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Rhabdomyosarcoma, Ewing Sarcoma, and Other Round Cell Sarcomas

Journal of clinical oncology, 2018-01, Vol.36 (2), p.168-179

2018

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Germline Mutations in Predisposition Genes in Pediatric Cancer

The New England journal of medicine, 2015-12, Vol.373 (24), p.2336-2346

2015

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A risk-based treatment strategy for non-rhabdomyosarcoma soft-tissue sarcomas in patients younger than 30 years (ARST0332): a Children's Oncology Group prospective study

The lancet oncology, 2020-01, Vol.21 (1), p.145-161

2020

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R1507, a Monoclonal Antibody to the Insulin-Like Growth Factor 1 Receptor, in Patients With Recurrent or Refractory Ewing Sarcoma Family of Tumors: Results of a Phase II Sarcoma Alliance for Research Through Collaboration Study

Journal of clinical oncology, 2011-12, Vol.29 (34), p.4541-4547

2011

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Analysis of Prognostic Factors in Patients With Nonmetastatic Rhabdomyosarcoma Treated on Intergroup Rhabdomyosarcoma Studies III and IV: The Children's Oncology Group

Journal of clinical oncology, 2006-08, Vol.24 (24), p.3844-3851

2006

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Feasibility of indocyanine green‐guided localization of pulmonary nodules in children with solid tumors

Pediatric blood & cancer, 2023-10, Vol.70 (10), p.e30437-n/a

2023

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Surgical Management of Wild-Type Gastrointestinal Stromal Tumors: A Report From the National Institutes of Health Pediatric and Wildtype GIST Clinic

Journal of clinical oncology, 2017-02, Vol.35 (5), p.523-528

2017

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Malignant rhabdoid tumors originating within and outside the central nervous system are clinically and molecularly heterogeneous

Acta neuropathologica, 2018-08, Vol.136 (2), p.315-326

2018

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Germline genomic findings in children and young adults with melanocytic tumors

Pediatric blood & cancer, 2023-07, Vol.70 (7), p.e30361-n/a

2023

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A phase II trial evaluating the feasibility of adding bevacizumab to standard osteosarcoma therapy

International journal of cancer, 2017-10, Vol.141 (7), p.1469-1477

2017

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Treatment Outcomes in Black and White Children With Cancer: Results From the SEER Database and St Jude Children's Research Hospital, 1992 Through 2007

Journal of clinical oncology, 2012-06, Vol.30 (16), p.2005-2012

2012

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Two Consecutive Phase II Window Trials of Irinotecan Alone or in Combination With Vincristine for the Treatment of Metastatic Rhabdomyosarcoma: The Children's Oncology Group

Journal of clinical oncology, 2007-02, Vol.25 (4), p.362-369

2007

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Infrequent Tumor Initiative of the Children's Oncology Group: Initial Lessons Learned and Their Impact on Future Plans

Journal of clinical oncology, 2010-11, Vol.28 (33), p.5011-5016

2010

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Pediatric Gastrointestinal Stromal Tumors

Hematology/oncology clinics of North America, 2009-02, Vol.23 (1), p.15-34

2009

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Ocular Manifestations of Hypoxia-Inducible Factor-2α Paraganglioma-Somatostatinoma-Polycythemia Syndrome

Ophthalmology (Rochester, Minn.), 2014-11, Vol.121 (11), p.2291-2293

2014

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Larotrectinib for paediatric solid tumours harbouring NTRK gene fusions: phase 1 results from a multicentre, open-label, phase 1/2 study

The lancet oncology, 2018-05, Vol.19 (5), p.705-714

2018

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Prognostic Factors and Clinical Outcomes in Children and Adolescents With Metastatic Rhabdomyosarcoma—A Report From the Intergroup Rhabdomyosarcoma Study IV

Journal of clinical oncology, 2003-01, Vol.21 (1), p.78-84

2003

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Longitudinal NK cell kinetics and cytotoxicity in children with neuroblastoma enrolled in a clinical phase II trial

Journal for immunotherapy of cancer, 2020-03, Vol.8 (1), p.e000176

2020

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Mesenchymal Chondrosarcoma in Children and Young Adults: A Single Institution Retrospective Review

Complexity (New York, N.Y.), 2015, Vol.2015 (2015), p.1-6

2015

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The use of neoadjuvant larotrectinib in the management of children with locally advanced TRK fusion sarcomas

Cancer, 2018-11, Vol.124 (21), p.4241-4247

2018

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Top advances of the year: Pediatric oncology

Cancer, 2022-10, Vol.128 (20), p.3593-3596

2022

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A Pilot Trial of Humanized Anti-GD2 Monoclonal Antibody (hu14.18K322A) with Chemotherapy and Natural Killer Cells in Children with Recurrent/Refractory Neuroblastoma

Clinical cancer research, 2017-11, Vol.23 (21), p.6441-6449

2017

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Pooled Analysis of Phase II Window Studies in Children With Contemporary High-Risk Metastatic Rhabdomyosarcoma: A Report From the Soft Tissue Sarcoma Committee of the Children's Oncology Group

Journal of clinical oncology, 2006-07, Vol.24 (21), p.3415-3422

2006

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Treatment of Childhood Nasopharyngeal Carcinoma With Induction Chemotherapy and Concurrent Chemoradiotherapy: Results of the Children's Oncology Group ARAR0331 Study

Journal of clinical oncology, 2019-12, Vol.37 (35), p.3369-3376

2019

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Rhabdomyosarcoma, Ewing Sarcoma, and Other Round Cell Sarcomas

Germline Mutations in Predisposition Genes in Pediatric Cancer

A risk-based treatment strategy for non-rhabdomyosarcoma soft-tissue sarcomas in patients younger than 30 years (ARST0332): a Children's Oncology Group prospective study

R1507, a Monoclonal Antibody to the Insulin-Like Growth Factor 1 Receptor, in Patients With Recurrent or Refractory Ewing Sarcoma Family of Tumors: Results of a Phase II Sarcoma Alliance for Research Through Collaboration Study

Analysis of Prognostic Factors in Patients With Nonmetastatic Rhabdomyosarcoma Treated on Intergroup Rhabdomyosarcoma Studies III and IV: The Children's Oncology Group

Feasibility of indocyanine green‐guided localization of pulmonary nodules in children with solid tumors

Surgical Management of Wild-Type Gastrointestinal Stromal Tumors: A Report From the National Institutes of Health Pediatric and Wildtype GIST Clinic

Malignant rhabdoid tumors originating within and outside the central nervous system are clinically and molecularly heterogeneous

Germline genomic findings in children and young adults with melanocytic tumors

A phase II trial evaluating the feasibility of adding bevacizumab to standard osteosarcoma therapy

Treatment Outcomes in Black and White Children With Cancer: Results From the SEER Database and St Jude Children's Research Hospital, 1992 Through 2007

Two Consecutive Phase II Window Trials of Irinotecan Alone or in Combination With Vincristine for the Treatment of Metastatic Rhabdomyosarcoma: The Children's Oncology Group

Infrequent Tumor Initiative of the Children's Oncology Group: Initial Lessons Learned and Their Impact on Future Plans

Pediatric Gastrointestinal Stromal Tumors

Ocular Manifestations of Hypoxia-Inducible Factor-2α Paraganglioma-Somatostatinoma-Polycythemia Syndrome

Larotrectinib for paediatric solid tumours harbouring NTRK gene fusions: phase 1 results from a multicentre, open-label, phase 1/2 study

Prognostic Factors and Clinical Outcomes in Children and Adolescents With Metastatic Rhabdomyosarcoma—A Report From the Intergroup Rhabdomyosarcoma Study IV

Larotrectinib in patients with TRK fusion-positive solid tumours: a pooled analysis of three phase 1/2 clinical trials

Longitudinal NK cell kinetics and cytotoxicity in children with neuroblastoma enrolled in a clinical phase II trial

Mesenchymal Chondrosarcoma in Children and Young Adults: A Single Institution Retrospective Review

The use of neoadjuvant larotrectinib in the management of children with locally advanced TRK fusion sarcomas

Top advances of the year: Pediatric oncology

A Pilot Trial of Humanized Anti-GD2 Monoclonal Antibody (hu14.18K322A) with Chemotherapy and Natural Killer Cells in Children with Recurrent/Refractory Neuroblastoma

Pooled Analysis of Phase II Window Studies in Children With Contemporary High-Risk Metastatic Rhabdomyosarcoma: A Report From the Soft Tissue Sarcoma Committee of the Children's Oncology Group

Treatment of Childhood Nasopharyngeal Carcinoma With Induction Chemotherapy and Concurrent Chemoradiotherapy: Results of the Children's Oncology Group ARAR0331 Study

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