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Prevalence and Clinical Implications of Mismatch Repair-Proficient Colorectal Cancer in Patients With Lynch Syndrome.
Ranganathan, Megha; Sacca, Rosalba E; Trottier, Magan; Maio, Anna; Kemel, Yelena; Salo-Mullen, Erin; Catchings, Amanda; Kane, Sarah; Wang, Chiyun; Ravichandran, Vignesh; Ptashkin, Ryan; Mehta, Nikita; Garcia-Aguilar, Julio; Weiser, Martin R; Donoghue, Mark T A; Berger, Michael F; Mandelker, Diana; Walsh, Michael F; Carlo, Maria; Liu, Ying L; Cercek, Andrea; Yaeger, Rona; Saltz, Leonard; Segal, Neil H; Mendelsohn, Robin B; Markowitz, Arnold J; Offit, Kenneth; Shia, Jinru; Stadler, Zsofia K; Latham, Alicia.
Afiliação
  • Ranganathan M; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Sacca RE; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Trottier M; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Maio A; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Kemel Y; Niehaus Center for Inherited Cancer Genomics, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Salo-Mullen E; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Catchings A; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Kane S; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Wang C; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Ravichandran V; Niehaus Center for Inherited Cancer Genomics, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Ptashkin R; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Mehta N; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Garcia-Aguilar J; Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Weiser MR; Department of Surgery, Weill Cornell Medical College, New York, NY.
  • Donoghue MTA; Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Berger MF; Department of Surgery, Weill Cornell Medical College, New York, NY.
  • Mandelker D; Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Walsh MF; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Carlo M; Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Liu YL; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Cercek A; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Yaeger R; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Saltz L; Niehaus Center for Inherited Cancer Genomics, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Segal NH; Department of Medicine, Weill Cornell Medical College, New York, NY.
  • Mendelsohn RB; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Markowitz AJ; Niehaus Center for Inherited Cancer Genomics, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Offit K; Department of Medicine, Weill Cornell Medical College, New York, NY.
  • Shia J; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Stadler ZK; Niehaus Center for Inherited Cancer Genomics, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Latham A; Department of Medicine, Weill Cornell Medical College, New York, NY.
JCO Precis Oncol ; 7: e2200675, 2023 05.
Article em En | MEDLINE | ID: mdl-37262391
PURPOSE: Lynch syndrome (LS)-associated colorectal cancer (CRC) is characterized by mismatch repair-deficiency (MMR-D) and/or microsatellite instability (MSI). However, with increasing utilization of germline testing, MMR-proficient (MMR-P) and/or microsatellite stable (MSS) CRC has also been observed. We sought to characterize MMR-P/MSS CRC among patients with LS. METHODS: Patients with solid tumors with germline MMR pathogenic/likely pathogenic (P/LP) variants were identified on a prospective matched tumor-normal next-generation sequencing (NGS) protocol. CRCs were evaluated for MMR-D via immunohistochemical (IHC) staining and/or MSI via NGS. Clinical variables were correlated with MMR status using nonparametric tests. RESULTS: Among 17,617 patients with solid tumors, 1.4% (n = 242) had LS. A total of 36% (86 of 242) of patients with LS had at least one CRC that underwent NGS profiling, amounting to 99 pooled CRCs assessed. A total of 10% (10 of 99) of CRCs were MMR-P, with 100% concordance between MSS status and retained MMR protein staining. A total of 89% (8 of 9) of patients in the MMR-P group had MSH6 or PMS2 variants, compared with 30% (23 of 77) in the MMR-D group (P = .001). A total of 46% (6 of 13) of PMS2+ patients had MMR-P CRC. The median age of onset was 58 and 43 years for MMR-P and MMR-D CRC, respectively (P = .07). Despite the later median age of onset, 40% (4 of 10) of MMR-P CRCs were diagnosed <50. A total of 60% (6 of 10) of MMR-P CRCs were metastatic compared with 13% (12 of 89) of MMR-D CRCs (P = .002). A total of 33% (3 of 9) of patients with MMR-P CRC did not meet LS testing criteria. CONCLUSION: Patients with LS remained at risk for MMR-P CRC, which was more prevalent among patients with MSH6 and PMS2 variants. MMR-P CRC was later onset and more commonly metastatic compared with MMR-D CRC. Confirmation of tumor MMR/MSI status is critical for patient management and familial risk estimation.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: JCO Precis Oncol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: JCO Precis Oncol Ano de publicação: 2023 Tipo de documento: Article