Natural history and evaluation of abnormal or nonreportable NIPT results and its association with maternal neoplasia
Natural history and evaluation of abnormal or nonreportable NIPT results and its association with maternal neoplasia
批准号:
10691112
负责人:
Diana Bianchi
金额:
$6.25万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
AmniocentesisAneuploidyAwardBenignBiochemistryBiocompatible MaterialsBiologicalBloodBlood CirculationCOVID-19 pandemicCase StudyChorionic Villi SamplingChromosomesClinicalClinical ManagementClinical OncologyCommunicationDNADNA analysisDNA sequencingDetectionDiagnosisDiagnosticDiagnostic testsEnrollmentEvaluationFetusGenomicsGuidelinesHematopoiesisHematopoietic SystemImageIndividualInstitutional Review BoardsInternationalInterviewJournalsKaryotypeLaboratoriesLightningMalignant NeoplasmsMedicalMosaicismNatural HistoryNeonatalNeoplasmsNurse MidwivesOncologistParticipantPatau&aposs syndromePatient RecruitmentsPerinatalPhysiciansPlacentaPlasmaPositive Test ResultPostpartum PeriodPredictive ValuePregnancyPregnant WomenPrenatal DiagnosisProtocols documentationProviderProxyPublishingReportingRetrospective StudiesRiskSamplingScreening ResultSerumSocietiesSolid NeoplasmSourceSuggestionTest ResultTestingTimeTravelUnited StatesUnited States National Institutes of HealthUterine FibroidsVisitWomanWorkacronymscell free DNAcell free fetal DNAcirculating DNAclinical careclinical centerclinical diagnosisclinical sequencingeditorialfetalfollow-upmeetingsmultidisciplinaryneoplastic cellpostersprenatalprenatal testingpreventprospectiverecruitresearch clinical testingsymposiumtreatment planningtumorultrasound
中文摘要
本研究的首字母缩略词是IDENTIFY研究:通过非侵入性细胞游离DNA分析偶然检测母体肿瘤。在NIH IRB最终批准本方案后,第一个IDENTIFY研究参与者于2019年12月入组。招聘虽然最初受到COVID大流行的影响,但已被接受。参与者在临床中心接受初步评估,以诊断可能的肿瘤。所有收集的临床、实验室和影像学信息在每月的多学科小组会议上进行讨论。如果发现肿瘤,结果将与参与者和转诊医生共享,并且是可操作的。参与者将在产后随访数年,以收集所有可用的医疗信息。
英文摘要
The acronym for this study is the IDENTIFY Study: Incidental DEtection of maternal Neoplasia Through non-Invasive cell Free DNA analYsis. Following final NIH IRB approval of this protocol, the first IDENTIFY study participant enrolled in December 2019. Recruitment, although initially impacted by the COVID pandemic, has been acceptable. Participants undergo an initial evaluation at the Clinical Center to diagnose possible neoplasia. All collected clinical, laboratory and imaging information is discussed in monthly multidisciplinary team meetings. If neoplasia is discovered, results are shared with participants and referring physicians and are actionable. Participants will be followed for several years post-partum to collect all available medical information.
To date, we have observed a variety of biological explanations for participants abnormal or non-reportable NIPT results, including confined placental mosaicism, clonal hematopoiesis, benign uterine leiomyomas, and malignant neoplasms. Participants with cancer have been diagnosed with a range of tumor types and stages.
In addition to completing a clinical evaluation to diagnose possible neoplasia, participants engage in qualitative interviews to help us understand the personal impact of receiving NIPT results suggestive of maternal malignancy and being offered a clinical evaluation to detect possible cancer during pregnancy. Individuals are interviewed before their visit to the NIH and after they have learned the results of their clinical evaluations. We presented our preliminary findings as a poster and Lightning Communication (5-minute talk) at the International Society for Prenatal Diagnosis Conference in Montreal (June 2022). Our poster Receiving Prenatal Screening Results Suggestive of Maternal Cancer: A Qualitative Exploration of Participants in the NIH Identify Study tied for the Best Poster Award.
Ongoing challenges to recruitment include prospective participants reluctance to travel, falsely reassuring medical advice and falsely reassuring incomplete workups provided by local providers, oncologists, obstetricians and nurse-midwives that prevented further follow-up. We continue to reach out to key stakeholders through local, national and international presentations to establish sources of participant recruitment and to emphasize the importance of a timely and thorough clinical evaluation when NIPT results are suggestive of maternal malignancy. This was also the topic of an editorial we published in the Journal of Clinical Oncology that highlights the barriers to implementing a coordinated diagnostic and treatment plan for pregnant women who receive malignancy suspicious NIPT results in the United States.
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Natural history and evaluation of abnormal or nonreportable NIPT results and its association with maternal neoplasia
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批准号:10920214
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项目类别:
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资助金额:$7.16万
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财政年份:--
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负责人:Diana Bianchi
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依托单位:
Natural history and evaluation of abnormal or nonreportable NIPT results and its association with maternal neoplasia
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批准号:10267124
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项目类别:
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资助金额:$6.24万
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财政年份:--
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负责人:Diana Bianchi
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依托单位:
Prenatal Treatment of Down Syndrome to Improve Brain Development and Neurocognition
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批准号:9589746
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项目类别:
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资助金额:$117.42万
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财政年份:--
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负责人:Diana Bianchi
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依托单位:
Natural history and evaluation of abnormal or nonreportable NIPT results and its association with maternal neoplasia
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批准号:10022465
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项目类别:
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资助金额:$5.86万
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财政年份:--
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负责人:Diana Bianchi
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依托单位:
Prenatal Treatment of Down Syndrome to Improve Brain Development and Neurocognition
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批准号:10022464
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项目类别:
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资助金额:$111.38万
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财政年份:--
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负责人:Diana Bianchi
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依托单位:
Prenatal Treatment of Down Syndrome to Improve Brain Development and Neurocognition
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批准号:10920213
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项目类别:
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资助金额:$136.01万
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财政年份:--
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负责人:Diana Bianchi
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依托单位:
Prenatal Treatment of Down Syndrome to Improve Brain Development and Neurocognition
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批准号:10267123
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项目类别:
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资助金额:$118.62万
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财政年份:--
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负责人:Diana Bianchi
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依托单位:
Prenatal Treatment of Down Syndrome to Improve Brain Development and Neurocognition
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批准号:10691111
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项目类别:
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资助金额:$118.7万
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财政年份:--
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负责人:Diana Bianchi
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依托单位:
海外基金