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Bone biopsy protocol for advanced prostate cancer in the era of precision medicine.
Sailer, Verena; Schiffman, Marc H; Kossai, Myriam; Cyrta, Joanna; Beg, Shaham; Sullivan, Brian; Pua, Bradley B; Lee, Kyungmouk Steve; Talenfeld, Adam D; Nanus, David M; Tagawa, Scott T; Robinson, Brian D; Rao, Rema A; Pauli, Chantal; Bareja, Rohan; Beltran, Luis S; Sigaras, Alexandros; Eng, Kenneth Wa; Elemento, Olivier; Sboner, Andrea; Rubin, Mark A; Beltran, Himisha; Mosquera, Juan Miguel.
Affiliation
  • Sailer V; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York.
  • Schiffman MH; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine and New York Presbyterian, New York, New York.
  • Kossai M; Department of Radiology, Weill Cornell Medicine, New York, New York.
  • Cyrta J; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York.
  • Beg S; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine and New York Presbyterian, New York, New York.
  • Sullivan B; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York.
  • Pua BB; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine and New York Presbyterian, New York, New York.
  • Lee KS; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York.
  • Talenfeld AD; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine and New York Presbyterian, New York, New York.
  • Nanus DM; Department of Radiology, Weill Cornell Medicine, New York, New York.
  • Tagawa ST; Department of Radiology, Weill Cornell Medicine, New York, New York.
  • Robinson BD; Department of Radiology, Weill Cornell Medicine, New York, New York.
  • Rao RA; Department of Radiology, Weill Cornell Medicine, New York, New York.
  • Pauli C; Sandra and Edward Meyer Cancer Center, Weill Cornell Medicine and New York Presbyterian, New York, New York.
  • Bareja R; Division of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medicine, New York, New York.
  • Beltran LS; Sandra and Edward Meyer Cancer Center, Weill Cornell Medicine and New York Presbyterian, New York, New York.
  • Sigaras A; Division of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medicine, New York, New York.
  • Eng KW; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York.
  • Elemento O; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine and New York Presbyterian, New York, New York.
  • Sboner A; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York.
  • Rubin MA; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine and New York Presbyterian, New York, New York.
  • Beltran H; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York.
  • Mosquera JM; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine and New York Presbyterian, New York, New York.
Cancer ; 124(5): 1008-1015, 2018 03 01.
Article in En | MEDLINE | ID: mdl-29266381
ABSTRACT

BACKGROUND:

Metastatic biopsies are increasingly being performed in patients with advanced prostate cancer to search for actionable targets and/or to identify emerging resistance mechanisms. Due to a predominance of bone metastases and their sclerotic nature, obtaining sufficient tissue for clinical and genomic studies is challenging.

METHODS:

Patients with prostate cancer bone metastases were enrolled between February 2013 and March 2017 on an institutional review board-approved protocol for prospective image-guided bone biopsy. Bone biopsies and blood clots were collected fresh. Compact bone was subjected to formalin with a decalcifying agent for diagnosis; bone marrow and blood clots were frozen in optimum cutting temperature formulation for next-generation sequencing. Frozen slides were cut from optimum cutting temperature cryomolds and evaluated for tumor histology and purity. Tissue was macrodissected for DNA and RNA extraction, and whole-exome sequencing and RNA sequencing were performed.

RESULTS:

Seventy bone biopsies from 64 patients were performed. Diagnostic material confirming prostate cancer was successful in 60 of 70 cases (85.7%). The median DNA/RNA yield was 25.5 ng/µL and 16.2 ng/µL, respectively. Whole-exome sequencing was performed successfully in 49 of 60 cases (81.7%), with additional RNA sequencing performed in 20 of 60 cases (33.3%). Recurrent alterations were as expected, including those involving the AR, PTEN, TP53, BRCA2, and SPOP genes.

CONCLUSIONS:

This prostate cancer bone biopsy protocol ensures a valuable source for high-quality DNA and RNA for tumor sequencing and may be used to detect actionable alterations and resistance mechanisms in patients with bone metastases. Cancer 2018;1241008-15. © 2017 American Cancer Society.
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Full text: 1 Database: MEDLINE Main subject: Prostate / Prostatic Neoplasms / Bone and Bones / Bone Neoplasms Type of study: Guideline / Observational_studies / Risk_factors_studies Limits: Aged / Aged80 / Humans / Male / Middle aged Language: En Year: 2018 Type: Article

Full text: 1 Database: MEDLINE Main subject: Prostate / Prostatic Neoplasms / Bone and Bones / Bone Neoplasms Type of study: Guideline / Observational_studies / Risk_factors_studies Limits: Aged / Aged80 / Humans / Male / Middle aged Language: En Year: 2018 Type: Article