo: Up to 6 months
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The mean of number of slices per sample when no punch was used are reported.
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Up to 6 months
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Median Time Between Receipt of Samples and Determination of Result by "In-house" Analytical Method
Prazo: Up to 6 months
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This In-house analytical method measured the time between receipt of samples to the result determination.
It measured the time in days.
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Up to 6 months
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Technician Work Time Between DNA Extraction and Result by "In-house" Analytical Method
Prazo: Up to 6 months
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The working time required by the technician from the time of DNA extraction to the time to obtain the results was measured in hours.
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Up to 6 months
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Mean DNA Concentration as Measured by COBAS 4800 BRAF V600 Mutation Test-Analytical Method
Prazo: Up to 6 months
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The DNA concentration as assessed by COBAS 4800 BRAF V600 Mutation assay was reported.
The unit used to measure the DNA concentration was nanogram/microlitre (ng/mcl)
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Up to 6 months
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Punch Used for Cobas 4800 BRAF V600 Mutation Test- Analytical Method
Prazo: Up to 6 months
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The punch done during Cobas 4800 BRAF V600 Mutation Test on the sample was described as Yes or No.
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Up to 6 months
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Number of Slices Used When No Punch Was Used for Cobas 4800 BRAF V600 Mutation Test- Analytical Method
Prazo: Up to 6 months
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This describes the Cobas 4800 BRAF V600 Mutation Test, for the mean of number of slices when No punch method, was used.
Of the 420 samples, punch was Yes, for 45 samples and punch was No, for 375 samples.
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Up to 6 months
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Median Time Between Receipt of Sample and Determination of Result by Cobas 4800 BRAF V600 Mutation Test -Analytical Method
Prazo: Up to 6 months
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This analytical method for cobas 4800 BRAF V600 Mutation Test measured the time between receipt of samples to the result determination.
It measured the time in days.
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Up to 6 months
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Technician Work Time Between DNA Extraction and Result by Cobas 4800 BRAF V600 Mutation Test - Analytical Method
Prazo: Up to 6 months
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This cobas 4800 BRAF V600 Mutation Test analytical method measures the working time required by the technician from the time of DNA extraction to the time to obtain the results.
The time duration was measured in hours.
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Up to 6 months
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Management of Discordance- Method Used to Manage Discordance
Prazo: Up to 6 months
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Crossing DNA, DNA from In-House method analysed with cobas, SNaPshot, DNA from cobas analysed with In-House method, external site control test, Sanger sequencing, Kit CE-IVD Therascreen RGQ Qiagen, Kit Therascreen RGQ BRAF + Pyrosequencing by another platform (PF), Pyrosequencing, Mutation detection On Another Block, (primitive tumor [prm.
tmr]), Sequencing And Therascreen kit (Qiagen) were used for management of discordance between "in-house" method and Cobas 4800 mutation test.
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Up to 6 months
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Management of Discordance-Final Result for BRAF V600 Mutation Detection
Prazo: Up to 6 months
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The final results obtained by discordance management of the 28 discordant samples were BRAF V600 mutation, No BRAF V600 mutation and Non-evaluable.
These results were further assessed by the Investigator and interpreted as final result.
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Up to 6 months
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Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo
1 de dezembro de 2012
Conclusão Primária (Real)
1 de abril de 2013
Conclusão do estudo (Real)
1 de abril de 2013
Datas de inscrição no estudo
Enviado pela primeira vez
6 de dezembro de 2012
Enviado pela primeira vez que atendeu aos critérios de CQ
6 de dezembro de 2012
Primeira postagem (Estimativa)
7 de dezembro de 2012
Atualizações de registro de estudo
Última Atualização Postada (Estimativa)
28 de março de 2016
Última atualização enviada que atendeu aos critérios de controle de qualidade
25 de fevereiro de 2016
Última verificação
1 de novembro de 2015
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- ML28471
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