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Gentherapie und Kombinationschemotherapie bei der Behandlung von Patienten mit AIDS-assoziiertem Non-Hodgkin-Lymphom

30. September 2026 aktualisiert von: City of Hope Medical Center

Sicherheit und Durchführbarkeit des Gentransfers von Stammzellen nach R-EPOCH für Non-Hodgkin-Lymphom bei AIDS-Patienten unter Verwendung von peripheren Blutstamm-/Vorläuferzellen, die mit einem Lentivirus-Vektor behandelt wurden, der mehrere Anti-HIV-RNAs codiert

This pilot clinical trial studies gene therapy following combination chemotherapy in treating patients with acquired immune deficiency syndrome (AIDS)-related non-Hodgkin lymphoma. Placing genes that have been shown in the laboratory to inhibit the growth and spread of the immunodeficiency virus (HIV) into the patient's peripheral blood stem cells may improve the body's ability to fight HIV. Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving gene therapy after combination chemotherapy may improve the body's ability to fight HIV and AIDS-related non-Hodgkin lymphoma.

Studienübersicht

Status

Aktiv, nicht rekrutierend

Bedingungen

Intervention / Behandlung

Detaillierte Beschreibung

PRIMARY OBJECTIVE:

I. To demonstrate the safety and feasibility of rHIV7-shI-TAR-CCR5RZ-treated hematopoietic stem progenitor cells (HSPC) (lentivirus vector rHIV7-shI-TAR-CCR5RZ-transduced hematopoietic progenitor cells) transplantation in AIDS patients completing treatment for non-Hodgkin lymphoma (NHL).

SECONDARY OBJECTIVES:

I. To determine the effect of HIV infection on the presence of gene-marked blood cells as measured by woodchuck post-transcriptional regulatory element (WPRE) deoxyribonucleic acid (DNA) polymerase chain reaction (PCR) performed before, during, and after ATI.

II. To demonstrate the engraftment of gene-modified progeny cells following such treatment.

III. To determine if selection of these gene-modified progeny cells occurs during analytical treatment interruption (ATI) of combination anti-retroviral therapy (cART).

OUTLINE:

Patients receive prednisone orally (PO) twice daily (BID) on days 1-5; rituximab intravenously (IV) on day 1; etoposide, doxorubicin hydrochloride and vincristine sulfate IV over 96 hours on days 1-4; and cyclophosphamide IV over 30-60 minutes on day 5. Patients then receive filgrastim subcutaneously (SC) once daily (QD) beginning on day 6 and continuing until absolute neutrophil count recovers. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity.

Patients then receive lentivirus vector rHIV7-shI-TAR-CCR5RZ-transduced hematopoietic stem/progenitor cells IV on day 0 (48 hours after the final combination chemotherapy course).

After completion of study treatment, patients are followed up at 1, 2, 3, 6, 9, 12, 18, and 24 months, every 6 months for 3 years, and then annually for 10 years.

Studientyp

Interventionell

Einschreibung (Geschätzt)

10

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Maryland
      • Bethesda, Maryland, Vereinigte Staaten, 20892
        • NCI Lymphoid Malignancies Branch

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre bis 65 Jahre (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • HIV seropositive at or before the time of lymphoma diagnosis; all HIV positive patients are eligible regardless of HIV viral load or antiviral therapy (ART) status; all patients on study will receive ART as per standard guidelines
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 - 2
  • Biopsy proven lymphoma for which rituximab, etoposide, prednisone, vincristine sulfate, cyclophosphamide, and doxorubicin hydrochloride (R-EPOCH) is appropriate frontline therapy, e.g., Burkitt lymphoma or diffuse large B-cell lymphoma (DLBCL) NHL, including plasmablastic lymphoma and primary effusion lymphoma but not T-cell lymphoma; tissue histology will be reviewed at the treating institution
  • No psychosocial conditions that would hinder study compliance and follow-up
  • Pretreatment serum glutamic oxaloacetic transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT) =< 2.5 x institutional upper limit of normal (ULN)
  • Pretreatment serum bilirubin =< 2.5 x ULN or total bilirubin < 4.5 mg/dl with direct fraction =< 0.3 mg/dl in patients for whom these abnormalities are felt to be due to protease inhibitor therapy
  • Patients with evidence of hepatitis C virus (HCV) or hepatitis B virus (HBV) infection must have no clinical evidence of cirrhosis
  • Serum creatinine < 2 x the institutional ULN; however, if serum creatinine > 1.5 x ULN, a 24 hour urine creatinine clearance must be > 50 ml/min unless there is renal involvement by lymphoma
  • Absence of clinically significant cardiomyopathy, congestive heart failure
  • If the subject is female and of child bearing potential, subject must have negative serum or urine pregnancy test within 7 days of treatment with research agent; men with partners of child-bearing potential and women of child-bearing potential must be willing to use medically effective birth control methods, e.g. contraceptive pill, condom, or diaphragm and continue this for one year post HSPC infusion
  • Subjects must be on a prophylactic regimen for Pneumocystis carinii pneumonia, or agree to begin such treatment and remain on treatment until after completion of therapy and until the cluster of differentiation (CD)4 cells are greater than 200/mm^3
  • Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control or abstinence) prior to study entry and for 12 months following stem cell infusion; should a woman become pregnant or suspect that she is pregnant while participating on the trial, she should inform her treating physician immediately
  • All subjects must have the ability to understand and the willingness to sign a written informed consent

ELIGIBILITY CRITERIA FOR HSPC TRANSPLANTATION

  • Patients must demonstrate >= 75% disease reduction on computed tomography (CT) scan (confirmed by PET scan) after the third cycle of R-EPOCH relative to baseline, with no evidence of disease progression after the fifth cycle
  • Subjects must complete the filgrastim (G-CSF)/plerixafor mobilization of peripheral blood progenitor cells, and subjects must have collected at least 5 x 10^6 CD34+ cells/kg by apheresis after Cycle 4

Exclusion Criteria:

  • Any AIDS-related opportunistic infection occurring within the past year and for which treatment has been unsuccessful would be considered exclusionary, but this is done on a case-by-case basis as determined by the principal investigator (PI)

  • Active cytomegalovirus (CMV) retinitis or other active CMV-related organ dysfunction; patients with a history of treated CMV infection are not excluded

  • AIDS-related syndromes, infectious or otherwise, if perceived to cause excessive risk for morbidity post-HSPC infusion, as determined by the PI; examples include, but not limited to:

    • Severe AIDS-related wasting
    • Severe intractable diarrhea
    • Active inadequately treated opportunistic infection of the central nervous system (CNS)
    • Primary CNS lymphoma
  • Pregnant or nursing women

  • Any history of HIV-associated encephalopathy; dementia of any kind; seizures in the past 12 months

  • Any perceived inability to directly provide informed consent (note: consent may not be obtained by means of a legal guardian)

  • Any medical or physical contraindication or other inability to undergo HSPC collection

  • Patients should not have any uncontrolled illness including ongoing or active infection other than HIV

  • Patients may not be receiving any other investigational agents, or concurrent biological, chemotherapy, or radiation therapy

  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to G-CSF/filgrastim (E. coli producing cell line) and plerixafor

  • Patients with other active malignancies; however, patients with skin cancers, namely basal cell or squamous cell carcinoma, and malignancies treated with curative intent having no known active disease present for >= 2 years, may be eligible

  • Subjects, who in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Treatment (R-EPOCH, rHIV7-shI-TAR-CCR5RZ-transduced HSPC)

Patients receive prednisone PO BID on days 1-5; rituximab IV on day 1; etoposide IV over 96 hours, doxorubicin hydrochloride IV over 96 hours and vincristine sulfate IV over 96 hours on days 1-4; and cyclophosphamide IV over 30-60 minutes on day 5. Patients then receive filgrastim SC QD beginning on day 6 and continuing until absolute neutrophil count recovers. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity.

Patients then receive lentivirus vector rHIV7-shI-TAR-CCR5RZ-transduced hematopoietic stem/progenitor cells IV on day 0 (48 hours after the final combination chemotherapy course.)

Given IV

Given IV

Andere Namen:
  • Adriamycin

Given PO

Given IV

Andere Namen:
  • MOAB IDEC-C2B8

Given IV

Andere Namen:
  • Videorecorder
  • Oncovin
  • Kyokristin
  • Vincasar

Given IV

Andere Namen:
  • Lastet
  • VP 16

Given SC

Andere Namen:
  • G-CSF
  • r-metHuG-CSF
  • Neupogen
  • Nivestim

Given IV

Andere Namen:
  • Lentivirus-transduzierte hämatopoetische Vorläuferzellen

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Fähigkeit, eine geeignete Anzahl von mit lentiviralen Vektoren behandelten HSPC zu erhalten, wie durch die Zellzahl bestimmt
Zeitfenster: Bis Tag -2 (vor der Infusion)
Bis Tag -2 (vor der Infusion)
Vorhandensein von Transgen im peripheren Blut durch digitale Tröpfchen-PCR
Zeitfenster: Bis zu 2 Jahre
Bis zu 2 Jahre
Incidence of adverse events related to R-EPOCH, graded using the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 4.03
Zeitfenster: Up to 2 years after completion of treatment

Tables will be created to summarize these toxicities and side effects by dose and by course.

Up to 2 years after completion of treatment
Incidence of adverse events related to lentivirus vector rHIV7-shI-TAR-CCR5RZ-transduced hematopoietic stem/progenitor cells infusion, graded using the NCI CTCAE version 4.03
Zeitfenster: Up to 2 years

All toxicities, related and unrelated, observed after each stem cell infusion will be summarized in terms of type (organ affected or laboratory determination such as absolute neutrophil count), severity (by NCI CTCAE and nadir or maximum values for the laboratory measures), time of onset (i.e. course number), duration, and reversibility or outcome. Tables will be created to summarize these toxicities and side effects by dose and by course.

Up to 2 years

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Transgene Ribonukleinsäure-Expression durch Northern Blotting/Hybridisierung und quantitativen Echtzeit-PCR-Assay
Zeitfenster: Bis zu 15 Jahre
Bis zu 15 Jahre
HIV-Reservoir, bestimmt durch HIV-1-Reverse Transkriptase (RT)-PCR, DNA-PCR und DNA-2-Long-Terminal-Repeat-Circle-PCR
Zeitfenster: Bis 15 Jahre und während ATI
Bis 15 Jahre und während ATI
Vektortransgensequenzen in peripheren mononukleären Blutzellen
Zeitfenster: Bis 2 Jahre, evtl. bis 15 Jahre
Bis 2 Jahre, evtl. bis 15 Jahre
Veränderung von shI-TAR-CCR5RZ-markierten Zellen im Knochenmark
Zeitfenster: Baseline bis zu 18 Monate
Baseline bis zu 18 Monate
HIV integration analysis by number of reads and loci
Zeitfenster: Up to 15 years

Integration analyses will be done at month 6 and 12, and at week 16 of ATI, and at times when there is a clinical syndrome that suggests clonal expansion of hematopoietic cells.

Up to 15 years

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Mitarbeiter

Ermittler

  • Hauptermittler: Mark J. Roschewski, MD, NCI Lymphoid Malignancy Branch
  • Hauptermittler: Amrita Krishnan, MD, City of Hope Medical Center

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

20. November 2015

Primärer Abschluss (Geschätzt)

9. August 2027

Studienabschluss (Geschätzt)

9. August 2027

Studienanmeldedaten

Zuerst eingereicht

23. Dezember 2014

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

9. Januar 2015

Zuerst gepostet (Geschätzt)

14. Januar 2015

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

1. Oktober 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

30. September 2026

Zuletzt verifiziert

1. September 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Zusätzliche relevante MeSH-Bedingungen

Andere Studien-ID-Nummern

  • 14004
  • NCI-2014-02416 (Registrierungskennung: CTRP (Clinical Trial Reporting Program))
  • U01CA183012 (US NIH Stipendium/Vertrag)
  • 14004 (Andere Kennung: City of Hope Medical Center)

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