Cargando…
Efficacy and Safety of Nanosomal Docetaxel Lipid Suspension (NDLS) versus Conventional Docetaxel as Neoadjuvant and Adjuvant Therapy for Primary Operable Breast Cancer
OBJECTIVE: Nanosomal docetaxel lipid suspension (NDLS) is a novel formulation developed to overcome toxicity issues caused by excipients (polysorbate 80 and ethanol) present in commercially available docetaxel formulation. We conducted a prospective, observational study to compare the outcomes of na...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10075221/ https://www.ncbi.nlm.nih.gov/pubmed/37033671 http://dx.doi.org/10.2147/OTT.S400824 |
_version_ | 1785019878207389696 |
---|---|
author | Badiginchala, Revathi Dattatreya, Palanki Satya Suresh, Attili Venkata Satya Nirni, Sharanabasappa Somanath Andra, Vindhya Vasini Bunger, Deepak Chaturvedi, Alok |
author_facet | Badiginchala, Revathi Dattatreya, Palanki Satya Suresh, Attili Venkata Satya Nirni, Sharanabasappa Somanath Andra, Vindhya Vasini Bunger, Deepak Chaturvedi, Alok |
author_sort | Badiginchala, Revathi |
collection | PubMed |
description | OBJECTIVE: Nanosomal docetaxel lipid suspension (NDLS) is a novel formulation developed to overcome toxicity issues caused by excipients (polysorbate 80 and ethanol) present in commercially available docetaxel formulation. We conducted a prospective, observational study to compare the outcomes of nanosomal docetaxel lipid suspension (NDLS)-based versus conventional docetaxel-based chemotherapy in primary operable breast cancer. METHODS: Sixty adult women with newly diagnosed stage IIb-III breast cancer were included. Patients received NDLS-based (n=30) or docetaxel-based (n=30) chemotherapy. Patients received (1) four cycles of preoperative doxorubicin and cyclophosphamide (AC) followed by four cycles of NDLS or docetaxel (T) and surgery (neoadjuvant AC→NDLS [n=9], or neoadjuvant AC→T [n=10]), or (2) four cycles of preoperative AC followed by surgery and postoperative NDLS or T (neoadjuvant AC→adjuvant NDLS [n=14], or neoadjuvant AC→adjuvant T [n=15]), or (3) surgery followed by postoperative AC→NDLS or T (adjuvant AC→NDLS [n=7], or adjuvant AC→T [n=5]) regimens. The study outcomes were pathological complete response (pCR) rates, clinical overall response rates (ORR), disease-free survival (DFS), overall survival (OS), and adverse event (AE) profile. RESULTS: For neoadjuvant AC→T (n=10) vs neoadjuvant AC→NDLS (n=9), the pCR rates were 100% each, and the ORR were 100% vs 88.9% (p=1.0). All patients were alive at 6 months, and the median OS was not reached. Three patients had progressive disease (T: n=2, NDLS: n=1) with a DFS of 12 weeks in all three patients. Grade 3 infusion-related reactions were seen in five patients (16.7%) in T vs none in NDLS arms. CONCLUSION: NDLS-based neo/adjuvant chemotherapy was efficacious in the treatment of primary operable breast cancer and showed comparable pCR, ORR, DFS and OS rates versus conventional docetaxel. NDLS was better tolerated than conventional docetaxel. |
format | Online Article Text |
id | pubmed-10075221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-100752212023-04-06 Efficacy and Safety of Nanosomal Docetaxel Lipid Suspension (NDLS) versus Conventional Docetaxel as Neoadjuvant and Adjuvant Therapy for Primary Operable Breast Cancer Badiginchala, Revathi Dattatreya, Palanki Satya Suresh, Attili Venkata Satya Nirni, Sharanabasappa Somanath Andra, Vindhya Vasini Bunger, Deepak Chaturvedi, Alok Onco Targets Ther Original Research OBJECTIVE: Nanosomal docetaxel lipid suspension (NDLS) is a novel formulation developed to overcome toxicity issues caused by excipients (polysorbate 80 and ethanol) present in commercially available docetaxel formulation. We conducted a prospective, observational study to compare the outcomes of nanosomal docetaxel lipid suspension (NDLS)-based versus conventional docetaxel-based chemotherapy in primary operable breast cancer. METHODS: Sixty adult women with newly diagnosed stage IIb-III breast cancer were included. Patients received NDLS-based (n=30) or docetaxel-based (n=30) chemotherapy. Patients received (1) four cycles of preoperative doxorubicin and cyclophosphamide (AC) followed by four cycles of NDLS or docetaxel (T) and surgery (neoadjuvant AC→NDLS [n=9], or neoadjuvant AC→T [n=10]), or (2) four cycles of preoperative AC followed by surgery and postoperative NDLS or T (neoadjuvant AC→adjuvant NDLS [n=14], or neoadjuvant AC→adjuvant T [n=15]), or (3) surgery followed by postoperative AC→NDLS or T (adjuvant AC→NDLS [n=7], or adjuvant AC→T [n=5]) regimens. The study outcomes were pathological complete response (pCR) rates, clinical overall response rates (ORR), disease-free survival (DFS), overall survival (OS), and adverse event (AE) profile. RESULTS: For neoadjuvant AC→T (n=10) vs neoadjuvant AC→NDLS (n=9), the pCR rates were 100% each, and the ORR were 100% vs 88.9% (p=1.0). All patients were alive at 6 months, and the median OS was not reached. Three patients had progressive disease (T: n=2, NDLS: n=1) with a DFS of 12 weeks in all three patients. Grade 3 infusion-related reactions were seen in five patients (16.7%) in T vs none in NDLS arms. CONCLUSION: NDLS-based neo/adjuvant chemotherapy was efficacious in the treatment of primary operable breast cancer and showed comparable pCR, ORR, DFS and OS rates versus conventional docetaxel. NDLS was better tolerated than conventional docetaxel. Dove 2023-04-01 /pmc/articles/PMC10075221/ /pubmed/37033671 http://dx.doi.org/10.2147/OTT.S400824 Text en © 2023 Badiginchala et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Badiginchala, Revathi Dattatreya, Palanki Satya Suresh, Attili Venkata Satya Nirni, Sharanabasappa Somanath Andra, Vindhya Vasini Bunger, Deepak Chaturvedi, Alok Efficacy and Safety of Nanosomal Docetaxel Lipid Suspension (NDLS) versus Conventional Docetaxel as Neoadjuvant and Adjuvant Therapy for Primary Operable Breast Cancer |
title | Efficacy and Safety of Nanosomal Docetaxel Lipid Suspension (NDLS) versus Conventional Docetaxel as Neoadjuvant and Adjuvant Therapy for Primary Operable Breast Cancer |
title_full | Efficacy and Safety of Nanosomal Docetaxel Lipid Suspension (NDLS) versus Conventional Docetaxel as Neoadjuvant and Adjuvant Therapy for Primary Operable Breast Cancer |
title_fullStr | Efficacy and Safety of Nanosomal Docetaxel Lipid Suspension (NDLS) versus Conventional Docetaxel as Neoadjuvant and Adjuvant Therapy for Primary Operable Breast Cancer |
title_full_unstemmed | Efficacy and Safety of Nanosomal Docetaxel Lipid Suspension (NDLS) versus Conventional Docetaxel as Neoadjuvant and Adjuvant Therapy for Primary Operable Breast Cancer |
title_short | Efficacy and Safety of Nanosomal Docetaxel Lipid Suspension (NDLS) versus Conventional Docetaxel as Neoadjuvant and Adjuvant Therapy for Primary Operable Breast Cancer |
title_sort | efficacy and safety of nanosomal docetaxel lipid suspension (ndls) versus conventional docetaxel as neoadjuvant and adjuvant therapy for primary operable breast cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10075221/ https://www.ncbi.nlm.nih.gov/pubmed/37033671 http://dx.doi.org/10.2147/OTT.S400824 |
work_keys_str_mv | AT badiginchalarevathi efficacyandsafetyofnanosomaldocetaxellipidsuspensionndlsversusconventionaldocetaxelasneoadjuvantandadjuvanttherapyforprimaryoperablebreastcancer AT dattatreyapalankisatya efficacyandsafetyofnanosomaldocetaxellipidsuspensionndlsversusconventionaldocetaxelasneoadjuvantandadjuvanttherapyforprimaryoperablebreastcancer AT sureshattilivenkatasatya efficacyandsafetyofnanosomaldocetaxellipidsuspensionndlsversusconventionaldocetaxelasneoadjuvantandadjuvanttherapyforprimaryoperablebreastcancer AT nirnisharanabasappasomanath efficacyandsafetyofnanosomaldocetaxellipidsuspensionndlsversusconventionaldocetaxelasneoadjuvantandadjuvanttherapyforprimaryoperablebreastcancer AT andravindhyavasini efficacyandsafetyofnanosomaldocetaxellipidsuspensionndlsversusconventionaldocetaxelasneoadjuvantandadjuvanttherapyforprimaryoperablebreastcancer AT bungerdeepak efficacyandsafetyofnanosomaldocetaxellipidsuspensionndlsversusconventionaldocetaxelasneoadjuvantandadjuvanttherapyforprimaryoperablebreastcancer AT chaturvedialok efficacyandsafetyofnanosomaldocetaxellipidsuspensionndlsversusconventionaldocetaxelasneoadjuvantandadjuvanttherapyforprimaryoperablebreastcancer |