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Therapeutic Implications of Germline Testing in Patients With Advanced Cancers.
Stadler, Zsofia K; Maio, Anna; Chakravarty, Debyani; Kemel, Yelena; Sheehan, Margaret; Salo-Mullen, Erin; Tkachuk, Kaitlyn; Fong, Christopher J; Nguyen, Bastien; Erakky, Amanda; Cadoo, Karen; Liu, Ying; Carlo, Maria I; Latham, Alicia; Zhang, Hongxin; Kundra, Ritika; Smith, Shaleigh; Galle, Jesse; Aghajanian, Carol; Abu-Rustum, Nadeem; Varghese, Anna; O'Reilly, Eileen M; Morris, Michael; Abida, Wassim; Walsh, Michael; Drilon, Alexander; Jayakumaran, Gowtham; Zehir, Ahmet; Ladanyi, Marc; Ceyhan-Birsoy, Ozge; Solit, David B; Schultz, Nikolaus; Berger, Michael F; Mandelker, Diana; Diaz, Luis A; Offit, Kenneth; Robson, Mark E.
Afiliação
  • Stadler ZK; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Maio A; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Chakravarty D; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Kemel Y; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Sheehan M; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Salo-Mullen E; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Tkachuk K; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Fong CJ; Computational Oncology, Department of Epidemiology and Statistics, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Nguyen B; Computational Oncology, Department of Epidemiology and Statistics, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Erakky A; David M. Rubinstein Center for Pancreatic Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Cadoo K; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Liu Y; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Carlo MI; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Latham A; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Zhang H; Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Kundra R; Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Smith S; Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Galle J; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Aghajanian C; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Abu-Rustum N; Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Varghese A; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • O'Reilly EM; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Morris M; David M. Rubinstein Center for Pancreatic Cancer Research, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Abida W; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Walsh M; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Drilon A; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Jayakumaran G; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Zehir A; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Ladanyi M; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Ceyhan-Birsoy O; Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Solit DB; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Schultz N; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Berger MF; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Mandelker D; Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Diaz LA; Computational Oncology, Department of Epidemiology and Statistics, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Offit K; Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Robson ME; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY.
J Clin Oncol ; 39(24): 2698-2709, 2021 08 20.
Article em En | MEDLINE | ID: mdl-34133209
ABSTRACT

PURPOSE:

Tumor mutational profiling is increasingly performed in patients with advanced cancer. We determined the extent to which germline mutation profiling guides therapy selection in patients with advanced cancer.

METHODS:

Patients with cancer undergoing tumor genomic profiling were prospectively consented for germline cancer predisposition gene analysis (2015-2019). In patients harboring germline likely pathogenic or pathogenic (LP/P) alterations, therapeutic actionability was classified using a precision oncology knowledge base. Patients with metastatic or recurrent cancer receiving germline genotype-directed therapy were determined.

RESULTS:

Among 11,947 patients across > 50 malignancies, 17% (n = 2,037) harbored a germline LP/P variant. By oncology knowledge base classification, 9% (n = 1042) had an LP/P variant in a gene with therapeutic implications (4% level 1; 4% level 3B; < 1% level 4). BRCA1/2 variants accounted for 42% of therapeutically actionable findings, followed by CHEK2 (13%), ATM (12%), mismatch repair genes (11%), and PALB2 (5%). When limited to the 9,079 patients with metastatic or recurrent cancer, 8% (n = 710) harbored level 1 or 3B genetic findings and 3.2% (n = 289) received germline genotype-directed therapy. Germline genotype-directed therapy was received by 61% and 18% of metastatic cancer patients with level 1 and level 3B findings, respectively, and by 54% of BRCA1/2, 75% of mismatch repair, 43% of PALB2, 35% of RAD51C/D, 24% of BRIP1, and 19% of ATM carriers. Of BRCA1/2 patients receiving a poly(ADP-ribose) polymerase inhibitor, 45% (84 of 188) had tumors other than breast or ovarian cancer, wherein the drug, at time of delivery, was delivered in an investigational setting.

CONCLUSION:

In a pan-cancer analysis, 8% of patients with advanced cancer harbored a germline variant with therapeutic actionability with 40% of these patients receiving germline genotype-directed treatment. Germline sequence analysis is additive to tumor sequence analysis for therapy selection and should be considered for all patients with advanced cancer.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação em Linhagem Germinativa / Neoplasias Tipo de estudo: Observational_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: J Clin Oncol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação em Linhagem Germinativa / Neoplasias Tipo de estudo: Observational_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: J Clin Oncol Ano de publicação: 2021 Tipo de documento: Article