Rechallenges without desensitization following platinum-based chemotherapy reactions

Author:

Young Fernanda D12ORCID,Aung Sidney3,Tang Monica4,Anstey Karen M5,Lee Michael C6,Alfaro Emely7,Cinar Pelin89,Ho Hansen10,Otani Iris M4

Affiliation:

1. National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA

2. Allergy and Immunology Fellowship Training Program, Department of Medicine, UCSF, San Francisco, CA, USA

3. Internal Medicine Residency Training Program, Department of Medicine, UCSF, San Francisco, CA, USA

4. Division of Pulmonary, Critical Care, Allergy, and Sleep Medicine, Department of Medicine, UCSF, San Francisco, CA, USA

5. Division of Pulmonary and Critical Care, Section of Allergy and Clinical Immunology, OHSU, Portland, OR, USA

6. Division of Allergy, Asthma, and Immunology, Scripps Clinic, San Diego, CA, USA

7. Adult Infusion Services, UCSF Medical Center, San Francisco, CA

8. UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, CA

9. Gilead Sciences Inc, Foster City, CA, USA

10. University of California San Francisco School of Pharmacy, San Francisco, CA, USA

Abstract

Background There is increasing interest in non-desensitization protocols as a potential way to reintroduce chemotherapy following hypersensitivity reactions (HSR). Objective To provide insight into the potential utility of non-desensitization reintroduction, particularly at institutions where allergy consultation may not be available. Methods For 70 patients with platinum HSR who underwent rechallenge with standard (≤2 hours), extended (1-bag, 1-step, 4–6 hours), or titrated (4-to-5-bag and -step, 6–7.5 hours) infusions between 1/2014 and 7/2019, demographics and clinical characteristics were reviewed and initial and breakthrough reactions (BTR) were graded using Common Terminology Criteria for Adverse Events version 5.0 (CTCAE v5.0). Tolerance (no BTR) and completion (dose completed despite BTR) were compared using Fisher's exact test. Results Patients (mean [standard deviation] age 57 [13] years, initial HSR grade 2 [1]), were rechallenged with standard ( n = 8), extended ( n = 23), or titrated ( n = 22) infusions after oxaliplatin HSR; and standard ( n = 5) or titrated ( n = 12) after carboplatin HSR. Tolerance and completion were higher for extended versus (vs) standard (tolerance-87%-vs-8%, p < 0.005; completion-96%-vs-38%, p < 0.005) and titrated versus standard (tolerance-76%-vs-8%, p < 0.005; completion-79%-vs-38%, p < 0.05) infusions. Conclusions Extended and titrated infusions may increase reintroduction safety compared to standard infusions. Further investigation into extended infusions may provide a safe alternative to standard infusions in patients who may not have access to desensitization at their institution.

Funder

Division of Intramural Research, National Institute of Allergy and Infectious Diseases

Publisher

SAGE Publications

Reference7 articles.

1. National Comprehensive Cancer Network NCC. NCCN clinical practice guidelines in oncology (NCCN Guidelines®) ovarian cancer including fallopian tube cancer and primary peritoneal cancer, 2013

2. Controversies in Allergy: Chemotherapy Reactions, Desensitize, or Delabel?

3. Hypersensitivity Reactions to Platinum Agents and Taxanes

4. National Cancer Institute (U.S.). Common terminology criteria for adverse events (CTCAE). Rev. ed. Bethesda, MD: U.S. Dept. of Health and Human Services, National Institutes of Health, National Cancer Institute, 2009, p.194.

5. Hypersensitivity Reactions to Oxaliplatin and the Application of a Desensitization Protocol

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