Department of Plastic Surgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Department of Surgical Oncology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Medicine (Baltimore). 2023 Nov 17;102(46):e35928. doi: 10.1097/MD.0000000000035928.
This study aimed to conduct a comparative analysis of the efficacy and safety of neoadjuvant chemotherapy combined with endocrine therapy against the backdrop of single neoadjuvant chemotherapy or endocrine therapy, specifically in the context of hormone receptor-positive (HR+) breast cancer treatment.
We conducted a thorough literature search across several databases, including China National Knowledge Infrastructure, Wanfang, Weipu, Chinese Journal Full-text Database, PubMed, Web of Science, Cochrane Library, and EMBASE, adhering to the guidelines outlined in the PRISMA statement. Our specific focus was on identifying randomized controlled trials that directly compared the combined approach of neoadjuvant chemotherapy and endocrine therapy with single chemotherapy or endocrine therapy in the context of treating HR+ breast cancer. Subsequently, we utilized statistical packages implemented in R software to perform comparative analyses of key clinical indicators, encompassing the complete response, objective response rate (ORR), disease control rate, pathological complete response (pCR), and adverse reactions.
A total of 11 randomized controlled trials, involving 1359 patients, all of whom met our inclusion criteria and were thus included in our comprehensive analysis. Within this cohort, 688 patients (50.63%) administered neoadjuvant chemotherapy combined with endocrine therapy (NCET), 642 patients (47.24%) received neoadjuvant chemotherapy (NCT) alone, while 29 patients (2.13%) underwent neoadjuvant endocrine therapy (NET) alone. The results of our meta-analysis revealed that NCET exhibited a statistically significant enhancement in both ORR and pCR (P < .05). Nonetheless, when compared to NCT or NET, NCET did not yield a significant impact on complete response, disease control rate, and safety (P > .05). In addition, NCET demonstrated a significant improvement in ORR among patients with HR+, HER2-negative breast cancer (P < .05). However, it was also linked to a heightened incidence of serious adverse reactions within this particular patient subgroup (P < .05).
The combination of Neoadjuvant chemotherapy and endocrine therapy stands out as a significant contributor to enhancing the ORR and pCR for HR+ breast cancer patients. For breast cancer patients with HER2- status, NCET demonstrates a remarkable improvement in ORR but is also associated with the emergence of adverse reactions.
本研究旨在针对激素受体阳性(HR+)乳腺癌的治疗,对新辅助化疗联合内分泌治疗与单一新辅助化疗或内分泌治疗相比的疗效和安全性进行对比分析。
我们通过中国知网、万方、维普、中国生物医学文献数据库、PubMed、Web of Science、Cochrane 图书馆和 EMBASE 等数据库进行了全面的文献检索,遵循 PRISMA 声明中的指南。我们的重点是确定直接比较新辅助化疗联合内分泌治疗与单一化疗或内分泌治疗在治疗 HR+乳腺癌方面的联合方法的随机对照试验。随后,我们使用 R 软件中的统计软件包对关键临床指标进行了对比分析,包括完全缓解率、客观缓解率(ORR)、疾病控制率、病理完全缓解率(pCR)和不良反应。
共纳入 11 项随机对照试验,共纳入 1359 例患者,所有患者均符合纳入标准,并纳入我们的综合分析。在这一队列中,688 例患者(50.63%)接受了新辅助化疗联合内分泌治疗(NCET),642 例患者(47.24%)接受了新辅助化疗(NCT),29 例患者(2.13%)接受了新辅助内分泌治疗(NET)。我们的荟萃分析结果表明,NCET 在 ORR 和 pCR 方面均有显著提高(P<0.05)。然而,与 NCT 或 NET 相比,NCET 对完全缓解率、疾病控制率和安全性没有显著影响(P>0.05)。此外,NCET 显著提高了 HR+、HER2-阴性乳腺癌患者的 ORR(P<0.05)。然而,在这一特定患者亚组中,NCET 也与严重不良反应发生率的增加有关(P<0.05)。
新辅助化疗联合内分泌治疗显著提高了 HR+乳腺癌患者的 ORR 和 pCR。对于 HR+、HER2-状态的乳腺癌患者,NCET 显著提高了 ORR,但也与不良反应的发生有关。