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| ID | Type | Description | Link |
|---|---|---|---|
| UID 4907 | Other Identifier | Clinical Trial Office - Istituto Europeo di oncologia |
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Few data about the impact of emotional distress (ED) on treatment efficacy in patients with metastatic breast cancer (mBC) are available.
Aim of this study is to assess the outcomes of patients with mBC receiving first-line treatment according to the presence of baseline ED.
Metastatic breast cancer (mBC) is the most incident and prevalent cancer in the world and, according to a recent meta-analysis, 50% of patients with BC report emotional distress (ED).
In patients with cancer, ED negatively impacts treatment adherence, ability to self-manage the physical and emotional consequences of cancer symptoms and treatment-related adverse events, and overall quality of life. ED has been shown to directly affect treatment outcomes in patients with breast cancer, with studies demonstrating that psychological well-being plays a critical role in therapeutic success.
Furthermore, recent studies showed that baseline ED is associated with a lower efficacy of immunotherapy in patients with non-small cell lung cancer (NSCLC) or melanoma.
Few data about the impact of ED on treatment efficacy in patients with mBC are available. In the first line setting patients receive endocrine therapy, chemotherapy, immunotherapy and/or targeted therapy according to the disease subtype. These agents display different mechanisms of action, which involve the immune system at different levels. However, the role of ED on the efficacy of these treatments according to the BC subtype is unknown.
Aim of this study is to assess the outcomes of patients with mBC receiving first-line treatment according to the presence of baseline ED.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Cohort A (HR-/HER2-, PD-L1+) | Triple-negative Programmed Cell Death Ligand 1 (PD-L1)+ mBC patients receiving chemotherapy with immune checkpoint inhibitors (ICIs) |
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| Cohort B (HR-/HER2-, PD-L1-) | Triple-negative PD-L1- mBC patients receiving chemotherapy |
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| Cohort C (HR+/HER2-) | HR+/HER2- mBC patients receiving Cyclin-Dependent Kinase 4/6 (CDK4/6) inhibitor + endocrine therapy |
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| Cohort D (HER2+) | HER2+ mBC patients receiving chemotherapy + trastuzumab and pertuzumab |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ED and quality of life assessment | Behavioral | Patients will undergo ED and quality of life assessments through specific questionnaires completion |
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| Measure | Description | Time Frame |
|---|---|---|
| Progression-free survival (PFS), according to the presence of ED at T0, in cohort A | Time from T0 (Cycle 1 Day 1) to disease progression or death | 2 years |
| Measure | Description | Time Frame |
|---|---|---|
| Progression-free survival (PFS), according to the presence of ED at T0, in cohort B, C and D | Time from T0 (Cycle 1 Day 1) to disease progression or death | 2 years |
| Progression-free survival (PFS), according to the presence of ED at T1 (Cycle 3 Day 1) |
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Inclusion Criteria:
Age over 18 years
Confirmed histological diagnosis of breast cancer
No prior treatment for advanced/metastatic cancer
Indication to receive first-line therapy as per standard clinical practice based on the disease subtype:
Presence of measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST) v.1.1 and/or Positron Emission Tomography Response Criteria in Solid Tumors (PERCIST) criteria
Able to provide full informed consent for the study
Exclusion Criteria:
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Patients with mBC eligible for standard 1st line treatment
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Gabriella Pravettoni, MD, PhD | Contact | +39 0257489731 | gabriella.pravettoni@ieo.it | |
| Mara Negri | Contact | +39 0257489536 | mara.negri@ieo.it |
| Name | Affiliation | Role |
|---|---|---|
| Gabriella Pravettoni, MD, PhD | European Istitute of Oncology | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Ospedali Riuniti di Ancona | Not yet recruiting | Ancona | Italy |
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Time from T0 (Cycle 1 Day 1) to disease progression or death |
| 2 years |
| Objective response rate (ORR), according to the presence of ED at T0 and T1 | Number of partial response or complete response achieved | 2 years |
| Quality of life evaluation | Completion of European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire (QLQ) EORTC-QLQ-C30 (minimum value: 1, maximum value: 4 - higher scores mean a greater agreement with the statement) | 3 months |
| Fear of cancer progression evaluation | Completion of Fear of Progression Questionnaire (FoP Q) (minimum value: 1, maximum value: 5 - higher total score reflects a higher level of fear of disease progression) | 3 months |
| CRO (Centro di Riferimento Oncologico) | Not yet recruiting | Aviano | Italy |
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| Azienda Usl Toscana centro - Ospedale Santa Maria Annunziata | Recruiting | Bagno a Ripoli | Italy |
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| IRCCS Istituto Tumori Giovanni Paolo II | Not yet recruiting | Bari | Italy |
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| ASST Papa Giovanni XXIII | Not yet recruiting | Bergamo | Italy |
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| ASST Spedali Civili | Not yet recruiting | Brescia | Italy |
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| Ospedale A. Perrino | Not yet recruiting | Brindisi | Italy |
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| ASST della Valle Olona | Not yet recruiting | Busto Arsizio | Italy |
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| Ospedale Valduce | Not yet recruiting | Como | Italy |
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| Ospedale Careggi | Not yet recruiting | Florence | Italy |
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| Ospedale Policlinico San Martino | Not yet recruiting | Genova | Italy |
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| AOU Gaetano Martino di Messina | Recruiting | Messina | Italy |
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| European Institute of Oncology | Recruiting | Milan | 20141 | Italy |
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| ASST Fatebenefratelli Sacco | Not yet recruiting | Milan | Italy |
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| Fondazione IRCCS Istituto Nazionale dei Tumori | Not yet recruiting | Milan | Italy |
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| IRCCS Ospedale San Raffaele | Not yet recruiting | Milan | Italy |
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| Ospedale Niguarda | Not yet recruiting | Milan | Italy |
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| Ospedale San Giuseppe MultiMedica | Not yet recruiting | Milan | Italy |
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| Policlinico di Milano | Not yet recruiting | Milan | Italy |
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| Azienda Ospedaliero-Universitaria di Modena | Not yet recruiting | Modena | Italy |
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| Azienda Ospedaliera Universitaria Federico II | Not yet recruiting | Naples | Italy |
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| Istituto Nazionale Tumori IRCCS Fondazione G. Pascale | Not yet recruiting | Naples | Italy |
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| Ospedale Maggiore di Novara | Not yet recruiting | Novara | Italy |
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| Policlinico Universitario Paolo Giaccone | Not yet recruiting | Palermo | Italy |
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| Policlinico San Matteo | Not yet recruiting | Pavia | Italy |
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| Azienda Ospedaliero Universitaria Pisana | Not yet recruiting | Pisa | Italy |
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| Azienda Ospedaliero Universitaria Pisana | Recruiting | Pisa | Italy |
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| Azienda Usl Toscana centro - Ospedale di Prato Santo Stefano | Recruiting | Prato | Italy |
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| Ospedale Infermi | Not yet recruiting | Rimini | Italy |
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| Policlinico Universitario Campus Bio-Medico | Not yet recruiting | Roma | Italy |
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| Policlinico Umberto I | Not yet recruiting | Rome | Italy |
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| Policlinico Universitario Agostino Gemelli IRCCS | Recruiting | Rome | Italy |
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| Azienda Ospedaliero Universitaria di Sassari | Recruiting | Sassari | Italy |
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| ASL CN2 - Ospedale Michele e Pietro Ferrero | Recruiting | Verduno | Italy |
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| Azienda Ospedaliera Universitaria Integrata Verona | Not yet recruiting | Verona | Italy |
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| Ospedale Sacro Cuore Don Calabria - Negrar | Not yet recruiting | Verona | Italy |
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| ASST Brianza | Not yet recruiting | Vimercate | Italy |
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| ID | Term |
|---|---|
| D001943 | Breast Neoplasms |
| ID | Term |
|---|---|
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D001941 | Breast Diseases |
| D012871 | Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |
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