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Aboulafia, Albert J.

0000-0002-1211-9506

Mayo Clinic

MedStar Franklin Square Medical Center

Citations 2

PPP6R3‐USP6 amplification: Novel oncogenic mechanism in malignant nodular fasciitis
Guo, Ruifeng, Chou, Margaret M. , Asmann, Yan W. , Wenger, Doris E. , Al‐Ibraheemi, Alyaa , Molavi, Diana Weedman, Aboulafia, Albert J. , Jin, Long , Fritchie, Karen , Oliveira, Jennifer L. , Jenkins, Robert B. , Dong, Jie , Oliveira, André M. , Guo, Ruifeng , Herrick, Jennifer L. , Wang, Xiaoke, Asmann, Yan, Al-Ibraheemi, Alyaa, Guo, Ruifeng, Wang, Xiaoke, Westendorf, Jennifer J. , Guo, Ruifeng

Genes, Chromosomes and Cancer | April 27, 2016 | Volume: 55 | Issue: 8 | Pages: 640-649

10.1002/gcc.22366 Get It

Nodular fasciitis (NF) is a clonal self‐limited neoplastic proliferation characterized by rearrangements of the USP6 locus in most examples. To our knowledge well‐documented malignant behavior has never been previously observed in NF. In this report we present an unusual case of NF with classical histologic features that showed a protracted clinical course characterized by multiple recurrences and eventual metastatic behavior over a period of 10 years. Molecular analyses revealed the presence and amplification of the novel PPPR6‐USP6 gene fusion, which resulted in USP6 mRNA transcriptional upregulation. These findings further support the oncogenic role of the USP6 protease in mesenchymal neoplasia and expand the biologic potential of NF. © 2016 Wiley Periodicals, Inc.
Treatment Planning and Fracture Prediction in Patients with Skeletal Metastasis with CT-Based Rigidity Analysis
Entezari, Vahid , Calderon, Nathan, Hipp, John A. , Villa‐Camacho, Juan C., Cheung, Felix H., Aboulafia, Albert J. , Turcotte, Robert , Anderson, Megan E. , Gebhardt, Mark C., Terek, Richard M. , Yaszemski, Michael J. , Snyder, Brian D. , Yaszemski, Michael, Nazarian, Ara , Zurakowski, David , Lin, Patrick P. , Cheng, Edward Y. , Damron, Timothy A.

Clinical Cancer Research | February 27, 2015 | Volume: 21 | Issue: 11 | Pages: 2514-2519

10.1158/1078-0432.ccr-14-2668 Get It

Abstract Purpose: Pathologic fractures could be prevented if reliable methods of fracture risk assessment were available. A multicenter prospective study was conducted to identify significant predictors of physicians' treatment plan for skeletal metastasis based on clinical fracture risk assessments and the proposed CT-based Rigidity Analysis (CTRA). Experimental Design: Orthopedic oncologists selected a treatment plan for 124 patients with 149 metastatic lesions based on the Mirels method. Then, CTRA was performed, and the results were provided to the physicians, who were asked to reassess their treatment plan. The pre- and post-CTRA treatment plans were compared to identify cases in which the treatment plan was changed based on the CTRA report. Patients were followed for a 4-month period to establish the incidence of pathologic fractures. Results: Pain, lesion type, and lesion size were significant predictors of the pre-CTRA plan. After providing the CTRA results, physicians changed their plan for 36 patients. CTRA results, pain, and primary source of metastasis were significant predictors of the post-CTRA plan. Follow-up of patients who did not undergo fixation resulted in 7 fractures; CTRA predicted these fractures with 100% sensitivity and 90% specificity, whereas the Mirels method was 71% sensitive and 50% specific. Conclusions: Lesion type and size and pain level influenced the physicians' plans for the management of metastatic lesions. Physicians' treatment plans and fracture risk predictions were significantly influenced by the availability of CTRA results. Due to its high sensitivity and specificity, CTRA could potentially be used as a screening method for pathologic fractures. Clin Cancer Res; 21(11); 2514–9. ©2015 AACR.