Management of cancer-associated anemia with erythropoiesis-stimulating agents: ASCO/ASH clinical practice guideline update

Author:

Bohlius Julia1,Bohlke Kari2,Castelli Roberto3,Djulbegovic Benjamin4,Lustberg Maryam B.5,Martino Massimo6,Mountzios Giannis7,Peswani Namrata8,Porter Laura9,Tanaka Tiffany N.10,Trifirò Gianluca11,Yang Hushan12,Lazo-Langner Alejandro13

Affiliation:

1. University of Bern, Bern, Switzerland;

2. American Society of Clinical Oncology, Alexandria, VA;

3. University of Milan, Milan, Italy;

4. City of Hope, Duarte, CA;

5. Ohio State University, Columbus, OH;

6. Azienda Ospedaliera Bianchi Melacrino Morelli, Reggio Calabria, Italy;

7. Henry Dunant Hospital Center, Athens, Greece;

8. Advocate Medical Group, Orland Park, IL;

9. Independent Patient Advocate, Washington, DC;

10. UC San Diego Moores Cancer Center, La Jolla, CA;

11. University of Messina, Messina, Italy;

12. Thomas Jefferson University, Philadelphia, PA; and

13. Western University, London, ON, Canada

Abstract

Abstract Purpose: To update the American Society of Clinical Oncology (ASCO)/American Society of Hematology (ASH) recommendations for use of erythropoiesis-stimulating agents (ESAs) in patients with cancer. Methods: PubMed and the Cochrane Library were searched for randomized controlled trials (RCTs) and meta-analyses of RCTs in patients with cancer published from January 31, 2010, through May 14, 2018. For biosimilar ESAs, the literature search was expanded to include meta-analyses and RCTs in patients with cancer or chronic kidney disease and cohort studies in patients with cancer due to limited RCT evidence in the cancer setting. ASCO and ASH convened an Expert Panel to review the evidence and revise previous recommendations as needed. Results: The primary literature review included 15 meta-analyses of RCTs and two RCTs. A growing body of evidence suggests that adding iron to treatment with an ESA may improve hematopoietic response and reduce the likelihood of RBC transfusion. The biosimilar literature review suggested that biosimilars of epoetin alfa have similar efficacy and safety to reference products, although evidence in cancer remains limited. Recommendations: ESAs (including biosimilars) may be offered to patients with chemotherapy-associated anemia whose cancer treatment is not curative in intent and whose hemoglobin has declined to < 10 g/dL. RBC transfusion is also an option. With the exception of selected patients with myelodysplastic syndromes, ESAs should not be offered to most patients with nonchemotherapy-associated anemia. During ESA treatment, hemoglobin may be increased to the lowest concentration needed to avoid transfusions. Iron replacement may be used to improve hemoglobin response and reduce RBC transfusions for patients receiving ESA with or without iron deficiency. Additional information is available at www.asco.org/supportive-care-guidelines and www.hematology.org/guidelines.

Publisher

American Society of Hematology

Subject

Hematology

Reference54 articles.

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5. PREPARE trial: A randomized phase III trial comparing preoperative, dose-dense, dose-intensified chemotherapy with epirubicin, paclitaxel, and CMF versus a standard-dosed epirubicin-cyclophosphamide followed by paclitaxel with or without darbepoetin alfa in primary breast cancer--outcome on prognosis;Untch;Ann Oncol,2011

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