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Surgery
Protocol
Protocol of a retrospective, multicentre observational study on hyperthermic intrathoracic chemotherapy in Germany
  1. Till Markowiak1,
  2. Michael Koller2,
  3. Florian Zeman2,
  4. Gunnar Huppertz2,
  5. Hans-Stefan Hofmann1,
  6. Michael Ried1
  7. HITOC Study Group
    1. 1Department of Thoracic Surgery, Universitätsklinikum Regensburg, Regensburg, Bayern, Germany
    2. 2Center for Clinical Studies, Universitätsklinikum Regensburg, Regensburg, Bayern, Germany
    1. Correspondence to Professor Michael Ried; michael.ried{at}ukr.de

    Abstract

    Introduction Objective of the ‘German hyperthermic intrathoracic chemotherapy (HITOC) study’ is to evaluate the HITOC as additional treatment after surgical cytoreduction for malignant pleural tumours. Even though HITOC is applied with increasing frequency, there is no standardised therapy protocol concerning the technique of HITOC, the selection as well as dosage of chemotherapeutic agents and perioperative management in order to provide a safe and comparable, standardised treatment regime.

    Methods and analysis This trial is a retrospective, multicentre observational study, which is funded by the German Research Foundation. Approximately 300 patients will be included. Four departments of thoracic surgery, which are performing the most HITOC procedures in Germany, are contributing to this study: Center for Thoracic Surgery at the University Hospital Regensburg, Thoracic Clinic Heidelberg of the University of Heidelberg, Center for Thoracic Surgery of the Hospital University of Munich and the Department of Thoracic Surgery at the University Hospital Freiburg. All patients who underwent surgical cytoreduction and subsequent HITOC at one of the four centres between starting the HITOC programme in 2008 and December 2019 will be included. Information on the performed HITOC will be obtained, focusing on the technique as well as the applied perfusion solution including the chemotherapeutic agent. Furthermore, parameters of the patient’s postoperative recovery will be analysed to determine 30-day morbidity and mortality.

    Ethics and dissemination The approvals by the local ethics committee of the respective clinic and the three participating clinics have been obtained. The results will be presented in conferences and published in a peer-reviewed journal.

    Trial registration number German Clinical Trials Registry (DRKS00015012; Pre-results).

    • thoracic surgery
    • thoracic medicine
    • adult oncology
    http://creativecommons.org/licenses/by-nc/4.0/

    This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

    https://doi.org/10.1136/bmjopen-2020-041511

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      Strengths and limitations of this study

      • The results of this retrospective, multicentre study should allow a better standardisation of the hyperthermic intrathoracic chemotherapy (HITOC) procedure including perioperative safety measures and also validate the existing clinical experience.

      • In the long term, it could be the basis for survival analyses and further prospective studies.

      • Due to the retrospective nature of our study, the implementation of HITOC was not uniform, which affects the analysis of 30-day morbidity and mortality.

      • To the best of our knowledge, this study will represent the largest cohort of patients with surgical cytoreduction and HITOC.

      Introduction

      Hyperthermic intrathoracic chemotherapy (HITOC) is a local, intraoperative perfusion of the thoracic cavity with a chemotherapeutic agent after surgical cytoreduction of malignant pleural tumours. The HITOC represents an additional therapeutic option in a multimodality treatment concept especially for patients with malignant pleural mesothelioma (MPM), thymic tumours with pleural spread (stage IVa) and even in highly selected patients with pleural carcinosis.1 2 The spreading growth pattern of these malignant tumours along the pleura impairs a microscopically complete resection, and small residues of the tumour often lead to local recurrence.2 With the application of the HITOC after macroscopic complete pleural tumour resection, it is expected to obtain better local tumour control, and thereby improve progression-free as well as overall survival.2–4 The few existing case series or single-centre retrospective studies in patients with MPM and thymic tumours have shown some encouraging results in this regard.2 5–9 However, a prospective study showing an advantage in survival does not yet exist.

      A survey of the German Society for Thoracic Surgery on the application of HITOC confirmed that approximately 350 HITOC procedures have already been performed in Germany from 2008 to 2017. Most of the procedures were conducted at University Thoracic Surgery Centers in Munich, Heidelberg, Freiburg, Regensburg and Cologne (Witten-Herdecke).10

      Although HITOC is performed routinely in some experienced departments of thoracic surgery in Germany, only feasibility studies, case series and retrospective studies with small numbers of patients have been published so far evaluating perioperative management, technique, the selection and dosage of chemotherapeutic agents and postoperative complications1 11 12 (table 1). There is no standardised procedure of HITOC concerning the administration of chemotherapeutic agents, the dosage of the drugs, duration and temperature of the perfusion as well as the perioperative management of these patients including safety measures for the personal. As a result, clinics performing HITOC follow internationally reported experiences and developed individual protocols.10 In 2019, a clinical practice guideline on HITOC within the guideline system of the Association of the Scientific Medical Societies in Germany was published. Due to the lack of empirical data, this guideline was based on an expert consensus (so called S1-guideline). The group of experts agreed on the key aspects of applying HITOC in thoracic surgery (table 2).13

      View this table:
      Table 1

      Study overview

      View this table:
      Table 2

      Consensus-based expert recommendation (excerpt)13

      Before performing the HITOC, all patients underwent surgical cytoreduction of the pleural tumour. Therefore, pleurectomy/decortication (P/D), extended P/D (eP/D) with partial and/or complete resection of the pericardium and/or diaphragm or extrapleural pneumonectomy (EPP) are carried out to achieve a macroscopic complete resection whenever possible.14 The outcome of lung-saving procedures (P/D and eP/D) turned out to be equivalent to EPP with significantly less complications, so that these procedures should preferably be performed.8

      Usually HITOC and tumour resection are performed in the same session. Apical inflow and basal outflow drainages are placed in the thoracic cavity. The following perfusion can be carried out with an open (before wound closure) or closed (after wound closure) chest, while the procedure on the closed chest is more common. Its advantage is that no cytostatic agent can leak out of the thoracic cavity during circulation, which would be a safety risk for the practitioner.7 10 The drainages are then connected to an external perfusion system. A stable circulation is established with a priming-volume, and the perfusion solution is heated to a targeted temperature of 40°C–43°C.9 15 The chemotherapeutic agents are added to the perfusate and the circulation is performed between 60 min and 120 min. Subsequently, the perfusion solution is passively drained.

      This retrospective, multicentre study will provide the first-time opportunity to enrol a substantial number of study participants from experienced German centres regarding HITOC to validate the clinical experience of the individual centres and possibly to form the basis for a standardised procedure with an adequate perioperative management in patients who underwent HITOC. In the long term, this database might be used for survival analyses with respect to the different tumour entities and may serve to design a prospective study.

      Methods and analysis

      Study design

      This is a retrospective, multicentre observational study to evaluate HITOC at university thoracic surgery clinics with the most performed operations including HITOC in Germany. The participating clinics include the Thoracic Surgery Center Regensburg (University Hospital Regensburg, Hospital Barmherzige Brüder Regensburg), the Department of Thoracic Surgery, Thoracic Clinic Heidelberg (University of Heidelberg), the Department of Thoracic Surgery, Medical Center, University of Freiburg and the Thoracic Surgery Center Munich, Hospital of the University of Munich (Ludwig Maximilians University, Campus Großhadern; Asklepios Lung Clinic Gauting). Estimating the number of patients of each participating clinic at the time of designing, this study resulted in a total number of approximately 350 patients in the period between January 2008 and December 2019 and who could be retrospectively included in this study. This will represent the largest cohort of patients who received HITOC compared with the recent international literature (table 1).9

      Inclusion and exclusion criteria

      The study will examine patients with malignant pleural tumours who received HITOC after surgical cytoreduction between beginning of the HITOC programme in 2008 and the end of December 2019 at all study centres. Patients without HITOC or without surgical cytoreduction will not be included (table 3). Informed consent is not an eligibility criterion because data will be processed in a pseudonymised manner in accordance with European Union General Data Protection Regulation (EU-GDPR) and Bavarian Hospital Law (BayKrG).

      View this table:
      Table 3

      Inclusion and exclusion criteria

      Study endpoints

      This study aims at quality assurance and evaluation of HITOC after surgical cytoreduction at the thoracic surgical university hospitals with most experience with HITOC in Germany. For this broad assessment, a compound of endpoints was defined as shown in box 1.

      Box 1

      Study endpoints (quality assurance and implementation of intraoperative HITOC after surgical cytoreduction)

      Study endpoints

      • Dosing of the intrathoracic chemotherapeutic agent.

      • Postoperative renal failure (dependence on cisplatin dosage).

      • 30-day morbidity and mortality.

      • Development of the technique, perioperative management and complication spectrum over time of HITOC.

      HITOC, hyperthermic intrathoracic chemotherapy.

      Central element of the study will be the evaluation of parameters concerning the implementation of HITOC. In particular, the selection of chemotherapeutic agents by the respective clinics will be assessed by showing which and how often certain combinations and dosages were used at leading German clinics in this field, since the approach varies internationally (table 1). In this regard, the association of the administered cisplatin dosage with the occurrence and severity (according to the Kidney Disease Improving Global Outcomes (KDIGO) classification) of postoperative renal insufficiency will be analysed. Also the incidence and severity (according to the Clavien-Dindo classification) as well as the spectrum of postoperative complications after HITOC will be determined. To further evaluate the safety of the procedure, 30-day mortality will be another element of the assessment. Finally, the development of this procedure in Germany concerning the technique, perioperative management and safety over a time span of approximately 11 years will be demonstrated (figure 1).

      Figure 1
      Figure 1

      Flowchart of the study design. HITOC, hyperthermic intrathoracic chemotherapy.

      Documentation and database

      After identifying all patients who meet all criteria shown in table 3, data will be documented in an electronic database. In this database, information on the performed surgery and additional HITOC will be obtained, focusing on the technique as well as the applied perfusion solution. Therefore, participating clinics will enter parameters regarding the patient characteristics (age, Eastern Cooperative Oncology Group (ECOG) stage, American Society of Anaesthesiologists (ASA) stage, tumour entity, tumour stage, date of first diagnosis), performed surgery (localisation, extend of surgical cytoreduction, complications), HITOC (combination and dosage of chemotherapeutics, perfusion volume, temperature, flow rate, duration of chemotherapy perfusion, complications) and perioperative management (weaning, fluid balancing, care on the intensive care unit). Data from the postoperative period (30-day morbidity) also include complications assigned to the Clavien-Dindo classification with special respect to postoperative renal insufficiency, required surgical revisions, duration of intensive medical care, hospitalisation and 30-day mortality.16 In addition, first data regarding progression-free and overall survival are warranted to be analysed (box 2).

      Box 2

      Overview of data collection with respect to subgroups

      Subgroups of data collection

      • Demographic data.

      • Physical examination.

      • Performance status.

      • Tumour specific data.

      • Surgery specific data (intraoperative, postoperative).

      • HITOC specific data.

      • Renal function.

      • Information on hospitalisation.

      • Follow-up.

      HITOC, hyperthermic intrathoracic chemotherapy.

      Data management

      The Center for Clinical Studies (ZKS) of the University Medical Center Regensburg is establishing a web-based, central and uniform database, using a common Clinical Database Management System. This system provides the capability to perform major data management activities within a consistent, auditable, integrated and EU-GDPR compliant environment. Data quality checks (regarding data ranges, validity and consistency) will be carried out regularly. In case of necessary corrections or existing data inconsistencies, a data manager will generate data queries consecutively. All data entries will be routinely recorded via audit trail as well as data modifications and data corrections.

      Statistical analyses

      Subsequently, the statistical data evaluation of the study is also carried out by the ZKS of the University Hospital Regensburg.

      Patient characteristics, quality assurance parameters and evaluation of HITOC after surgical cytoreduction (box 1) will be summarised descriptively, using absolute and relative frequencies for categorical data and mean, SD, median, IQR, minimum and maximum for metric data.

      Risk factors (eg, HITOC parameters) for 30-day mortality, in-hospital mortality and postoperative complications will be assessed by using binary logistic regression models. With regard to all outcome measurements, reference values for optimal HITOC parameters will be provided. The level of significance will be set at 5% for all statistical tests.

      The results of this retrospective study are intended to contribute to a standardisation of the perioperative procedure including safety measurements. To establish quality assurance in patients with HITOC, benchmarks are to be defined on the basis of the study. The rate of lung-sparing resections as well as the rate of postoperative renal insufficiency, wound infections as well as the length of hospital stay after surgical cytoreduction including HITOC and the 30-day mortality will be determined and thus provide reference for clinics performing this combined procedure.

      Ethics and dissemination

      The study was funded by the German Research Foundation (Deutsche Forschungsgemeinschaft—DFG; GZ: RI 2905/3-1) and will be supported for 12 months after its start in January 2020. The trial is registered in the German Register of Clinical Studies (date of registration: 03 August 2018). The approvals by the local ethics committee of the respective clinic and the three participating clinics have been obtained (reference number University Regensburg: 18-1119-104). Each patient will be assigned an identification number for pseudonymisation. The study ends regularly in December 2020 when the study parameters have been evaluated and published. The results are planned to be published in a peer-reviewed journal.

      Patient and public involvement

      In this study, patients or the public were not involved in the design, conduct, reporting or dissemination of research.

      Discussion

      There are different approaches in the international literature regarding the implementation and perioperative management of HITOC after surgical cytoreduction.9 A common standard for the procedure of HITOC does not yet exist, so that clinics performing this procedure orientate their protocols towards a small number of studies with often few participants (table 1).

      The available single-centre studies demonstrated that the rate of complications could be acceptable with an appropriate perioperative management.1 11 12 To perform HITOC safely and keep HITOC-specific complications low, adequate perioperative management and an interdisciplinary approach are essential, especially between surgery, anaesthesia and intensive care.17

      In the published research, cisplatin is always part of the perfusion solution. However, the dose administered varies, but usually it is applied in doses lower than 175 mg/m2 body surface area (BSA) (table 1).1 10 18–20 The application of higher doses of cisplatin seems to be associated with better overall survival, but also might cause more complications. Our study group described that the cisplatin concentration in patient serum increases to only about 2% of the intrathoracic concentration, although if the cisplatin dosage is increased up to 150 mg/m2 BSA.6 21 As a result, much higher concentrations can be achieved locally in the tissue than with systemic administration.15 However, high intrathoracic concentrations lead to an increased incidence of postoperative complications (eg, renal insufficiency), for which reason the maximum tolerable dose of cisplatin was identified at 225 mg/m2 BSA.6 Concerning postoperative renal insufficiency, the use of protective measures such as nephroprotective agents and fluid balancing may have a preventive effect.22 First introduced by Sugarbaker et al1 in HITOC, it is currently also being practised in a few more studies.6 22

      The application of a second chemotherapeutic agent is also heterogeneous. The considerations of applied agents were guided by the experience in systemic therapy. Superiority over systemic cisplatin monotherapy has been demonstrated in both patients with MPM and thymoma.23 24 In some clinics, cisplatin is combined with doxorubicin, epirubicin, gemcitabine or mitomycin, whereas other clinics use cisplatin alone.5 18 25

      Another factor where the protocols differ in international compare is the target temperature of the chemotherapeutic solution. During perfusion, it is constantly measured using two probes at the inflow and outflow drainages.6 It has been shown that the penetration depth of cisplatin into the tissue increases with the temperature of the intrathoracic solution. Applied temperatures of 40°C–43°C are described in the literature.1 26–28 Intrapleural temperatures above 43°C are supposed with an increased risk of pulmonary oedema and should therefore be avoided.29 Also, high temperatures of the perfusate lead to an increased risk of systemic hyperthermia.17 Regarding the optimal duration of perfusion, only little research exists and thus varies between 60 min and 120 min.19 25

      Conclusion

      In summary, the German HITOC study will include the biggest study population with surgical cytoreduction and HITOC since now. It will retrospectively evaluate the additional HITOC procedure with main respect to quality assurance and it will support a standardisation of the procedure. Results are expected in 2021.

      Trial status

      At the time of manuscript submission, database is finished and data collection started in April 2020. The following analyses are planned to be completed by the end of 2020.

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      Footnotes

      • Collaborators HITOC Study Group:Hauke Winter; Martin Eichhorn; Laura Klotz; Rudolf Hatz; Julia Zimmermann; Julia Kovacs; Bernward Passlick; Severin Schmid; Mohamed Hassan.

      • Contributors TM and MR wrote the manuscript. FZ, GH and MK proved the manuscript regarding the study design and the described statistical analysis. H-SH and all collaborators of the HITOC Study Group revised the manuscript critically. All authors approved the final version of the manuscript.

      • Funding This work was supported by the German Research Foundation, Kennedyallee 40, 53170, Bonn, Germany (Grant number GZ: RI 2905/3-1).

      • Competing interests None declared.

      • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting or dissemination plans of this research.

      • Patient consent for publication Not required.

      • Provenance and peer review Not commissioned; peer reviewed for ethical and funding approval prior to submission.