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Articles by Julia Bohlius
Impact of the 2013 WHO guidelines for screening and treatment of cervical precancerous lesions on womens screening rates, by HIV-status, in East and Southern Africa: A regression discontinuity design analysis
The authors declare no competing interests. Olivia Keiser was supported by the Swiss National Science Foundation (grant no 202660). I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Non-Specific Effects of Bacillus Calmette-Guérin: A Systematic Review and Meta-Analysis of Randomized Controlled Trials
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Cervical cancer in women living in South Africa: a record linkage study of the National Health Laboratory Service and the National Cancer Registry
Tafadzwa Dhokotera1,2,3, Serra Asangbeh2,3, Julia Bohlius3,4,5, Elvira Singh1,6, Matthias Egger5,7,8, Eliane Rohner5, Jabulani Ncayiyana6,9, Gary M Clifford10, Victor Olago1,6 and Mazvita Sengayi-Muchengeti1,6,11 1National Cancer Registry, National Health Laboratory Science, 1 Modderfontein Road, Sandringham, Johannesburg 2192, South Africa 2Graduate School for Cellular and Biomedical Sciences, University of Bern, Uni Mittelstrasse, Mittelstrasse 43, CH-3012 Bern, Switzerland 3Swiss Tropical...
Management of Cancer-Associated Anemia With Erythropoiesis-Stimulating Agents: ASCO/ASH Clinical Practice Guideline Update
Journal of Oncology Practice
Management of cancer-associated anemia with erythropoiesis-stimulating agents: ASCO/ASH clinical practice guideline update
Julia Bohlius, Kari Bohlke, Roberto Castelli, Benjamin Djulbegovic, Maryam B. Lustberg, Massimo Martino, Giannis Mountzios, Namrata Peswani, Laura Porter, Tiffany N.
Management of Cancer-Associated Anemia With Erythropoiesis-Stimulating Agents: ASCO/ASH Clinical Practice Guideline Update
Use of erythropoiesis-stimulating agents (ESAs) to manage anemia raises hemoglobin (HgB) levels and reduces the need for RBC transfusions, but increases the risk of thromboembolic events.1,2 Studies have also reported decreased survival, increased mortality during active study phase, and/or an increased risk of cancer progression or recurrence with the use of ESAs in patients with cancer.3-6 The risks of ESAs prompted multiple regulatory actions by the US Food and Drug Administration (FDA)...
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