CIRT is a prospective, multicenter, single-device, noninterventional study of patients with liver tumors treated with radioembolization in daily routine practice as a standard of care. The primary objective is to observe the real-life clinical application of radioembolization and the impact of the treatment in clinical practice. This objective is described by: type of liver cancer, intention of treatment, prior hepatic procedures, associated systemic therapy, and postradioembolization hepatic procedures.

Secondary objectives are effectiveness, safety, technical considerations, and patient-reported outcome measures (see Textbox 1).

Sites that incorporated radioembolization in their standard of care armamentarium and had a minimum amount of experience with the procedures were considered for invitations to participate in the study (ie, 10 or more treatments in the last 12 months and a career history of at least 40 cases). The selected sites were limited to centers in the European Union, Switzerland, Turkey, and Israel. A multidisciplinary steering committee containing experts from the field of medical oncology, diagnostic and interventional radiology, hepatology, surgery, and nuclear medicine developed a list of sites that met the selection criteria and continued to update this list throughout the course of the study. All sites that met the selection criteria were invited directly by the steering committee.

Eligible patients consist of any adult patients treated with radioembolization with 90Y resin microspheres for primary or secondary liver tumors that have signed the informed consent form. No formal sample size calculation was made. The steering committee reasoned that about 1000 patients could be recruited during a period of 3 years, and this would be sufficient to observe the real-life clinical application of radioembolization.

Site enrollment was from August 2014 until April 2017. Patients were included from January 2015 until December 2017. Follow-up data collection ended in December 2019.

This study was performed in accordance with the Declaration of Helsinki and Good Clinical Practice Guidelines. This study was approved by the local ethics committees of participating centers.

Patients enter the study by accepting participation and signing the informed consent form. Baseline data is collected upon allocation. Data on how the treatment was performed and its day-of-treatment outcomes are collected on the day of treatment. The patient is then followed for a maximum of 24 months or until study exit (see Figure 1). Guidelines for radioembolization advise that posttreatment assessments should be performed every 3 months [22]. However, the final decisions on treatment and follow-up schedules are determined by the site-specific medical teams.

Baseline assessments included patient demographics, medical history related to the underlying disease and cancer treatment, as well as cancer type and stage for patients with HCC (Table 1). The technical aspects that may determine how radioembolization is performed or impacts procedure-related outcomes were documented at the time of treatment. Time to event end points and safety end points were collected at every follow-up. In addition to demographic and clinical data, patient-reported outcomes are measured using the European Organisation for the Research and Treatment of Cancer (EORTC) quality of life questionnaire C30 (QLQ-C30) [23,24]. The questionnaire was provided before the treatment, shortly after the treatment, and at every follow-up. When this was not feasible on site, patients were approached via letters or phone calls organized by the study center responsible for the patient. For patients with HCC, in addition to the QLQ-C30, the HCC module was provided to assess factors related to chronic liver disease, as well as issues related to the primary tumor and its treatment [25]. The QLQ-C30 and HCC module were made available to each patient in their local language, using questionnaires translated and validated by EORTC [26-28].

Demographic and clinical data obtained from medical examinations, medical records, and QOL forms were transferred into an electronic case report form (e-CRF). Patient data was pseudonymized by each site without a centralized pseudonymization policy, and data collection was done according to the General Data Protection Regulation and stored in an encrypted form on a state-of-the-art server in Vienna, Austria. The e-CRF was accessible through a custom-built online database developed by ConexSys Inc (Lincoln, RI) and installed on the CIRSE server in Vienna, Austria. Access to the system is password protected. Statistical analysis will be performed by an independent statistician.

Data quality was ensured through regular remote monitoring of data entered into the database. Remote monitoring includes regular information on data quality (query reports), inclusion of patients, and follow-ups. No on-site monitoring or source data verification was performed due to limited resources.

All patients who were found eligible, enrolled in the registry, underwent radioembolization treatment, and have the minimum amount of data required will be included in analysis. Patients for which the amount of data collected is too scarce to warrant meaningful analysis will be excluded. The number of excluded patients and reason for exclusion will be reported.

Data regarding the primary end point, safety, and technical considerations will be presented by summaries (eg, counts, means, standard deviations) and descriptive statistics. The number of missing observations will be given in all summary tables. Time to event end points will be described graphically through the Kaplan-Meier analysis (including 95% CIs for median survival). The Cox regression will be used to assess the impact of the covariates for time to event end points (Table 2).

Hazard ratios and their 95% CIs will be presented together with P values. Sensitivity analyses of time to event data will be performed where censored patients with less than 6 weeks of follow-up will be included as worst case (ie, death or progression).

Table 2

Covariates for time to event end points.

QOL is measured with the EORTC QLQ-C30, a questionnaire developed to assess the QOL in patients with cancer. The QLQ-C30 includes five functional scales, three symptom scales, a global health status scale, and six single items. The functional and symptom status of the QLQ-C30 will be assessed according to the scoring manual developed and validated by EORTC [29]. Patients who die during follow-up will be included in the QOL analyses until their date of death. The focus of these analyses will be on patients who are alive at the time point of analysis.

To document the safety and effectiveness of radioembolization and subsequent surgical or interventional procedures, the data will be broken down into subgroups as defined for the covariate analyses above.

Missing data can be expected in the event of a study site failing to enter certain data into the e-CRF, or a patient’s withdrawal of consent or being lost to follow-up. Given the descriptive and exploratory nature of CIRT, all available data will be used, and no imputations of missing data will be made. The amount of missing data will be summarized and the subset of patients with missing data will be compared with patients included in the analysis.

In the effectiveness analyses, patients withdrawing consent or being lost to follow-up will be censored at the last time they were observed as being alive (overall survival) or at the time of their last magnetic resonance imaging scan from which disease progression could have been determined (progression-free survival [PFS]). Patients who die during the course of their follow-up in the registry will be regarded as having disease progression in the analyses of PFS and liver-specific PFS.

Missing data for QOL will be handled in line with the suggestions in the EORTC scoring manual for QLQ-C30; the amount of and reasons for completely missing forms will be analyzed and multiple imputations will be used for a part of the completely missing forms (ie, forms considered to be missing at random or due to administrative failure) [29].

CIRT is the first European-wide prospective observational study of patients with liver tumors treated with radioembolization as the standard of care and will provide an important addition to the body of knowledge on radioembolization treatment.

Data from several large RCTs on mCRC and HCC were published while CIRT was already ongoing and more can be expected in the future [12,30,31]. However, these studies provide insufficient data with respect to “real life” clinical practice since there may be patient cohorts that benefit more from radioembolization than the patient cohorts included in these trials [32-34]. CIRT was designed to also explore patient cohorts for which less data is available. The writing group hopes that the outcomes of CIRT would provide valuable insights in these less explored patient populations to gain further insight into real world clinical practice of radioembolization. The extent to which this data relates to the overall body of data available on radioembolization will be discussed in the results publication.

The single-arm observational study nature of the study design implies that several limitations need to be considered. The absence of a contemporaneous comparator group may limit our interpretation of the clinical data reported. Despite this, important positive features of the study are the long-term data collection for patients included and the valuable information collected on health-related QOL. The size of the study should enhance patient selection by providing new information on the patient subgroups that benefit most from this treatment in day-to-day clinical practice.

Furthermore, selection bias could occur at several stages of the study. An element of site selection was introduced when the Steering Committee created a list of sites that met the selection criteria of minimal expertise with radioembolization treatment. The potential of patient selection bias is addressed by a contractual agreed upon prospective design, whereby sites agreed to present the possibility to participate in the CIRT to all eligible patients consecutively.

Another source for bias relates to drop-out during follow-up. The sites included in the study have been advised to continue patient follow-up at least 24 months after the first treatment. However, patients may be lost to follow-up or withdraw their consent at any time. Loss to follow-up may relate to the course of disease or site procedures; for example, when a patient is treated at a participating site but followed-up by their referring physician, sometimes in another country. It will therefore not always be possible for study sites to collect additional follow-up data and the patient will be reported as lost to follow-up. Baseline characteristics will be compared between those lost to follow-up and those who have follow-up data to assess differences with the potential to bias results. Notable differences on a background characteristic will prompt additional analyses where the sensitivity of the results to that background characteristic will be further assessed.

To date, the CIRT is the largest observational study on the use of radioembolization with 90Y resin microspheres. The objective of the study was to observe the real-life clinical application of radioembolization and its impact in clinical practice. Currently, radioembolization has a position in the guidelines for the treatment of HCC, cholangiocarcinoma, and mCRC, and more data is warranted on the possibilities that this treatment has for these diseases. Furthermore, additional data is needed for the effects of other lines of therapy and treatment of liver metastatic disease from other primary sites. Observing a large study population may reveal treatment aspects that would justify a wider application of this innovative treatment.