Literature DB >> 27098551

Intravenous versus oral dexamethasone for prophylaxis of paclitaxel-associated hypersensitivity reaction in patients with primary ovarian, fallopian tube and peritoneal cancer: A double-blind randomized controlled trial.

Marut Yanaranop1,2, Surasith Chaithongwongwatthana3.   

Abstract

AIM: To compare the efficacies and side effects of intravenous and oral dexamethasone (IV-D and PO-D) for paclitaxel-associated hypersensitivity reaction (P-HSR) prophylaxis in patients with primary ovarian, fallopian tube and peritoneal carcinomas (POC/PFTC/PPC) receiving a first cycle of paclitaxel plus carboplatin (TC).
METHODS: In this double-blind randomized controlled trial, patients with POC/PFTC/PPC receiving a first cycle of TC were randomly allocated in a 1:1 ratio to either the IV-D or PO-D groups. Those were followed at 28 days. Primary outcomes were incidence of overall and severe P-HSRs. Secondary outcomes included incidence of dexamethasone-related side effects, other chemotherapy-related adverse events (AEs), and quality-of-life (QoL).
RESULTS: A total of 288 patients were enrolled from February to July 2015, of whom 281 were eligible for analysis, including 140 allocated to IV-D and 141 to PO-D. There was no significant difference in P-HSR rate between the IV-D and PO-D groups (17.9% vs. 19.1%, P = 0.780). Severe P-HSR occurred in one women in the IV-D group (0.7% vs. 0%, P = 0.498). There were no significant differences in other chemotherapy-related AEs and QoL scores. However, women in the PO-D had more side effects from short-term corticosteroid use than those in the IV-D group, especially acne (10.6% vs. 2.1%, P = 0.004).
CONCLUSIONS: IV-D and PO-D have similar efficacies for preventing P-HSR. However, short-term IV-D may be associated with fewer side effects than PO-D. IV-D is thus suggested for P-HSR prophylaxis in patients with POC/PFTC/PPC receiving a first cycle of TC.
© 2016 John Wiley & Sons Australia, Ltd.

Entities:  

Keywords:  dexamethasone; hypersensitivity reaction; ovarian cancer; paclitaxel

Mesh:

Substances:

Year:  2016        PMID: 27098551     DOI: 10.1111/ajco.12495

Source DB:  PubMed          Journal:  Asia Pac J Clin Oncol        ISSN: 1743-7555            Impact factor:   2.601


  4 in total

1.  Pre-medication protocols for the prevention of paclitaxel-induced infusion related reactions: a systematic review and meta-analysis.

Authors:  Samuel Dubinsky; Deep Patel; Xiang Wang; Amirrtha Srikanthan; Terry L Ng; Corey Tsang
Journal:  Support Care Cancer       Date:  2022-02-12       Impact factor: 3.603

Review 2.  Productive Cross-Talk with the Microenvironment: A Critical Step in Ovarian Cancer Metastasis.

Authors:  Mohamed A Abd El Aziz; Komal Agarwal; Subramanyam Dasari; And Anirban K Mitra
Journal:  Cancers (Basel)       Date:  2019-10-21       Impact factor: 6.639

3.  The natural compound n-butylidenephthalide kills high-grade serous ovarian cancer stem cells by activating intrinsic apoptosis signaling pathways.

Authors:  Yu-Hsun Chang; Kun-Chi Wu; Dah-Ching Ding
Journal:  J Cancer       Date:  2021-03-30       Impact factor: 4.207

Review 4.  Premedications for Cancer Therapies: A Primer for the Hematology/Oncology Provider.

Authors:  Amber Clemmons; Arpita Gandhi; Andrea Clarke; Sarah Jimenez; Thuy Le; Germame Ajebo
Journal:  J Adv Pract Oncol       Date:  2021-11-01
  4 in total

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