3.1. Overall design
The MAMETIC Trial is a multicenter, retrospective and prospective observational investigation (Fig. 1).
- The retrospective part of the study concerns all patients enrolled with a diagnosis of metastatic disease, treated in RT centers of the Campania Region. RT was performed through several approaches including three-dimensional conformal radiation therapy (3DCRT), intensity-modulated radiation therapy (IMRT), volumetric modulated arc therapy (VMAT), stereotactic body radiation therapy (SBRT). Treatments were performed from January 2019 to July 2020.
Because in 2019, about 12.500 patients have been treated in the centers and it is estimated that 20-30% of the above-mentioned patients had metastasis, approximately 2.560 patients are expected to be enrolled.
- The prospective part of the study is going to involve all the metastatic patients with indication of palliative RT, treated with 3DCRT, IMRT, VMAT, SBRT techniques from December 2020 to December 2025. Considering regional epidemiological data, we expect an enrollment of patients between 500 - 4.200 patients per year, 12.500-21.000 in 5 years.
3.2. Study setting
RT centers joining the study can enter patient data in appropriate eCRFs. An eCRF will be provided for the retrospective part of the study. About the prospective part, RT centers can choose 3 levels of membership:
- Level A: epidemiological data entry on clinical features (metastatic cancers) and RT offered.
- Level B: level A plus pain features and analgesic therapy data.
- Level C: adds to the two previous levels data on HRQoL.
We have chosen to offer a different membership option to collect the greatest number of epidemiological information (primary objective). From the centers that will be able to enter the most complete data (Level B and level C), it will be possible to obtain data to achieve the secondary objectives.
3.3. Outcome measures
The primary objective of the study is focused on the data collection concerning metastatic cancers in the Campania region. This objective regards both the retrospective and prospective phases of the study.
For this purpose, will be recorded:
- Epidemiological data (patient/disease):
- Patient data
- Cancer type
- Metastasis
- Incidence of metastatic disease at diagnosis
- Time between first diagnosis and the onset of metastases
Secondary objectives of the study are:
- Characterization of palliative RT offered
- Cancer pain features
- Patients’ HRQoL
3.4. Study population
Eligible candidates for MAMETIC are metastatic patients candidates for palliative RT.
- Patients with bone metastases. They are about 70% of cancer patients in advanced stage of disease 5. They often have complicated lesions, with tumor tissue invading the muscle or nerve structures close to the bone. These lesions usually cause constant or intermittent pain, with a neuropathic component. In addition to baseline pain, the patient may have episodes of BTcP (Breakthrough cancer Pain) that compromise the HRQoL. As a result, they may have severe movement restrictions and an increased risk of pathological bone fracture6-9.
- Patients with metastases affecting the thoracic district with primary or secondary locally advanced disease. Symptoms such as dyspnea, chest pain, cough, hemoptysis, and dysphagia can be controlled with radiation treatments in 2/3 of these patients. Palliative mediastinal RT can improve obstructive dysphagia in locally advanced esophageal cancer10. At the same time, it can improve esophageal function after insertion of a stent11. Again, in patients with mediastinal syndrome, radiant treatment of the whole or part of mediastinum can ameliorate the HRQoL.
- Patients with bleeding, who may have neoplastic bleeding in the gastrointestinal, genitourinary, upper respiratory tract, or pelvic tract. For these patients, RT can have an important hemostatic effect and consequently can improve symptoms and hematological values. Radiant treatment can be used for hemostatic purposes in patients with bladder, rectal or gynecological malignancies with an improvement of the symptoms in 50-75% of cases.
- Patients with brain or spinal cord metastases. This category includes patients with symptomatic or asymptomatic brain metastases, patients with symptomatic or asymptomatic bone marrow compression, and those with cauda equina syndrome. In patients with paraplegia caused by spinal cord compression, 10% of motility can be recover if treatment is early. The presence of brain metastases can cause severe symptoms such as epilepsy, focal neurological symptoms, or intracranial hypertension symptoms such as nausea, vomiting, or headache12.
- Patients with symptomatic lymph node lesions who may have neck lymph node packages or pelvic district.
Eligibility criteria are summarized in Table 1
Table 1. MAMETIC Trial Eligibility criteria
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Inclusion criteria
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Exclusion criteria
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· Patients aged > 18 years resident in the Campania Region
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· Patients aged < 18 years
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· Patients diagnosed with metastatic disease candidates for radiotherapy
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· Patients who are unable to express consent to sensitive data and radiant treatment
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· Metastatic patients candidates for radiotherapy re-treatment
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· Oligometastatic patients candidates for radiotherapy
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· Patients who have given their consent
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3.5. Clinical Variables
Clinical characteristics of patients will be collected from hospital clinical documentation and RT treatment plans, according to data needed for the study. Data will be identified in the medical record and collected in specific eCRF:
- RETROSPECTIVE STUDY:
- Address
- Weight
- Height
- Primary tumor
- Date of the first diagnosis
- Stage c / pTNM at diagnosis
- Therapies carried out for the primary tumor (surgery, chemotherapy, hormone therapy, immunotherapy, target therapies, RT)
- Metastatic disease diagnosis date
- Pre-treatment radiotherapy visit date
- Start and end date of palliative RT
- Possible request for rapid access to RT
- Indications for palliative RT (bone marrow compression, mediastinal syndrome, hemostasis, bone metastasis painful, painless bone metastasis, compression or infiltration pain, bone - lung - liver - lymph node - adrenal oligometastasis, brain metastases, primitive encephalic with expired PS)
- Type of treatment: RT flash, SBRT
- Prescribed dose and fractions
- Re-treatment.
- PROSPECTIVE STUDY
- Level A. The same epidemiological/RT data recorded in the retrospective study
- Level B: Epidemiological/RT data plus:
- Type of pain (neuropathic, nociceptive, mixed) and intensity measured through the Numeric Rating Scale (NRS) score. This latter is an 11-point scale (from 0 to 10), with higher scores indicating greater pain intensity.
- Breakthrough cancer pain (BTcP) [defined as ‘a transitory flare of pain that occurs on a background of relatively well-controlled baseline pain’13] in terms of number of episodes/day; pain intensity14.
- Pain flare (a transient worsening of the bone pain after RT) in terms of intensity (NRS).
- Data about pain therapy: drugs (adjuvant drugs, opioids, non-opioid analgesics) and doses.
- Adverse events of the pain therapy.
- For the pain evaluation, patients will report pain data (NRS, episodes of BTcP) and therapy in a Pain Diary. Follow-ups will be performed on the 15th (telephone revaluation) and 30th day (outpatient revaluation) after the end of RT treatment.
- Level C. In addition to what is specified for levels A and B, the following tools for assessing the patients’ HRQoL will be adopted before starting and at the end of the RT treatment:
- The European Organization for Research and Treatment of Cancer (EORTC) QLQC15-PAL questionnaire15, and Palliative Performance Score (PPS)16 for all patients.
- The EORTC QLQ-BM2217 questionnaire; van der Linden Score18; Mizumoto Prognostic Score19 for assessing the HRQoL in patients with bone metastases.
- The Spinal Instability Neoplastic Score (SINS)20 used for investigating the incidence of spinal instability in patients with spinal metastases.
- The American Spinal Injury Association (ASIA) Score21 for evaluation of the functional impairment as a result of the spinal cord injury/compression.
- The Mini-Mental State Examination (MMSE)22 for assessing cognitive function in patients with brain metastases.
3.6. Data collecting and Statistical considerations
The data collection and registration procedures will be carried out through specific CRFs organized on an electronic platform managed by the coordinating center which will be responsible for the privacy of sensitive data. The platform was created with a management software developed with Microsoft Net technology, Web App made with Internet Information Services (IIS 10) pattern, MVC, Razor syntax, Jquery 3.4.1 scripting language. Net framework version 4.8. SQL Server 2019 database version 15. Crystal Reporting for Visual Studio 2019.
The data will be transmitted to the coordinating center when each form is completed by the operator of the individual center. Every 3 months a report of the total amount of patients entered in the platform will be sent by the coordinating center to every center participating in the study.
A descriptive analysis will summarize the total number and stratification of patients with metastatic disease by place of residence and tumor location. Metastatic tumors at diagnosis will be differentiated from metastatic disease developed later. Every center is going to fill a form for each patient with mandatory socio-demographic and anamnestic information (Level A) and information on pain and HRQoL (Levels B and C). This process lets the study produce a compliance survey by a single center and carry on a comparative analysis for subsequent levels on qualitative variables (presence of pain; typology and characterization of pain) through the Chi-Square Test and quantitative variables (pain scale, scores on quality of life) with T-test and ANOVA. Nonparametric tests will be provided where the population distribution does not have a known form (normal Gaussian). The significance of the tests is fixed with p <0.05.
3.7. Ethics considerations
The MAMETIC Trial is promoted by the Division of Radiotherapy of National Cancer Institute - IRCCS Fondazione Pascale, Naples (Italy), in collaboration with the Divisions of Anesthesia and Pain Medicine, Uro-Gynecological Medical Oncology, Epidemiology and Biostatistics of the Fondazione Pascale, and with the Cancer Registry Unit ASL-Napoli 3 South. The local Ethics Committee approved the protocol on July 8, 2020 (n. 868/2020).
Each interested center will submit the protocol to its ethics committee to be approved before accrual. After approval, the center will receive a dedicated electronic case report form (CRF). Eligible patients who provided consent and meet the inclusion criteria are anonymously registered on the CRF by assigning a numerical code.
The Trial will be conducted in accordance with the approved protocol and the Helsinki Declaration (1996), the Guidelines for Good Clinical Practice CPM / ICH135 / 95-DM 15/7/97, in compliance with Legislative Decree n. 200 of 6 November 2007, Implementation of Directive 2005/2 // EC Article 3 and GDPR EU Regulation no. 2016/679.