Combination of chemotherapeutic agents and biological response modifiers (immunotherapy) in triple-negative/Her2( +) breast cancer, multiple myeloma, and non-small-cell lung cancer.

IF 2.1 Q3 ONCOLOGY
William Morse, Haroon Nawaz, Ayesha A Choudhry
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引用次数: 2

Abstract

Hypothesis: Biological response modifiers (immunotherapy) in combination to chemotherapy are superior to that of chemotherapy in treatment of breast cancer (triple-negative/HER-2 ( +)), multiple myeloma, and non-small-cell lung cancer.

Methods: This review article consists of a total of eighteen independent randomized controlled clinical trials ranging from phases one to three. Patients were randomly selected for immunomodulatory treatment or chemotherapy and assessed for a specific mutation expression that the immunomodulatory agent targets. Kaplan-Meier plots, swimmer plots, and bar graphs depict overall/progression-free survival, objective response, and clinical response rates. The data collected was assessed by using 95% confidence interval and a p value of 0.05. Patients were treated until disease progression.

Results: Biological response modifiers (immunotherapy) resulted in significantly longer median progression-free survival in PD-L1-positive breast cancer (7.5 months compared to 5.0 months in control group), multiple myeloma (60.7% compared to 26.9% in the daratumumab and placebo groups, respectively), and in non-small-cell lung cancer (median progression-free survival was 10.3 months in the pembrolizumab group compared to 6.0 months in the chemotherapy group): higher complete responses in multiple myeloma (79% and 66% in the elotuzumab and control groups, respectively) and lower disease progression in PD-L1-positive non-small-cell lung cancer (62.1% of pembrolizumab versus 50.3% of chemotherapy patients had no disease progression at 6 months).

Conclusion: Combination biological response modifiers (immunotherapy) and chemotherapy displayed benefit in overall/progression-free survival, response rate, duration of response, clinical benefit, and invasive disease-free survival in triple-negative/HER2-2( +) breast cancer, multiple myeloma, and non-small-cell lung cancer.

化疗药物和生物反应调节剂(免疫疗法)联合治疗三阴性/Her2(+)乳腺癌、多发性骨髓瘤和非小细胞肺癌。
假设:生物反应调节剂(免疫疗法)联合化疗治疗乳腺癌(三阴性/HER-2(+))、多发性骨髓瘤和非小细胞肺癌优于化疗。方法:这篇综述文章包括18个独立的随机对照临床试验,从一期到三期。随机选择患者进行免疫调节治疗或化疗,并评估免疫调节剂靶向的特定突变表达。Kaplan-Meier图、swimmer图和柱状图描述了总体/无进展生存期、客观反应和临床反应率。收集的资料采用95%置信区间和p值0.05进行评估。患者接受治疗直至疾病进展。结果:生物反应修饰剂(免疫治疗)显著延长了pd - l1阳性乳腺癌(7.5个月,对照组5.0个月)、多发性骨髓瘤(60.7%,达拉单抗组26.9%,安慰剂组分别)和非小细胞肺癌(派姆单抗组中位无进展生存期为10.3个月,化疗组为6.0个月)的中位无进展生存期。多发性骨髓瘤患者的完全缓解率更高(elotuzumab组和对照组分别为79%和66%),pd - l1阳性非小细胞肺癌患者的疾病进展率更低(62.1%的派姆单抗和50.3%的化疗患者在6个月时没有疾病进展)。结论:联合生物反应修饰剂(免疫治疗)和化疗在三阴性/HER2-2(+)乳腺癌、多发性骨髓瘤和非小细胞肺癌的总/无进展生存期、反应率、反应持续时间、临床获益和侵袭性无病生存期均有益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
46
审稿时长
11 weeks
期刊介绍: As the official publication of the National Cancer Institute, Cairo University, the Journal of the Egyptian National Cancer Institute (JENCI) is an open access peer-reviewed journal that publishes on the latest innovations in oncology and thereby, providing academics and clinicians a leading research platform. JENCI welcomes submissions pertaining to all fields of basic, applied and clinical cancer research. Main topics of interest include: local and systemic anticancer therapy (with specific interest on applied cancer research from developing countries); experimental oncology; early cancer detection; randomized trials (including negatives ones); and key emerging fields of personalized medicine, such as molecular pathology, bioinformatics, and biotechnologies.
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