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Metastatic Triple-negative Breast CancerTIPNCT05831553

TIP in Patients Affected by Metastatic TNBC

An observational study of Metastatic Triple-negative Breast Cancer, run by Fondazione per la Medicina Personalizzata at 6 sites in Italy.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Triple-negative breast cancer (TNBC) is defined by the absence of estrogen receptor (ER), progesterone receptor (PgR), and human epidermal growth factor receptor 2 (HER2) expression on cancer cells. Read more about this study

Who is it for?
Ages 18 years and older, women only
Conditions the study is for
Metastatic Triple-negative Breast Cancer
What is being tested?
Tissue Immune Profile
How many people
100 participants
Where
6 sitesItaly
Study dates
16 Sep 2022to 16 Sep 2025
How long will I take part?
24 Months
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • Adult, Older adult

Study population: Female patients affected by metastatic TNBC (PDL1>1%) treated with upfront atezolizumab plus nab-paclitaxel

Who may be able to join

  • Patients able and willing to provide a written informed consent to participate to the study;
  • Histological confirmed diagnosis of PD-L1 positive TNBC (> 1%)
  • Confirmed radiological or histological diagnosis of metastatic TNBC
  • Availability of tumor specimen in order to perform the requested analysis
  • Patients eligible for or treated with atezolizumab plus nab-paclitaxel first line as requested for clinical practice
  • Availability of complete clinical data on duration, efficacy and safety of the treatment

Who cannot join

  • Sample not sufficient to perform the requested tissue analysis
  • Patients unable to provide informed consent or with possible poor compliance with protocol procedures
  • Patients with any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule;
  • Patients treated with the following drugs, because of the risk of immunosuppression: Chronic or high-dose oral corticosteroid therapy, TNF-inhibitors and Anti-T cell antibodies
  • Patients participating in other clinical studies.

Trial locations and contacts

6 sites in 1 country.

6 sites in 1 country

Italy6 sites, 5 recruiting
  • IRCCS Istituto Europeo di Oncologia IEO

    Milan, MI, 20141

    Suspended
  • Istituto Nazionale per lo Studio e la Cura dei Tumori - Fondazione S. Pascale

    Naples, 80131

    Roberta Caputo, dr

    Recruiting
  • Ospedale Santo Stefano

    Prato, FI, 59100

    Emanuela Risi, dr

    Recruiting
  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

    Roma, RM, 00168

    Ida Paris

    Recruiting
  • Azienda Ospedaliero Universitaria Policlinico Umberto I

    Roma, RM, 00198

    Andrea Botticelli

    Recruiting
  • ospedale Belcolle

    Viterbo, VT, 01100

    Agnese Fabbri, dr

    Not yet recruiting

Other trials in Italy

About this study

Official title: Evaluation of a Tissue Immune Profile (TIP) in Patients Affected by Metastatic TNBC Treated With Upfront Atezolizumab Plus Nab-paclitaxel (TIP)

Triple-negative breast cancer (TNBC) is defined by the absence of estrogen receptor (ER), progesterone receptor (PgR), and human epidermal growth factor receptor 2 (HER2) expression on cancer cells. TNBCs accounts for 15-20% of all breast cancers (BC).1 It is characterized by a worse prognosis, increased risk of metastasis to vital organs and a relative lack of therapeutic target if compared to other BC subtypes.2 Therefore, the identification of new molecular targets and therapeutic strategies is a critical need in both early and metastatic setting. TNBC appears to be more immunogenic compared to other BC6. Immunotherapy has recently changed the landscape of therapeutic options in TNBC. Recent clinical trials have shown a significant clinical benefit in patients with metastatic TNBC treated with a combination of chemotherapy and anti PD-1 agents.11-12-13-14-15 In particular, results from IMPASSION 130 trial showed a significant benefit in both progression free survival (PFS) and overall survival (OS) in PD-L1 positive (PD-L1+) patients treated with a combination of atezolizumab and nab-paclitaxel.20 However, about 70% of PD-L1+ patients has experienced a disease progression after one year and about 50% was alive at 2 year. Moreover, no difference in survival endpoint has been seen in PD-L1 negative (PD-L1-) population, with an increase of toxicity and costs related to the addition of a checkpoint-inhibitor. Therefore, the identification of novel biomarkers in addition to PD-L1 and the combination of several biomarkers in a profile with higher predictive capacity is considered an area of urgent clinical need. Some immune-related features that can be identified in tumor microenvironment have been demonstrated to be independent prognostic and predictive factors: TILs, PD-L1, CD73.

  1. Tumour-infiltrating lymphocytes (TILs) control the clinical progression of various types of cancer7. Breast cancer with higher levels of infiltrating CD8+ cytotoxic T cells have been associated with better patient survival8. Moreover, high levels of stromal CD8+ TILs (sTILs) correlate with higher probability of pCR9. Not only quantitative, but also qualitative analysis of TILs is a promising research area. Some studies suggest that different subtypes of TILs may have an opposite role in tumor microenvironment allowing the induction of both immune activating (es. CD8+) or immune suppressive (es FOXP3+) environment8-9-10.
  2. The interaction between programmed cell death protein 1 (PD-1) and its ligand (PD-L1) represents one of the principal mechanisms of immune escape and a therapeutic target for several malignancies13-14. PD-1/PD-L1 interaction attenuates lymphocyte activation and promotes T-regulatory cell development and function, allowing to terminate the immune response15. In breast cancer the prognostic role of PD-1/PD-L1 axis is still uncertain with limited and contrasting data. PD-L1 positivity (≥1%) on immune cells (IC) is the clinical most used threshold, according to the results of IMPASSION 130 trial.18-24
  3. Recently, CD73 has been identified as a possible further molecular immunosuppressive target in triple negative breast cancer28. CD73 is expressed on the surface of tumoral cells, stromal cells and immunological cells. By increasing extracellular levels of adenosine monophosphate , CD73 suppresses immune responses. CD73 has been found to be overexpressed in several types of human cancers, and it has been associated with a poor prognosis29-30-31. Particularly Loi et al demonstrated that high CD73 expression is associated with poor prognosis in TNBC and to a low rate of pathological complete response32.

We defined a tissue immune profile positive (TIP+) as the simultaneous presence of TILs≥50%, CD73≤40% and PD-L1≥1%. Any other combination was defined as TIP negative (TIP-) In conclusion, we will evaluate the association between TIP and clinical outcomes (ORR, PFS, OS).

Being tested
Tissue Immune Profile
Medical subject headings
Triple Negative Breast Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Tissue Immune ProfileDiagnostic test

    Tissue samples of the patients will be analized for the presence of TILs, CD73 and PDL1 (>=1%)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Progression Free Survival

    After 12 months from patient enrollment, the presence of disease progression will be assessed

    Measured: 12 months

Secondary outcomes (2)
  1. months of Overall Response Rate

    To evaluate the association between immune profile (TIP) and Objective Response Rate

    Measured: through study completion, an average of 1 year

  2. months of Overall Survival

    To evaluate the association between immune profile (TIP) and Overall Survival

    Measured: through study completion, an average of 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Apr 2023
  2. Study start16 Sep 2022
  3. Primary completion16 Sep 2025 (estimated)
  4. Study completion16 Sep 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Other
Enrolment
100 participants (estimated)
Target duration
24 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT05831553
Sponsor's protocol ID
FMP-2020-01-TIP
Acronym
TIP
Status last verified
May 2023
First submitted
20 Mar 2023
Last updated
6 May 2023
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Metastatic Triple-negative Breast Cancer, run by Fondazione per la Medicina Personalizzata at 6 sites in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 6 May 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 6 sites in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Paolo Marchetti (+393356105946, coordinamentofmp@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Progression Free Survival (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 May 2023.

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