Superior vena cava syndrome often occurs in malignant diseases, especially bronchial cancer, lymphoma and metastatic tumor [9].Reconstruction of the superior vena cava and bypass grafting can be used as adjuvant treatments for malignant superior vena cava syndrome. However, due to the large trauma, the high risk of anesthesia, and the general inability of patients to tolerate it, they have been rarely used [10, 11]. At present, medical radiotherapy and chemotherapy are still the main treatment options for patients with tumors combined with superior vena cava syndrome, because they can treat the primary tumor, reduce the lesion area and reduce the compression of the superior vena cava, thereby alleviating the patient's clinical symptoms. In recent years, the treatment of malignant superior vena cava obstruction by stent placement has been frequently reported. Kuo et al. pointed out that stent placement should be used as the first-line treatment for malignant superior vena cava obstruction, rather than reserved for rescue treatment after radiotherapy or chemotherapy [12]. Wei et al. believe that although stents combined with targeted drugs as secondary SVCS treatment for lung cancer cannot prolong the survival of patients, they can benefit patients [13]. In this study, the success rate of stent implantation technology was 100%, and all patients' clinical symptoms were significantly relieved after surgery, which is similar to the results reported by Mokry, Maleux and Fagedet [14, 15, 16].
In this study, we observed that the restenosis of the superior vena cava in patients with Wallstent stent (3/12) was higher than that in the ELuminexx stent group (2/18). There is no research showing that two stents are effective in the treatment of superior vena cava syndrome. The advantages and disadvantages of the Wallstent stent, we believe that it may be related to the Wallstent stent wire is thinner and the mesh is large, which may easily lead to endothelialization of the stent, and its supporting force is relatively weak, which is also one of the reasons that easily cause restenosis. Gwon et al. found that the cumulative stent patency rate of the covered stent group was significantly higher than that of the non-covered stent group, but there was no significant difference in the survival rate between the covered stent group and the non-covered stent group [17]. In this study, 2 patients underwent stent graft implantation, and there were no complications related to stent implantation. However, stent graft placement may block collateral circulation, and the risk of stent displacement is higher and the cost is higher. Therefore, we believe that the clinical use should be carefully selected according to the disease.
Regarding the choice of puncture approach, puncturing the right femoral vein is more common. Because of its simple and convenient puncture, the angle from the femoral vein to the bilateral brachiocephalic vein is small, and it is easy to selectively intubate or open the superior vena cava. For those who have difficulty in opening the superior vena cava or whose lesions simultaneously involve the subclavian vein and internal jugular vein on the same side, the upper limb vein combined with the femoral vein two-way approach should be adopted to improve the efficiency of opening. For patients with indwelling central venous access, there is no need to re-puncture without affecting subsequent operations. In this study, 1 patient had lesions involving the right subclavian and right internal jugular vein, and the two-way approach was adopted for the right main vein and the right femoral vein to successfully open the occluded blood vessel; 2 patients were under the right subclavian CVC (Central venous catheter) was placed in the vein, so we did not choose to re-puncture the femoral vein.
Related literature reports that intravascular stent placement treatment has complications such as stent displacement, secondary thrombosis in the stent, restenosis, pulmonary thromboembolism, acute right heart insufficiency, and superior vena cava rupture, with an average incidence of 3.2% To 7.8% [18, 19]. Usually superior vena cava restenosis is the most important complication, because tumor progression will increase the compression of the superior vena cava, and even grow into the cavity through the stent network. Takahara et al. believe that even in patients with poor general conditions, additional superior vena cava stent placement is an option for the treatment of restenosis [20]. For patients with recurrent stenosis after stent placement, interventional therapy can be performed again, balloon dilation of the stenosis segment or another placement of a stent to restore brachiocephalic venous return. For tumorous lesions, reinsertion of a stent can achieve a longer-term patency rate and better clinical efficacy than balloon dilatation. Another common complication of stent placement is secondary thrombosis in the stent. Therefore, patients in our center routinely use anticoagulant drugs after stent placement. For patients with acute thrombosis in stents, balloon dilation and indwelling catheter thrombolytic therapy can also achieve better results. Under normal circumstances, there is no need to re-stent. Fagedet et al. found that stents with a diameter of more than 16 mm are more likely to cause thrombosis in the stent [16]. At the same time, small stent diameter, long stent length, and superior vena cava endothelial injury are high-risk factors for superior vena cava restenosis. In this study, most patients use stents with a diameter of 16 mm or less (34/37), with low complications and no serious complications related to surgery.
Although stent placement can effectively alleviate related symptoms caused by superior vena cava obstruction, follow-up treatment for the primary cause cannot be ignored. In this study, all patients received anti-tumor therapy after stent placement. After stent placement, combined with active anti-tumor therapy, such as radiotherapy, chemotherapy and molecular targeted drugs, is a more appropriate choice.
This study has certain limitations. First of all, this is a retrospective study with a limited number of cases. Secondly, due to the poor prognosis of malignant tumors, the follow-up time is limited, and the long-term patency rate is unknown. Further randomized controlled experiments are needed to confirm this conclusion.