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Fase II Palbociclib + Ibrutinib i mantelcellelymfom

1. oktober 2026 oppdatert av: Alliance Foundation Trials, LLC.

En fase II-studie av Palbociclib (PD-0332991) i kombinasjon med Ibrutinib hos pasienter med tidligere behandlet mantelcellelymfom

The proposed study is a single-arm, multi-center, open-label phase II study of the combination of palbociclib and ibrutinib in patients with previously treated mantle cell lymphoma to evaluate the efficacy of this combination, with the primary objective of the study being to assess median PFS and the secondary objectives to include ORR, CR, DOR, OS and toxicity. Subjects will be enrolled and treated with palbociclib and ibrutinib with each cycle of therapy being 28 days. Treatment will be based on the recommended phase II dose (RP2D) from the phase I combination trial.

Studieoversikt

Status

Aktiv, ikke rekrutterende

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

Treatment will consist of:

  • Palbociclib administered at 100 mg oral once daily for 21 days on followed by 7 days off
  • Ibrutinib administered at 560 mg oral continuously

Patients will continue to receive study drugs until disease progression, unacceptable toxicity, or withdrawal of consent. If at any time one of the agents is held due to toxicity, the other agent may be continued in those patients who are receiving clinical benefit.

Response will be assessed by PET/CT and/or CT every 3 cycles while on therapy for the first year and then every 6 cycles thereafter until disease progression or at the investigator's discretion if otherwise medically indicated. A PET will be required to confirm CR. A bone marrow biopsy will be performed in patients with bone marrow involvement at the start of therapy to confirm complete response once patients have otherwise met criteria for CR.

Studietype

Intervensjonell

Registrering (Faktiske)

39

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • California
      • Duarte, California, Forente stater, 91010
        • City of Hope National Medical Center
    • Maryland
      • Baltimore, Maryland, Forente stater, 21201
        • University of Maryland, Greenebaum Comprehensive Cancer Center
    • Massachusetts
      • Boston, Massachusetts, Forente stater, 02114
        • Massachusetts General Hospital
    • Michigan
      • Ypsilanti, Michigan, Forente stater, 48197
        • St. Joseph Mercy Hospital Cancer Care Center
    • New York
      • Buffalo, New York, Forente stater, 14263
        • Roswell Park Comprehensive Cancer Center
      • New York, New York, Forente stater, 10065
        • Weill Cornell Medical College
    • North Carolina
      • Chapel Hill, North Carolina, Forente stater, 27599
        • University of North Carolina
    • Ohio
      • Columbus, Ohio, Forente stater, 43210
        • Ohio State University
    • South Carolina
      • Charleston, South Carolina, Forente stater, 29425
        • Medical University of South Carolina - Hollings Cancer Center

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  1. Subjects must have histologically or cytologically confirmed MCL as defined by the World Health Organization. All patients must have either t(11;14) by karyotype or fluorescent in-situ hybridization (FISH) or positive immunohistochemistry (IHC) for cyclin D1.

  2. Subjects must have measurable disease defined as at least one tumor lesion of at least 1.5 cm by CT or MRI, PET positive lesion(s) or a peripheral blood CD5+, CD19+ lymphocyte count of at least 5,000 cells/µL.

  3. Subjects must have received at least one prior systemic therapy.

  4. Subjects who have received prior autologous stem cell transplant are eligible. Patients that have undergone prior allogeneic stem cell transplant will only be eligible if the patient is no longer taking immunosuppressive therapy and there are no significant ongoing transplant-related adverse effects.

  5. Subjects must be age ≥ 18 years

  6. ECOG performance status ≤ 2

  7. Patients must have normal organ and marrow function as defined below:

  8. Laboratory Values:

    • ANC ≥ 1000 cells/μL, unless bone marrow involvement in MCL, then ANC >500 cells/μL;
    • Platelets ≥ 75,000 cells/μL, unless bone marrow involvement in MCL, then platelets >30,000 cells/μL;
    • Calculated creatinine clearance ≥30mL/min;
    • AST or ALT ≤ 2.5x ULN;
    • Total bilirubin ≤ 1.5x ULN;
    • QTc ≤ 480 ms
  9. Subjects must be able to provide written, informed consent

  10. Subjects must have recovered from adverse events to ≤ grade 1 from prior therapies

  11. Subjects must be able and willing to swallow and retain oral medication without a condition that would interfere with enteric absorption

  12. Subjects may be receiving prednisone at a maximum dose of 20 mg orally daily for symptom control.

  13. Serum or urine pregnancy test must be negative within 7 days of starting study treatment in women of childbearing potential. Women of childbearing potential and men with female partners who are able to become pregnant are required to use a highly effective form of barrier contraception for the duration of the study and for 90 days after the last dose of study drug. Adequate contraception is defined as abstinence or two forms non hormonal contraception, which is a combination of two forms of the following:

    • Condom with spermicidal foam/gel/cream/suppository
    • occlusive cap (diaphragm or cervical vault caps) with spermicidal
    • non hormonal intrauterine device (IVD)
  14. No evidence of active hepatitis B or C infections (i.e., no positive serology for anti-HBc or anti-HCV antibodies)

  15. HBV seropositive patients (HBsAg +) are eligible if they are closely monitored for evidence of active HBV infection by HBV DNA testing and receive suppressive therapy with lamivudine or other HBV suppressive therapy until 6 months after the last rituximab dose.

  16. Patients with HIV infection are eligible, provided they meet the following:

    • No evidence of coinfection with hepatitis B or C
    • CD4+ cell count ≥ 400/mm3
    • No evidence of resistant strains of HIV
    • If not on anti-HIV therapy, HIV viral load < 10,000 copies HIV RNA/mL If on anti-HIV therapy, HIV viral load < 50 copies HIV RNA/mL
    • No history of AIDS-defining conditions
    • No use of strong CYP3A4/5 inhibitors or inducers

Exclusion Criteria:

  1. Subjects that have received prior CDK4/6 inhibitor will not be eligible.
  2. Subjects that have received any prior BTK inhibitor > 90 days prior to enrollment will not be eligible.
  3. Subjects with known or suspected CNS involvement.
  4. Concurrent therapy with other investigational products.
  5. History of allergic reactions attributed to compounds of chemical or biologic composition similar to palbociclib.
  6. Subjects receiving any medications or substances that are strong or moderate inhibitors or strong inducers of CYP3A isoenzymes within 7 days of starting study treatment (See Appendix II).
  7. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, diabetes, or psychiatric illness/social situations that would limit compliance with study requirements.
  8. Subjects with myocardial infarction within 6 months prior to enrollment or has New York Heart Association (NYHA) Class III or IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities are not eligible. Prior to study entry, any ECG abnormality at screening has to be documented by the investigator as not medically relevant.
  9. Pregnant women, or women of childbearing potential without a negative pregnancy test (serum or urine) within 7 days prior to registration, irrespective of the method of contraception used, are excluded from this study because the effect of palbociclib on a developing fetus is unknown. Breastfeeding should be discontinued prior to study entry.
  10. Subjects must agree to use barrier contraceptive methods throughout the study period up until at least 90 days post last palbociclib dose.
  11. Subjects with clinically significant history of liver disease, including viral or other known hepatitis, current alcohol abuse, or cirrhosis, etc.
  12. Subjects with another active malignancy that limits survival.
  13. Subjects with a bleeding diathesis are not eligible.
  14. Subjects with transfusion-dependent thrombocytopenia are not eligible.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Single Arm

All patients will receive palbociclib at 100 mg oral once a day for 21 days, followed by 7 days off.

Ibrutinib will be administered at 560 mg oral continuously.

Taken at 100 mg once daily for 21 days, followed by 7 days off

Andre navn:
  • Ibrance; PD-0332991

560 mg taken orally all patients throughout the study

Andre navn:
  • Imbruvica

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Progression free survival
Tidsramme: 42 months

Time interval between registration and progression or death

42 months

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Overall survival
Tidsramme: 42 months

time from registration to death due to any cause

42 months
Duration of response
Tidsramme: 42 months

Time from documentation of tumor response to disease progression

42 months
Overall Response Rate
Tidsramme: 42 Months

Proportion of patients with reduction in tumor burden of a predefined amount

42 Months
Complete Response
Tidsramme: 42 Months

Disappearance of all non-target lesions and normalization of tumor marker level

42 Months
Toxicity: Incidence and severity of adverse events by summaries of toxicity data/contingency tables
Tidsramme: 42 Months

Evaluation of incidence and severity of adverse events by summaries of toxicity data/contingency tables

42 Months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Samarbeidspartnere

Etterforskere

  • Studiestol: Kami Maddocks, MD, Ohio State University
  • Hovedetterforsker: Evanthia Galanis, MD, Alliance Foundation Trials, LLC.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

11. september 2018

Primær fullføring (Faktiske)

19. desember 2025

Studiet fullført (Antatt)

30. juli 2027

Datoer for studieregistrering

Først innsendt

21. mars 2018

Først innsendt som oppfylte QC-kriteriene

26. mars 2018

Først lagt ut (Faktiske)

27. mars 2018

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

2. oktober 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

1. oktober 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • AFT-32

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

UBESLUTTE

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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