Central venous access related adverse events after trabectedin infusions in soft tissue sarcoma patients; experience and management in a nationwide multi-center study
© The Author(s) 2017
Received: 21 November 2016
Accepted: 9 January 2017
Published: 31 January 2017
Trabectedin has shown efficacy against soft tissue sarcomas (STS) and has manageable toxicity. Trabectedin is administered through central venous access devices (VAD), such as subcutaneous ports with tunneled catheters, Hickman catheters and PICC lines. Venous access related adverse events are common, but have not yet been reported in detail.
A retrospective analysis of patient files of STS patients receiving trabectedin monotherapy between 1999 and 2014 was performed in all five STS referral centers in the Netherlands. This survey focused on adverse events related to the VAD and the actions taken in response to these events.
In the 127 patients included in this analysis, 102 venous access ports (VAP), 15 Hickman catheters and 10 PICC lines were used as primary means of central venous access. The most frequently reported adverse events at the VAD site were erythema (30.7%), pain (28.3%), inflammation (11.8%) and thrombosis (11.0%). Actions taken towards these adverse events include oral antibiotics (17.3%), VAD replacement (15.0%) or a wait-and-see policy (13.4%). In total, 45 patients (35.4%) with a subcutaneous port developed a varying degree of inflammation along the trajectory of the tunneled catheter. In all but three patients, this was a sterile inflammation, which was considered a unique phenomenon for trabectedin. Microscopic leakage of trabectedin along the venous access device and catheter was considered the most plausible cause for this adverse event. Placing the catheter deeper under the skin resolved the issue almost completely.
Trabectedin infusion commonly leads to central venous access related adverse events. Sterile inflammation along the catheter trajectory is one of the most common adverse events and can be prevented by placing the catheter deeper under the skin.
KeywordsTrabectedin Central venous catheters Adverse events Soft tissue sarcoma
Cytostatic drugs infused directly into peripheral veins can have very damaging effects on these blood vessels. To ensure safe and durable administration of such agents, several methods have been developed in the past, like the arteriovenous shunt, which is no longer used for the infusion of chemotherapy . In 1982, a central venous access device was introduced, that used a subcutaneous reservoir and a tunneled catheter to provide access to the superior vena cava . This type of central venous catheters (CVC) allows for easy access to a patient’s circulation, incur minimal restriction in normal activities and usually at a low risk of complications . Next to VAPs, other methods have also been introduced, such as the Hickman catheter and peripherally inserted CVC (PICC) lines [4, 5]. However, all devices constitute some risk of venous access related adverse events (VARAE).
As anticancer drug, trabectedin stands out as a drug with a unique mechanism of action, having effect both at the level of tumor DNA and on the tumor microenvironment . It is one of the few drugs active in STS . The drug has a manageable toxicity profile, but life-threatening toxicity due to uncommon adverse events has been reported . Thus far several papers have mentioned VARAE, including reports on trabectedin extravasation and associated thrombi on the line tip, but no papers focusing on VARAE in detail have been published [9–12]. This article aims to systematically study VARAE observed in 127 consecutive sarcoma patients treated with trabectedin and to evaluate the measures taken to handle these problems.
A retrospective analysis of VARAE in all patients treated with trabectedin was performed in all five participating Dutch sarcoma referral centers: the Leiden University Medical Center (LUMC), the Netherlands Cancer Institute Antoni van Leeuwenhoek (NKI-AvL), the Erasmus MC Cancer Institute (EMC), the Radboud University Medical Center (RUMC) and the University Medical Center Groningen (UMCG). Patients were eligible when treated with trabectedin monotherapy for advanced STS. Data on patient characteristics were reported as well as the type of venous access device, its placement, adverse events related to its usage and the interventions to counter these events. Adverse events related to the VAD placement were ignored, as these have no direct relation with trabectedin infusions. Hence, all events described occurred after at least one cycle of trabectedin had been given.
To test for a difference in the number of cycles per VAD, a Kruskal–Wallis non-parametric test was used. To assess differences between VARAE per VAD cross tables and the Chi square were computed. All statistical analyses were performed using SPSS version 20.
WHO performance score
The VAP was used in 102 (80.3%) patients, of which 87 were identified as a Smith Medical Port-a-Cath®. Hickman catheters and PICC lines were inserted in 15 (11.8%) and 10 (7.9%) of patients, respectively. A total of 540 cycles of trabectedin were given with a median number of 4 cycles for the entire patient group. The number of cycles given did not differ significantly per VAD (data not shown).
Each hospital had a clear preference for a particular type of VAD that was initially inserted; in the LUMC VAPs (100% of patients), in the NKI-AvL VAPs (95%), in the EMC the Hickman catheter (100%), in the RUMC a PICC line (66.7%) and in the UMCG VAPs (100%). VADs were inserted by a dedicated team of health care workers to ensure low incidence of complications related to the VAD placement.
Of all patients, only three patients with a Hickman catheter requested their VAD to be replaced by another type of VAD. Two of these patients preferred a VAP, but did not have a VARAE at the time of replacement. In another patient, the catheter was chronically obstructed due to a thrombus at the catheter tip, which required catheter flushing by a radiologist, despite adequate antithrombotic treatment.
Sterile inflammation along the catheter trajectory
In the first instances these symptoms were deemed a result of cellulitis and oral antibiotics were prescribed (flucloxacillin 500 mg four times daily). However, the symptoms abated only mildly and the erythema remained unchanged for weeks and existed even after the discontinuation of trabectedin therapy. Extra intravenous infusion of normal saline fluids during trabectedin infusion appeared to ease the symptoms, especially the pain.
Remarkably, this complication appeared only in patients from one hospital and only after receiving several trabectedin cycles, and did not occur with any other type of cytostatic agent. As the same brand and type of VAD was used in another hospital without this complication, the dedicated teams compared their respective methods of VAD insertion. The only apparent difference found, was in the depth of the subcutaneous insertion for tunneling the catheter. Catheter insertion can be performed more or less deeper under the skin and the latter method was associated with the sterile inflammation along the catheter trajectory. Upon changing the local protocol to deepen the tunneling of the catheter, no further events of sterile inflammation of the catheter trajectory were observed.
Adverse events related to VAD
Adverse events at VAD site/trajectory per venous access device
Venous access port (102)
Hickman line (15)
PICC line (10)
Interventions for VARAE
Interventions for VAD related adverse events per venous access device
Venous access port (102)
Hickman line (15)
PICC line (10)
Trabectedin is one of the proven active drugs in the treatment of soft tissue sarcoma and is given through a central venous catheter to avoid peripheral vein damage. As treatment continues until progressive disease or unacceptable toxicity, is it important to evaluate catheter related complications. The sterile inflammation along the catheter trajectory found in this study was an unexpected VARAE and was initially poorly understood. Erythema or pain is usually taken as a sign of skin infection and treated as such. However, there were no other signs of infection such as positive cultures, and the severity of the skin complications appeared to be related to the administration of trabectedin. In addition, the erythema was most prominent along the catheter trajectory, which made a porous catheter likely to be the cause. A direct effect of trabectedin on the tissue surrounding the catheter could cause the inflammation, but this catheter porosity implies that only a small quantity of trabectedin permeates. This small quantity leads to fewer symptoms compared to a full trabectedin extravasation, as has been reported in literature .
To investigate the hypothesis of catheter porosity, the manufacturer of trabectedin, PharmaMar, offered to test a used catheter. A VAP was available that was previously used in a patient who had received several cycles of trabectedin with symptoms of sterile inflammation alongside the catheter trajectory and from whom the VAP was removed because of disease progression. The objective of the test was to determine if trabectedin permeates from the internal surface to the outside of the catheter during a 24 h infusion. High-performance liquid chromatography with diode array detection (HPLC–DAD) and multi-syringe flow injection system (MS-FIA) methods were used for detection of trabectedin in the dextrose 5% solution the VAP was submerged in. Neither test could detect trabectedin in samples taken from the dextrose 5% solution, which ruled out gross catheter porosity (PharmaMar communication). In our view, however, this could not rule out sub lower-limit of quantification leakage.
Non-infectious inflammation of the VAD site of various severity was also reported by Hoicyk et al. in addition of thrombi at the catheter tip. It was hypothesized that increased resistance due to small thrombi may be associated with drug backspill . In the current study, neither an association of sterile inflammation and thrombosis was found, nor was reduced flow through the catheter observed. Catheter thrombosis occurred in several patients, which was treated by flushing the catheter with an urokinase solution. Thrombosis prophylaxis was not initiated at the start of trabectedin therapy in any of the participating centres.
In the patient cohort only a small number of patients had PICC lines. A larger retrospective series of STS and ovarian cancer patients was reported by Martella and colleagues. Out of 45 patients with a PICC line receiving trabectedin a device dislocation was reported in two patients and an infection in another two. PICC line malfunction or VARAE requiring VAD removal did not occur . This implies that PICC lines may have lower incidence of associated toxicity than our current cohort suggests. However, the number of VARAE in patients using a PORT was also lower. Due to the retrospective nature of this patient series, relative underreporting compared to our study may have occurred, as almost all patient in this cohort where treated as part of a clinical trial.
The usage of a disposable elastomeric pump to administer a 24-h trabectedin infusion has been described . Patients could choose for a regular VAP or a Baxter LV10 Pump which allowed patients to spend the night at home. Out of 28 patients 21 chose the ambulatory pump. This method was considered feasible and safe. However, most patients will receive trabectedin trough conventional VAPs reported on in this paper, and no data is available comparing these different techniques.
Compared to published safety data, the rate of observed trabectedin extravasation of 0.8% in our series was similar to 0.5% reported in large pooled analysis of 1132 patients who received single agent trabectedin .
Despite the use of central venous access devices, trabectedin can cause local sterile inflammation along the catheter trajectory, in particular in venous access ports. Positioning the port’s catheter deeper in the subcutis appears to be the most efficient way to prevent this complication.
soft tissue sarcomas
venous access devices (any type)
- PICC line:
peripherally inserted CVC line
central venous catheter
venous access ports (such as a Port-a-Cath)
venous access related adverse events
HG designed the study, MV collected, analysed the data and drafted the first manuscript, all authors participated in patient care and manuscript writing. All authors read and approved the final manuscript.
HG: PharmaMar provided a research grant to the Leiden University Medical Center to perform a health outcomes study, which was also supported by a ZonMW grant. This study is a sub-study of the health outcomes study. MV: PharmaMar provided a research grant to perform this study, as sub-study of a health outcomes study. None for the other authors.
Availability of data and materials
The patients information used for this study is not publicly available due to privacy regulations.
Consent for publication
For all patients receiving trabectedin when it was an experimental drug, written informed consent was obtained. For patients who received trabectedin as standard treatment, informed consent is not necessary.
Ethics approval and consent to participate
Almost all patients were treated in a observational phase IV study or the phase IIb TRUSTS trial and written informed consent was obtained from all patients. Some patients were treated during early development pharmacokinetics studies with written informed consent. A copy of these written informed consent papers is available for review by the Editor-in-Chief of this journal. A final group was treated with trabectedin at a time when this drug was approved for clinical use in the Netherlands and this treatment was not considered experimental and no ethics approval or consent to participate is necessary.
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