Badiginchala Revathi, Dattatreya Palanki Satya, Suresh Attili Venkata Satya, Nirni Sharanabasappa Somanath, Andra Vindhya Vasini, Bunger Deepak, Chaturvedi Alok
Medical Oncology, Omega Hospitals, Hyderabad, Telangana, India.
Medical Affairs, Intas Pharmaceuticals Limited, Ahmedabad, India.
Onco Targets Ther. 2023 Apr 1;16:215-225. doi: 10.2147/OTT.S400824. eCollection 2023.
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.
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.
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.
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.
纳米粒多西他赛脂质混悬液(NDLS)是一种新开发的制剂,旨在克服市售多西他赛制剂中辅料(聚山梨酯80和乙醇)引起的毒性问题。我们进行了一项前瞻性观察性研究,以比较纳米粒多西他赛脂质混悬液(NDLS)为基础的化疗与传统多西他赛为基础的化疗在原发性可手术乳腺癌中的疗效。
纳入60例新诊断为IIb-III期乳腺癌的成年女性患者。患者接受基于NDLS(n = 30)或基于多西他赛(n = 30)的化疗。患者接受(1)四个周期的术前阿霉素和环磷酰胺(AC),随后四个周期的NDLS或多西他赛(T)以及手术(新辅助AC→NDLS [n = 9],或新辅助AC→T [n = 10]),或(2)四个周期的术前AC,随后手术及术后NDLS或T(新辅助AC→辅助NDLS [n = 14],或新辅助AC→辅助T [n = 15]),或(3)手术,随后术后AC→NDLS或T(辅助AC→NDLS [n = 7],或辅助AC→T [n = 5])方案。研究结果包括病理完全缓解(pCR)率、临床总缓解率(ORR)、无病生存期(DFS)、总生存期(OS)和不良事件(AE)情况。
对于新辅助AC→T(n = 10)与新辅助AC→NDLS(n = 9),pCR率均为100%,ORR分别为100%和88.9%(p = 1.0)。所有患者在6个月时均存活,中位OS未达到。3例患者出现疾病进展(T组:n = 2,NDLS组:n = 1),所有3例患者的DFS为12周。T组有5例患者(16.7%)出现3级输液相关反应,而NDLS组无。
基于NDLS的新辅助/辅助化疗在原发性可手术乳腺癌治疗中有效,与传统多西他赛相比,pCR、ORR、DFS和OS率相当。NDLS的耐受性优于传统多西他赛