Martella Francesca, Salutari Vanda, Marchetti Claudia, Pisano Carmela, Di Napoli Marilena, Pietta Francesca, Centineo Dina, Caringella Anna M, Musella Angela, Fioretto Luisa
aOncology Department, Azienda Sanitaria Firenze, Istituto Toscano Tumori, Florence bGynecologic Oncology Unit, Policlinico Gemelli, Cattolica University cDepartment of Gynecological and Obstetrical Sciences and Urological Sciences, Policlinico Umberto I, La Sapienza University, Rome dDivision of Oncology, Department of Urology and Gynecology, Istituto Nazionale Tumori "Fondazione G. Pascale" IRCCS, Naples eOncology Department, Azienda Ospedaliero Universitaria, Modena fDepartment of Obstetrics and Gynecology II, Azienda Ospedaliera Policlinico Universitario, Bari, Italy.
Anticancer Drugs. 2015 Oct;26(9):990-4. doi: 10.1097/CAD.0000000000000275.
The European Medicines Agency strongly recommends administration of trabectedin through a central venous catheter (CVC) to minimize the risk of extravasation. However, CVCs place patients at risk of catheter-related complications and have a significant budgetary impact for oncology departments. The most frequently used CVCs are subcutaneously implanted PORT-chamber catheters (PORTs); peripherally inserted central venous catheters (PICCs) are relatively new. We reviewed data of trabectedin-treated patients to evaluate the relative cost-effectiveness of the use of PORTs and PICCs in six Italian centres. Data on 102 trabectedin-treated patients (20 with sarcoma, 80 with ovarian cancer and two with cervical cancer) were evaluated. Forty-five patients received trabectedin by a PICC, inserted by trained nurses using an ultrasound-guided technique at the bedside, whereas 57 patients received trabectedin infusion by a PORT, requiring a day surgery procedure in the hospital by a surgeon. Device dislocation and infections were reported in four patients, equally distributed between PORT or PICC users. Thrombosis occurred in a single patient with a PORT. Complications requiring devices removal were not reported during any of the 509 cycles of therapy (median 5; range 1-20). PICC misplacement or early malfunctions were not reported during trabectedin infusion. The cost-efficiency ratio favours PORT over PICC only when the device is used for more than 1 year. Our data suggest that trabectedin infusion by PICC is safe and well accepted, with a preferable cost-efficiency ratio compared with PORT in patients requiring short-term use of the device (≤1 year).
欧洲药品管理局强烈建议通过中心静脉导管(CVC)给予曲贝替定,以将外渗风险降至最低。然而,中心静脉导管会使患者面临与导管相关并发症的风险,并且对肿瘤科的预算有重大影响。最常用的中心静脉导管是皮下植入的输液港(PORT);外周静脉穿刺中心静脉导管(PICC)相对较新。我们回顾了接受曲贝替定治疗患者的数据,以评估在六个意大利中心使用输液港和外周静脉穿刺中心静脉导管的相对成本效益。评估了102例接受曲贝替定治疗患者的数据(20例患有肉瘤,80例患有卵巢癌,2例患有宫颈癌)。45例患者通过外周静脉穿刺中心静脉导管接受曲贝替定治疗,由经过培训的护士在床边采用超声引导技术插入,而57例患者通过输液港接受曲贝替定输注,这需要外科医生在医院进行日间手术。4例患者报告了装置移位和感染,在输液港或外周静脉穿刺中心静脉导管使用者之间分布均匀。1例使用输液港的患者发生了血栓形成。在509个治疗周期(中位数5;范围1 - 20)中的任何一个周期内均未报告需要移除装置的并发症。在曲贝替定输注期间未报告外周静脉穿刺中心静脉导管误置或早期故障。仅当装置使用超过1年时,成本效益比才有利于输液港而非外周静脉穿刺中心静脉导管。我们的数据表明,对于需要短期使用该装置(≤1年)的患者,通过外周静脉穿刺中心静脉导管输注曲贝替定是安全且易于接受的,与输液港相比具有更优的成本效益比。