(2022) A Post-Marketing Surveillance Study to Evaluate the Safety Profile of Alvotere (R) (Docetaxel) in Iranian Patients Diagnosed with Different Types of Cancers Receiving Chemotherapy. Current Therapeutic Research-Clinical and Experimental. p. 5. ISSN 0011-393X
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Abstract
Background: Docetaxel is a clinically well established antimitotic chemotherapy medication. Labeled docetaxel indications are breast cancer, gastric cancer, head and neck cancer, non-small cell lung cancer, and prostate cancer. Objective: This is a Phase IV study to evaluate the safety profile of docetaxel (Alvotere; NanoAlvand, Iran) in Iranian patients diagnosed with different types of cancers receiving chemotherapy regimens with docetaxel. Methods: Patients who received Alvotere as a part of their chemotherapy regimen were enrolled in this Phase IV, observational, multicenter, open-label study. Alvotere was administrated as a single agent or in combination with other chemotherapy agents. Safety parameters in each cycle were assessed, and the related data were recorded in booklets. Findings: A total of 411 patients with different types of cancers were enrolled from 25 centers in Iran. The most common malignancies among participants were breast cancer (49.88), followed by gastric cancer (22.63). Participants' mean age was 53.33 years, and the mean total dose used in each cycle was 132 mg. According to the results, 341 patients experienced at least 1 adverse event, that the most common was alopecia (41.12). In total, 92 (22.38) patients had at least 1 adverse event of grade 3 or 4, and 25 (6.08) patients showed 54 serious adverse events, which the causality assessment for all was possibly related to Alvotere. There was a significant difference between men and women in the incidence of skin and subcutaneous tissue disorders (55.63 in women vs 41.73 in men; P=0.009). Also, the incidence of gastrointestinal disorders, nervous system disorders, skin and subcutaneous tissue disorders, hepatic enzymes increase, and fluid retention was significantly higher (P < 0.05) in patients receiving anthracyclines in their chemotherapy regimens. Conclusions: The findings of this open-label, observational, multicenter, postmarketing surveillance showed that Alvotere appears to have an acceptable safety profile in Iranian cancer patients receiving chemotherapeutic regimens. (C) 2022 Elsevier HS Journals, Inc. (C) 2021 Published by Elsevier Inc.
Item Type: | Article |
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Keywords: | Alvotere cancer observational Phase IV safety phase-iii trial adjuvant therapy prostate-cancer fluorouracil population cisplatin toxicity Research & Experimental Medicine Pharmacology & Pharmacy |
Divisions: | Education Vice-Chancellor Department > Faculty of Medicine > Departments of Clinical Sciences > Department of Internal |
Page Range: | p. 5 |
Journal or Publication Title: | Current Therapeutic Research-Clinical and Experimental |
Journal Index: | ISI, Pubmed |
Volume: | 96 |
Identification Number: | https://doi.org/10.1016/j.curtheres.2021.100659 |
ISSN: | 0011-393X |
Depositing User: | خانم مهتاب اکبری |
URI: | http://eprints.rums.ac.ir/id/eprint/29795 |
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