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使用经基因改造以释放沙格司亭的全细胞疫苗后,不同部位转移性乳腺癌的客观临床消退情况

Objective clinical regression of metastatic breast cancer in disparate sites after use of whole-cell vaccine genetically modified to release sargramostim.

作者信息

Wiseman Charles L, Kharazi Alex

机构信息

Immunotherapy Laboratory, St Vincent Medical Center, Los Angeles, CA 90057, USA.

出版信息

Breast J. 2006 Sep-Oct;12(5):475-80. doi: 10.1111/j.1075-122X.2006.00319.x.


DOI:10.1111/j.1075-122X.2006.00319.x
PMID:16958969
Abstract

A patient with recurrent breast cancer metastases following initial response to chemotherapy and hormonal maintenance was treated with a whole-cell tumor vaccine, resulting in a prompt objective complete remission of a lung lesion on computed tomography (CT) scans and near-complete regression of multiple breast lesions on magnetic resonance imaging (MRI). Three months after completion of the protocol, metastases were again found in the breast and lung, with new lesions in the brain and liver. Reinstitution of vaccine inoculation resulted in major regression of the brain and breast lesions, improvement in all other areas, and no indication of new lesions. Therapy consisted of inoculation of 20 x 10(6) SV-BR-1-GM cells, a unique breast cancer cell line transfected to release sargramostim (granulocyte macrophage colony-stimulating factor [GM-CSF]). Following lethal irradiation to 200 cGy, vaccine was injected intradermally in four divided doses to the back and thighs, every 2 weeks x 3, then every month x 3. Each treatment was preceded 48 hours earlier with low-dose cyclophosphamide 300 mg/m2 to abrogate regulatory T-cell activity. Interferon (IFN)-alpha, 20,000 IU, was injected into each inoculation site at 48 and 96 hours postinoculation to provide an additional "danger signal." The patient developed positive delayed-type hypersensitivity responses and also antibody reactivity to the vaccine cells.

摘要

一名乳腺癌患者在对化疗和激素维持治疗初始有反应后出现复发转移,接受了全细胞肿瘤疫苗治疗,计算机断层扫描(CT)显示肺部病灶迅速达到客观完全缓解,磁共振成像(MRI)显示多个乳腺病灶近乎完全消退。方案完成三个月后,乳腺和肺部再次发现转移灶,同时脑部和肝脏出现新病灶。重新接种疫苗后,脑部和乳腺病灶大幅消退,其他所有部位病情改善,且未发现新病灶迹象。治疗方法为接种20×10⁶个SV-BR-1-GM细胞,这是一种经转染以释放沙格司亭(粒细胞巨噬细胞集落刺激因子[GM-CSF])的独特乳腺癌细胞系。在接受200 cGy的致死性照射后,将疫苗分四次皮内注射到背部和大腿,每2周一次,共3次,然后每月一次,共3次。每次治疗前48小时给予低剂量环磷酰胺300 mg/m²以消除调节性T细胞活性。在接种后48小时和96小时,在每个接种部位注射20,000 IU干扰素(IFN)-α,以提供额外的“危险信号”。该患者出现了阳性迟发型超敏反应,并且对疫苗细胞产生了抗体反应。

相似文献

[1]
Objective clinical regression of metastatic breast cancer in disparate sites after use of whole-cell vaccine genetically modified to release sargramostim.

Breast J. 2006

[2]
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[5]
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J Immunother. 2008-1

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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Results of a phase I/IIa trial of SV-BR-1-GM inoculation with low-dose cyclophosphamide and interferon alpha (Bria-IMT) in metastatic breast cancer.

Hum Vaccin Immunother. 2024-12-31

[2]
Regression of Breast Cancer Metastases Following Treatment with Irradiated SV-BR-1-GM, a GM-CSF Overexpressing Breast Cancer Cell Line: Intellectual Property and Immune Markers of Response.

Recent Pat Anticancer Drug Discov. 2022

[3]
Reversing an Oncogenic Epithelial-to-Mesenchymal Transition Program in Breast Cancer Reveals Actionable Immune Suppressive Pathways.

Pharmaceuticals (Basel). 2021-11-2

[4]
Dormant Tumor Cell Vaccination: A Mathematical Model of Immunological Dormancy in Triple-Negative Breast Cancer.

Cancers (Basel). 2021-1-11

[5]
SV-BR-1-GM, a Clinically Effective GM-CSF-Secreting Breast Cancer Cell Line, Expresses an Immune Signature and Directly Activates CD4 T Lymphocytes.

Front Immunol. 2018-5-15

[6]
Improving alloreactive CTL immunotherapy for malignant gliomas using a simulation model of their interactive dynamics.

Cancer Immunol Immunother. 2008-3

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