Skip to main content

Advertisement

Log in

Cross-sensitivity between taxanes in patients with breast cancer

  • Brief Research Articles
  • Published:
Clinical and Translational Oncology Aims and scope Submit manuscript

Abstract

Aim

This study was a retrospective analysis of our experience with severe cross-hypersensitivity reactions (HSR) to the taxanes paclitaxel (P) and docetaxel (D) in patients with breast cancer.

Patients and methods

We evaluated patients with breast cancer treated with P or D who experienced severe HSR to one of the two taxanes. Severe HSR was defined as any reaction severe enough to warrant discontinuation of the drug. Initial intravenous premedication for paclitaxel was dexamethasone (20 mg), ranitidine (50 mg) and dexchlorpheniramine (10 mg). For docetaxel, dexamethasone (4 mg) orally every 12 hours was administered the day before infusion and dexamethasone (20 mg) was administered intravenously prior to infusion. After severe HSR to the taxane and 30 minutes before infusion of another taxane, we administered dexamethasone (20 mg), ranitidine (50 mg) and dexchlorpheniramine (10 mg) iv as a premedication, and we also increased the time of the infusion.

Results

Between March 2009 and April 2010, 23 patients experienced an initial severe HSR to taxane (12 P, 11 D). Substitution of another taxane was conducted in 17 patients in the two weeks following the initial HSR. Eight patients had an initial HSR with P, and three had a cross-HSR to D. Nine patients had an initial HSR to D, and four of these patients had a cross-HSR to P. Among the 17 patients who received both taxanes, 7 (41%) had a cross-HSR. All cross-HSRs were sufficiently severe (grade 3–4) to suspend taxane treatment permanently. In the remaining 6 patients, a desensitisation protocol to taxanes was performed by increasing the dose of the diluted drug (4 P, 2 D), which resulted in administration of the drug without complications in all cases. There were no treatment-related deaths.

Conclusion

Severe cross-HSR between P and D occurred in a significant proportion of our patients with breast cancer, so care must be taken when substituting taxanes (paclitaxel and docetaxel). A desensitisation protocol can be an effective alternative to decrease the risk of a new HSR.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Crown J, O’Leary M, Ooi WS (2004) Docetaxel and paclitaxel in the treatment of breast cancer: a review of clinical experience. Oncologist 9[Suppl 2]:24–32

    Article  PubMed  CAS  Google Scholar 

  2. Weiss RB, Donehower RC, Wiernik PH et al (1990) Hypersensitivity reactions from taxol. J Clin Oncol 8:1263–1268

    PubMed  CAS  Google Scholar 

  3. Dizon DS, Schwartz J, Rojan A et al (2006) Cross-sensitivity between paclitaxel and docetaxel in a women’s cancers program. Gynecol Oncol 100:149–151

    Article  PubMed  CAS  Google Scholar 

  4. Moon C, Verschraegen CF, Bevers M et al (2000) Use of docetaxel (Taxotere) in patients with paclitaxel (Taxol) hypersensitivity. Anticancer Drugs 11:565–568

    Article  PubMed  CAS  Google Scholar 

  5. Lokich J, Anderson N (1998) Paclitaxel hypersensitivity reactions: a role for docetaxel substitution. Ann Oncol 9:573

    Article  PubMed  CAS  Google Scholar 

  6. Denman JP, Gilbar PJ, Abdi EA (2002) Hypersensitivity reaction (HSR) to docetaxel after a previous HSR to paclitaxel. J Clin Oncol 20:2760–2761

    PubMed  Google Scholar 

  7. Essayan DM, Kagey-Sobotka A, Colarusso PJ et al (1996) Successful parenteral desensitization to paclitaxel. J Allergy Clin Immunol 97:42–46

    Article  PubMed  CAS  Google Scholar 

  8. Feldweg AM, Lee CW, Matulonis UA, Castells M (2005) Rapid desensitization for hypersensitivity reactions to paclitaxel and docetaxel: a new standard protocol used in 77 successful treatments. Gynecol Oncol 96:824–829

    Article  PubMed  CAS  Google Scholar 

  9. Fishman A, Gold T, Goldberg A et al (1999) Effective desensitization protocol to paclitaxel following hypersensitivity reaction. Int J Gynecol Cancer 9:156–159

    Article  PubMed  Google Scholar 

  10. Castells MC, Tennant NM, Sloane DE et al (2008) Hypersensitivity reactions to chemotherapy: outcomes and safety of rapid desensitization in 413 cases. J Allergy Clin Immunol 122:574–580

    Article  PubMed  CAS  Google Scholar 

  11. Gradishar WJ, Tjulandin S, Davidson N et al (2005) Phase III trial of nanoparticle albuminbound paclitaxel compared with polyethylated castor oil-based paclitaxel in women with breast cancer. J Clin Oncol 23:7794–7803

    Article  PubMed  CAS  Google Scholar 

  12. Gradishar WJ, Krasnojon D, Cheporov S et al (2009) Significantly longer progression-free survival with nab-paclitaxel compared with docetaxel as first-line therapy for metastatic breast cancer. J Clin Oncol 27:3611–3619

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Alfonso Sánchez-Muñoz.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sánchez-Muñoz, A., Jiménez, B., García-Tapiador, A. et al. Cross-sensitivity between taxanes in patients with breast cancer. Clin Transl Oncol 13, 904–906 (2011). https://doi.org/10.1007/s12094-011-0753-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12094-011-0753-3

Keywords

Navigation