Division of Thoracic Surgery and Interventional Pulmonology, Swedish Cancer Institute, 1101 Madison Street, Suite 900, Seattle, WA, 98104, USA.
Support Care Cancer. 2018 May;26(5):1525-1531. doi: 10.1007/s00520-017-3989-9. Epub 2017 Nov 29.
Concerns for infections resulting from antineoplastic therapy-associated immunosuppression may deter referral for symptom palliation with a tunneled pleural catheter (TPC) in patients with malignant/para-malignant pleural effusions (MPE/PMPE). While rates of TPC-related infections range from 1 to 21%, those in patients receiving antineoplastic therapy with correlation to immune status has not been established. We aimed to assess TPC-related infection rates in patients on antineoplastic therapy, determine relation to immune system competency, and assess impact on the patient.
Patients with a MPE/PMPE undergoing TPC management associated with antineoplastic therapy, from 2008 to 2016, were reviewed and categorized into those with an immunocompromised versus immunocompetent immune status.
Of the 150 patients, a TPC-related infection developed in 13 (9%): pleural space in 11 (7%) and superficial in 2 (1%). Ninety-three percent (139/150) were identified to be immunocompromised during their antineoplastic therapy. No difference in TPC-related infections was seen in patients with an immunocompromised (9%, 12/139) versus immunocompetent status (9%, 1/11); p = 0.614. The presence of a catheter-related infection did not negatively impact overall survival over a median follow-up of 144 days (interquartile range 41-341); p = 0.740.
These results suggest that antineoplastic therapy may not significantly increase the overall risk of TPC-related infections, as the rate remains low and comparable to rates in patients not undergoing antineoplastic therapy. Regardless of immune status, the presence of a catheter-related infection did not negatively impact overall survival. These results should reassure clinicians that the need to initiate antineoplastic therapy should not delay definitive pleural palliation with a TPC.
抗肿瘤治疗相关免疫抑制引起的感染问题可能会阻碍对恶性/恶性间皮瘤胸腔积液(MPE/PMPE)患者进行症状缓解的经皮胸腔导管(TPC)治疗。虽然 TPC 相关感染的发生率为 1%至 21%,但在接受抗肿瘤治疗且与免疫状态相关的患者中尚未确定这一数据。我们旨在评估接受抗肿瘤治疗患者的 TPC 相关感染率,确定与免疫系统功能的关系,并评估其对患者的影响。
回顾了 2008 年至 2016 年间接受 TPC 治疗且接受抗肿瘤治疗的 MPE/PMPE 患者,并根据免疫抑制状态将其分为免疫抑制组和免疫正常组。
在 150 例患者中,有 13 例(9%)发生 TPC 相关感染:11 例(7%)为胸腔内感染,2 例(1%)为浅表感染。93%(139/150)在接受抗肿瘤治疗期间被确定为免疫抑制。免疫抑制组(9%,12/139)与免疫正常组(9%,1/11)TPC 相关感染发生率无差异(p=0.614)。导管相关感染的存在并未对中位随访 144 天(四分位距 41-341)内的总体生存率产生负面影响(p=0.740)。
这些结果表明,抗肿瘤治疗可能不会显著增加 TPC 相关感染的总体风险,因为其发生率仍然较低,且与未接受抗肿瘤治疗的患者的感染率相当。无论免疫状态如何,导管相关感染的存在并未对总体生存率产生负面影响。这些结果应使临床医生放心,不应因需要启动抗肿瘤治疗而延迟使用 TPC 进行明确的胸腔缓解治疗。