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Clinical utility of RT-PCR in assessing HER 2 gene expression versus traditional IHC and FISH in breast cancer patients.
Suryavanshi, Moushumi; Mehta, Anurag; Jaipuria, Jiten; Kumar, Dushyant; Vishwakarma, Gayatri; Panigrahi, Manoj Kumar; Verma, Haristuti; Saifi, Mumtaz; Sharma, Sanjeev; Tandon, Simran; Doval, D C; Das, Bhudev C.
Afiliação
  • Suryavanshi M; Centre for Molecular Diagnostic and Cell Biology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, 110085, India. moushumisuryavanshi@gmail.com.
  • Mehta A; Lab Services, Blood Transfusion & Molecular, Rajiv Gandhi Cancer Institute and research Centre, New Delhi, 110085, India.
  • Jaipuria J; Department of Urogynaeoncology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, 110085, India.
  • Kumar D; Centre for Molecular Diagnostic and Cell Biology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, 110085, India.
  • Vishwakarma G; Department of Research, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, 110085, India.
  • Panigrahi MK; Centre for Molecular Diagnostic and Cell Biology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, 110085, India.
  • Verma H; Centre for Molecular Diagnostic and Cell Biology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, 110085, India.
  • Saifi M; Centre for Molecular Diagnostic and Cell Biology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, 110085, India.
  • Sharma S; Centre for Molecular Diagnostic and Cell Biology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, 110085, India.
  • Tandon S; Amity Institute of Molecular Medicine and Stem Cell Research (AIMMSCR) Amity University, Uttar Pradesh Campus, Sector-125, Noida, 201313, India.
  • Doval DC; Medical Oncology, Rajiv Gandhi Cancer Institute and Research Centre, New Delhi, 110085, India.
  • Das BC; Amity Institute of Molecular Medicine and Stem Cell Research (AIMMSCR) Amity University, Uttar Pradesh Campus, Sector-125, Noida, 201313, India.
Breast Cancer ; 25(4): 416-430, 2018 Jul.
Article em En | MEDLINE | ID: mdl-29427123
BACKGROUND: IHC and FISH are used for categorizing HER 2 status in breast cancer at the protein and DNA level, respectively. HER 2 expression at the RNA level is quantitative, cheaper, easier to standardize and free from interobserver variation. METHODS: 115 consecutive patients were tested by IHC, FISH and RT-PCR (test cohort). Assuming FISH result to be the response variable, ROC curves for RT-PCR ratio were analyzed to label HER 2 negative, equivocal and positive cases as RT-PCR score 1, 2 and 3, respectively. Inter-relationships between RT-PCR, IHC and FISH were defined. 'Clinical benefit' of a test was defined as proportion of patients labeled unequivocally as HER 2 positive or negative. Population for 1 year was simulated constraint to previous reports of HER 2 positivity and IHC category distribution by a meta-analysis of previous studies that evaluated concordance between IHC and FISH to determine HER 2 status (simulation cohort). Four diagnostic pathways in the simulation cohort were defined-(1) initial IHC, followed by FISH (conventional pathway); (2) initial RT-PCR, followed by FISH; (3) initial IHC, followed by RT-PCR and then by FISH; (4) initial RT-PCR, followed by IHC and then by FISH. The clinical benefit of IHC and RT-PCR in the four pathways was analyzed and sensitivity analysis for incremental cost-effectiveness ratio and cost-benefit comapring RT-PCR against IHC, both as first-line tests and among those with IHC score 2 as a reflex second-line test was performed by the Monte Carlo technique. FINDINGS: 115 patients comprised the study population. While none with IHC score of 0 or 1 was FISH positive for HER 2, all cases with IHC score of 3 were FISH positive. 43 cases were assigned IHC score of 2. Thus, 72 patients benefited from the initial IHC testing [clinical benefit 62.6%], with the overall concordance between IHC and FISH being 100% for those with IHC score of 0, 1 and 3 (conclusive IHC categories). For RT-PCR with 100% concordance, 15.7% (115-97 = 18) patients would have benefited from RT-PCR testing if it was used as a first-line test. If RT-PCR would have been used as a second-line test among those with IHC score 2 (n = 43), then only 6 patients would have been assigned a conclusive RT-PCR category (category 1 or 3) translating to a clinical benefit of 14% (6/43) as a second-line test. As a second-line test it had 51% probability to prove more cost-effective than the conventional pathway, provided the cost of RT-PCR was 0.4 times the cost of IHC. Also in a three-step pathway, RT-PCR upfront would have 56% probability of higher cost-benefit provided the cost of RT-PCR was 0.1 times the cost of IHC. CONCLUSION: RT-PCR results were found to be suboptimal to IHC in terms of discriminative ability and clinical benefit; thus, it is unlikely to replace IHC as a first-line test in the near future.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Imuno-Histoquímica / Hibridização in Situ Fluorescente / Receptor ErbB-2 / Reação em Cadeia da Polimerase Via Transcriptase Reversa Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Imuno-Histoquímica / Hibridização in Situ Fluorescente / Receptor ErbB-2 / Reação em Cadeia da Polimerase Via Transcriptase Reversa Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article