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Lifileucel (TIL) Therapy After PD-1 Blockade Failure in Kidney Cancer

3 listopada 2026 zaktualizowane przez: David J. Einstein, Beth Israel Deaconess Medical Center

A Phase II Trial of Autologous Ex Vivo Expanded Tumor-Infiltrating Lymphocyte (TIL) Therapy With Lifileucel After Failure of PD-1 Blockade in Kidney Cancer.

This study aims to evaluate autologous ex vivo expanded tumor-infiltrating lymphocyte therapy (lifileucel/LN-145) for kidney cancer after failure of PD-1 blockade.

Przegląd badań

Status

Jeszcze nie rekrutacja

Warunki

Interwencja / Leczenie

Szczegółowy opis

This is a Phase II single-arm trial of tumor-infiltrating lymphocyte (TIL) therapy in kidney cancer. Briefly, participants who meet eligibility criteria undergo surgical removal of a metastasis or primary tumor to provide material for generation of the TIL product in a lab, which involves growing and expanding the immune cells contained in the tumor before infusing the TIL product into the patient.

Baseline evaluations occur before tumor harvest, and participants who proceed on study undergo tumor resection so tissue can be shipped to a manufacturing facility to create the autologous TIL product LN-145/lifileucel. The treatment plan includes 5 days of lymphodepleting chemotherapy before TIL infusion, using cyclophosphamide and fludarabine, followed by LN-145 infusion on Day 0 and IL-2 (aldesleukin) afterward. The study calendar includes post-treatment visits around Day 14, Day 28, Weeks 8, 12, and 18, then every 3 months starting at Month 6, with long-term follow-up by telephone continuing until study end or withdrawal, up to Month 36. Participants undergo screening and tumor resection to obtain tissue for manufacture of the TIL product. If treatment proceeds, participants receive lymphodepleting chemotherapy with cyclophosphamide and fludarabine, followed by LN-145 infusion and IL-2 (aldesleukin). Participants complete scheduled clinic-based assessments and longer-term follow-up, including telephone follow-up approximately every 3 months for up to about 3 years

Typ studiów

Interwencyjne

Zapisy (Szacowany)

10

Faza

  • Faza 2

Kontakty i lokalizacje

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

Kontakt w sprawie studiów

Lokalizacje studiów

    • Massachusetts
      • Boston, Massachusetts, Stany Zjednoczone, 02115
      • Boston, Massachusetts, Stany Zjednoczone, 02115
      • Boston, Massachusetts, Stany Zjednoczone, 02115
        • Beth Israel Deaconess Medical Center (BIDMC)
        • Kontakt:

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

18 lat i starsze (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Tak

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

  • Histologically or cytologically confirmed, advanced or metastatic renal cell carcinoma with clear cell, papillary, sarcomatoid (with or without other subtypes present), or unclassified histology. Other non-clear cell subtypes are also eligible if the patient has had a prior documented response to immune checkpoint inhibitor therapy.

    • Participants must have measurable disease with at least two malignant lesions, one for disease monitoring as response to therapy and one for TIL harvest.
    • Age ≥18 years
    • Received one of the following regimens:
    • Anti-PD-(L)1 immune checkpoint inhibitor (ICI) with or without an anti-CTLA-4 ICI or VEGF tyrosine kinase inhibitor (TKI) for treatment of advanced/metastatic disease, and experienced either (1) radiographic progression of disease while on treatment or (2) best response of stable disease after at least 6 months
    • Adjuvant anti-PD-(L)1 ICI after nephrectomy for localized disease and had either (1) disease recurrence while receiving adjuvant ICI or (2) disease recurrence within 6 months of the final dose of any amount of adjuvant ICI
    • Prior HIF2α inhibitor exposure in the adjuvant or advanced/metastatic setting is allowed but not required
    • Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 and an estimated life expectancy of ≥ 3 months in the opinion of the Investigator.
    • Participants must have adequate organ and marrow function as defined in the protocol.
    • Patients with definitively treated brain metastases may be considered for enrollment if the patient is clinically stable for ≥ 14 days, with no lesions on follow-up imaging and no requirement for ongoing steroid treatment.
    • Participants must have a washout period from any anticancer therapy prior to tumor harvest. The protocol contains provisions for optional use of "bridging" TKI between tumor harvest and lymphodepleting chemotherapy.
    • Palliative radiation therapy is permitted as long as it does not involve lesions being selected for resection for TIL manufacturing, or being assessed radiographically as target lesions.
    • Participants must have recovered from all prior anti-cancer therapy-related adverse events (AEs), as defined in the protocol.
    • Participants of childbearing potential or those with partners of childbearing potential must be willing to practice an approved method of highly effective birth control.
    • Previous surgical procedure(s) is/are permitted provided that wound healing has occurred, all complications have resolved, and at least 14 days have elapsed (for major operative procedures) prior to the tumor resection.

Exclusion Criteria:

  • Patients who have received an organ allograft or prior cell transfer therapy within the past 20 years that included a non-myeloablative or myeloablative chemotherapy regimen.
  • Patients who have a history of hypersensitivity to any component of the study intervention.
  • Patients with rapidly progressive disease or symptomatic disease requiring urgent treatment per investigator discretion.
  • Patients with symptomatic and/or untreated brain metastases.
  • Patients who are on chronic systemic steroid therapy except for those requiring steroid therapy for management of adrenal insufficiency.
  • Patients who are pregnant or breastfeeding.
  • Patients who have any form of primary immunodeficiency (such as severe combined immunodeficiency disease [SCID] and acquired immunodeficiency syndrome [AIDS]).
  • Patients with any other primary malignancy that is radiographically visible or is expected to require treatment within the next three years.
  • Patients who are hypoxemic (oxygen saturation <90%) on room air at baseline or who require supplemental oxygen.

Other protocol-defined inclusion/exclusion criteria may apply.

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

  • Główny cel: Leczenie
  • Przydział: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Lifileucel (LN-145) TIL regimen

Participants undergo tumor resection for TIL manufacturing, then receive lymphodepleting cyclophosphamide and fludarabine, followed byLN-145/lifileucel infusion and IL-2 (aldesleukin), with scheduled post-treatment clinic visits and long-term follow-up

Part of the lymphodepleting chemotherapy given before LN-145 infusion

Part of the lymphodepleting chemotherapy given before LN-145 infusion.

Administered after LN-145 infusion as part of the treatment regimen.

Surgical removal of tumor tissue for TIL production/manufacture

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Radiographic Objective Response Rate
Ramy czasowe: Participants will be followed thought out the course of the trial for 3 years

HCC-centrally assessed Objective Response Rate per RECIST 1.1 of the efficacy evaluable population Primary analysis is performed on patients who receive TIL.

Participants will be followed thought out the course of the trial for 3 years

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Radiographic change in target lesions
Ramy czasowe: Participants will be followed thought out the course of the trial for 3 years

Longitudinal and best change in target lesion measurements. Target lesions are measured at baseline and followed per RECIST 1.1

Participants will be followed thought out the course of the trial for 3 years
Radiographic Disease Control Rate (SD + PR + CR)
Ramy czasowe: Participants will be followed thought out the course of the trial for 3 years

Disease control rate is listed as a secondary endpoint and will be summarized in the efficacy cohort.

Participants will be followed thought out the course of the trial for 3 years
Duration of response
Ramy czasowe: Participants will be followed thought out the course of the trial for 3 years

Duration of overall response is measured from the first time CR or PR criteria are met until the first date recurrent or progressive disease is objectively documented, or death due to any cause

Participants will be followed thought out the course of the trial for 3 years
Progression-free survival
Ramy czasowe: Participants will be followed thought out the course of the trial for 3 years

Progression-free survival is a listed secondary endpoint for both the efficacy evaluable population and the total population. Time-to-event variables are calculated from TIL infusion; PFS is also calculated for the total population from trial enrollment.

Participants will be followed thought out the course of the trial for 3 years
Toxicity per CTCAE v6.0
Ramy czasowe: Participants will be followed thought out the course of the trial for 3 years

Adverse events are graded using NCI Common Terminology Criteria for Adverse Events version 6.0.

Participants will be followed thought out the course of the trial for 3 years
Feasibility
Ramy czasowe: Assessed at time of TIL infusion (D0)

Feasibility is defined as the proportion of patients who successfully undergo tumor harvest, ex vivo TIL expansion, lymphodepletion, and TIL infusion, regardless of number of IL-2 doses given post-TIL.

Assessed at time of TIL infusion (D0)

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Sponsor

Współpracownicy

Śledczy

  • Główny śledczy: David Einstein, MD, Beth Israel Deaconess Medical Center

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 (Szacowany)

26 kwietnia 2027

Zakończenie podstawowe (Szacowany)

1 sierpnia 2029

Ukończenie studiów (Szacowany)

1 marca 2030

Daty rejestracji na studia

Pierwszy przesłany

28 października 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

3 listopada 2026

Pierwszy wysłany (Rzeczywisty)

9 listopada 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

9 listopada 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

3 listopada 2026

Ostatnia weryfikacja

1 listopada 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

TAK

Opis planu IPD

The Harvard Cancer Consortium encourages and supports the responsible and ethical sharing of data from clinical trials. De-identified participant data from the final research dataset used in the published manuscript may only be shared under the terms of a Data Use Agreement. Requests may be directed to: [contact information for Sponsor Investigator or designee]. The protocol and statistical analysis plan will be made available on Clinicaltrials.gov only as required by federal regulation or as a condition of awards and agreements supporting the research.

Typ informacji pomocniczych dotyczących udostępniania IPD

  • PROTOKÓŁ BADANIA
  • SOK ROŚLINNY

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Tak

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

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