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Table of Contents

EDITORIAL

BLOOD COMMENTARIES

SPECIAL REPORT

Joachim Yahalom,on behalf of the International Lymphoma Radiation Oncology Group (ILROG),Bouthaina Shbib Dabaja,on behalf of the International Lymphoma Radiation Oncology Group (ILROG),Umberto Ricardi,on behalf of the International Lymphoma Radiation Oncology Group (ILROG),Andrea Ng,on behalf of the International Lymphoma Radiation Oncology Group (ILROG),N. George Mikhaeel,on behalf of the International Lymphoma Radiation Oncology Group (ILROG),Ivan R. Vogelius,on behalf of the International Lymphoma Radiation Oncology Group (ILROG),Tim Illidge,on behalf of the International Lymphoma Radiation Oncology Group (ILROG),Shunan Qi,on behalf of the International Lymphoma Radiation Oncology Group (ILROG),Andrew Wirth,on behalf of the International Lymphoma Radiation Oncology Group (ILROG),Lena Specht,on behalf of the International Lymphoma Radiation Oncology Group (ILROG)

The International Lymphoma Radiation Oncology Group provides evidence-supported options for adjusting radiation therapy timing and delivery for patients with selected hematological malignancies in the COVID-19 pandemic, while maintaining efficacy and safety.

CLINICAL TRIALS AND OBSERVATIONS

Virginie Royal,for the International Kidney and Monoclonal Gammopathy Research Group,Nelson Leung,for the International Kidney and Monoclonal Gammopathy Research Group,Stéphan Troyanov,for the International Kidney and Monoclonal Gammopathy Research Group,Samih H. Nasr,for the International Kidney and Monoclonal Gammopathy Research Group,Laure Écotière,for the International Kidney and Monoclonal Gammopathy Research Group,Richard LeBlanc,for the International Kidney and Monoclonal Gammopathy Research Group,Benjamin A. Adam,for the International Kidney and Monoclonal Gammopathy Research Group,Andrea Angioi,for the International Kidney and Monoclonal Gammopathy Research Group,Mariam P. Alexander,for the International Kidney and Monoclonal Gammopathy Research Group,Anna Maria Asunis,for the International Kidney and Monoclonal Gammopathy Research Group,Antonella Barreca,for the International Kidney and Monoclonal Gammopathy Research Group,Paola Bianco,for the International Kidney and Monoclonal Gammopathy Research Group,Camille Cohen,for the International Kidney and Monoclonal Gammopathy Research Group,Maria E. Drosou,for the International Kidney and Monoclonal Gammopathy Research Group,Huma Fatima,for the International Kidney and Monoclonal Gammopathy Research Group,Roberta Fenoglio,for the International Kidney and Monoclonal Gammopathy Research Group,François Gougeon,for the International Kidney and Monoclonal Gammopathy Research Group,Jean-Michel Goujon,for the International Kidney and Monoclonal Gammopathy Research Group,Guillermo A. Herrera,for the International Kidney and Monoclonal Gammopathy Research Group,Bertrand Knebelmann,for the International Kidney and Monoclonal Gammopathy Research Group,Nicola Lepori,for the International Kidney and Monoclonal Gammopathy Research Group,Francesca Maletta,for the International Kidney and Monoclonal Gammopathy Research Group,Rita Manso,for the International Kidney and Monoclonal Gammopathy Research Group,Shveta S. Motwani,for the International Kidney and Monoclonal Gammopathy Research Group,Antonello Pani,for the International Kidney and Monoclonal Gammopathy Research Group,Marion Rabant,for the International Kidney and Monoclonal Gammopathy Research Group,Helmut G. Rennke,for the International Kidney and Monoclonal Gammopathy Research Group,Dario Rocatello,for the International Kidney and Monoclonal Gammopathy Research Group,Frida Rosenblum,for the International Kidney and Monoclonal Gammopathy Research Group,Paul W. Sanders,for the International Kidney and Monoclonal Gammopathy Research Group,Afonso Santos,for the International Kidney and Monoclonal Gammopathy Research Group,Karina Soto,for the International Kidney and Monoclonal Gammopathy Research Group,Banu Sis,for the International Kidney and Monoclonal Gammopathy Research Group,Guy Touchard,for the International Kidney and Monoclonal Gammopathy Research Group,Christopher P. Venner,for the International Kidney and Monoclonal Gammopathy Research Group,Frank Bridoux,for the International Kidney and Monoclonal Gammopathy Research Group

In this month’s CME article, Royal and colleagues report on light chain cast nephropathy in 178 patients with myeloma and demonstrate that the extent of cast formation and interstital fibrosis/tubular atrophy predicts the quality of renal response to therapy, which, in turn, is associated with overall survival.

HEMATOPOIESIS AND STEM CELLS

Investigators from St. Jude Children’s Research Hospital provide a valuable resource for understanding the long-term health of pediatric stem cell transplant survivors by analyzing both detailed patient-reported and clinically assessed outcomes and comparing these with similar data for patients receiving nontransplant regimens and normal controls.

LYMPHOID NEOPLASIA

A key question for many patients when first diagnosed with early-stage chronic lymphocytic leukemia is, “When will I need therapy?” Condoluci and an international consortium report a validated algorithm comprising clinical and laboratory measures to estimate the probability of requiring therapy within 5 years for individual patients.

Most Epstein-Barr virus (EBV)–associated lymphomas express viral proteins that are poorly immunogenic. Dalton and colleagues used a high-throughput screen to identify decitabine as a potent inducer of immunogenic EBV antigens and validate the drug’s ability to sensitize lymphomas to EBV-cytotoxic T lymphocytes in vitro and in vivo.

MYELOID NEOPLASIA

Simon and colleagues report their investigations into whether mutations in RUNX1 observed in a series of 430 acute myeloid leukemia (AML) samples are somatic or germline. They revealed a surprisingly high frequency of germline mutations that should prompt further exploration.

PLATELETS AND THROMBOPOIESIS

Using a murine model, Pal and colleagues demonstrated that MYH9-RD mutations observed in patients impair megakaryocyte chemotaxis, disrupting migration towards the vasculature and interfering with proplatelet release, thereby causing macrothrombocytopenia.

THROMBOSIS AND HEMOSTASIS

Producing recombinant factor VIII in mammalian cells is inefficient. Poothong and colleagues provide novel insight into mechanisms that limit factor VIII secretion through endoplasmic reticulum stress, with implications for ongoing hemophilia A gene therapy clinical trials.

LETTER TO BLOOD

Treon et al provide early clinical data supporting a theoretical rationale for continuing ibrutinib in patients receiving the drug during COVID-19 illness.

BLOOD WORK

CONTINUING MEDICAL EDUCATION (CME) QUESTIONS

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