Your browser doesn't support javascript.
loading
Real-World Performance of a Comprehensive Genomic Profiling Test Optimized for Small Tumor Samples.
Tomlins, Scott A; Hovelson, Daniel H; Suga, Jennifer M; Anderson, Daniel M; Koh, Han A; Dees, Elizabeth C; McNulty, Brendan; Burkard, Mark E; Guarino, Michael; Khatri, Jamil; Safa, Malek M; Matrana, Marc R; Yang, Eddy S; Menter, Alex R; Parsons, Benjamin M; Slim, Jennifer N; Thompson, Michael A; Hwang, Leon; Edenfield, William J; Nair, Suresh; Onitilo, Adedayo; Siegel, Robert; Miller, Alan; Wassenaar, Timothy; Irvin, William J; Schulz, William; Padmanabhan, Arvinda; Harish, Vallathucherry; Gonzalez, Anneliese; Mansoor, Abdul Hai; Kellum, Andrew; Harms, Paul; Drewery, Stephanie; Falkner, Jayson; Fischer, Andrew; Hipp, Jennifer; Kwiatkowski, Kat; Lazo de la Vega, Lorena; Mitchell, Khalis; Reeder, Travis; Siddiqui, Javed; Vakil, Hana; Johnson, D Bryan; Rhodes, Daniel R.
Afiliação
  • Tomlins SA; Strata Oncology, Ann Arbor, MI.
  • Hovelson DH; Strata Oncology, Ann Arbor, MI.
  • Suga JM; Kaiser Permanente, Dept of Medical Oncology, Vallejo, CA.
  • Anderson DM; Metro-Minnesota Community Oncology Research Consortium (MMCORC), St Louis Park, MN.
  • Koh HA; Kaiser Permanente, Bellflower, CA.
  • Dees EC; The University of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC.
  • McNulty B; UNC Rex Healthcare, Raleigh, NC.
  • Burkard ME; University of Wisconsin Carbone Cancer Center, Madison, WI.
  • Guarino M; ChristianaCare's Helen F. Graham Cancer Center & Research Institute, Newark, DE.
  • Khatri J; ChristianaCare's Helen F. Graham Cancer Center & Research Institute, Newark, DE.
  • Safa MM; Kettering Cancer Center, Kettering, OH.
  • Matrana MR; Ochsner Cancer Institute, New Orleans, LA.
  • Yang ES; University of Alabama at Birmingham, Birmingham, AL.
  • Menter AR; Kaiser Permanente Medical Group, Denver, CO.
  • Parsons BM; Gundersen Health System, La Crosse, WI.
  • Slim JN; MultiCare, Auburn, WA.
  • Thompson MA; Advocate Aurora Health Care, Milwaukee, WI.
  • Hwang L; Kaiser Permanente Mid Atlantic, Rockville, MD.
  • Edenfield WJ; Prisma Health Cancer Institute, Greenville, SC.
  • Nair S; Lehigh Valley Health Network, Allentown, PA.
  • Onitilo A; Marshfield Clinic, Marshfield WI.
  • Siegel R; Bon Secours St Francis Cancer Center, Greenville, SC.
  • Miller A; SCL Health Colorado, Broomfield, CO.
  • Wassenaar T; ProHealth Care, Waukesha, WI.
  • Irvin WJ; Bon Secours St Francis Medical Center Midlothian, Midlothian, VA.
  • Schulz W; Swedish American, Rockford, IL.
  • Padmanabhan A; Baptist Health, Lexington, KY.
  • Harish V; High Point Medical Center, High Point, NC.
  • Gonzalez A; UT Health-Memorial Hermann Cancer Institute, Houston, TX.
  • Mansoor AH; Kaiser Permanente Northwest, Portland, OR.
  • Kellum A; North Mississippi Medical Center, Tupelo, MS.
  • Harms P; University of Michigan Health Systems, Ann Arbor, MI.
  • Drewery S; Strata Oncology, Ann Arbor, MI.
  • Falkner J; Strata Oncology, Ann Arbor, MI.
  • Fischer A; Strata Oncology, Ann Arbor, MI.
  • Hipp J; Strata Oncology, Ann Arbor, MI.
  • Kwiatkowski K; Strata Oncology, Ann Arbor, MI.
  • Lazo de la Vega L; Strata Oncology, Ann Arbor, MI.
  • Mitchell K; Current address: Brigham & Women's Hospital, Boston, MA.
  • Reeder T; Strata Oncology, Ann Arbor, MI.
  • Siddiqui J; Strata Oncology, Ann Arbor, MI.
  • Vakil H; Strata Oncology, Ann Arbor, MI.
  • Johnson DB; Strata Oncology, Ann Arbor, MI.
  • Rhodes DR; Strata Oncology, Ann Arbor, MI.
JCO Precis Oncol ; 52021 08.
Article em En | MEDLINE | ID: mdl-34476329
ABSTRACT

PURPOSE:

Tissue-based comprehensive genomic profiling (CGP) is increasingly used for treatment selection in patients with advanced cancer; however, tissue availability may limit widespread implementation. Here, we established real-world CGP tissue availability and assessed CGP performance on consecutively received samples. MATERIALS AND

METHODS:

We conducted a post hoc, nonprespecified analysis of 32,048 consecutive tumor tissue samples received for StrataNGS, a multiplex polymerase chain reaction (PCR)-based comprehensive genomic profiling (PCR-CGP) test, as part of an ongoing observational trial (NCT03061305). Sample characteristics and PCR-CGP performance were assessed across all tested samples, including exception samples not meeting minimum input quality control (QC) requirements (< 20% tumor content [TC], < 2 mm2 tumor surface area [TSA], DNA or RNA yield < 1 ng/µL, or specimen age > 5 years). Tests reporting ≥ 1 prioritized alteration or meeting TC and sequencing QC were considered successful. For prostate carcinoma and lung adenocarcinoma, tests reporting ≥ 1 actionable or informative alteration or meeting TC and sequencing QC were considered actionable.

RESULTS:

Among 31,165 (97.2%) samples where PCR-CGP was attempted, 10.7% had < 20% TC and 59.2% were small (< 25 mm2 tumor surface area). Of 31,101 samples evaluable for input requirements, 8,089 (26.0%) were exceptions not meeting requirements. However, 94.2% of the 31,101 tested samples were successfully reported, including 80.5% of exception samples. Positive predictive value of PCR-CGP for ERBB2 amplification in exceptions and/or sequencing QC-failure breast cancer samples was 96.7%. Importantly, 84.0% of tested prostate carcinomas and 87.9% of lung adenocarcinomas yielded results informing treatment selection.

CONCLUSION:

Most real-world tissue samples from patients with advanced cancer desiring CGP are limited, requiring optimized CGP approaches to produce meaningful results. An optimized PCR-CGP test, coupled with an inclusive exception testing policy, delivered reportable results for > 94% of samples, potentially expanding the proportion of CGP-testable patients and impact of biomarker-guided therapies.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genoma Humano / Neoplasias Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: JCO Precis Oncol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genoma Humano / Neoplasias Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: JCO Precis Oncol Ano de publicação: 2021 Tipo de documento: Article