Analysis of increased paclitaxel hypersensitivity at a single institution in setting of COVID 19 vaccination.

Authors

null

Nikita Jain

Northwestern Medicine, Mchenry, IL

Nikita Jain, Anika Bhargava, Kelly Weaver, Lesley Volz, Brette Conliffe, Lauren Ingles, Brian Dong

Organizations

Northwestern Medicine, Mchenry, IL, University of Louisville, Louisville, KY, James Graham Brown Cancer Center, Louisville, KY, UofL Health: University of Louisville Hospital/Brown Cancer Center, Louisville, KY, Brown Cancer Center, Louisville, KY, James Graham Brown Cancer Center, University of Louisville, Louisville, KY

Research Funding

No funding received
None.

Background: Paclitaxel is a commonly used chemotherapy agent effective in various malignancies. It is known to cause serious and potentially life-threatening hypersensitivity reactions (HRs). Pre-medication protocols have been employed, however approximately 10% of patients will still experience these reactions (1). On an internal review at the University of Louisville, Brown Cancer Center (UofL, BCC) there has been a considerable increase in the incidence of paclitaxel HRs from 4.2% in March 2020 - March 2021 to 14.8% in March 2021 - April 2022. Identifying risk factors that may predispose patients to these reactions is an area of interest in an effort to reduce these events. In this study we investigated clinical characteristics between patients that tolerated paclitaxel versus those who had a HR within the last year with a particular focus on the COVID-19 vaccine given the recent pandemic. Methods: This is a single center retrospective case-control study done at the UofL, BCC. Data was collected on patients who received cycle one day one paclitaxel from March 2021 to April 2022 (n = 135), and patients who developed a reaction were identified. Patient characteristics including demographics, COVID vaccination status, and prior allergies were also collected (table). A T-test analysis was performed between the two groups – those who had a HR and those who did not. Results: Of the 135 patients, 20 were found to have a HR. Absolute lymphocyte count (ALC) was found to be significantly higher with an average of 1125 in the HR group versus 853 in the no reaction group (p = 0.0357). Patients in the HR group also had fewer lines of chemotherapy with an average of 1.15 versus the no reaction group of 1.4 (p = 0.039). There was no significant difference between patients who received the COVID-19 vaccine and those who did not (table). Conclusions: Patients who experienced paclitaxel HRs were found to have higher levels of ALC and tend to be earlier in their treatment course with having undergone fewer lines of chemotherapy. Of note COVID-19 vaccination status appears to have no association with those experiencing paclitaxel HRs. The clinical implications of this requires further exploration in future studies

Statistical analysis of patient characteristics between those who experienced a paclitaxel HR versus those who did not.

Characteristics
Paclitaxel Reaction

(n = 20)
No Reaction

(n = 113)
P Value
Age, mean
62.1
63.4
0.589
Stage, mean
3.15
2.94
0.381
Sex


 Male
4
23
0.957
 Female
16
89
Lines of Treatment, mean
1.15
1.4
0.039
COVID-19 Vaccine Received


 Yes
14
83
0.719
 No
6
29
# COVID Vaccine Doses, mean
2.36
2.49
0.53
WBC, mean
8.14
8.01
0.881
ANC, mean
6310
4589
0.053
ALC, mean
1125
853
0.0357
AEC, mean
140
79
0.203
Prior Allergies

 Yes
11
64
0.863
 No
9
48
Days from 1st Vaccine to Paclitaxel, mean
173
241.5
0.118

References Weiss RB, et al. Hypersensitivity Reactions to the Taxanes Paclitaxel and Docetaxel. J of Clin Oncol. 1990; 8(7):1263-8.

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Abstract Details

Meeting

2022 ASCO Quality Care Symposium

Session Type

Poster Session

Session Title

Poster Session B

Track

Palliative and Supportive Care,Technology and Innovation in Quality of Care,Quality, Safety, and Implementation Science

Sub Track

Quality Improvement Research and Implementation Science

Citation

J Clin Oncol 40, 2022 (suppl 28; abstr 364)

DOI

10.1200/JCO.2022.40.28_suppl.364

Abstract #

364

Poster Bd #

E7

Abstract Disclosures

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