Reported categories of somatic mutations (A) and germline mutations (B) are shown. Germline testing for autosomal recessive carrier mutations was performed if requested by the parents at the time of study enrollment. PCG indicates pharmacogenetic; VUS, variant of uncertain significance. The image in panel B was adapted from the study by Scollon et al,7 an open access article. For more information on the categorization of TSC2 frameshift as a category II mutation, see Perry et al,8 Krueger et al,9 and Iyer et al.10
A, Highest category of somatic mutation per participant identified by tumor whole-exome sequencing (WES). Data for the subsets of children with central nervous system (CNS) tumors (n = 40) and non-CNS tumors (n = 81) are shown in addition to the entire patient cohort with tumor samples available (n = 121). I indicates category I mutation; II, category II mutation; III, category III mutation; IV, category IV or no mutation. B, Genes targeted by recurrent somatic mutations in patients for whom tumor WES was performed.
Mutations with known or potential clinical implications identified by tumor and germline WES of children with newly diagnosed solid tumors. Each slice represents a different patient undergoing both tumor and germline sequencing (n = 121), and each concentric ring a category of somatic or germline mutation.
eMethods. Variant Categorization Based on Clinical Utility
eFigure 1. Tumor Whole Exome Sequencing Analysis Pipeline
eFigure 2. Overview of the BASIC3 Clinical Study
eTable 1. Somatic Variant Filters
eTable 2. Familial Cancer Gene List
eTable 3. Somatic Category I Genes and Mutations
eTable 4. Somatic Category II Genes
eTable 5. Somatic Category III Genes
eTable 6. Patient Demographics and Clinical Characteristics
eTable 7. Validated Somatic Mutations Detected by Tumor Whole Exome Sequencing
eTable 8. Number of Somatic Mutations Reported by Clinical Category
eTable 9. Diagnostic Germline Findings Related to Patient Phenotype (expanded)
eTable 10. Single Recessive Mutations in Genes Related to Patient Phenotype
eTable 11. Incidental Findings Identified by Whole Exome Sequencing
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Parsons DW, Roy A, Yang Y, et al. Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors. JAMA Oncol. 2016;2(5):616–624. doi:10.1001/jamaoncol.2015.5699
Whole-exome sequencing (WES) has the potential to reveal tumor and germline mutations of clinical relevance, but the diagnostic yield for pediatric patients with solid tumors is unknown.
To characterize the diagnostic yield of combined tumor and germline WES for children with solid tumors.
Unselected children with newly diagnosed and previously untreated central nervous system (CNS) and non-CNS solid tumors were prospectively enrolled in the BASIC3 study at a large academic children’s hospital during a 23-month period from August 2012 through June 2014. Blood and tumor samples underwent WES in a certified clinical laboratory with genetic results categorized on the basis of perceived clinical relevance and entered in the electronic health record.
Main Outcomes and Measures
Clinical categorization of somatic mutations; frequencies of deleterious germline mutations related to patient phenotype and incidental medically-actionable mutations.
Of the first 150 participants (80 boys and 70 girls, mean age, 7.4 years), tumor samples adequate for WES were available from 121 patients (81%). Somatic mutations of established clinical utility (category I) were reported in 4 (3%) of 121 patients, with mutations of potential utility (category II) detected in an additional 29 (24%) of 121 patients. CTNNB1 was the gene most frequently mutated, with recurrent mutations in KIT, TSC2, and MAPK pathway genes (BRAF, KRAS, and NRAS) also identified. Mutations in consensus cancer genes (category III) were found in an additional 24 (20%) of 121 tumors. Fewer than half of somatic mutations identified were in genes known to be recurrently mutated in the tumor type tested. Diagnostic germline findings related to patient phenotype were discovered in 15 (10%) of 150 cases: 13 pathogenic or likely pathogenic dominant mutations in adult and pediatric cancer susceptibility genes (including 2 each in TP53, VHL, and BRCA1), 1 recessive liver disorder with hepatocellular carcinoma (TJP2), and 1 renal diagnosis (CLCN5). Incidental findings were reported in 8 (5%) of 150 patients. Most patients harbored germline uncertain variants in cancer genes (98%), pharmacogenetic variants (89%), and recessive carrier mutations (85%).
Conclusions and Relevance
Tumor and germline WES revealed mutations in a broad spectrum of genes previously implicated in both adult and pediatric cancers. Combined reporting of tumor and germline WES identified diagnostic and/or potentially actionable findings in nearly 40% of newly diagnosed pediatric patients with solid tumors.
Genome-scale sequencing methods such as whole-exome sequencing (WES) have provided significant insight into the pathogenesis of cancer as well as a wide spectrum of human diseases.1 Recent studies have begun to establish the yield of WES for the diagnosis of Mendelian disorders and the discovery of incidental (non–phenotype-related) medically actionable findings.2-4 However, experience with the use of these tests in the care of patients with cancer remains limited.
Sequencing of tumor and matched normal samples can reveal multiple types of results with implications for clinical practice. The identification of somatic (tumor-specific) mutations has the potential to offer diagnostic and prognostic information and inform selection of therapies, particularly for patients with relapsed or refractory tumors.5 Detection of germline mutations in cancer susceptibility genes may prompt further genetic testing and guide cancer surveillance strategies for both the patient and family members.6 Germline mutations may also explain noncancer phenotypes, predict drug responses, or provide reproductive counseling information for parents (Figure 1).7-11
The BASIC3 (Baylor College of Medicine Advancing Sequencing in Childhood Cancer Care) study is a Clinical Sequencing Exploratory Research (CSER) consortium project funded by the National Genome Human Research Institute (NHGRI) and National Cancer Institute (NCI) focusing on prospective implementation of clinical WES in the pediatric oncology clinic.12 To characterize the diagnostic yield of combined tumor and germline WES for children with newly diagnosed solid tumors, we report here the results for 150 consecutive BASIC3 study patients sequenced in a laboratory certified by the College of American Pathologists (CAP) and Clinical Laboratory Improvement Act (CLIA).
Question: What is the feasibility and diagnostic yield of clinical tumor and germline whole-exome sequencing (WES) in an unselected cohort of children with newly diagnosed solid tumors of both the central nervous system and elsewhere?
Findings: Somatic mutations of established or potential clinical utility were identified in 27% of patients, and pathogenic or likely pathogenic germline mutations in adult and pediatric cancer susceptibility genes were identified in more than 8% of patients. Combined reporting of tumor and germline WES identified diagnostic and/or potentially actionable findings in nearly 40% of newly diagnosed pediatric patients with solid tumors.
Meaning: This study highlights the diversity of tumor and germline results detectable by clinical WES, including many genes not previously associated with the specific pediatric tumor diagnosed in the patient.
The BASIC3 study was approved by the institutional review board of Baylor College of Medicine. Study enrollment was offered to all patients having diagnostic tumor surgery or biopsy at Texas Children’s Hospital for newly diagnosed and previously untreated central nervous system (CNS) and non-CNS solid tumors who had at least 1 English- or Spanish-speaking parent and planned ongoing oncology care at Texas Children’s Cancer Center.7 Written informed consent was obtained for all study participants. Patients with benign non-CNS tumors not requiring ongoing oncology care were excluded.
At study entry, the study medical geneticist or genetic counselor reviewed the age, cancer diagnosis, medical record (including family history), and parental surveys and determined whether clinical genetic testing would be considered as part of routine care, and if so, which specific test(s) would be used. The Texas Children’s Hospital electronic health record was reviewed for all patients as of April 1, 2015, for any germline genetic or molecular tumor testing ordered.
Peripheral blood samples were obtained from all study patients and requested from parents. Fresh tumor from pretreatment diagnostic specimens, if available, was snap frozen for the study by the consultant pathologist. A confirmatory pathology review was conducted for each tumor sample. Study genetic counselors completed a clinical WES requisition form for each patient including tumor diagnosis, other medical diagnoses, and family history.
Whole-exome sequencing was performed in the CAP- and CLIA-certified Whole Genome Laboratory at Baylor College of Medicine following a previously described protocol,2,3 including library construction, exome capture by VCRome, version 2.113 (Roche NimbleGen), and paired-end sequencing on an Illumina HiSeq instrument (Illumina Inc). Tumor and germline library pairs were sequenced on a single lane of a HiSeq 2000/2500, with a mean coverage of 272× and a target base coverage of 20× at 97.3%. Germline-only samples were run 3 per lane.
Data analysis for germline samples was performed as previously described.2,3 Tumor exomes were similarly analyzed using the Mercury v.3 pipeline,14 including variant calling and annotation (eFigure 1 in Supplement 1). A somatic variant list was generated for each patient by subtracting the germline .vcf from the tumor .vcf and applying somatic filters (eTable 1 in Supplement 2) to the merged file with a tumor variant ratio cutoff of 0.05 or greater. Somatic mutations were annotated with information from the Catalog of Somatic Mutations in Cancer (COSMIC) database.15,16 A FamCan (Familial Cancer) variant list was also populated with germline variants in a list of cancer predisposition syndrome genes (eTable 2 in Supplement 2) to allow detection of biallelic mutations (second hits) in the tumor or loss of heterozygosity (LOH) in autosomal dominant cancer genes. An increase in variant allele fraction of 0.20 in the tumor was considered evidence of LOH.17
Germline variants remaining after filtering were classified and interpreted in the context of patient phenotype(s) to generate a germline WES report, as previously described.2,3 For the present study, these reports included variants confirmed by Sanger sequencing in 4 categories (Figure 1): pathogenic or likely pathogenic mutations in disease genes related to cancer susceptibility or other patient phenotype; variants of uncertain significance (VUS) in phenotype-associated disease genes; incidental medically actionable mutations (including the mitochondrial genome); and a limited panel of pharmacogenetic variant alleles.3 Parents were given the option to have their child’s report include carrier status results for any recessive disorder for which genetic testing is currently available. Parental blood samples, if available, underwent Sanger sequencing for specific germline mutations identified in the patient sample. Germline WES reports did not include disease-associated mutations that were not considered actionable in the absence of a phenotype.
Somatic and FamCan variants were imported into an in-house-developed variant review program and subjected to additional filters (eFigure 1 in Supplement 1 and eTable 1 in Supplement 2) followed by inspection of read alignments on the Integrative Genomics Viewer.18 An algorithm for variant ranking based on perceived clinical utility was used to assign somatic mutations to 1 of 4 categories (Figure 1 and eTables 3 to 5 in Supplement 2): established clinical utility (I); potential clinical utility (II); mutations in consensus cancer genes (III); and all other mutations (IV). For a more detailed description of the algorithm see eMethods in Supplement 1. Category I to III somatic mutations were confirmed by Sanger sequencing and reported with accompanying interpretative text.
The Fisher exact test was used to compare the frequencies of category I and II somatic mutations in CNS vs non-CNS tumors and to compare the frequencies of cancer susceptibility variants between study participants and a cohort of 2000 consecutive germline exomes reported from the Baylor College of Medicine Whole Genome Laboratory.3
Study enrollment began in August 2012. Two hundred eligible patients were identified and offered study enrollment following a previously reported informed consent process,7 of whom 150 (75%) agreed to participate in the study (eFigure 2 in Supplement 1). Patient clinical characteristics and demographics are summarized in eTable 6 in Supplement 2. Enrolled patients were diagnosed with a diverse representation of pediatric CNS (n = 56, 37%) and non-CNS (n = 94, 63%) solid tumors (Table 1). Blood samples were collected from all participants, and adequate tumor samples for WES were obtained from 121 (81%) of the 150 participants, including 40 (71%) of 56 with CNS tumors and 81 (86%) of 94 with non-CNS tumors (eFigure 2 in Supplement 1). The last WES results described here were reported in September 2014 (n = 150 germline reports and n = 121 tumor reports).
Aggregating the results from 121 tumor WES reports revealed validated somatic mutations that were designated as having established clinical utility (category I) in 4 patients (3%) and potential utility (category II) in an additional 29 patients (24%) (Figure 2A and eTables 7 and 8 in Supplement 2). The fraction of patients with CNS tumors who had category I and II mutations (7 of 40, 17%) was numerically but not statistically lower than that for non-CNS tumors (26 of 81, 32%) (Figure 2A, P = .13). The 37 recurrent category I and II mutations detected included CTNNB1 (in 10 of 121 participants, 8.3%), BRAF (5 of 121, 4.1%), KIT, KRAS, NRAS, and TSC2 (2 of 121 each, 1.7%) (Figure 2B and eTable 7 in Supplement 2). Only 4 (11%) of these 37 mutations were previously detected by routine clinical molecular testing: an ALK hotspot mutation in a neuroblastoma and BRAF V600E mutations in 3 gliomas. An equal number were identified in genes that are now becoming routinely tested in the patient’s tumor type (CTNNB1 in 3 medulloblastomas and H3F3A in a glioblastoma) although not at the time of diagnosis.19 A total of 25 of 37 category I or II mutations (68%) were either oncogene alterations previously reported in the COSMIC database or inactivating mutations in tumor suppressor genes (eTable 7 in Supplement 2).15
The tumor reports of an additional 24 of 121 patients (20%) included at least 1 somatic mutation in a consensus cancer gene (category III), most frequently TP53 (7 of 121, 6%), BCOR, DDX3X, and MED12 (3 of 121 each, 2.5%), while 64 (53%) of 121 patients had no category I to III mutations reported (Figure 2; eTables 7 and 8 in Supplement 2). Only 22 (59%) of 37 category I and II mutations and 18 (33%) of 54 (33%) category III mutations were in genes known to be mutated at greater than 2% frequency in the tumor type tested; for example, BRAF, JAK3, KRAS, MET, and TSC2 mutations are all rare events in neuroblastoma.15,20,21 A total of 1111 mutations in category IV genes were also identified by WES, but not further validated, in 112 (93%) of 121 patients.
Pathogenic or likely pathogenic mutations underlying the patient’s phenotype were identified in 15 (10%) of 150 patients (Table 2 and eTable 9 in Supplement 2). For 8 (62%) of 13 patients with dominant cancer susceptibility mutations, the gene in which the mutation was reported was known to be associated with childhood cancer risk (VHL × 2, TP53 × 2, DICER1, MSH2, WT1, and KRAS). However, in 3 of these 8 cases, the clinical team caring for the child had not considered genetic testing because (1) the positive family history suggestive of Lynch syndrome was not elicited by the team caring for the child with glioblastoma multiforme and MSH2 mutation; (2) the clinical features had not previously resulted in a Noonan syndrome diagnosis in the child with KRAS mutation; and (3) 1 child with unilateral Wilms tumor and no congenital anomalies or developmental delay was mosaic for WT1 mutation. In addition, the remaining 5 patients with dominant mutations had tumor diagnoses not previously associated with the mutated gene (BRCA1 × 2, BRCA2, SMARCA4, and CHEK2). There was also a single autosomal recessive diagnosis (TJP2 deficiency) in a patient with severe liver disease and hepatocellular carcinoma (HCC). This case (in addition to another concurrent finding at another institution) was the first report of an association of TJP2 deficiency and HCC.22 Finally, 1 patient with previously unexplained proteinuria was found to carry an X-linked CLCN5 mutation. Parental samples were available for testing in 13 of these 15 diagnostic cases. Sanger validation revealed the diagnostic mutation to be inherited from a parent in 11 (85%); the only exceptions were the mosaic WT1 mutation and de novo KRAS mutation.
An additional 10 participants (6%) were found to have a single pathogenic mutation in a gene associated with an autosomal recessive cancer syndrome (eTable 10 in Supplement 2), including several genes in the Fanconi anemia pathway, with no further evidence of the disorder noted by the oncologist or found in the medical record. Of this group, only 1 participant, with Wilms tumor and a single DIS3L2 mutation, had the tumor type most commonly associated with the recessive condition, Perlman syndrome.23
We further explored the possibility of second events, either somatic mutation or LOH in the tumor WES data of patients with germline findings (Table 2; eTables 9 and 10 in Supplement 2). No somatic mutations in the same gene were detected. However, tumor LOH was documented in 6 patients. Of note, there was no evidence of LOH in the 3 tumors with germline BRCA1 or BRCA2 mutations or any of the single recessive cancer mutations other than LOH of DIS3L2 in the Wilms tumor sample.
Finally, we performed comparisons of some of the recurring mutations found in the BASIC3 cohort with 2000 clinical exomes reported3 by our same testing laboratory in a primarily pediatric noncancer clinical population. There was only a modest increased rate of BRCA1/2 mutations in the BASIC3 cohort (3 of 150, 2% vs 14 of 2000, 0.7%; P = .10). Summing across all the 14 Fanconi genes, we found no evidence that putative loss-of-function mutations were enriched in the BASIC3 cohort (P > .99). However, 1 recurrent FANCL frameshift mutation was found in 0.5% of the 2000 exome data set vs 3 of 150 among the BASIC3 participants (P = .19); thus, evaluation of the significance of this finding requires a larger data set.
Twelve patients had clinical germline gene testing outside of WES (the majority being TP53 comprehensive analysis) with no additional sequence-based mutations reported. The WES report does not include deletions, and a large deletion of the SMARCB1 gene was reported in a single patient with an atypical teratoid/rhabdoid tumor of the CNS. In addition, WES revealed the germline nature of a TP53 mutation previously reported from a tumor mutation panel.
Medically actionable incidental findings reported included those genes recommended by the American College of Medical Genetics and Genomics (ACMG)24 and additional findings (including mitochondrial DNA), as recently described.2,3 Eight (5%) of 150 patients had incidental findings, including 5 in genes on the ACMG list (eTable 11 in Supplement 2). Two findings were specifically reported as being actionable for an oncology patient: an immunodeficiency allele and a mitochondrial DNA allele associated with aminoglycoside toxic effects. The remaining patient was diagnosed incidentally with the MELAS mitochondrial disorder (mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes).
The germline exome report includes 3 additional categories. The laboratory reports VUS in genes related to the patient’s phenotype, which included the cancer susceptibility genes listed in eTable 2 in Supplement 2. One hundred forty-four (96%) of 150 patients had at least 1 (median of 3) VUS on their report, which is consistent with previous reports of 2 VUS per study participants using a much smaller gene panel.25 In addition, the WES reports include the common variants recommended by the US Food and Drug Administration for dosing in VKORC1/ CYP2C9 (altered warfarin metabolism) and CYP2C19 (altered Plavix metabolism), with 133 (89%) of 150 patients having at least 1 pharmacogenetic variant reported (median of 1). Finally, parents are provided the option of reporting of carrier status (pathogenic mutations only) for the very large number of autosomal recessive disorders currently available for single gene testing. Of the 137 probands whose parents requested reporting (91%), 115 (84%) had at least 1 recessive carrier finding (median of 2).
In combination, tumor and germline WES revealed potentially clinically relevant alterations (category I or II somatic mutations, pathogenic germline mutations in genes related to cancer or other patient phenotype [excluding single recessive mutations], or medically actionable incidental germline mutations) in 47 (39%) of 121 patients (Figure 3).
Here we report that clinical tumor WES in children with newly diagnosed solid tumors revealed somatic mutations of established or potential clinical utility (category I and II) in approximately one-quarter of patients and mutations in cancer genes not classified as targetable (category III) in a similar number (Figure 2A and eTable 8 in Supplement 2). The vast majority of these mutations had not been detected by targeted molecular testing as part of routine clinical care. Consistent with this current practice, tumor WES revealed somatic mutations of established clinical utility (category I) in only a small minority of patients, with far more tumors harboring mutations of potential clinical utility (category II). To our knowledge, this is the first study to investigate the diagnostic yield of WES in the wide spectrum of childhood solid tumors routinely seen in a large children’s hospital. Further studies in larger cohorts of patients will be required to evaluate the yield of such testing for specific tumor types.
Our tumor WES data highlight several points regarding the use of genomic tests for children with solid tumors. First, despite being less frequently mutated than most adult cancers, pediatric solid tumors harbor potentially attractive targets for therapy, prominently including mitogen-activated protein kinase (MAPK) signaling and MTOR/PI3K pathway mutations (eTable 7 in Supplement 2). As expected, given that children with cancer are typically initially treated on clinical trials or following established treatment regimens, the mutations detected did not alter the management of the newly diagnosed cancer in this cohort. Further studies will be required to assess their potential relevance in the context of refractory and relapsed cancers.
Second, although pediatric solid tumors share common genetic alterations with adult epithelial cancers, mutations in developmental pathways such as Wnt/Wingless signaling (eg, CTNNB1, the most frequently mutated gene in this unselected cohort) are particularly prominent in pediatric solid tumors. Accordingly, both pediatric cancer-specific mutation panels and novel therapeutic strategies for targeting these key pediatric cancer pathways are needed.
Third, 56% (51/91) of mutations were found in genes not known to be recurrently mutated in that specific tumor type, demonstrating the potential value of testing strategies and clinical trials based on molecular alterations rather than tumor histology.26
Fourth, to maximize the yield of such strategies, genomic testing to detect alterations outside of known hotspots is necessary, such as the inactivating TSC2 mutations observed in this cohort. The clinical relevance of noncanonical mutations in oncogenes, such as the detected missense kinase domain mutations in JAK2 and FGFR1, is currently unclear and will require further study.
Fifth, many potentially actionable mutations were found in a small fraction of patients (eg, mutation of FGFR1 in <1%), indicating that effective pediatric precision oncology approaches will require access to a large number of targeted agents.
The clinical categorization of mutations in tumor WES reports was based on expert opinion, using knowledge of mutations, genes, and availability of molecularly targeted agents. For example, the reported category III mutations include variants with diagnostic or prognostic utility (eg, DDX3X mutations in Wnt subtype medulloblastoma)27,28 and others that may be predictive of drug response, such as mutations in BRCA1 and BRCA2 and poly-ADP ribose polymerase (PARP) inhibitors.29 The development of standardized definitions for clinical categorization of somatic mutations will be critical to allow comparative analyses between different genomic testing platforms and patient populations.
We determined the yield of germline WES and whether those findings would have been revealed by a genetic evaluation. The gene most frequently considered for testing by the BASIC3 genetics study team was TP53 (n = 23), although only 2 TP53 germline mutations were identified in this cohort. Substantial heterogeneity was observed in the distribution of cancer susceptibility mutations, with most genes mutated only in a single case. Overall, 5 of the 15 genetic diagnoses in this cohort had specifically been considered for testing by the teams caring for the patient. For many of the remaining diagnoses, the mutations occurred in genes not previously associated with the child’s cancer diagnosis. This may partially relate to recently described disease genes with limited data, eg SMARCA4, which was first described in 2010 in rhabdoid tumors30 and identified in a child with neuroblastoma in this study. Consistent with the somatic mutation analysis, our data suggest that a pediatric hereditary cancer gene panel would also need to be broadly constituted to be an effective test platform. In addition, cancer risk may be influenced by gene-by-gene interactions, as may be the case for the Wilms tumor found in the patient with heterozygous CHEK2, FANCC, and DIS3L2 mutations. In addition, the transmission of cancer susceptibility mutations in these families suggests that the population genetics of childhood cancer susceptibility may be distinct from that of other disease populations; for example, 85% of patients in our study inherited the cancer susceptibility mutation from a parent, with only 1 de novo and 1 mosaic mutation detected in contrast to a 70% de novo rate observed in children with neurodevelopmental disorders.3 This high rate of inheritance has also resulted in rapid targeted testing of at-risk siblings, with cancer screening initiated for those found to carry the identified disease mutation.
A number of children carried pathogenic mutations in adult-onset cancer genes, in particular 3 (2%) of 150 participants with BRCA1 or BRCA2 mutations. Polymorphisms in BARD1, which encodes a BRCA1-interacting protein, have been associated with neuroblastoma risk,31 but 1 study reported no increase in childhood cancer diagnosis in breast cancer kindreds with BRCA1/2 mutations.32 The 3 different tumor types, the absence of LOH, and no statistically significant increase in BRCA1/2 mutations compared with a nonpediatric cancer cohort would suggest that this may be an incidental finding. The discovery here of both germline (n = 3) and somatic (n = 2) BRCA1/2 mutations by WES, as well as the clarification that a TP53 mutation initially identified on a tumor mutation panel was germline, demonstrates the value of sequencing matched normal samples as part of tumor genomic testing.33 The integration of paired tumor and normal sequencing analyses can also be useful for interpretation of germline data, including evaluation of tumor LOH in cases with germline mutations in cancer susceptibility genes, such as our patient with a likely pathogenic TP53 mutation.
Combined reporting of tumor and germline WES results in an unselected cohort of 150 children with newly diagnosed solid tumors revealed potentially actionable findings in nearly 40% of patients across a spectrum of genes previously implicated in both pediatric and adult cancers. The further integration of methods to detect copy number abnormalities and fusion genes will increase the diagnostic yield of these tests, particularly for tumor types that are known to harbor few mutations detectable by WES. Strategies to effectively and responsibly use these diverse results are required to incorporate WES and other genomic tests into childhood cancer care and clinical trials.
Corresponding Authors: D. Williams Parsons, MD, PhD (firstname.lastname@example.org), or Sharon E. Plon, MD, PhD (email@example.com), Texas Children’s Cancer Center, Department of Pediatrics, Baylor College of Medicine, 1102 Bates Ave, Ste 1030.15 (Parsons) or 1200 (Plon), Houston, TX 77030.
Correction: This article was corrected on March 3, 2016, to add the Open Access note.
Published Online: January 28, 2016. doi:10.1001/jamaoncol.2015.5699.
Open Access: This article is published under the JAMA Oncology open access model and is free to read on the day of publication.
Author Contributions: Drs Parsons and Plon had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Drs Parsons and Plon served as co–senior authors, each with equal contribution to this report.
Study concept and design: Parsons, Monzon, Hicks, McGuire, Muzny, Berg, Gibbs, Plon.
Acquisition, analysis, or interpretation of data: All authors.
Drafting of the manuscript: Parsons, Roy, Bergstrom, Kerstein, Petersen, Hicks, Eldin, Ramamurthy, Berg, Plon.
Critical revision of the manuscript for important intellectual content: Parsons, Roy, Yang, Wang, Scollon, Bergstrom, Gutierrez, Bavle, Lin, López-Terrada, Monzon, Hicks, Quintanilla, Adesina, Mohila, Whitehead, Jea, Vasudevan, Nuchtern, McGuire, Hilsenbeck, Reid, Muzny, Wheeler, Berg, Chintagumpala, Eng, Gibbs, Plon.
Statistical analysis: Wang, Petersen, Hilsenbeck.
Obtained funding: Parsons, Berg, Gibbs, Plon.
Administrative, technical, or material support: Parsons, Roy, Yang, Bergstrom, Kerstein, Gutierrez, Lin, López-Terrada, Monzon, Hicks, Adesina, Jea, Nuchtern, Ramamurthy, Reid, Muzny, Chintagumpala, Eng, Gibbs.
Study supervision: Parsons, López-Terrada, Monzon, Hicks, Wheeler, Chintagumpala, Plon.
Conflict of Interest Disclosures: As of February 2015 Baylor College of Medicine and Miraca Holdings Inc have formed a joint venture with shared ownership and governance of the Baylor Miraca Genetics Laboratories, which performs exome sequencing. Dr Gibbs is the Chief Scientific Officer; Dr Eng is the Vice President and Executive Laboratory Director; and Dr Plon is a member of the scientific advisory board of Baylor Miraca Genetics Laboratories. No other conflicts are reported.
Funding/Support: This study is a Clinical Sequencing Exploratory Research (CSER) program project supported by the National Human Genome Research Institute and the National Cancer Institute grant U01HG006485 (Drs Parsons and Plon).
Role of the Funder/Sponsor: The sponsors had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Additional Contributions: The authors are grateful to the patients and families, pediatric oncologists, and clinical staff at Texas Children’s Cancer Center for their participation in the study. The authors also thank Dr Ramamurthy’s team from the Dan L. Duncan Institute for Clinical and Translational Research, who developed and maintained the BASIC3 study database: Medha Naik, MS, Xingquan Lu, MS, and Vivek Ramanathan, MS. They received no compensation beyond their salaries as full-time Baylor College of Medicine employees.
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