ASH Clinical News July 2017 Bonus Issue | Page 38

TRAINING and EDUCATION You Make the Call Each month in “You Make the Call,” we’ll pick a challenging clinical question submitted through ASH’s Consult a Colleague program and post the expert’s response, but we also want to know what you would do. Send in your responses to next month’s clinical dilemma and see how your answer matches up to the experts’ in the next print issue. This month, David Straus, MD, discusses treatment options for a patient with c-Myc positive diffuse large B-cell lymphoma. Clinical Dilemma: A 54-year-old previously healthy male with recent abdominal pain had a computed tomography (CT) scan that showed a 5 cm mesenteric mass. The CT core biopsy revealed diffuse large B-cell lymphoma of the germinal center B-cell phenotype that was c-Myc positive. A positron emission tomography scan showed this to be the only site of disease and the bone marrow is negative. Would you recommend R-CHOP x6 or x3-4 with radiation? Or a different regimen given the c-Myc positivity? Consult a Colleague Through ASH Expert Opinion Consult a Colleague is a service for ASH members that helps facilitate the exchange of information between hematologists and their peers. ASH members can seek consultation on clinical cases from qualified experts in 11 categories: David Straus, MD Internist and Hematologic Oncologist Memorial Sloan Kettering Cancer Center New York, New York • Anemias This is probably a high-grade diffuse large B-cell lymphoma. I would obtain fluorescence in situ hybrid- ization to see if there is a c-Myc translocation as well as c-Myc over- expression by immunohistochemis- try. Researchers from the National Cancer Institute (NCI) reported promising early results with dose- adjusted EPOCH-R for treatment of patients with aggressive B-cell lym- phomas with MYC-rearrangement at the 2014 ASH Annual Meeting. 1 This is being explored further in an NCI Cancer Therapy Evaluation Program clinical trial. 2 If his lactate dehydrogenase is normal, he may be eligible for short course treatment with three cycles of RR-EPOCH-R. These regimens are described in the New England Journal of Medicine manuscript on Burkitt lymphoma treatment. 3 • Hematopoietic cell transplantation • Hemoglobinopathies • Hemostasis/thrombosis • Lymphomas • Lymphoproliferative disorders • Leukemias • Multiple myeloma & Waldenström macroglobulinemia • Myeloproliferative disorders • Myelodysplastic syndromes • Thrombocytopenias Assigned volunteers (“colleagues”) will respond to inquiries within two business days (either by email or phone). Have a puzzling clinical dilemma? Submit a question, and read more about Consult a Colleague volunteers at hematology.org/Clinicians/Consult.aspx or scan the QR code. References 1. Dunleavy K, Fanale M, LaCasce A, et al. Preliminary report of a multicenter prospective phase II study of DA-EPOCH-R in MYC-rearranged aggressive B-cell lymphoma. Blood. 2014;124:395. 2. ClinicalTrials.gov. Phase II study of dose-adjusted EPOCH- rituximab in adults with untreated Burkitt lymphoma and c-MYC+ diffuse large B-Cell lymphoma (NCT01092182). 3. Dunleavy K, Pittaluga S, and Shovlin M, et al. Low-intensity therapy in adults with Burkitt’s lymphoma. N Engl J Med. 2013;369:1915-25. Next Month’s Clinical Dilemma: A 30-year-old man with aplastic anemia presented with rapidly progressive exercise intolerance over a 2-week period. White blood cell (WBC) count is 2.2×10 9 /L with an absolute neutrophil count of 450/μL. Hemoglobin is 5.5 g/dl, and platelet count is 3,000/μL. Lactate de- hydrogenase is 180/μL and erythrocyte sedimentation rate is 89 mm/hr. Kidney and liver function is normal. A bone marrow (BM) biopsy shows scant lymphocytes and BM stromal cells. Hematopoietic elements are virtually absent. No signs of paroxysmal nocturnal hemoglobinuria 36 ASH Clinical News by flow cytometry. The patient refuses packed red blood cells or platelet transfusions for religious reasons. We have started immunosuppressive treatment with anti- thymocyte globulin, steroids, and cyclosporine. Since the patient does not wish to receive transfusions, BM transplant is probably out of the question. Do you think it is reasonable to add erythropoietin, eltrombopag, or granulocyte colony-stimulating factor upfront? Is there anything else I am not thinking about? How would you respond? Email us at ashclinicalnews@ hematology.org. ● *If you have a request related to a hematologic disorder not listed here, please email your recommendation to  [email protected] so it can be considered for addition in the future. DISCLAIMER: ASH does not recommend or endorse any specific tests, physicians, products, procedures, or opinions, and disclaims any representation, warranty, or guaranty as to the same. Reliance on any information provided in this article is solely at your own risk. July 2017 Bonus Mid-Year Edition