Thomas Arthur Olson
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Thomas Arthur Olson has a total of 117 co-authors. Here are the top co-authors by number of shared publications:
- Dominik T. Schneider
Clinic of Pediatrics Klinikum Dortmund University Witten/Herdecke Dortmund Germany
7 shared publications Giovanni Cecchetto
University of Padua
4 shared publications- A. Lindsay Frazier
Dana Farber Cancer Institute , Boston, MA
2 shared publications - Bryan J. Dicken
Stollery Children's Hospital Edmonton Alberta Canada
2 shared publications - Carlos Rodriguez-Galindo
Department of Global Pediatric Medicine St. Jude Children's Research Hospital Memphis Tennessee USA
2 shared publications Deborah F. Billmire
Riley Hospital for Children Indianapolis Indiana USA
2 shared publications
Latest Publications
- 14 September 2025
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 72 (12) , e32033
Outcome of Children With Intermediate‐Risk Extracranial Malignant Germ Cell Tumors by Response Status at the End of Induction Chemotherapy: A Report From the Children's Oncology Group
Background: In many pediatric malignant germ cell tumor (MGCT) protocols, patients who do not achieve a complete response (CR; normal tumor markers, no radiological/histological residual) after three cisplatin–etoposide–bleomycin (PEb) cycles receive two to three “consolidation” cycles of the same regimen. Evidence for this practice is limited, and historical outcomes for non‑CR patients remain poor. Methods: We retrospectively reviewed patients diagnosed with intermediate‐risk MGCT, enrolled in AGCT0132, between 2003 and 2011. All patients received three cycles of PEb and underwent response assessment at the end of induction. Patients not in CR were prescribed three additional cycles of PEb as consolidation. We compared event‐free survival (EFS) and overall survival (OS) for patients who did and did not receive consolidation. Results: Among 210 patients enrolled, two patients were excluded from analyses: one without complete information, and one had rapid progressive disease (PD) and did not complete induction therapy. Out of 208 patients, 193 had a CR after three cycles of induction chemotherapy, and their post‐induction 4‐year EFS and OS were 93% and 99%. Fifteen patients were not in CR at the end of the first three cycles. Twelve received consolidated chemotherapy as mandated per protocol, and their 4‐year EFS and OS were 61% and 65%, respectively. Three patients were deemed to have progressive disease at the end of induction and received second‐line therapy. Conclusion: Children with MGCTs who did not achieve CR after the first three cycles of chemotherapy had an inferior outcome compared to those with a CR, despite receiving additional cycles of PEb chemotherapy. We conclude that consolidation is of unclear benefit. We suggest that pediatric MGCT patients who fail to achieve a CR after standard induction chemotherapy may receive a salvage regimen with different agents rather than consolidation with more of the same chemotherapy.
- 14 September 2025
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 72 (12) , e32033
Outcome of Children With Intermediate‐Risk Extracranial Malignant Germ Cell Tumors by Response Status at the End of Induction Chemotherapy: A Report From the Children's Oncology Group
Background: In many pediatric malignant germ cell tumor (MGCT) protocols, patients who do not achieve a complete response (CR; normal tumor markers, no radiological/histological residual) after three cisplatin–etoposide–bleomycin (PEb) cycles receive two to three “consolidation” cycles of the same regimen. Evidence for this practice is limited, and historical outcomes for non‑CR patients remain poor. Methods: We retrospectively reviewed patients diagnosed with intermediate‐risk MGCT, enrolled in AGCT0132, between 2003 and 2011. All patients received three cycles of PEb and underwent response assessment at the end of induction. Patients not in CR were prescribed three additional cycles of PEb as consolidation. We compared event‐free survival (EFS) and overall survival (OS) for patients who did and did not receive consolidation. Results: Among 210 patients enrolled, two patients were excluded from analyses: one without complete information, and one had rapid progressive disease (PD) and did not complete induction therapy. Out of 208 patients, 193 had a CR after three cycles of induction chemotherapy, and their post‐induction 4‐year EFS and OS were 93% and 99%. Fifteen patients were not in CR at the end of the first three cycles. Twelve received consolidated chemotherapy as mandated per protocol, and their 4‐year EFS and OS were 61% and 65%, respectively. Three patients were deemed to have progressive disease at the end of induction and received second‐line therapy. Conclusion: Children with MGCTs who did not achieve CR after the first three cycles of chemotherapy had an inferior outcome compared to those with a CR, despite receiving additional cycles of PEb chemotherapy. We conclude that consolidation is of unclear benefit. We suggest that pediatric MGCT patients who fail to achieve a CR after standard induction chemotherapy may receive a salvage regimen with different agents rather than consolidation with more of the same chemotherapy.
- 16 January 2025
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 72 (4) , e31545
Multicenter Retrospective Analysis of Pediatric Differentiated Thyroid Carcinoma: Treatment Practices and Outcomes Prior to Pediatric American Thyroid Association Guidelines Implementation
Background: Differentiated thyroid carcinoma (DTC) is the most common pediatric thyroid malignancy, with papillary thyroid carcinoma (PTC) representing 90% of the cases. In 2015, the American Thyroid Association (ATA) developed management guidelines for pediatric DTC.Procedure: Patients less than 21 years of age diagnosed with DTC between 2000 and 2015 at Texas Children's Hospital, Seattle Children's Hospital, Children's Healthcare of Atlanta, Children's Hospital Colorado, and Nationwide Children's Hospital were retrospectively analyzed to evaluate treatment practices before the implementation of the ATA guidelines.Results: We included 216 pediatric patients with DTC. A majority were female (76%) with a median age at diagnosis of 14.8 years. Neck swelling (56%) and palpable nodules (49%) were common presenting symptoms. Diagnostic evaluations typically included thyroid ultrasound, with common features being microcalcifications (47.7%) and hypoechogenicity (39.0%). Fine‐needle aspiration cytology confirmed diagnosis in 50.5%. The majority of patients underwent total thyroidectomy (78.7%) and lymph node dissection (75.5%). ATA risk stratification was low, intermediate, and high risk in 111 (51.4%), 29 (13.4%), and 76 patients (35.2%), respectively. Upfront radioactive iodine (RAI) was administered in 83%. At 1‐year follow‐up, 46% were disease‐free (66% low risk, 59% intermediate risk, and 13% high risk). The 5‐year progression‐free survival for low, intermediate, and high risk were 86%, 53%, and 43%, respectively. The disease‐related overall survival was 100%.Conclusions: Prior to the introduction of the ATA guidelines, a majority of patients underwent total thyroidectomy with lymph node dissection followed by RAI. Selective use of RAI for low‐risk disease as recommended in the current guidelines may be appropriate.
- 16 January 2025
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 72 (4) , e31545
Multicenter Retrospective Analysis of Pediatric Differentiated Thyroid Carcinoma: Treatment Practices and Outcomes Prior to Pediatric American Thyroid Association Guidelines Implementation
Background: Differentiated thyroid carcinoma (DTC) is the most common pediatric thyroid malignancy, with papillary thyroid carcinoma (PTC) representing 90% of the cases. In 2015, the American Thyroid Association (ATA) developed management guidelines for pediatric DTC.Procedure: Patients less than 21 years of age diagnosed with DTC between 2000 and 2015 at Texas Children's Hospital, Seattle Children's Hospital, Children's Healthcare of Atlanta, Children's Hospital Colorado, and Nationwide Children's Hospital were retrospectively analyzed to evaluate treatment practices before the implementation of the ATA guidelines.Results: We included 216 pediatric patients with DTC. A majority were female (76%) with a median age at diagnosis of 14.8 years. Neck swelling (56%) and palpable nodules (49%) were common presenting symptoms. Diagnostic evaluations typically included thyroid ultrasound, with common features being microcalcifications (47.7%) and hypoechogenicity (39.0%). Fine‐needle aspiration cytology confirmed diagnosis in 50.5%. The majority of patients underwent total thyroidectomy (78.7%) and lymph node dissection (75.5%). ATA risk stratification was low, intermediate, and high risk in 111 (51.4%), 29 (13.4%), and 76 patients (35.2%), respectively. Upfront radioactive iodine (RAI) was administered in 83%. At 1‐year follow‐up, 46% were disease‐free (66% low risk, 59% intermediate risk, and 13% high risk). The 5‐year progression‐free survival for low, intermediate, and high risk were 86%, 53%, and 43%, respectively. The disease‐related overall survival was 100%.Conclusions: Prior to the introduction of the ATA guidelines, a majority of patients underwent total thyroidectomy with lymph node dissection followed by RAI. Selective use of RAI for low‐risk disease as recommended in the current guidelines may be appropriate.
- 24 April 2022
- Published by Springer Nature
- p. 107-111
Germ Cell Tumors of the Head and Neck
- 24 April 2022
- Published by Springer Nature
- p. 301-389
Gonadal and Extragonadal Germ Cell Tumors, Sex Cord Stromal and Rare Gonadal Tumors
- 24 April 2022
- Published by Springer Nature
- p. 301-389
Gonadal and Extragonadal Germ Cell Tumors, Sex Cord Stromal and Rare Gonadal Tumors
- 24 April 2022
- Published by Springer Nature
- p. 149-157
Mediastinal Germ Cell Tumors
- 24 April 2022
- Published by Springer Nature
- p. 593-598
Tumors of Unknown Primary Site
- Open Access
- 11 April 2022
- Published by SAGE Publications in OMICS: A Journal of Integrative Biology
- Vol. 26 (4) , 236-245
How to Maintain a Healthy Gut Microbiome in Children with Cancer? Gut Microbiome Association with Diet in Children with Solid Tumors Postchemotherapy
Malnutrition is a common complication in children with cancer. Cancer treatment and malnutrition can disrupt gut microbiome diversity and composition. The gut microbiome is of broad interest to better understand the mechanisms of malnutrition in cancer therapy. This study aimed to compare the gut microbiome between children with solid tumors postchemotherapy and healthy controls, and investigated the association of the putative microbiome differences with diet. Study participants were 27 children (7–18 years) with solid tumors within the first year after the completion of chemotherapy and 22 healthy controls. The study groups did not have a statistically significant difference in age, race, sex, and body mass index. At study intake, the participants completed the Block Kids Food Screener for dietary intakes in the past week. Fecal specimens were collected and analyzed for the gut microbiome. The cancer and control groups differed in gut microbial β-diversity and abundance analyses. The macronutrient intakes such as carbohydrates, fiber, beta-carotene, and vitamin B6 were positively associated with α-diversity. Children with adequate vitamin B6 had a higher Chao1 diversity index than children with inadequate or excessive intake ( p = 0.0004). Children with excessive selenium intake had a trend for higher Pielou's_e index than children with inadequate intake ( p = 0.091). Maintaining a healthy gut microbiome is critical among children with cancer. This study provides new insights on the linkages between dietary intakes and the gut microbiome in children with solid tumors postchemotherapy. These findings, if replicated in future independent studies, may help anticipate malnutrition and plan for personalized nutrition approaches during chemotherapy in pediatric cancers.
- 11 April 2022
- Published by SAGE Publications in OMICS: A Journal of Integrative Biology
- Vol. 26 (4) , 236-245
Open AccessHow to Maintain a Healthy Gut Microbiome in Children with Cancer? Gut Microbiome Association with Diet in Children with Solid Tumors Postchemotherapy
Malnutrition is a common complication in children with cancer. Cancer treatment and malnutrition can disrupt gut microbiome diversity and composition. The gut microbiome is of broad interest to better understand the mechanisms of malnutrition in cancer therapy. This study aimed to compare the gut microbiome between children with solid tumors postchemotherapy and healthy controls, and investigated the association of the putative microbiome differences with diet. Study participants were 27 children (7–18 years) with solid tumors within the first year after the completion of chemotherapy and 22 healthy controls. The study groups did not have a statistically significant difference in age, race, sex, and body mass index. At study intake, the participants completed the Block Kids Food Screener for dietary intakes in the past week. Fecal specimens were collected and analyzed for the gut microbiome. The cancer and control groups differed in gut microbial β-diversity and abundance analyses. The macronutrient intakes such as carbohydrates, fiber, beta-carotene, and vitamin B6 were positively associated with α-diversity. Children with adequate vitamin B6 had a higher Chao1 diversity index than children with inadequate or excessive intake ( p = 0.0004). Children with excessive selenium intake had a trend for higher Pielou's_e index than children with inadequate intake ( p = 0.091). Maintaining a healthy gut microbiome is critical among children with cancer. This study provides new insights on the linkages between dietary intakes and the gut microbiome in children with solid tumors postchemotherapy. These findings, if replicated in future independent studies, may help anticipate malnutrition and plan for personalized nutrition approaches during chemotherapy in pediatric cancers.
- 16 December 2021
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 69 (3) , e29529
Intraventricular topotecan in the successful treatment of recurrent CNS pleuropulmonary blastoma
Pleuropulmonary blastoma (PPB) is a rare pediatric tumor of the pleura and pulmonary mesenchyme, associated with pathogenic germline DICER1 mutations. Although the most common site of metastasis is the central nervous system (CNS), patients with CNS metastasis have dismal outcome. We report a case of a patient presenting with type II PPB and intracranial and bone metastases. We describe a multimodal therapy approach and highlight the use of intraventricular topotecan for isolated CNS recurrence. In addition, a new pathogenic germline mutation heterozygous for the c.1234delT of DICER1 was identified. Patient remains in remission 3 years after recurrence.
- 16 December 2021
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 69 (3) , e29529
Intraventricular topotecan in the successful treatment of recurrent CNS pleuropulmonary blastoma
Pleuropulmonary blastoma (PPB) is a rare pediatric tumor of the pleura and pulmonary mesenchyme, associated with pathogenic germline DICER1 mutations. Although the most common site of metastasis is the central nervous system (CNS), patients with CNS metastasis have dismal outcome. We report a case of a patient presenting with type II PPB and intracranial and bone metastases. We describe a multimodal therapy approach and highlight the use of intraventricular topotecan for isolated CNS recurrence. In addition, a new pathogenic germline mutation heterozygous for the c.1234delT of DICER1 was identified. Patient remains in remission 3 years after recurrence.
- 9 December 2021
- Published by Institute of Electrical and Electronics Engineers (IEEE)
- p. 1679-1681
Examining Mental Illness Trends in the United States From 2006 to 2019
We investigate the characteristics of medical expenditures associated with mental illness hospitalizations using the Truven Health MarketScan Database. We focus on the inpatient admissions due to mental illness of adults aged 1S to 64 between 2006 to 2019. We aim to answer the following questions: (1) Did the financial crisis of 2008 impact mental health in the U.S.?(2) What are the other macro-level (socioeconomic and regulartory) and micro-level (individualpatient related) factors that affect the cost of inpatient care due to mental illness; (3) Did mental illness affect men and women differently? (4) How were different regions within the U.S. affected by mental illness?
- 9 December 2021
- Published by Institute of Electrical and Electronics Engineers (IEEE)
- p. 1679-1681
Examining Mental Illness Trends in the United States From 2006 to 2019
We investigate the characteristics of medical expenditures associated with mental illness hospitalizations using the Truven Health MarketScan Database. We focus on the inpatient admissions due to mental illness of adults aged 1S to 64 between 2006 to 2019. We aim to answer the following questions: (1) Did the financial crisis of 2008 impact mental health in the U.S.?(2) What are the other macro-level (socioeconomic and regulartory) and micro-level (individualpatient related) factors that affect the cost of inpatient care due to mental illness; (3) Did mental illness affect men and women differently? (4) How were different regions within the U.S. affected by mental illness?
- 14 July 2021
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 68 (10) , e29241
Adjuvant chemoradiation for high‐grade cardiac leiomyosarcoma in a child: Case report and review of literature
A 13‐year‐old healthy girl presented with dizziness and palpitations, found to have a left atrial mass. An 8‐cm tumor was removed en bloc. Pathology confirmed grade 3 leiomyosarcoma with multifocal positive margins. She received adjuvant ifosfamide and doxorubicin, followed by concurrent proton radiotherapy and ifosfamide. Radiotherapy included 66 Gy (RBE) in 33 fractions to the operative bed. Prospectively graded toxicities included Grade 2 esophagitis and Grade 1 anorexia, dermatitis, and fatigue. She completed six cycles of ifosfamide. Two years post operation, she had no evidence of disease, intermittent palpitations with normal cardiac function, and no other cardiopulmonary or esophageal symptoms.
- 14 July 2021
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 68 (10) , e29241
Adjuvant chemoradiation for high‐grade cardiac leiomyosarcoma in a child: Case report and review of literature
A 13‐year‐old healthy girl presented with dizziness and palpitations, found to have a left atrial mass. An 8‐cm tumor was removed en bloc. Pathology confirmed grade 3 leiomyosarcoma with multifocal positive margins. She received adjuvant ifosfamide and doxorubicin, followed by concurrent proton radiotherapy and ifosfamide. Radiotherapy included 66 Gy (RBE) in 33 fractions to the operative bed. Prospectively graded toxicities included Grade 2 esophagitis and Grade 1 anorexia, dermatitis, and fatigue. She completed six cycles of ifosfamide. Two years post operation, she had no evidence of disease, intermittent palpitations with normal cardiac function, and no other cardiopulmonary or esophageal symptoms.