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  1. Article ; Online: Beyond the three P's: adrenal involvement in MEN1.

    Clemente-Gutierrez, Uriel / Pieterman, Carolina R C / Lui, Michael S / Yamashita, Thomas Szabo / Tame-Elorduy, Andrés / Huang, Bernice L / Shirali, Aditya S / Erstad, Derek J / Lee, Jeffrey E / Fisher, Sarah B / Graham, Paul H / Grubbs, Elizabeth G / Waguespack, Steven G / Ng, Chaan S / Perrier, Nancy

    Endocrine-related cancer

    2024  Volume 31, Issue 2

    Abstract: Adrenal lesions (ALs) are often detected in patients with multiple endocrine neoplasia type 1 (MEN1). However, they are not well described in MEN1, making their clinical management unclear. This study examined the prevalence and outcomes of ALs found in ... ...

    Abstract Adrenal lesions (ALs) are often detected in patients with multiple endocrine neoplasia type 1 (MEN1). However, they are not well described in MEN1, making their clinical management unclear. This study examined the prevalence and outcomes of ALs found in MEN1. We performed a retrospective chart review of patients diagnosed with MEN1 from 1990 to 2021. ALs were diagnosed using abdominal or thoracic imaging and classified as being unilateral or bilateral, having single or multiple nodules, and as having diffuse enlargement or not. Measurable nodular lesions were analyzed for their size and growth over time. Patients' clinical and radiographic characteristics were collected. We identified 382 patients with MEN1, 89 (23.3%) of whom had ALs. The mean age at detection was 47 ± 11.9 years. We documented 101 measurable nodular lesions (mean size, 17.5 mm; range, 3-123 mm). Twenty-seven nodules (26.7%) were smaller than 1 cm. Watchful waiting was indicated in 79 (78.2%) patients, of whom 28 (35.4%) had growing lesions. Functional lesions were diagnosed in 6 (15.8%) of 38 that had functional work-up (diagnoses: pheochromocytoma (n = 2), adrenocorticotropic hormone-dependent hypercortisolism (n = 2), hyperandrogenism (n = 1), hyperaldosteronism (n = 1)); surgery was indicated for 5 (83.3%; n = 12 nodules), 2 of whom had bilateral, diffuse adrenal enlargement. Two patients were diagnosed with adrenocortical carcinoma and two with neoplasms of uncertain malignant potential. Radiographic or clinical progression of ALs is uncommon. Malignancy should be suspected on the basis of a lesion's growth rate and size. A baseline hormonal work-up is recommended, and no further biochemical work-up is suggested when the initial assessment shows nonfunctioning lesions.
    MeSH term(s) Humans ; Adult ; Middle Aged ; Multiple Endocrine Neoplasia Type 1/pathology ; Retrospective Studies ; Adrenal Gland Neoplasms/epidemiology ; Adrenocortical Carcinoma ; Adrenal Cortex Neoplasms
    Language English
    Publishing date 2024-01-16
    Publishing country England
    Document type Journal Article
    ZDB-ID 1218450-0
    ISSN 1479-6821 ; 1351-0088
    ISSN (online) 1479-6821
    ISSN 1351-0088
    DOI 10.1530/ERC-23-0162
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Next-Generation Sequencing in Sporadic Medullary Thyroid Cancer Patients: Mutation Profile and Disease Aggressiveness.

    Shirali, Aditya S / Hu, Mimi I / Chiang, Yi-Ju / Graham, Paul H / Fisher, Sarah B / Sosa, Julie Ann / Perrier, Nancy / Brown, Spandana / Holla, Vijaykumar R / Dadu, Ramona / Busaidy, Naifa / Sherman, Steven I / Cabanillas, Maria / Waguespack, Steven G / Zafereo, Mark E / Grubbs, Elizabeth G

    Journal of the Endocrine Society

    2024  Volume 8, Issue 6, Page(s) bvae048

    Abstract: Context: Next-generation sequencing (NGS) analysis of sporadic medullary thyroid carcinoma (sMTC) has led to increased detection of somatic mutations, including : Objective: This study aimed to determine the association between clinicopathologic ... ...

    Abstract Context: Next-generation sequencing (NGS) analysis of sporadic medullary thyroid carcinoma (sMTC) has led to increased detection of somatic mutations, including
    Objective: This study aimed to determine the association between clinicopathologic behavior and somatic mutation identified on clinically motivated NGS.
    Methods: In this retrospective cohort study, patients with sMTC who underwent NGS to identify somatic mutations for treatment planning were identified. Clinicopathologic factors, time to distant metastatic disease (DMD), disease-specific survival (DSS), and overall survival (OS) were compared between somatic mutations.
    Results: Somatic mutations were identified in 191 sMTC tumors, including
    Conclusion: Somatic
    Language English
    Publishing date 2024-04-24
    Publishing country United States
    Document type Journal Article
    ISSN 2472-1972
    ISSN (online) 2472-1972
    DOI 10.1210/jendso/bvae048
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: High-Specific-Activity 131I-MIBG for the Treatment of Advanced Pheochromocytoma and Paraganglioma.

    Al-Ward, Ruaa / Brondani, Vania Balderrama / Sawani, Sahar / Potter, Cheryl L / Xu, Guofan / Waguespack, Steven G / Varghese, Jeena / Habra, Mouhammed Amir / Lu, Yang / Jimenez, Camilo

    Clinical nuclear medicine

    2024  

    Abstract: Patients and methods: The primary endpoints were objective response rate (ORR) and disease control rate (DCR). Secondary endpoints were duration of response, blood pressure control, safety, overall and progression-free survival rates, MIBG uptake, and ... ...

    Abstract Patients and methods: The primary endpoints were objective response rate (ORR) and disease control rate (DCR). Secondary endpoints were duration of response, blood pressure control, safety, overall and progression-free survival rates, MIBG uptake, and correlations with genetic background.
    Results: The study included 25 patients. Twenty-four patients had distant metastases, 17 (68%) had hormonally active tumors, and 13 (52%) had previously received antineoplastic treatment. In 24 evaluable patients, the ORR was 38%, including 2 patients with complete response, and the DCR was 83%; median time to response was 12.5 months (95% confidence interval, 4.6-25.1). Twelve patients had sporadic disease, among whom the ORR was 25% and DCR was 83%. Twelve patients had hereditary disease (SDHB, VHL, RET); among these, the ORR was 50%, and DCR was 83%. Plasma metanephrines normalized in 30% of patients and improved by greater than 50% in 46%. Sixteen patients had hormonally active tumors and hypertension; in 9 (56%) of these, blood pressure normalized, leading to discontinuation of antihypertensive therapy.The most common adverse events were grades 1-2 nausea/vomiting and transient bone marrow suppression. One patient developed premature ovarian failure. Reversible grades 3-4 myelosuppression were seen in 7 patients (28%). One patient had fatal pneumonitis.
    Conclusions: HSA-131I-MIBG is associated with a high DCR in patients with MPPGL, regardless of underlying genetic mutation.
    Language English
    Publishing date 2024-04-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 197628-x
    ISSN 1536-0229 ; 0363-9762
    ISSN (online) 1536-0229
    ISSN 0363-9762
    DOI 10.1097/RLU.0000000000005184
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Guidelines for surveillance of patients with von Hippel-Lindau disease: Consensus statement of the International VHL Surveillance Guidelines Consortium and VHL Alliance.

    Daniels, Anthony B / Tirosh, Amit / Huntoon, Kristin / Mehta, Gautam U / Spiess, Philippe E / Friedman, Debra L / Waguespack, Steven G / Kilkelly, Jill E / Rednam, Surya / Pruthi, Sumit / Jonasch, Eric A / Baum, Laura / Chahoud, Jad

    Cancer

    2023  Volume 129, Issue 19, Page(s) 2927–2940

    MeSH term(s) Humans ; von Hippel-Lindau Disease/complications ; von Hippel-Lindau Disease/diagnosis ; Von Hippel-Lindau Tumor Suppressor Protein/genetics ; Patients
    Chemical Substances Von Hippel-Lindau Tumor Suppressor Protein (EC 2.3.2.27) ; VHL protein, human (EC 6.3.2.-)
    Language English
    Publishing date 2023-06-19
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1429-1
    ISSN 1097-0142 ; 0008-543X ; 1934-662X
    ISSN (online) 1097-0142
    ISSN 0008-543X ; 1934-662X
    DOI 10.1002/cncr.34896
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Decreasing utilization for postoperative radiation therapy in locoregionally advanced medullary thyroid cancer.

    Maniakas, Anastasios / Sullivan, Andrew / Hu, Mimi I / Busaidy, Naifa L / Cabanillas, Maria E / Dadu, Ramona / Waguespack, Steven G / Fisher, Sarah B / Graham, Paul H / Gross, Neil D / Grubbs, Elizabeth G / Perrier, Nancy D / Wang, Jennifer R / Gunn, Brandon / Garden, Adam S / Megahed, Romy / Navuluri, Sriram / Li, Xu / Williams, Michelle D /
    Zafereo, Mark

    Head & neck

    2023  Volume 46, Issue 2, Page(s) 328–335

    Abstract: Background: Use of postoperative radiation therapy (PORT) in locoregionally advanced medullary thyroid cancer (MTC) remains controversial. The objective was to evaluate the effect of PORT on locoregional control (LRC) and overall survival (OS).: ... ...

    Abstract Background: Use of postoperative radiation therapy (PORT) in locoregionally advanced medullary thyroid cancer (MTC) remains controversial. The objective was to evaluate the effect of PORT on locoregional control (LRC) and overall survival (OS).
    Methods: Retrospective cohort study of 346 MTC patients separated into PORT and no-PORT cohorts. Relative indications for PORT, as well as changes in patterns of treatment, were recorded.
    Results: 49/346 (14%) received PORT. PORT was associated with worse OS; adjusted HR = 2.0 (95%CI 1.3-3.3). PORT was not associated with improved LRC, even when adjusting for advanced stage (Stage III p = 0.892; Stage IV p = 0.101). PORT and targeted therapy were not associated with improved OS compared to targeted therapy alone; adjusted HR = 1.2 (95%CI 0.3-4.1).
    Conclusions: Use of PORT in MTC has decreased and its indications have become more selective, coinciding with the advent of effective targeted therapies. Overall, PORT was not associated with improved LRC or OS.
    MeSH term(s) Humans ; Retrospective Studies ; Thyroid Neoplasms/radiotherapy ; Thyroid Neoplasms/surgery ; Carcinoma, Neuroendocrine/radiotherapy ; Carcinoma, Neuroendocrine/surgery ; Neoplasm Staging ; Radiotherapy, Adjuvant
    Language English
    Publishing date 2023-11-27
    Publishing country United States
    Document type Journal Article
    ZDB-ID 645165-2
    ISSN 1097-0347 ; 0148-6403 ; 1043-3074
    ISSN (online) 1097-0347
    ISSN 0148-6403 ; 1043-3074
    DOI 10.1002/hed.27584
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: It's not a mystery, it's in the history: Multidisciplinary management of multiple endocrine neoplasia type 1.

    Shirali, Aditya S / Pieterman, Carolina R C / Lewis, Mark A / Hyde, Samuel M / Makawita, Shalini / Dasari, Arvind / Thosani, Nirav / Ikoma, Naruhiko / McCutcheon, Ian E / Waguespack, Steven G / Perrier, Nancy D

    CA: a cancer journal for clinicians

    2021  Volume 71, Issue 5, Page(s) 369–380

    MeSH term(s) Adult ; Child, Preschool ; Diagnostic Self Evaluation ; Genetic Testing ; Humans ; Male ; Medical History Taking ; Multiple Endocrine Neoplasia Type 1/complications ; Multiple Endocrine Neoplasia Type 1/diagnosis ; Multiple Endocrine Neoplasia Type 1/genetics ; Multiple Endocrine Neoplasia Type 1/therapy ; Patient Care Team
    Language English
    Publishing date 2021-06-01
    Publishing country United States
    Document type Case Reports ; Journal Article ; Personal Narrative
    ZDB-ID 603553-x
    ISSN 1542-4863 ; 0007-9235
    ISSN (online) 1542-4863
    ISSN 0007-9235
    DOI 10.3322/caac.21673
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Steroid Cell Ovarian Tumor in a Case of von Hippel-Lindau Disease: Demonstrating Lipid Content of the Mass with MR Imaging.

    Morani, Ajaykumar C / Mubarak, Ahmad Iyad / Bhosale, Hrishabh R / Ramani, Nisha S / Waguespack, Steven G / Ying, Anita

    Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine

    2019  Volume 18, Issue 4, Page(s) 251–252

    Language English
    Publishing date 2019-01-31
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 2217833-8
    ISSN 1880-2206 ; 1347-3182
    ISSN (online) 1880-2206
    ISSN 1347-3182
    DOI 10.2463/mrms.ci.2018-0104
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Imaging features of adrenal gland masses in the pediatric population.

    Hanafy, Abdelrahman K / Mujtaba, Bilal / Roman-Colon, Alicia M / Elsayes, Khaled M / Harrison, Douglas / Ramani, Nisha S / Waguespack, Steven G / Morani, Ajaykumar C

    Abdominal radiology (New York)

    2019  Volume 45, Issue 4, Page(s) 964–981

    Abstract: The spectrum of adrenal masses in the pediatric population markedly differs from that in the adult population. Imaging plays a crucial role in detecting adrenal masses, differentiating malignant from benign lesions, recognizing extra-adrenal lesions in ... ...

    Abstract The spectrum of adrenal masses in the pediatric population markedly differs from that in the adult population. Imaging plays a crucial role in detecting adrenal masses, differentiating malignant from benign lesions, recognizing extra-adrenal lesions in the suprarenal fossa, and directing further management. Ultrasound is the primary imaging modality of choice for the evaluation of adrenal masses in the neonatal period, whereas MRI or CT is used as a problem-solving tool. In older children, computed tomography or magnetic resonance imaging is often required after initial sonographic evaluation for further characterization of a lesion. Herein, we discuss the salient imaging features along with pathophysiology and clinical features of pediatric adrenal masses.
    MeSH term(s) Adrenal Gland Neoplasms/congenital ; Adrenal Gland Neoplasms/diagnostic imaging ; Adrenal Gland Neoplasms/pathology ; Child ; Diagnosis, Differential ; Humans
    Language English
    Publishing date 2019-09-19
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2839786-1
    ISSN 2366-0058 ; 2366-004X
    ISSN (online) 2366-0058
    ISSN 2366-004X
    DOI 10.1007/s00261-019-02213-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Decision Making When Cancer Becomes Chronic: Needs Assessment for a Web-Based Medullary Thyroid Carcinoma Patient Decision Aid.

    Shojaie, Danielle / Hoffman, Aubri S / Amaku, Ruth / Cabanillas, Maria E / Sosa, Julie Ann / Waguespack, Steven G / Zafereo, Mark E / Hu, Mimi I / Grubbs, Elizabeth E

    JMIR formative research

    2021  Volume 5, Issue 7, Page(s) e27484

    Abstract: Background: In cancers with a chronic phase, patients and family caregivers face difficult decisions such as whether to start a novel therapy, whether to enroll in a clinical trial, and when to stop treatment. These decisions are complex, require an ... ...

    Abstract Background: In cancers with a chronic phase, patients and family caregivers face difficult decisions such as whether to start a novel therapy, whether to enroll in a clinical trial, and when to stop treatment. These decisions are complex, require an understanding of uncertainty, and necessitate the consideration of patients' informed preferences. For some cancers, such as medullary thyroid carcinoma, these decisions may also involve significant out-of-pocket costs and effects on family members. Providers have expressed a need for web-based interventions that can be delivered between consultations to provide education and prepare patients and families to discuss these decisions. To ensure that these tools are effective, usable, and understandable, studies are needed to identify patients', families', and providers' decision-making needs and optimal design strategies for a web-based patient decision aid.
    Objective: Following the international guidelines for the development of a web-based patient decision aid, the objectives of this study are to engage potential users to guide development; review the existing literature and available tools; assess users' decision-making experiences, needs, and design recommendations; and identify shared decision-making approaches to address each need.
    Methods: This study used the decisional needs assessment approach, which included creating a stakeholder advisory panel, mapping decision pathways, conducting an environmental scan of existing materials, and administering a decisional needs assessment questionnaire. Thematic analyses identified current decision-making pathways, unmet decision-making needs, and decision support strategies for meeting each need.
    Results: The stakeholders reported wide heterogeneity in decision timing and pathways. Relevant existing materials included 2 systematic reviews, 9 additional papers, and multiple educational websites, but none of these met the criteria for a patient decision aid. Patients and family members (n=54) emphasized the need for plain language (46/54, 85%), shared decision making (45/54, 83%), and help with family discussions (39/54, 72%). Additional needs included information about uncertainty, lived experience, and costs. Providers (n=10) reported needing interventions that address misinformation (9/10, 90%), foster realistic expectations (9/10, 90%), and address mistrust in clinical trials (5/10, 50%). Additional needs included provider tools that support shared decision making. Both groups recommended designing a web-based patient decision aid that can be tailored to (64/64, 100%) and delivered on a hospital website (53/64, 83%), focuses on quality of life (45/64, 70%), and provides step-by-step guidance (43/64, 67%). The study team identified best practices to meet each need, which are presented in the proposed decision support design guide.
    Conclusions: Patients, families, and providers report multifaceted decision support needs during the chronic phase of cancer. Web-based patient decision aids that provide tailored support over time and explicitly address uncertainty, quality of life, realistic expectations, and effects on families are needed.
    Language English
    Publishing date 2021-07-16
    Publishing country Canada
    Document type Journal Article
    ISSN 2561-326X
    ISSN (online) 2561-326X
    DOI 10.2196/27484
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Biomechanical effects of a novel posteriorly placed sacroiliac joint fusion device integrated with traditional lumbopelvic long-construct instrumentation.

    de Andrada Pereira, Bernardo / Lehrman, Jennifer N / Sawa, Anna G U / Lindsey, Derek P / Yerby, Scott A / Godzik, Jakub / Waguespack, Alexis M / Uribe, Juan S / Kelly, Brian P

    Journal of neurosurgery. Spine

    2021  Volume 35, Issue 3, Page(s) 320–329

    Abstract: Objective: S2-alar-iliac (S2AI) screw fixation effectively ensures stability and enhances fusion in long-segment constructs. Nevertheless, pelvic fixation is associated with a high rate of mechanical failure. Because of the transarticular nature of the ... ...

    Abstract Objective: S2-alar-iliac (S2AI) screw fixation effectively ensures stability and enhances fusion in long-segment constructs. Nevertheless, pelvic fixation is associated with a high rate of mechanical failure. Because of the transarticular nature of the S2AI screw, adding a second point of fixation may provide additional stability and attenuate strains. The objective of the study was to evaluate changes in stability and strain with the integration of a sacroiliac (SI) joint fusion device, implanted through a novel posterior SI approach, supplemental to posterior long-segment fusion.
    Methods: L1-pelvis human cadaveric specimens underwent pure moment (7.5 Nm) and compression (400 N) tests in the following conditions: 1) intact, 2) L2-S1 pedicle screw and rod fixation with L5-S1 interbody fusion, 3) added S2AI screws, and 4) added bilateral SI joint fixation (SIJF). The range of motion (ROM), rod strain, and screw bending moments (S1 and S2AI) were analyzed.
    Results: S2AI fixation decreased L2-S1 ROM in flexion-extension (p ≤ 0.04), L5-S1 ROM in flexion-extension and compression (p ≤ 0.004), and SI joint ROM during flexion-extension and lateral bending (p ≤ 0.03) compared with S1 fixation. SI joint ROM was significantly less with SIJF in place than with the intact joint, S1, and S2AI fixation in flexion-extension and lateral bending (p ≤ 0.01). The S1 screw bending moment decreased following S2AI fixation by as much as 78% in extension, but with statistical significance only in right axial rotation (p = 0.03). Extending fixation to S2AI significantly increased the rod strain at L5-S1 during flexion, axial rotation, and compression (p ≤ 0.048). SIJF was associated with a slight increase in rod strain versus S2AI fixation alone at L5-S1 during left lateral bending (p = 0.048). Compared with the S1 condition, fixation to S2AI increased the mean rod strain at L5-S1 during compression (p = 0.048). The rod strain at L5-S1 was not statistically different with SIJF compared with S2AI fixation (p ≥ 0.12).
    Conclusions: Constructs ending with an S2AI screw versus an S1 screw tended to be more stable, with reduced SI joint motion. S2AI fixation decreased the S1 screw bending moments compared with fixation ending at S1. These benefits were paired with increased rod strain at L5-S1. Supplementation of S2AI fixation with SIJF implants provided further reductions (approximately 30%) in the sagittal plane and lateral bending SI joint motion compared with fixation ending at the S2AI position. This stability was not paired with significant changes in rod or screw strains.
    Language English
    Publishing date 2021-06-18
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2158643-3
    ISSN 1547-5646 ; 1547-5654
    ISSN (online) 1547-5646
    ISSN 1547-5654
    DOI 10.3171/2020.11.SPINE201540
    Database MEDical Literature Analysis and Retrieval System OnLINE

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