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Clinically Actionable Tumor-Associated Antigens in Prostate Cancer

13 maja 2026 zaktualizowane przez: Yelin Mulati, Peking University First Hospital

Expression Profiles And Prognostic Implications Of Clinically Actionable Tumor-Associated Antigens Across Diverse Clinicopathological Subtypes of Prostate Cancer: a Bidirectional Cohort Study

The goal of this observational study is to evaluate and validate the expression and prognostic value of 15 ADC-targetable membrane proteins (PSMA, B7-H3, STEAP1, TROP2, KLK2, HER2, TF, HER3, DLL3, SEZ6, STEAP2, MUC1, NECTIN4, FAP, PDL1) in patients with diverse clinicopathological subtypes of prostate cancer (e.g. primary and different metastatic types，HSPC and CRPC， PC with neuroendocrine differentiation, cribriform/intraductal carcinoma).

The main questions it aims to answer are:

  1. What is the expression profile of 15 clinically actionable targes in tumor tissues from patients with diverse clinicopathological subtypes of prostate cancer?
  2. Can the prognostic value of these targets (e.g. association with overall survival) identified in a retrospective cohort be validated in an independent prospective cohort? Researchers will head-to-head compare the expression levels among different targets and across different disease stages/metastatic site. Researchers will also assess whether the targets showing prognostic significance in the retrospective cohort can also predict survival outcomes in the prospective cohort.

Participants in the retrospective cohort have already provided archived tissue samples and clinical data. Participants in the prospective cohort (metastatic prostate cancer patients) will be invited to provide residual tumor tissue samples obtained during standard care and will be followed up regularly for clinical outcomes.

Przegląd badań

Status

Aktywny, nie rekrutujący

Warunki

Interwencja / Leczenie

Szczegółowy opis

  1. Study Type This is a single-center, observational cohort study incorporating both retrospective and prospective components. It is a non-interventional study that does not involve assignment of participants to specific interventions.
  2. Objectives

Primary Objectives:

  1. To determine the protein expression profile (positive rate, expression level) of 15 membrane targets (PSMA, B7-H3, STEAP1, TROP2, KLK2, HER2, TF, HER3, DLL3, SEZ6, STEAP2, MUC1, NECTIN4, FAP, PDL1) in diverse clinicopathological subtypes of prostate cancer (HSPC and CRPC，primary and metastatic lesions include lymph node, bone and visceral metastasis, etc.).
  2. To characterize the molecular subtypes of prostate cancer based on the expression profiles of AR, PSA, PSMA, Syn, CgA, CD56, p53, RB1, and PTEN across different disease states and metastatic sites.
  3. To validate the association between the expression of prognostically significant targets (identified in the retrospective cohort) and overall survival (OS) in an independent, prospectively enrolled cohort of prostate cancer patients.

Secondary Objectives:

  1. To compare the expression of each target between matched CSPC and mCRPC samples from the same patients.
  2. To compare the expression of each target across different metastatic sites (e.g., bone, lymph node, viscera) in mCRPC.
  3. To analyze the association between target expression and clinical outcomes [biochemical recurrence-free survival (BFS), metastasis-free survival (MFS)] in patients with CSPC.
  4. To explore co-expression patterns of the targets and their correlation with clinicopathological features.

3.Study Design

Retrospective Cohort:

Population: Patients treated at Peking University First Hospital between 2000-2022.

Cohort 1: Primary Tumor Cohort - This cohort includes patients with CSPC or CRPC, or those with special pathological structures, for whom primary tumor tissue (from biopsy or surgery) is available.

Cohort 2: Lymph Node Metastasis Cohort - This cohort includes patients with CSPC or CRPC for whom lymph node metastasis tissue is available (from biopsy or surgery) .

Cohort 3: Bone Metastasis Cohort - This cohort includes patients with CSPC or CRPC, for whom bone metastasis tissue is available (from biopsy or surgery).

Cohort 4: Visceral Metastasis Cohort - This cohort includes patients with CSPC or CRPC, for whom visceral (e.g., liver, lung) metastasis tissue is available.

Procedures: Archived FFPE tissue blocks will be retrieved for immunohistochemistry (IHC) staining. Clinical and follow-up data will be extracted from medical records.

Prospective Cohort:

Population: Newly diagnosed metastatic prostate cancer patients at Peking University First Hospital from January 1, 2026.

Cohort 5: Prospective Validation Cohort - This cohort will consist of patients with metastatic prostate cancer (mHSPC or mCRPC), from whom tissue samples will be collected prospectively along with their clinical data.

Procedures: Eligible patients will provide informed consent. Residual tumor tissue obtained during standard-of-care biopsies or surgeries will be collected for IHC staining. Patients will be followed prospectively at defined intervals to collect treatment and outcome data.

4.Methods Laboratory Assessment (for both cohorts): IHC will be performed on FFPE tissue sections using validated antibodies against the eight targets (as specified in the protocol: e.g., HER2: ab2142275; TROP2: ab214488; etc.). Staining will be evaluated by pathologists blinded to clinical outcomes. IHC score 0-3,0=negative/none,1=weak,2=moderate,3=strong. A modified H-score ([1×% weak staining + 2×% moderate staining + 3×% strong staining], range 0-300) will be used for quantification.

Data Collection: Clinical data (demographics, laboratory assessment (tPSA、LDH levels)，imaging data(ultrasound, MRI, CT, PET, providing TNM staging results, treatment history, pathology reports) and outcome data (biochemical recurrence, metastasis, death) will be collected retrospectively from databases/records for the retrospective cohort and prospectively during follow-up visits for the prospective cohort.

Typ studiów

Obserwacyjny

Zapisy (Szacowany)

1600

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

  • Chiny
    • Beijing Municipality
      • Beijing, Beijing Municipality, Chiny, 100034
        • Peking University First Hospital

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Metoda próbkowania

Próbka bez prawdopodobieństwa

Badana populacja

  1. Retrospective Cohorts: These four groups are defined by the origin of the archived tumor tissue specimen at Peking University First Hospital (2000-2025). Each cohort includes patients across the spectrum of disease states (castration-sensitive [CSPC] and castration-resistant [CRPC] prostate cancer) and those with special clinicopathological subtypes (e.g., neuroendocrine differentiation, cribriform/intraductal carcinoma).
  2. Prospective Validation Cohort: This group will consist of patients with metastatic prostate cancer recruited at Peking University First Hospital starting January 1, 2026. Participants will provide informed consent for the use of residual tumor tissue (from any anatomic site) obtained during standard clinical care and for prospective clinical follow-up.

The core material for analysis is formalin-fixed, paraffin-embedded (FFPE) tumor tissue from all participants, which will be subjected to immunohistochemical (IHC) staining for biomarker evaluation.

Opis

Inclusion Criteria:

  • For the Retrospective Cohorts (mCRPC, CSPC, Special Pathology):

    1. Patients with a pathological diagnosis of prostate cancer.
    2. Treated at Peking University First Hospital between January 2000 and 2025.
    3. Availability of adequate, qualified formalin-fixed, paraffin-embedded (FFPE) tumor tissue blocks for research.
    4. Availability of essential clinical and follow-up data in medical records.

  • For the Prospective Cohort:

    1. Age ≥ 18 years.
    2. CSPC, primarily includes patients who underwent neoadjuvant therapy and have paired pre- and post-treatment biopsy and surgical specimens; or patients with special clinicopathological subtypes.
    3. metastatic prostate cancer patients.
    4. Planned or recent (within 6 months prior to enrollment) acquisition of tumor tissue (from metastasis or primary site) as part of standard clinical care, with sufficient residual tissue available for the study.
    5. Willing and able to provide written informed consent.

Exclusion Criteria:

  • For All Cohorts:

    1. Tumor tissue sample is of insufficient quality or quantity for immunohistochemical (IHC) analysis.
    2. Essential clinical or outcome data are missing or irretrievable, which would preclude meaningful analysis.

  • Specifically for the Prospective Cohort:

    1. Any condition that, in the investigator's judgment, would significantly compromise the patient's ability to provide informed consent or comply with the study follow-up procedures.
    2. Patient refusal to participate.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

Kohorty i interwencje

Grupa / Kohorta
Interwencja / Leczenie
Primary Tumor Cohort
This retrospective cohort consists of patients with prostate cancer (encompassing castration-sensitive [CSPC], castration-resistant [CRPC] disease states, and those with special clinicopathological subtypes) for whom primary tumor tissue (from biopsy or radical prostatectomy) is available. Archived FFPE specimens were obtained at Peking University First Hospital between 2000 and 2025. This is an observational cohort. No study intervention is administered.
Inny: Immunohistochemistry (IHC) Staining and Analysis
Immunohistochemistry staining will be performed on formalin-fixed, paraffin-embedded (FFPE) prostate cancer tissue sections to quantitatively assess the expression levels of eight membrane protein targets: PSMA, HER2, TROP2, NECTIN4, DLL3, STEAP1, B7-H3, and PDL1. This is a laboratory-based biomarker analysis and does not constitute a therapeutic intervention for participants.
Lymph Node Metastasis Cohort
This retrospective cohort consists of patients with prostate cancer (encompassing CSPC, CRPC disease states, and those with special clinicopathological subtypes) for whom lymph node metastasis tissue is available. Archived FFPE specimens were obtained at Peking University First Hospital between 2000 and 2025. This is an observational cohort. No study intervention is administered.
Inny: Immunohistochemistry (IHC) Staining and Analysis
Immunohistochemistry staining will be performed on formalin-fixed, paraffin-embedded (FFPE) prostate cancer tissue sections to quantitatively assess the expression levels of eight membrane protein targets: PSMA, HER2, TROP2, NECTIN4, DLL3, STEAP1, B7-H3, and PDL1. This is a laboratory-based biomarker analysis and does not constitute a therapeutic intervention for participants.
Bone Metastasis Cohort
This retrospective cohort consists of patients with prostate cancer (encompassing CSPC, CRPC disease states, and those with special clinicopathological subtypes) for whom bone metastasis tissue is available. Archived FFPE specimens were obtained at Peking University First Hospital between 2000 and 2025. This is an observational cohort. No study intervention is administered.
Inny: Immunohistochemistry (IHC) Staining and Analysis
Immunohistochemistry staining will be performed on formalin-fixed, paraffin-embedded (FFPE) prostate cancer tissue sections to quantitatively assess the expression levels of eight membrane protein targets: PSMA, HER2, TROP2, NECTIN4, DLL3, STEAP1, B7-H3, and PDL1. This is a laboratory-based biomarker analysis and does not constitute a therapeutic intervention for participants.
Visceral Metastasis Cohort
This retrospective cohort consists of patients with prostate cancer (encompassing CSPC, CRPC disease states, and those with special clinicopathological subtypes) for whom visceral metastasis (e.g., liver, lung) tissue is available. Archived FFPE specimens were obtained at Peking University First Hospital between 2000 and 2025. This is an observational cohort. No study intervention is administered.
Inny: Immunohistochemistry (IHC) Staining and Analysis
Immunohistochemistry staining will be performed on formalin-fixed, paraffin-embedded (FFPE) prostate cancer tissue sections to quantitatively assess the expression levels of eight membrane protein targets: PSMA, HER2, TROP2, NECTIN4, DLL3, STEAP1, B7-H3, and PDL1. This is a laboratory-based biomarker analysis and does not constitute a therapeutic intervention for participants.
Prospective Validation Cohort
This is a prospective, observational cohort. It will enroll metastatic prostate cancer patients (mHSPC or mCRPC) at Peking University First Hospital starting January 1, 2026. Participants will provide informed consent. Residual tumor tissue (from any site) obtained during standard-of-care procedures will be collected for biomarker analysis, and participants will be followed prospectively for clinical outcomes. No study intervention is administered.
Inny: Immunohistochemistry (IHC) Staining and Analysis
Immunohistochemistry staining will be performed on formalin-fixed, paraffin-embedded (FFPE) prostate cancer tissue sections to quantitatively assess the expression levels of eight membrane protein targets: PSMA, HER2, TROP2, NECTIN4, DLL3, STEAP1, B7-H3, and PDL1. This is a laboratory-based biomarker analysis and does not constitute a therapeutic intervention for participants.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Expression Profile in the Retrospective Prostate Cancer Cohort
Ramy czasowe: Baseline (at time of metastatic site sample acquisition)
The protein expression profiles of 15 tumor-associated antigens (PSMA, B7-H3, STEAP1, TROP2, KLK2, HER2, TF, HER3, DLL3, SEZ6, STEAP2, MUC1, NECTIN4, FAP, PDL1) and molecular subtype markers (AR, PSA, Syn, CgA, CD56, p53, RB1, and PTEN) in tumor tissues from the four retrospective site-based cohorts (Primary Tumor, Lymph Node Metastasis, Bone Metastasis, Visceral Metastasis). Measure: Expression level assessed by IHC score (0-3) , modified H-score (0-300) (positive expression defined as a H-score > 20) for each target within each cohort.
Baseline (at time of metastatic site sample acquisition)
Validation in the Prospective Cohort
Ramy czasowe: From date of prospective cohort enrollment until death from any cause, assessed up to 3 years

The association between the expression status (positive/negative or H-score level) of prognostically significant ADC targets (identified in the retrospective cohort) and Overall Survival (OS) in the prospectively enrolled mCRPC validation cohort. This is a confirmatory analysis.

Measure: Hazard Ratio (HR) with 95% Confidence Interval (CI) from Cox proportional hazards model.
From date of prospective cohort enrollment until death from any cause, assessed up to 3 years

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Target Expression Difference: Primary Tumor vs. Paired Metastasis
Ramy czasowe: Baseline (at time of matched sample acquisition)

The difference in expression level (IHC score or H-score) for each target between primary tumor and matched metastasis (from any site) from the same patients, where such paired samples are available in the retrospective cohorts.

Measure: IHC score or H-score.
Baseline (at time of matched sample acquisition)
Target Expression Difference: Across Different Metastatic Sites
Ramy czasowe: Baseline

The difference in expression level (IHC score or H-score) for each target among the different metastatic sites (Lymph Node, Bone, Viscera) in the retrospective cohorts.

Measure: IHC score or H-score.
Baseline
Target Expression in Special Clinicopathological Subtypes (Subgroup Analysis)
Ramy czasowe: Baseline

The expression profile of the 15 tumor-associated antigens in tumor tissues with neuroendocrine differentiation or cribriform/intraductal carcinoma (CF/IDC), analyzed as a subgroup across retrospective cohorts.

Measure: IHC score or H-score.
Baseline
Prognostic Association in Retrospective Prostate Cancer Cohort
Ramy czasowe: From date of radical prostatectomy until biochemical recurrence, metastasis, or death, assessed up to 10 years

The association between tumor-associated antigens expression status and clinical outcomes in the retrospective retrospective prostate cancer cohort, with sub-analysis by disease state (CSPC vs. CRPC).

Measure: Hazard Ratios (HR) for Metastasis-free Survival (MFS) and (for CSPC sub-group) Biochemical Recurrence-free Survival (BFS).
From date of radical prostatectomy until biochemical recurrence, metastasis, or death, assessed up to 10 years

Inne miary wyników

Miara wyniku
Opis środka
Ramy czasowe
Co-expression and Complementary Expression Patterns of ADC Targets
Ramy czasowe: Baseline
Exploration of co-expression patterns among the 15 tumor-associated antigens and their correlation with clinicopathological features. Characterization of molecular subtypes based on expression profiles of key markers (e.g., AR, Syn, etc.) across different anatomic sites and disease states
Baseline

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Peking University First Hospital

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

1 stycznia 2026

Zakończenie podstawowe (Szacowany)

1 stycznia 2029

Ukończenie studiów (Szacowany)

1 stycznia 2029

Daty rejestracji na studia

Pierwszy przesłany

13 maja 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

13 maja 2026

Pierwszy wysłany (Rzeczywisty)

19 maja 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

19 maja 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

13 maja 2026

Ostatnia weryfikacja

1 stycznia 2026

Więcej informacji

Terminy związane z tym badaniem

Słowa kluczowe

Dodatkowe istotne warunki MeSH

Inne numery identyfikacyjne badania

  • 2022CR16

Plan dla danych uczestnika indywidualnego (IPD)

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Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

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Badania kliniczne na Immunohistochemistry (IHC) Staining and Analysis

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