Hepatitis B Virus Screening and Management for Patients With Cancer Prior to Therapy: ASCO Provisional Clinical Opinion Update

Author:

Hwang Jessica P.1,Feld Jordan J.2,Hammond Sarah P.3,Wang Su H.4,Alston-Johnson Devena E.5,Cryer Donna R.6,Hershman Dawn L.7,Loehrer Andrew P.8,Sabichi Anita L.9,Symington Banu E.10,Terrault Norah11,Wong Melisa L.12,Somerfield Mark R.13,Artz Andrew S.14

Affiliation:

1. The University of Texas MD Anderson Cancer Center, Houston, TX

2. Toronto Centre for Liver Disease, University Health Network, University of Toronto, Toronto, Ontario, Canada

3. Dana Farber Cancer Institute, Boston, MA

4. Saint Barnabas Medical Center, Florham Park, NJ

5. Upstate Oncology Associates, Greenville, SC

6. American Liver Foundation, Washington, DC

7. Herbert Irving Comprehensive Cancer Center at Columbia University, New York, NY

8. Dartmouth-Hitchcock Medical Center, Lebanon, NH

9. Baylor College of Medicine, Houston, TX

10. Memorial Hospital of Sweetwater County, Rock Springs, WY

11. Keck School of Medicine, University of Southern California, Los Angeles, CA

12. University of California San Francisco, San Francisco, CA

13. American Society of Clinical Oncology, Alexandria, VA

14. City of Hope Comprehensive Cancer Center, Duarte, CA

Abstract

PURPOSE This Provisional Clinical Opinion update presents a clinically pragmatic approach to hepatitis B virus (HBV) screening and management. PROVISIONAL CLINICAL OPINION All patients anticipating systemic anticancer therapy should be tested for HBV by 3 tests—hepatitis B surface antigen (HBsAg), hepatitis B core antibody (anti-HBc) total immunoglobulin (Ig) or IgG, and antibody to hepatitis B surface antigen—but anticancer therapy should not be delayed. Findings of chronic HBV (HBsAg-positive) or past HBV (HBsAg-negative and anti-HBc–positive) infection require HBV reactivation risk assessment. Patients with chronic HBV receiving any systemic anticancer therapy should receive antiviral prophylactic therapy through and for minimum 12 months following anticancer therapy. Hormonal therapy alone should not pose a substantial risk of HBV reactivation in patients with chronic HBV receiving hormonal therapy alone; these patients may follow noncancer HBV monitoring and treatment guidance. Coordination of care with a clinician experienced in HBV management is recommended for patients with chronic HBV to determine HBV monitoring and long-term antiviral therapy after completion of anticancer therapy. Patients with past HBV infection undergoing anticancer therapies associated with a high risk of HBV reactivation, such as anti-CD20 monoclonal antibodies or stem-cell transplantation, should receive antiviral prophylaxis during and for minimum 12 months after anticancer therapy completion, with individualized management thereafter. Careful monitoring may be an alternative if patients and providers can adhere to frequent, consistent follow-up so antiviral therapy may begin at the earliest sign of reactivation. Patients with past HBV undergoing other systemic anticancer therapies not clearly associated with a high risk of HBV reactivation should be monitored with HBsAg and alanine aminotransferase during cancer treatment; antiviral therapy should commence if HBV reactivation occurs. Additional information is available at www.asco.org/supportive-care-guidelines .

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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