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胸腔灌注抗血管生成药物治疗恶性胸腔积液的研究进展
Research Progress in the Treatment of Malignant Pleural Effusion with Intrathoracic Perfusion of Antiangiogenic Drugs

DOI: 10.12677/ACM.2022.132170, PP. 123-1237

Keywords: 恶性胸腔积液,胸腔内灌注治疗,抗血管生成药,贝伐珠单抗,重组人血管内皮抑素
Malignant Pleural Effusion
, Intrathoracic Perfusion Therapy, Anti Angiogenic Agents, Bevacizumab, Recombinant Human Endostatin

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Abstract:

恶性胸腔积液(malignant pleural effusion, MPE)是晚期癌症的常见及严重并发症,可不同程度地引起胸闷、胸痛、呼吸困难等不适症状,这对于晚期癌症患者无疑是雪上加霜。此外,恶性胸腔积液的存在会降低患者的整体表现状态,从而影响他们接受可能延长生命的抗癌治疗的可能性。以往,多以反复胸腔内置管引流为恶性胸腔积液的主要治疗手段,但单纯的胸腔内置管引流一方面无法解决胸腔积液反复产生的问题;另一方面因多次进行胸腔穿刺将不可避免地导致胸腔内感染、组织纤维化等并发症。目前,针对恶性胸腔积液的主要治疗方法是,对原发恶性肿瘤进行全面系统的全身化疗,同时针对胸腔积液做局部治疗,其中,胸腔内药物灌注治疗正进一步成为控制恶性胸腔积液产生的主要手段。经国内外多项研究证明,铂类药物、贝伐珠单抗、重组人血管内皮抑素等药物对恶性胸腔积液的产生有抑制作用。本文讨论两种抗血管生成药物(贝伐珠单抗、重组人血管内皮抑素)胸腔内灌注治疗(intrapleural perfusion therapy, IPT)恶性胸腔积液的疗效及其安全性。旨在为恶性胸腔积液治疗提供些许思路。
Malignant pleural effusion (MPE) is a common and serious complication of advanced cancer, which can cause chest tightness, chest pain, dyspnea and other discomfort symptoms to varying degrees, which is undoubtedly worse for patients with advanced cancer. In addition, the presence of malig-nant pleural effusion will reduce the overall performance of patients, thus affecting their possibility of receiving anti-cancer treatment that may prolong life. In the past, the main treatment method for malignant pleural effusion was to drain the pleural effusion repeatedly, but on the one hand, the simple drainage of pleural effusion could not solve the problem of repeated pleural effusion; On the other hand, multiple thoracentesis will inevitably lead to complications such as intrathoracic infec-tion and tissue fibrosis. At present, the main treatment methods for malignant pleural effusion are comprehensive and systematic systemic chemotherapy for primary malignant tumors, and local treatment for pleural effusion. Among them, intrathoracic drug infusion therapy is further becom-ing the main means to control the production of malignant pleural effusion. Many studies at home and abroad have proved that platinum drugs, bevacizumab, recombinant human endostatin and other drugs can inhibit the production of malignant pleural effusion. This article discusses the effi-cacy and safety of two anti angiogenic drugs (bevacizumab and recombinant human endostatin) in the treatment of malignant pleural effusion (IPT). It aims to provide some ideas for the treatment of malignant pleural effusion.

References

[1]  李金金, 轩伟霞, 张晓菊. 恶性胸腔积液产生的机制研究进展[J]. 国际呼吸杂志, 2018, 38(10): 783-786.
[2]  Jany, B. and Welte, T. (2019) Pleural Effusion in Adults-Etiology, Diagnosis, and Treatment. Deutsches Arzteblatt International, 116, 377-386.
https://doi.org/10.3238/arztebl.2019.0377
[3]  Koegelenberg, C.F.N., Shaw, J.A., Irusen, E.M. and Gary Lee, Y.C. (2018) Contemporary Best Practice in the Management of Malignant Pleural Effu-sion. Therapeutic Advances in Respiratory Disease, 12.
https://doi.org/10.1177/1753466618785098
[4]  李克爱, 郝仲芳, 陈洪萍, 苗培田, 雒建雷. 腔内注射贝伐珠单抗联合奥沙利铂治疗肺癌恶性胸腔积液的效果[J]. 广东医学, 2019, 40(23): 3327-3330.
https://doi.org/10.13820/j.cnki.gdyx.20191241
[5]  Folkman, J. (1971) Tumor Angiogenesis: Therapeutic Impli-cations. The New England Journal of Medicine, 285, Article ID: 11826.
https://doi.org/10.1056/NEJM197111182852108
[6]  Bradshaw, M., Mansfield, A. and Peikert, T. (2013) The Role of Vascular Endothelial Growth Factor in the Pathogenesis, Diagnosis and Treatment of Malignant Pleural Effusion. Current Oncology Reports, 15, 207-216.
https://doi.org/10.1007/s11912-013-0315-7
[7]  Fafliora, E., Hatzoglou, C., Gourgoulianis, K.I., et al. (2016) Sys-tematic Review and Meta-Analysis of Vascular Endothelial Growth Factor as a Biomarker for Malignant Pleural Effu-sions. Physiological Reports, 4, e12978.
https://doi.org/10.14814/phy2.12978
[8]  Zachary, I. (2001) Signaling Mechanisms Mediating Vascular Protective Actions of Vascular Endothelial Growth Factor. American Journal of Physiology-Cell Physiology, 280, C1375-C1386.
https://doi.org/10.1152/ajpcell.2001.280.6.C1375
[9]  Bradshaw, M., Mansfield, A. and Peikert, T. (2013) The Role of Vascular Endothelial Growth Factor in the Pathogenesis, Diagnosis and Treatment of Malignant Pleural Effusion. Current Oncology Reports, 15, 207-216.
https://doi.org/10.1007/s11912-013-0315-7
[10]  Fujimoto, K., Hosotani, R., Wada, M., et al. (1998) Expression of Two Angiogenic Factors, Vascular Endothelial Growth Factor and Platelet-Derived Endothelial Cell Growth Factor in Human Pancreatic Cancer, and Its Relationship to Angiogenesis. European Journal of Cancer, 34, 1439-1447.
https://doi.org/10.1016/S0959-8049(98)00069-0
[11]  Ikeda, N., Adachi, M., Taki, T., et al. (1999) Prognostic Sig-nificance of Angiogenesis in Human Pancreatic Cancer. British Journal of Cancer, 79, 1553-1563.
https://doi.org/10.1038/sj.bjc.6690248
[12]  Maeda, K., Chung, Y.S., Ogawa, Y., et al. (1996) Prognostic Value of Vascular Endothelial Growth Factor Expression in Gastric Carcinoma. Cancer, 77, 858-863.
https://doi.org/10.1002/(SICI)1097-0142(19960301)77:5<858::AID-CNCR8>3.0.CO;2-A
[13]  Takahashi, Y., Cleary, K.R., Mai, M., et al. (1996) Significance of Vessel Count and Vascular Endothelial Growth Factor and Its Re-ceptor (KDR) in Intestinal-Type Gastric Cancer. Clinical Cancer Research, 2, 1679-1684.
[14]  Lee, J.C., Chow, N.H., Wang, S.T. and Huang, S.M. (2000) Prognostic Value of Vascular Endothelial Growth Factor Expression in Colorectal Cancer Patients. European Journal of Cancer, 36, 7453.
https://doi.org/10.1016/S0959-8049(00)00003-4
[15]  Takahashi, Y., Kitadai, Y., Bucana, C.D., et al. (1995) Ex-pression of Vascular Endothelial Growth Factor and Its Receptor, KDR, Correlates with Vascularity, Metastasis, and Proliferation of Human Colon Cancer. Cancer Research, 55, 3964-3968.
[16]  Hamed, E.A., El-Noweihi, A.M., Mo-hamed, A.Z. and Mahmoud, A. (2004) Vasoactive Mediators (VEGF and TNF- Alpha) in Patients with Malignant and Tuberculous Pleural Effusions. Respirology, 9, 816.
https://doi.org/10.1111/j.1440-1843.2003.00529.x
[17]  Gerber, H.P. and Ferrara, N. (2005) Pharmacology and Pharmacodynamics of Bevacizumab as Monotherapy or in Combination with Cytotoxic Therapy in Preclinical Studies. Cancer Research, 65, 671-680.
https://doi.org/10.1158/0008-5472.671.65.3
[18]  Numnum, T.M., Rocconi, R.P., Whitworth, J. and Barnes, M.N. (2006) The Use of Bevacizumab to Palliate Symptomatic Ascites in Patients with Refractory Ovarian Carcinoma. Gyne-cologic Oncology, 102, 4258.
https://doi.org/10.1016/j.ygyno.2006.05.018
[19]  Ferrara, N. and Henzel, W.J. (1989) Pituitary Follicular Cells Se-crete a Novel Heparin-Binding Growth Factor Specific for Vascular Endothelial Cells. Biochemical and Biophysical Re-search Communications, 161, 851-858.
https://doi.org/10.1016/0006-291X(89)92678-8
[20]  Ferrara, N., Gerber, H.P. and LeCouter, J. (2003) The Biolo-gy of VEGF and Its Receptors. Nature Medicine, 9, 669- 676.
https://doi.org/10.1038/nm0603-669
[21]  Hicklin, D.J. and Ellis, L.M. (2005) Role of the Vascular Endothelial Growth Factor Pathway in Tumor Growth and Angiogene-sis. Journal of Clinical Oncology, 23, 1011-1027.
https://doi.org/10.1200/JCO.2005.06.081
[22]  Ku, D.D., Zaleski, J.K., Liu, S. and Brock, T.A. (1993) Vascular Endothelial Growth Factor Induces EDRF-Dependent Relaxation in Coro-nary Arteries. American Journal of Physiology, 265, H586-H592.
https://doi.org/10.1152/ajpheart.1993.265.2.H586
[23]  Brown, L.F., Detmar, M., Claffey, K., et al. (1997) Vascu-lar Permeability Factor/Vascular Endothelial Growth Factor: A Multifunctional Angiogenic Cytokine. EXS, 79, 233-269.
https://doi.org/10.1007/978-3-0348-9006-9_10
[24]  Mohammed, K.A., Nasreen, N., Hardwick, J., et al. (2001) Bacterial Induction of Pleural Mesothelial Monolayer Barrier Dysfunction. The American Journal of Physiology-Lung Cellular and Molecular Physiology, 281, L119-L125.
https://doi.org/10.1152/ajplung.2001.281.1.L119
[25]  Ishii, H., Yazawa, T., Sato, H., et al. (2004) Enhancement of Pleural Dissemination and Lymph Node Metastasis of Intrathoracic Lung Cancer Cells by Vascular Endothelial Growth Factors (VEGFs). Lung Cancer, 45, 32537.
https://doi.org/10.1016/j.lungcan.2004.02.021
[26]  Yano, S., Shinohara, H., Herbst, R.S., Kuniyasu, H., Bucana, C.D., Ellis, L.M., et al. (2000) Production of Experimental Malignant Pleural Effusions Is Dependent on Invasion of the Pleura and Expression of Vascular Endothelial Growth Factor/Vascular Permeability Factor by Human Lung Cancer Cells. The American Journal of Pathology, 157, 1893- 1903.
https://doi.org/10.1016/S0002-9440(10)64828-6
[27]  Chellappan, D.K., Leng, K.H., Jia, L.J., et al. (2018) The Role of Bevacizumab on Tumour Angiogenesis and in the Management of Gynaecological Cancers: A Review. Biomedi-cine & Pharmacotherapy, 102, 1127-1144.
https://doi.org/10.1016/j.biopha.2018.03.061
[28]  Sandler, A. (2007) Bevacizumab in Non Small Cell Lung Cancer. Clinical Cancer Research, 13, s4613-s4617.
https://doi.org/10.1158/1078-0432.CCR-07-0647
[29]  Nie, K.K., Zhang, Z., You, Y.H., et al. (2020) A Random-ized Clinical Study to Compare Intrapleural Infusion with Intravenous Infusion of Bevacizumab in the Management of Malignant Pleural Effusion in Patients with Non-Small-Cell Lung Cancer. Thoracic Cancer, 11, 8-14.
https://doi.org/10.1111/1759-7714.13238
[30]  Bradshaw, M., Mansfifield, A. and Peikert, T. (2013) The Role of Vascular Endothelial Growth Factor in the Pathogenesis, Diagnosis and Treatment of Malignant Pleural Effusion. Cur-rent Oncology Reports, 15, 207-216.
https://doi.org/10.1007/s11912-013-0315-7
[31]  Song, X., Chen, D., Guo, J., et al. (2018) Better Efficacy of Intra-pleural Infusion of Bevacizumab with Pemetrexed for Malignant Pleural Effusion Mediated from Nonsquamous Non-Small Cell Lung Cancer. OncoTargets and Therapy, 11, 8421-8426.
https://doi.org/10.2147/OTT.S184030
[32]  Kitamura, K., Kubota, K. ando, M., et al. (2013) Bevacizumab plus Chemotherapy for Advanced Non-Squamous Non-Small-Cell Lung Cancer with Malignant Pleural Effusion. Cancer Chemotherapy and Pharmacology, 71, 457-461.
https://doi.org/10.1007/s00280-012-2026-4
[33]  Qi, N., Li, F., Li, X., et al. (2016) Combination Use of Paclitaxel and Avastin Enhances Treatment Effect for the NSCLC Patients with Malignant Pleural Effusion. Medicine (Baltimore), 95, e5392.
https://doi.org/10.1097/MD.0000000000005392
[34]  Wu, D., Cong, Y., Zhang, Z.R., et al. (2022) A Phase II Study of Bevacizumab in Non-Squamous, Non-Small-Cell Lung Cancer Patients with Malignant Pleural Effusion. Future Oncology (London, England), 18, 669-677.
https://doi.org/10.2217/fon-2021-1035
[35]  O’Reilly, M.S., Boehm, T., Shing, Y., et al. (1997) Endostatin: An Endogenous Inhibitor of Angiogenesis and Tumor Growth. Cell, 88, 277-285.
https://doi.org/10.1016/S0092-8674(00)81848-6
[36]  Nasreen, N., Mohammed, K.A., Sanders, K., et al. (2003) Pleural Mesothelial Cell (PMC) Defense Mechanisms against Malignancy. Oncology Research, 14, 155-161.
https://doi.org/10.3727/000000003771013053
[37]  Tian, P.W., Shen, Y.C., Feng, M., et al. (2015) Diagnostic Accuracy of Endostatin for Malignant Pleural Effusion: A Clinical Study and Meta-Analysis. Postgraduate Medicine, 127, 529-534.
https://doi.org/10.1080/00325481.2015.1048180
[38]  Wang, J.W., Sun, Y., Liu, Y.Y., et al. (2005) Results of Randomized, Multicenter, Double-Blind Phase III Trial of Rh-Endostatin (YH-16) in Treatment of Advanced Non-Small Cell Lung Cancer Patients. Chinese Journal of Lung Cancer, 8, 283-290.
[39]  Wang, X.J., Miao, K., Luo, Y., et al. (2018) Randomized Controlled Trial of Endostar Combined with Cisplatin/Pemetrexed Chemotherapy for Elderly Patients with Advanced Malignant Pleural Effusion of Lung Adenocarcinoma. Journal of B.U.O.N.: Official Journal of the Bal-kan Union of Oncology, 23, 92-97
[40]  Zhao, W.-Y. Chen, D.-Y., Chen, J.-H. and Ji, Z.-N. (2014) Effects of Intracavi-tary Administration of Endostar Combined with Cisplatin in Malignant Pleural Effusion and Ascites. Cell Biochemistry and Biophysics, 70, 623-628.
https://doi.org/10.1007/s12013-014-9965-9
[41]  Qin, S., Yang, L., Liang, J., et al. (2017) Prospective, Random-ized, Multicenter Clinical Study of Endometrial and Cisplatin in the Treatment of Malignant Pleural Effusion. Chinese Journal of Clinical Oncology, 22, 193-202. (In Chinese)
[42]  Hu, X., Shi, Y., Wang, H., et al. (2015) A Clinical Study on Intra-Thoracic Chemotherapy of Recombinant Human Endostatin Combined with Cisplatin for Malignant Pleural Ef-fusion. Clinical Medicine Journal, 3, 23-27.
[43]  Wei, H.M., Qin, S.K., Yin, X.J., et al. (2015) Endostar Inhibits Asci-tes Formation and Prolongs Survival in Mouse Models of Malignant Ascites. Oncology Letters, 9, 2694-2700.
https://doi.org/10.3892/ol.2015.3134
[44]  Ma, X.Q., Yao, Y.W., Yuan, D.M., Liu, H.B., et al. (2012) Recombi-nant Human Endostatin Endostar Suppresses Angiogenesis and Lymphangiogenesis of Malignant Pleural Effusion in Mice. PLOS ONE, 7, e53449.
https://doi.org/10.1371/journal.pone.0053449
[45]  Tong, R.T., et al. (2004) Vascular Normalization by Vascular Endothelial Growth Factor Receptor 2 Blockade Induces a Pressure Gradient across the Vasculature and Improves Drug Penetration in Tumors. Cancer Research, 64, 3731- 3736.
https://doi.org/10.1158/0008-5472.CAN-04-0074
[46]  Rong, B.X., Cai, X.G., Liu, H., Gao, W.L. and Yang, S.Y. (2016) Thoracic Perfusion of Recombinant Human Endostatin (Endostar) Combined with Chemotherapeutic Agents ver-sus Chemotherapeutic Agents Alone for Treating Malignant Pleural Effusions: A Systematic Evaluation and Me-ta-Analysis. BMC Cancer, 16, 888.
https://doi.org/10.1186/s12885-016-2935-4
[47]  林卫佳, 张亚平, 李峰, 项保利, 张秀珑, 张志华, 袁胜芳. 重组人血管内皮抑素对恶性胸腔积液的治疗效果[J]. 临床肺科杂志, 2022, 27(9): 1407-1410.
[48]  杨璞, 李反念, 豆瑞刚, 曹万乐, 刘扬, 朱梓铭, 高计林, 刘军校, 刘世伟. 不同剂量恩度胸腔灌注治疗肺癌恶性胸腔积液的效果及安全性观察[J]. 药学与临床研究, 2022, 30(4): 339-342.
https://doi.org/10.13664/j.cnki.pcr.2022.04.011

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