- Study protocol
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From prospective biobanking to precision medicine: BIO-RAIDs – an EU study protocol in cervical cancer
BMC Cancer volume 15, Article number: 842 (2015)
Cervical cancer (CC) is -second to breast cancer- a dominant cause of gynecological cancer-related deaths worldwide. CC tumor biopsies and blood samples are of easy access and vital for the development of future precision medicine strategies.
BIO-RAIDs is a prospective multicenter European study, presently recruiting patients in 6 EU countries. Tumor and liquid biopsies from patients with previously non-treated cervical cancer (stages IB2-IV) are collected at defined time points. Patients receive standard primary treatment according to the stage of their disease. 700 patients are planned to be enrolled. The main objectives are the discovery of -dominant molecular alterations, -signalling pathway activation, and -tumor micro-environment patterns that may predict response or resistance to treatment. An exhaustive molecular analysis is performed using 1° Next generation sequencing, 2° Reverse phase protein arrays and 3° Immuno-histochemistry.
The clinical study BIO-RAIDs is activated in all planned countries, 170 patients have been recruited till now. This study will make an important contribution towards precision medicine treatments in cervical cancer. The results will support the development of clinical practice guidelines for cervical cancer patients to improve their prognosis and their quality of life.
Clinicaltrials.gov: NCT02428842, registered 10 February 2015.
Cervical cancer (CC) is the second cause of gynecological cancer-related deaths worldwide . Incidence and mortality rates of CC are up to twelve times higher in Eastern Europe as compared to North/Western Europe due to previously inadequate or absent screening practices [1, 2].
HPV is commonly accepted as the major etiological cause of CC . Preventive vaccination is expected to impact incidence rates in more than 20 years from now when the first vaccinated adolescents will reach the age of peak incidence (35–50) of CC. In the meantime, women are at risk and there is an unmet medical need to improve the diagnosis and treatment of CC.
Diagnosis, standard treatment and prognosis of CC
FIGO (International Federation of Gynecology and Obstetrics) classification for CC was revised in 2009. The use of MRI imaging was encouraged towards improving staging accuracy (92 %) [4–7]. While screening has decreased the incidence of CC in Western EU countries, its treatment has not changed over the last 15 years, the most recent improvement being the association of radio-chemotherapy [8, 9]. Addition of Bevacizumab  or Gemcitabine  to chemotherapy did show small improvements, but these treatments are costly, have side effects and are not available in many countries in need.
In early stage disease (≤IB1) and in a subset of patients of stage IB2-IIA, a surgical approach may cure the patient [12–15]. For stages IB2 to III, concurrent chemo-radiation with a platinum-based reagent is the recommended standard of therapy . Unfortunately, advanced stage (III-IV) disease remains a significant public health problem . In on-going clinical trials, the impact of additional chemotherapy either as neo-adjuvant (INTERLACE trial  or adjuvant (OUTBACK trial: ASCO meeting 2012) strategies, are currently being assessed.
Precision medicine in CC and BIO-RAIDs objectives
Molecularly targeted agents in CC are still being tested in clinical trials. CC patients may have variable outcomes and specific genetic mutations have already been shown to impact clinical response to standard therapy by us  and others [19–21]. The Cetuxicol trial, a phase 2 trial sponsored by Institut Curie, showed that the addition of Cetuximab over a 6 week period, did not improve DFS. Of interest was the finding that PI3K pathway tumor mutations in the Cetuximab treatment arm led to a worse outcome (De la Rochefordiere 2015). We are presently lacking prognostic and predictive biomarkers for CC treatment and there is a growing need for the development of these to follow up the course of the disease. Due to the multiplicity of potential genetic alterations, retrospective molecular assessments in small patient populations are mostly inconclusive. For these reasons, we initiated BIO-RAIDs, a prospective study with extensive biobanking which aims to identify predictive biomarkers for treatment response of cervical cancers in both Western and Eastern European countries. To our knowledge, BIO-RAIDs is the first large prospective trial of this type in the field of CC. At the medical/scientific level, BIO-RAIDs will be crucial in setting the ground for future precision medicine studies by identifying a set of stratification criteria for cervical carcinomas as well as other cancers with similar molecular alterations.
The BIO-RAIDs study is at the core of the European project called RAIDs “Rational molecular Assessment Innovative Drug selection” coordinated by Institut Curie. RAIDs is based on an international multidisciplinary cooperation between academic hospitals, SMEs and platforms for translational research www.raids-fp7.eu/ (Fig. 1).
Institut Curie (France) is responsible for the overall coordination and management (study documents and data quality, statistical analyses). In countries other than France, the registration, management, and monitoring of clinical centers is delegated to a national coordinator.
Study design and objectives
BIO-RAIDs is a prospective European study, involving oncology centers from France, Germany, Serbia, the Netherlands, Romania and Moldova. 700 patients with previously untreated, advanced stage CC (stage IB2-IV) will be enrolled. The recommendations for standards of treatment by stage of disease as well as the timing of biopsies are shown in Fig. 2. The primary objective of the study is to assess dominant mutations and activation of signaling pathways in cervical cancers predictive of response to standard treatment. Secondary objectives of the study are: 1. The determination of PFS at 18 months as a function of dominant genetic or protein alterations; 2. The descriptive analysis of standard treatments applied in participating European countries; 3. A descriptive analysis of grade 3 and 4 side effects; 4. A descriptive analysis of the frequency of molecular alterations according to geographic location.
Ethical considerations and regulatory approvals
Approval for the BIO-RAIDs study has been obtained from ethics committees in all participating countries (Comité pour la protection des personnes (CPP) Ile de France in France, The Serbian Medical Society Belgrade in Serbia, The Protocol Toetsingscommissie of the Antoni van Leeuwenhoek (PTC) in the Netherlands, The Medizinische Hochschule Hannover Ethik-kommission in Germany, The National Ethics Committee of Health Ministry of Republic of Moldova, Academy of Medical Sciences National Ethics Committee for medicines and medical devices in Romania). BIO-RAIDs is conducted in accordance with the guidelines of the Declaration of Helsinki, and the principles of Good Clinical Practice as defined by the International Conference on Harmonization (ICH-E6, 17/07/96) as well as specific laws and regulations of the countries were the study is performed. Centers participating in BIO-RAIDs study are listed in the Table 1.
Patient recruitment, data collection and biobanking
Eligible patients with stage IB2-IV disease, scheduled for primary surgery, chemo-radiation or primary chemotherapy are invited to participate in this study. Table 2 details the inclusion and exclusion criteria. Documented informed consent is obtained for all patients. Patient data is anonymized and recorded in an electronic Case Report Form (eCRF) (Quanticsoft). The eCRF generates patient specific unique barcode numbers for each sample. At study entry, baseline demographic characteristics, medical history and findings of staging such as complete physical and gynecological examination, abdominal and pelvic CT, pelvic MRI (+/- optional PET-CT) are recorded. A central review of MRI imaging is planned to be performed in Serbia.
Biobanking: sample collection and procedures
Tumor and serum samples are collected at defined time points as shown in Table 3 and stored at −80 °C (mutational data) or at room T° in case of preparation of fixed paraffin embedded sections (IHC). Standard operating procedures have been established by the RAIDs consortium for biopsy handling as well as for blood and sera collections. All samples are centralized in the RAIDs biobank located in Morahollum (SeQomics, Hungary).
One biopsy composed of at least 3 tumor samples must be collected at baseline before any treatment. In the case of large cervical lesions, 2 additional tumor samples may be collected: 1 tumor sample will be paraffin-embedded (FFPE) for Immunohistochemistry analysis and 2 to 4 tumor samples will be instantly frozen in liquid nitrogen and stored at −80 °C. The minimum size for tumor sample is 0.3 cm3 (bite of 7*3*1.5 mm). The ideal size is however > 0.3 cm3, and preferably 0.5–1 cm3. In case of poor response during the primary treatment sequence (at the insertion of the brachytherapy device which is done under general anesthesia following radio chemotherapy or at in case of surgery), 2 additional tumor samples may be collected and instantly frozen in liquid nitrogen and stored at −80 °C. At the end of the patient’s primary treatment sequence and in case of accessible residual/recurrent disease, 2 residual tumor samples will be collected and instantly frozen in liquid nitrogen and stored at −80 °C.
Before treatment, 7 mL of blood is collected in EDTA tubes for DNA extraction and sequencing at Seqomics and 10 mL of blood collected in adapted tubes for serum preparation. At the end of treatment and during follow-up visits at 6 and 12 months 10 mL of blood will be collected in adapted tubes for serum preparation. Sera will be stored at −80 °C and centralized at Seqomics.
Each sample (tumor, blood or serum) is meticulously labeled with a unique 2D barcode provided by Institut Curie at the beginning of the study. For each label a patient specific kit number is assigned by the electronic CRF software at the time of patient inclusion.
Molecular profiling is performed as summarized in Fig. 3. Raw data of molecular profiling together with the clinical data of patients are integrated into a common repository (KDI: Knowledge and Data Integration) (Fig. 4), developed by Institut Curie and already successfully used for the European project MAARS - (261366) as well as for the SHIVA clinical trial at Institut Curie .
Early clinical follow up may vary according to the chosen treatment strategy and a function of the FIGO stage of the disease. Detailed clinical and imaging evaluations are carried out at the end of treatment and at 6, 12 and 18 months. All clinical, sampling and imaging data are registered in the eCRF.
Quality control for radiotherapy
Standardization for External Beam Radio-chemotherapy (EBRT) and Brachytherapy (BT) delineation in participating centers was improved through online workshops (ODW) according to the GEC-ESTRO recommendations  and the EMBRACE protocol (An International study on MRI-guided Brachytherapy in locally advanced CC: EMBRACE. https://www.embracestudy.dk/). Centers with deviations from the treatment protocol are being offered an on-site training period in a reference center. Contour evaluation methodology: Intraobserver variability between 3 contouring periods: 1. Quantitative differences: DICE index. 2. Qualitative assessment: target Volumes, areas contoured. Organs at Risk A: Optimal: > 0.81; B: Suboptimal: < = 0.81 (Breunig et al. IJROB 2012) A: Optimal: > 0.81 Target Vol. B: Average: 0.65 – 0.81 C: Suboptimal: < 0.65 (Dimopoulos et al. Radioth Oncol2009; Petersen et al. IJROB2007) Initial analyses demonstrated interobserver variability for baseline contouring. Quantitative analyses were performed between centers and years of experience. Qualitative analyses compared group contours with reference contours. ANOVA was applied for analysis based on DICE, the significance of: institution; organ at risk (OAR) versus target volume (TV); organ; participant’s years of experience (grouped in 2 levels: Residents vs. Specialists). As an example of results of contouring workshop: most centers have an average DICE index for each volume between 0.65 and 0.81. This loosely falls within the average (B) category. If the participants improve in the guideline and final contouring sessions, these centers are initially prepared to participate within the RAIDs study, and only would need to complete a dummy run to validate the dosimetry as well. Half of the RAIDs institutions have suboptimal (C) DICE indexes for the GTV-node volume. The qualitative analyses showed some conceptual errors: 1. delineating vessels or clinical nodal target volumes instead of the actual macroscopic lymph nodes. 2. these results are partly due to the clinical case itself: 1. paraaortic lymph node which on the computed tomography image set for contouring seemed enlarged, although the clinical information explicitly stated that no paraaortic lymph nodes were pathological. 2. suspicious lymph node in the left groin, which within the live sessions was deemed as inflammatory by an experienced radiotherapist.
Acute or delayed toxicities of treatment will be documented in the eCRF.
Bioinformatics and statistical analysis
We try to assess which are the dominant mutations and which signaling pathways are activated in cervical cancers based on potentially deleterious genomic or proteomic alterations (COSMIC database). Furthermore we want to ascertain which abnormalities will be predictive of response to standard treatment and outcome. Analysis of a large number of patients is necessary because if a specific driver mutation is present in only 7 % of patients, 700 patients need to be evaluated to detect this mutation in 50 patients. No statistical hypothesis applies, but appropriate statistical methods will be used to analyze the results.
Complete response (CR) is assessed by MRI at the end of treatment (latest at 6 months) based on RECIST criteria. In the case of surgery, complete response will be defined as a pathological complete response. Progression-free survival (PFS) is defined as the time from diagnosis to the date of the first progression or death. If patients are alive and free of progression, they will be censored and their PFS will be defined as the time from diagnosis to the date of last known follow-up visit. Overall survival (S) will be defined as the time from diagnosis to the date of death or last follow-up. Survival rates will be estimated using the Kaplan-Meier method. PFS and OS will be compared to molecular phenotypes or clinical factors using the log-rank test.
Univariate and multivariate analyses will be performed to evaluate the association between each set of biomarkers (gain or loss of function) and clinical outcome. If the outcome measure is CR, a logistic regression is used. If the outcome measure is PFS or OS, a Cox regression model is preferred using 95 % confidence intervals. Multivariate analyses will take into account correlations between the different factors allowing to define a genomic or proteomic “response signature”, capable to predict the different outcome measures as compared to the presently available criteria. The level of significance is fixed at 5 %. Corrections for multiple testing to correct for the occurrence of false positives will be by the Benjamini-Hochberg method. Stratification according to geographical location will take into account the heterogeneity of standard treatment. Analyses will be performed using R° software by the Biostatistics Department of Institut Curie.
The bioinformatics’ platform at Institut Curie together with SeQomics (Hungary) will ensure reliable downstream bioinformatics analysis of patient samples. The tumors will be characterized by a list of features such as: mutations, structural variants, protein expression +/- phosphorylation, and presence of an immune signature by IHC among others. In an unsupervised analysis, an exhaustive exploration of the molecular profiles, without an a priori model will be carried out to characterize the dominant molecular abnormalities. This approach will involve a principal component analysis, an independent component analysis as well as clustering. This exploratory analysis is meant to detect possible biases due to technological aspects or sample handling (batch effect). The supervised analysis will attempt to identify and validate biomarkers using machine learning techniques such as LASSO, ridge regression, elastic net or SVM. The prediction of the influence of specific molecular abnormalities on patient outcome needs to be validated by their impact on the major endpoints which have been defined above: 1° Complete Response (CR). 2° Progression-free survival (PFS); 3° Overall survival (OS). Finally, results of both the unsupervised and supervised analyses will be compared to published classifications.
The biomarkers identified in the second step will be integrated with well-known clinical (FIGO stage, node involvement etc.) and histological prognostic factors in a multivariate model as defined in the first step. Our objectives are to study correlations and prioritize markers for their distinctive ability to predict complete response, progression free survival and overall survival.
BIO-RAIDs is one of the first prospective studies including a substantial biobanking effort for molecular profiling using fresh frozen tumor material with high standards of quality control of both biological samples and clinical data. While the aim of this study is to assess the relevant impact of dominant genetic/proteomic or immune parameters on primary treatment outcome in a prospective well controlled patient population with sufficient numbers to draw valid conclusions, there were a number of shortcomings in the initiation phase of this trial.
The clinical study BIO-RAIDs is now activated in all planned countries -up to two years after the start of the EU project- and patient recruitment numbers are satisfactory. Multiple bottlenecks causing the delay in this international study initiation were identified. Significant delays in the provisional time frame guidelines were caused by 1° Regulatory aspects; 2° Insurance modalities; 3° Negotiation of sponsorship delegation contracts; 4° Site specific logistics for biobanking; 5° Clinical trials operational management. Based on our experience, we believe there is a real need to develop procedures that facilitate the implementation of trials with biobanking in the era of precision medicine.
Conclusion and perspectives
The present protocol may serve to model the relationship of molecular aberrations to outcome in cervical cancer. Moreover this may apply to other cancers as well, since treatment response and outcome of a variety of cancers does not segregate according to histological tumor type. Response to treatment may in fact be more closely related to molecular driver genes than to tumor histotype. The implication of this project for the clinical practice of the future is to stratify cancer patients for the most appropriate treatment option.
Knowing the relative risk of good or bad outcome of specific tumor deregulations will be instrumental in guiding us towards more specific and less toxic treatments while also allowing the right amount of supervision and treatment, appropriate for each patient. In the RAIDs project, 20 cell lines have been collected and have been analyzed for molecular markers and for treatment response to a large panel of drug combinations. These may serve as companion diagnostics tools in the future.
Catalogue of somatic mutations in cancer
Common terminology criteria for adverse events
Eastern cooperative oncology group
Electronic case report file
International Federation of Gynecology and Obstetrics
Gynecologic oncology group
Human papilloma virus
Clinical research organization
Knowledge and data integration
Magnetic resonance imaging
Rational assessment and innovative drug selection
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This project has received funding from the European Union’s Seventh Program for research, technological development and demonstration under grant agreement No. 304810. We acknowledge the great implication of Clinical Research department of Institut Curie (Sponsor of BIO-RAIDs study).
The authors declare that they have no competing interests.
CN conception and design of the study, patient recruitment, writing of manuscript. SS protocol design, patient recruitment and writing of manuscript. KB clinical study coordination and writing of manuscript. AS supervision of radiotherapy and review of manuscript. PH design of bioinformatics and review of manuscript. GK conception of study and review of manuscript. MP conception and design of the study and patient recruitment. NS conception and design of the study and patient recruitment. PT study supervision. HvdL coordination of the study, study monitoring, review of manuscript. ED conception and design of the study, coordinator of radiotherapy control. RR conception and design of the study, manuscript review. LB biostatistics study design, writing of manuscript. MK scientific coordination, scientific design and manuscript review. SS coordinator of project and corresponding author, conception and design of the study, coordination and writing of manuscript. RAIDs Consortium variety of tasks in the conception, design, execution, monitoring, quality control in this study. All authors read and approved the final manuscript.
Charlotte Ngo and Sanne Samuels contributed equally to this work.
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Ngo, C., Samuels, S., Bagrintseva, K. et al. From prospective biobanking to precision medicine: BIO-RAIDs – an EU study protocol in cervical cancer. BMC Cancer 15, 842 (2015). https://doi.org/10.1186/s12885-015-1801-0
- Prospective European biobanking study
- Precision medicine
- Molecular profiling
- Cervical cancer
- Next generation sequencing
- Reverse phase protein array
- Tumor micro environment
- Targeted therapy
- Patient stratification
- International trial
- Clinical trial operations
- Quality control of pelvic radiotherapy
- HPV typing