Suzanne Shusterman | Medical Services
Specialties
Programs & Services
Languages
- English
Suzanne Shusterman | Education
Internship
Pediatrics
Boston Children's Hospital
1994, Boston, MA
Medical School
University of Massachusetts
1993, Worcester, MA
Residency
Pediatrics
Boston Combined Residency Program (BCRP)
1996, Boston, MA
Undergraduate School
University of Pennsylvania
1989, Philadelphia, PA
Fellowship
Pediatric Hematology -Oncology
Children's Hospital of Philadelphia
2000, Philadelphia, PA
Suzanne Shusterman | Certifications
- American Board of Pediatrics (Hematology-Oncology)
Suzanne Shusterman | Publications
Hypofractionated Palliative Radiotherapy for Relapsed and Refractory High-Risk Neuroblastoma. Curr Oncol. 2025 Feb 22; 32(3). View Hypofractionated Palliative Radiotherapy for Relapsed and Refractory High-Risk Neuroblastoma. Abstract
A phase 1 dose-escalation study of LY3295668 erbumine as monotherapy and in combination with topotecan and cyclophosphamide in children with relapsed/refractory neuroblastoma. Cancer. 2025 Feb 15; 131(4):e35751. View A phase 1 dose-escalation study of LY3295668 erbumine as monotherapy and in combination with topotecan and cyclophosphamide in children with relapsed/refractory neuroblastoma. Abstract
Author Correction: Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. Nat Commun. 2024 Aug 22; 15(1):7218. View Author Correction: Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. Abstract
Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. Nat Commun. 2024 Jul 11; 15(1):5837. View Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. Abstract
Patterns of recurrence after radiotherapy for high-risk neuroblastoma: Implications for radiation dose and field. Radiother Oncol. 2024 09; 198:110384. View Patterns of recurrence after radiotherapy for high-risk neuroblastoma: Implications for radiation dose and field. Abstract
Factors influencing parents' choice of palliative treatment goals for children with relapsed or refractory neuroblastoma: A multi-site longitudinal survey study. Cancer. 2024 04 01; 130(7):1101-1111. View Factors influencing parents' choice of palliative treatment goals for children with relapsed or refractory neuroblastoma: A multi-site longitudinal survey study. Abstract
STK11 Adnexal Tumor in an Adolescent Female: Diagnostic Pitfalls of a Recently Described Entity. Pediatr Dev Pathol. 2023 Sep-Oct; 26(5):486-493. View STK11 Adnexal Tumor in an Adolescent Female: Diagnostic Pitfalls of a Recently Described Entity. Abstract
A single-institution pediatric and young adult interventional oncology collaborative: Novel therapeutic options for relapsed/refractory solid tumors. Cancer Med. 2023 06; 12(12):13300-13308. View A single-institution pediatric and young adult interventional oncology collaborative: Novel therapeutic options for relapsed/refractory solid tumors. Abstract
Lorlatinib with or without chemotherapy in ALK-driven refractory/relapsed neuroblastoma: phase 1 trial results. Nat Med. 2023 05; 29(5):1092-1102. View Lorlatinib with or without chemotherapy in ALK-driven refractory/relapsed neuroblastoma: phase 1 trial results. Abstract
Progression-Free Survival and Patterns of Response in Patients With Relapsed High-Risk Neuroblastoma Treated With Irinotecan/Temozolomide/Dinutuximab/Granulocyte-Macrophage Colony-Stimulating Factor. J Clin Oncol. 2023 01 20; 41(3):508-516. View Progression-Free Survival and Patterns of Response in Patients With Relapsed High-Risk Neuroblastoma Treated With Irinotecan/Temozolomide/Dinutuximab/Granulocyte-Macrophage Colony-Stimulating Factor. Abstract
Entrectinib in children and young adults with solid or primary CNS tumors harboring NTRK, ROS1, or ALK aberrations (STARTRK-NG). Neuro Oncol. 2022 10 03; 24(10):1776-1789. View Entrectinib in children and young adults with solid or primary CNS tumors harboring NTRK, ROS1, or ALK aberrations (STARTRK-NG). Abstract
Efficacy of post-induction therapy for high-risk neuroblastoma patients with end-induction residual disease. Cancer. 2022 08 01; 128(15):2967-2977. View Efficacy of post-induction therapy for high-risk neuroblastoma patients with end-induction residual disease. Abstract
Phase 1 study of sorafenib and irinotecan in pediatric patients with relapsed or refractory solid tumors. Pediatr Blood Cancer. 2021 11; 68(11):e29282. View Phase 1 study of sorafenib and irinotecan in pediatric patients with relapsed or refractory solid tumors. Abstract
Randomized Phase II Trial of MIBG Versus MIBG, Vincristine, and Irinotecan Versus MIBG and Vorinostat for Patients With Relapsed or Refractory Neuroblastoma: A Report From NANT Consortium. J Clin Oncol. 2021 11 01; 39(31):3506-3514. View Randomized Phase II Trial of MIBG Versus MIBG, Vincristine, and Irinotecan Versus MIBG and Vorinostat for Patients With Relapsed or Refractory Neuroblastoma: A Report From NANT Consortium. Abstract
Facial Paralysis From Post-transplant Lymphoproliferative Disorder. Otol Neurotol. 2021 06 01; 42(5):e605-e608. View Facial Paralysis From Post-transplant Lymphoproliferative Disorder. Abstract
Retrospective evaluation of single patient investigational new drug (IND) requests in pediatric oncology. Cancer Med. 2021 Apr; 10(7):2310-2318. View Retrospective evaluation of single patient investigational new drug (IND) requests in pediatric oncology. Abstract
The use of interval-compressed chemotherapy with the addition of vincristine, irinotecan, and temozolomide for pediatric patients with newly diagnosed desmoplastic small round cell tumor. Pediatr Blood Cancer. 2020 10; 67(10):e28559. View The use of interval-compressed chemotherapy with the addition of vincristine, irinotecan, and temozolomide for pediatric patients with newly diagnosed desmoplastic small round cell tumor. Abstract
Racial and Ethnic Differences in Communication and Care for Children With Advanced Cancer. J Pain Symptom Manage. 2020 10; 60(4):782-789. View Racial and Ethnic Differences in Communication and Care for Children With Advanced Cancer. Abstract
A Novel ALK Fusion in Pediatric Medullary Thyroid Carcinoma. Thyroid. 2019 11; 29(11):1704-1707. View A Novel ALK Fusion in Pediatric Medullary Thyroid Carcinoma. Abstract
Unrealistic parental expectations for cure in poor-prognosis childhood cancer. Cancer. 2020 01 15; 126(2):416-424. View Unrealistic parental expectations for cure in poor-prognosis childhood cancer. Abstract
Antitumor Activity and Tolerability of hu14.18-IL2 with GMCSF and Isotretinoin in Recurrent or Refractory Neuroblastoma: A Children's Oncology Group Phase II Study. Clin Cancer Res. 2019 10 15; 25(20):6044-6051. View Antitumor Activity and Tolerability of hu14.18-IL2 with GMCSF and Isotretinoin in Recurrent or Refractory Neuroblastoma: A Children's Oncology Group Phase II Study. Abstract
Evaluation of the utility of 99m Tc-MDP bone scintigraphy versus MIBG scintigraphy and cross-sectional imaging for staging patients with neuroblastoma. Pediatr Blood Cancer. 2017 Nov; 64(11). View Evaluation of the utility of 99m Tc-MDP bone scintigraphy versus MIBG scintigraphy and cross-sectional imaging for staging patients with neuroblastoma. Abstract
Patterns of Relapse in High-Risk Neuroblastoma Patients Treated With and Without Total Body Irradiation. Int J Radiat Oncol Biol Phys. 2017 02 01; 97(2):270-277. View Patterns of Relapse in High-Risk Neuroblastoma Patients Treated With and Without Total Body Irradiation. Abstract
Multicenter Feasibility Study of Tumor Molecular Profiling to Inform Therapeutic Decisions in Advanced Pediatric Solid Tumors: The Individualized Cancer Therapy (iCat) Study. JAMA Oncol. 2016 May 01; 2(5):608-615. View Multicenter Feasibility Study of Tumor Molecular Profiling to Inform Therapeutic Decisions in Advanced Pediatric Solid Tumors: The Individualized Cancer Therapy (iCat) Study. Abstract
A phase I trial combining decitabine/dendritic cell vaccine targeting MAGE-A1, MAGE-A3 and NY-ESO-1 for children with relapsed or therapy-refractory neuroblastoma and sarcoma. Cancer Immunol Immunother. 2015 Oct; 64(10):1251-60. View A phase I trial combining decitabine/dendritic cell vaccine targeting MAGE-A1, MAGE-A3 and NY-ESO-1 for children with relapsed or therapy-refractory neuroblastoma and sarcoma. Abstract
Phase 1 evaluation of EZN-2208, a polyethylene glycol conjugate of SN38, in children adolescents and young adults with relapsed or refractory solid tumors. Pediatr Blood Cancer. 2014 Oct; 61(10):1792-7. View Phase 1 evaluation of EZN-2208, a polyethylene glycol conjugate of SN38, in children adolescents and young adults with relapsed or refractory solid tumors. Abstract
Neuroblastoma presenting as facial nerve palsy and bulging tympanic membrane. Clin Pediatr (Phila). 2015 Feb; 54(2):183-5. View Neuroblastoma presenting as facial nerve palsy and bulging tympanic membrane. Abstract
Time to disease progression in children with relapsed or refractory neuroblastoma treated with ABT-751: a report from the Children's Oncology Group (ANBL0621). Pediatr Blood Cancer. 2014 Jun; 61(6):990-6. View Time to disease progression in children with relapsed or refractory neuroblastoma treated with ABT-751: a report from the Children's Oncology Group (ANBL0621). Abstract
Radiation exposure to family caregivers and nurses of pediatric neuroblastoma patients receiving 131I-metaiodobenzylguanidine (131I-MIBG) therapy. Clin Nucl Med. 2013 Aug; 38(8):604-7. View Radiation exposure to family caregivers and nurses of pediatric neuroblastoma patients receiving 131I-metaiodobenzylguanidine (131I-MIBG) therapy. Abstract
Adoptive transfer of autologous T cells improves T-cell repertoire diversity and long-term B-cell function in pediatric patients with neuroblastoma. Clin Cancer Res. 2012 12 15; 18(24):6732-41. View Adoptive transfer of autologous T cells improves T-cell repertoire diversity and long-term B-cell function in pediatric patients with neuroblastoma. Abstract
Tolerability and pharmacokinetic profile of a sunitinib powder formulation in pediatric patients with refractory solid tumors: a Children's Oncology Group study. Cancer Chemother Pharmacol. 2012 Apr; 69(4):1021-7. View Tolerability and pharmacokinetic profile of a sunitinib powder formulation in pediatric patients with refractory solid tumors: a Children's Oncology Group study. Abstract
Iodine-131-labeled meta-iodobenzylguanidine therapy of children with neuroblastoma: program planning and initial experience. Semin Nucl Med. 2011 Sep; 41(5):354-63. View Iodine-131-labeled meta-iodobenzylguanidine therapy of children with neuroblastoma: program planning and initial experience. Abstract
Phase I and pharmacokinetic study of sunitinib in pediatric patients with refractory solid tumors: a children's oncology group study. Clin Cancer Res. 2011 Aug 01; 17(15):5113-22. View Phase I and pharmacokinetic study of sunitinib in pediatric patients with refractory solid tumors: a children's oncology group study. Abstract
Phase I trial of lestaurtinib for children with refractory neuroblastoma: a new approaches to neuroblastoma therapy consortium study. Cancer Chemother Pharmacol. 2011 Oct; 68(4):1057-65. View Phase I trial of lestaurtinib for children with refractory neuroblastoma: a new approaches to neuroblastoma therapy consortium study. Abstract
Pediatric phase I trial and pharmacokinetic study of dasatinib: a report from the children's oncology group phase I consortium. J Clin Oncol. 2011 Mar 01; 29(7):839-44. View Pediatric phase I trial and pharmacokinetic study of dasatinib: a report from the children's oncology group phase I consortium. Abstract
Genotypes of NK cell KIR receptors, their ligands, and Fc? receptors in the response of neuroblastoma patients to Hu14.18-IL2 immunotherapy. Cancer Res. 2010 Dec 01; 70(23):9554-61. View Genotypes of NK cell KIR receptors, their ligands, and Fc? receptors in the response of neuroblastoma patients to Hu14.18-IL2 immunotherapy. Abstract
Antitumor activity of hu14.18-IL2 in patients with relapsed/refractory neuroblastoma: a Children's Oncology Group (COG) phase II study. J Clin Oncol. 2010 Nov 20; 28(33):4969-75. View Antitumor activity of hu14.18-IL2 in patients with relapsed/refractory neuroblastoma: a Children's Oncology Group (COG) phase II study. Abstract
Iodine-131--metaiodobenzylguanidine double infusion with autologous stem-cell rescue for neuroblastoma: a new approaches to neuroblastoma therapy phase I study. J Clin Oncol. 2009 Mar 01; 27(7):1020-5. View Iodine-131--metaiodobenzylguanidine double infusion with autologous stem-cell rescue for neuroblastoma: a new approaches to neuroblastoma therapy phase I study. Abstract
Integrative genomics identifies distinct molecular classes of neuroblastoma and shows that multiple genes are targeted by regional alterations in DNA copy number. Cancer Res. 2006 Jun 15; 66(12):6050-62. View Integrative genomics identifies distinct molecular classes of neuroblastoma and shows that multiple genes are targeted by regional alterations in DNA copy number. Abstract
Neuroblastoma. Holland JC and Frei E, editors. Cancer Medicine. 2006.
Expression profiling identifies BAI2, an endogenous inhibitor of angiogenesis, as a traget for somatic inactivation in high-risk neuroblastoma. Advances in Neuroblastoma Research Proceedings. 2006; 73.
131I-Metaiodobenzylguanidine(131I-MIBG) double infusion with autologous stem cell transplant (ASCT) for neuroblastoma: A New Approaches to Neuroblastoma Therapy (NANT) study. Advances in Neuroblastoma Research Proceedings. 2006; 123.
Prospects for therapeutic inhibition of neuroblastoma angiogenesis. Cancer Lett. 2005 Oct 18; 228(1-2):171-9. View Prospects for therapeutic inhibition of neuroblastoma angiogenesis. Abstract
Methionine aminopeptidase 2 inhibition is an effective treatment strategy for neuroblastoma in preclinical models. Clin Cancer Res. 2005 Apr 01; 11(7):2680-5. View Methionine aminopeptidase 2 inhibition is an effective treatment strategy for neuroblastoma in preclinical models. Abstract
Somatic Inactivation of brain-specific angiogenesis inhibitor-2 (BAI2) during the malignant evolution of high-risk neuroblastoma. Pediatric Blood and Cancer. 2005; 44(6).
131I-MIBG double infusiton with autologous stem cell transplant (ASCT) for neuroblastoma - a New Approaches to Neuroblastoma Therapy (NANT) study. Advances in Neuroblastoma Research Proceedings. 2004; 65.
Genome-wide transcriptome analysis for neuroblastoma gene discovery and refinement of clinical risk group prediction. Advances in Neuroblastoma Research Proceedings. 2004; 103.
Detection of single-copy chromosome 17q gain in human neuroblastomas using real-time quantitative polymerase chain reaction. Mod Pathol. 2003 Dec; 16(12):1248-56. View Detection of single-copy chromosome 17q gain in human neuroblastomas using real-time quantitative polymerase chain reaction. Abstract
Tumor suppression by a rationally designed reversible inhibitor of methionine aminopeptidase-2. Cancer Res. 2003 Nov 15; 63(22):7861-9. View Tumor suppression by a rationally designed reversible inhibitor of methionine aminopeptidase-2. Abstract
ID2 expression is not associated with MYCN amplification or expression in human neuroblastomas. Cancer Res. 2003 Apr 01; 63(7):1631-5. View ID2 expression is not associated with MYCN amplification or expression in human neuroblastomas. Abstract
Functional genomic analysis of neuroblastoma for high resolution mapping of 11q deletions. American Association for Cancer Research Proceedings. 2003; 44:1394.
Neuroblastoma. Holland JC and Frei E, editors. Cancer Medicine. 2003; 2263-76.
Increased incidence of TP53 mutations in post-treatment neuroblastomas. American Association for Cancer Research Proceedings. 2003; 44:809.
Transfusion of the patient with congenitally aquired coagulation defects. Hillyer CD and Silbersteing LE, editors. Principles of Blood Banking and Transfusion Medicine. 2003; 291-306.
Discovery of antiangiogenic targets induced by chemotherapy in a murine model of human neuroblastoma. American Association for Cancer Research Proceedings Late Breaking Abstracts. 2003.
A reversible methionine aminopeptidase inhibitor potently inhibits growth of human neuroblastoma in xenotransplantation models. American Association fo Cancer Research Proceedings. 2003; 44:809.
Transplantation in Hematology and Oncology II. 2003; 283-98.
Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13. Cancer Res. 2002 Nov 15; 62(22):6651-8. View Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13. Abstract
Chromosome 11q23.3-q24.1 deletions in neuroblastoma (NB). Advances in Neuroblastoma Research Proceedings. 2002; 18.
ID2 is a MYCN target gene, but expression is not correlated with MYCN gene amplification in human neuroblastomas. Advances in Neuroblastoma Research Proceedings. 2002; 50.
Angiogenesis inhibition is an effective adjuvant therapeutic strategy in neuroblastoma (NB) preclinical models. Advances in Neuroblastoma Research Proceeddings. 2002; 87.
A combined functional and expression profiling strategy for isolating neuroblastoma suppresso genes on chromosome 11. American Association for Cancer Research Proceedings. 2002; 43:343.
Prospective validation of real-time quantitative PCR for detection of MYCN amplifcation inprimary neuroblastoma specimens. Advances in Neuroblastoma Research Proceedings. 2002; 67.
A functional and expression profiling stratefy for isolating neuroblastoma (NB) supressor genes on chromosome 11. Advances in Neuroblastoma Research Proceedings. 2002; 18.
The angiogenesis inhibitor tnp-470 effectively inhibits human neuroblastoma xenograft growth, especially in the setting of subclinical disease. Clin Cancer Res. 2001 Apr; 7(4):977-84. View The angiogenesis inhibitor tnp-470 effectively inhibits human neuroblastoma xenograft growth, especially in the setting of subclinical disease. Abstract
Angiogenesis inhibitor TNP-470 during bone marrow transplant: safety in a preclinical model. Clin Cancer Res. 2001 Apr; 7(4):1026-32. View Angiogenesis inhibitor TNP-470 during bone marrow transplant: safety in a preclinical model. Abstract
The growth rate of human neuroblastoma xenografts is decreased through inhibition of multiple angiogenic signaling pathways with SU668. Journal of Pediatric Hematology/Oncology . 2001; 23:A1.
The angiogenesis inhibitor TNP-470 effectively inhibits human neuroblastoma xenograft growth especially in the setting of subclinical disease. Clinical Cancer Research. 2001; 7(4):977-84.
Inhibition of the VEGF, PDGF and bFGF signaling pathways with SU6668 decreases the growth rate of human neuroblastoma xenografts. American Association for Cancer Research Proceedings. 2001; 42:803.
Localization of a hereditary neuroblastoma predisposition gene to 16p12-p13. Med Pediatr Oncol. 2000 Dec; 35(6):526-30. View Localization of a hereditary neuroblastoma predisposition gene to 16p12-p13. Abstract
Inhibition of tumor growth in a human neuroblastoma xenograft model with TNP-470. Med Pediatr Oncol. 2000 Dec; 35(6):673-6. View Inhibition of tumor growth in a human neuroblastoma xenograft model with TNP-470. Abstract
Long term survivors of childhood leukemia. Curr Opin Hematol. 2000 Jul; 7(4):217-22. View Long term survivors of childhood leukemia. Abstract
Effects of TRK receptor expression on angiogenesis in neuroblastoma cells. American Association for Cancer Research Proceedings. 2000; 41:791.
Detection of unbalanced 17q gain in human neuroblastomas by real-time quantitative PCR. American Association for Cancer Research Proceedings. 2000; 41:791.
Use of real-time quantitative PCR to detect unbalanced 17q gain in neuroblastoma cell lines and primary tumors. Medical and Pediatric Oncology. 2000; 35:748.
Microcytic Anemia. Iron Deficiency Anemia. The 5 Minute Pediatric Consult. 2000.
Inhibitors of angiogenesis in minimal residual disease: safety post-BMT and efficacy in a preclinical model. Angiogenesis in Oncology and Hematology. 2000.
Preclinical evaluation of antiangiogenic therapy with TNP-470 for human neuroblastoma. Molecular Targets and Cancer Therapeutics. 1999; 5:3812s.
TNP-470 inhibits the growth rate and tumorigenicity of human neuroblastoma xenografts. Journal of Pediatric Hematology/Oncology. 1999; 21:326.
A 2.5-month-old girl with hyperbilirubinemia, hypoglycemia, and blindness. Curr Opin Pediatr. 1996 Aug; 8(4):411-6. View A 2.5-month-old girl with hyperbilirubinemia, hypoglycemia, and blindness. Abstract