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Lenalidomide Maintenance Therapy in Stage IIIB/IV Non-small Cell Lung Cancer

16. Januar 2018 aktualisiert von: Jun Zhang

A Pilot Study of Lenalidomide Maintenance Therapy in Stage IIIB/IV Non-small Cell Lung Cancer After First-line Chemotherapy

The purpose of this study is to investigate the safety and efficacy of maintenance therapy with daily low dose lenalidomide in patients with stage IIIB/IV non-small cell lung cancer (NSCLC) after first line chemotherapy. Investigators expect this treatment approach will delay disease progression by boosting the patient's anti-tumor immune response. Investigators hypothesize that 10 mg/day of lenalidomide can be administered safely as maintenance therapy and improve progression free survival time.

Studienübersicht

Status

Beendet

Intervention / Behandlung

Detaillierte Beschreibung

For patients with stage IIIB/IV non-small cell lung cancer, who did not progress after first line chemotherapy, lenalidomide 10mg/day orally will be administered as maintenance therapy until disease progression or death.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

7

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

    • Texas
      • Houston, Texas, Vereinigte Staaten, 77030
        • Baylor College of Medicine

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 und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Patients must have histologically or cytologically confirmed stage IIIB or stage IV NSCLC with measurable disease at initial presentation prior to chemotherapy. See Section 8.4.1 for measurable disease parameters.
  • Patients must have had a complete response (CR), partial response (PR) or stable disease (SD) after 4-6 cycles of first-line chemotherapy. Tumor response will be assessed by RECIST criteria version 1.1.
  • Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, or radiotherapy before entering this study.

    1. Myelosuppressive chemotherapy: At least 21 days elapsed from end of treatment before registration (42 days if prior nitrosourea).
    2. Hematopoietic growth factors: At least 7 days since the completion of therapy with a growth factor.
    3. Other: For agents that have known adverse events occurring beyond 7 days after administration, this period must be extended beyond the time during which adverse events are known to occur.
    4. XRT: > or = to 2 weeks for local palliative XRT (small port); 3 months must have elapsed if 50% radiation of pelvis; 6 weeks must have elapsed if other substantial bone marrow radiation.
  • Patients must be > or = 18 years of age.
  • ECOG performance status < or = to 1 (Karnofsky > 70%).
  • Organ Functions: Patients must have normal organ and marrow function as defined below within 28 days of registration:

    1. Leukocytes > or = 3,000/uL
    2. Absolute neutrophil count > or = 1,500/uL
    3. Hemoglobin > or = 8 g/dL
    4. Platelets > or = 100,000/uL
    5. Total bilirubin 1.5X institutional upper limit of normal (ULN)
    6. AST (SGOT) and ALT (SGPT) 1.5X institutional ULN
    7. Creatinine clearance > or = 60 mL/min/1.73 m2 for patients with creatinine levels > institutional normal
  • All study participants must be willing and agree to be registered into the mandatory REVLIMID REMS program, and be willing and able to comply with the requirements of REVLIMID REM. REVLIMID REMS registration does not need to be complete to determine study eligibility.
  • Females of childbearing potential (FCBP)* must have a negative serum or urine pregnancy test with a sensitivity of at least 50 mIU/mL within 10 - 14 days before registration. Treating investigator must affirm intention to perform another serum or urine UPT 24 hours before initiating lenalidomide treatment.

    *FCBP: A female of childbearing potential (FCBP) is a sexually mature female who: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months).

  • All patients must be counseled about pregnancy precautions, risks of fetal exposure and other risks. The counseling must be done before the initiation of the study and every 28 days before the study drug is dispensed to the subject. FCBP must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable methods of birth control, one highly effective method and one additional effective method AT THE SAME TIME, at least 28 days before she starts taking lenalidomide. FCBP must also agree to ongoing pregnancy testing. Men must agree to use a latex condom during sexual contact with a FCBP even if they have had a successful vasectomy. See Appendix D: Risks of Fetal Exposure, Pregnancy Testing Guidelines and Acceptable Birth Control Methods.
  • Able to take aspirin (81 mg) daily as prophylactic anticoagulation (Patients intolerant to ASA may use warfarin or low molecular weight heparin).
  • Able to understand and willing to sign a written informed consent document.
  • Life expectancy > or = 12 weeks

Exclusion Criteria

  • Concomitant Medications:

    1. Patients may not be receiving any other anti-cancer therapy.
    2. Patients may not be receiving any other investigational agents.
    3. Patients may not be receiving systemic steroids or other immunosuppressive drugs; however, steroid containing inhaler may be allowed after discussing with the Principal Investigator. Duration of 5 half-lives must have elapsed before the study registration if the patient was on systemic steroids or other immunosuppressive drugs.
  • Patients with untreated brain metastasis, or with treated brain metastasis but requiring steroids.
  • Patients with known EGFR mutation or EML-ALK fusion gene and with stage IV disease.
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to lenalidomide or thalidomide.
  • The development of erythema nodosum if characterized by a desquamating rash while taking thalidomide or similar drugs.
  • Uncontrolled inter-current illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, myocardial infarction within the last 6 months, unstable angina pectoris, cardiac arrhythmia, autoimmune disease or psychiatric illness/social situations that would limit compliance with study requirements.
  • Pregnant or breastfeeding women are excluded from this study because lenalidomide has the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with lenalidomide, breastfeeding should be discontinued if the mother is treated with lenalidomide.
  • Known sera-positive for or active viral infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV) or hepatitis C virus (HCV). Patients who are seropositive because of hepatitis B virus vaccine are eligible.
  • Any other clinically significant medical condition and/or organ dysfunction that will interfere with the administration of the therapy according to this protocol or which, in the views of investigator, preclude combination chemotherapy.

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: Lenalidomide
Oral lenalidomide 10 mg daily until disease progression
lenalidomide 10mg/day orally until disease progression
Andere Namen:
  • Revlimid

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Progression free survival
Zeitfenster: up to 6 months from the date of registration
Progression free survival is defined as the duration of time from the date starting lenalidomide to the date of documented radiographic progression or death.
up to 6 months from the date of registration

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Number of participants with adverse events
Zeitfenster: From date of registration to end of study, up to 3 years
From date of registration to end of study, up to 3 years
Change in circulating immune cells
Zeitfenster: Change from baseline at 1 week
Change from baseline at 1 week
Change in circulating immune cells
Zeitfenster: Change from baseline at 5 weeks
Change from baseline at 5 weeks
Change in circulating immune cells
Zeitfenster: Change from baseline at 9 weeks
Change from baseline at 9 weeks
Change in circulating immune cells
Zeitfenster: Change from baseline at 13, 17, 21 and 25 weeks
Change from baseline at 13, 17, 21 and 25 weeks
Change in circulating immune cells
Zeitfenster: Change from baseline to 6 months, 9 months and 1 year
Change from baseline to 6 months, 9 months and 1 year
Change in circulating immune cells
Zeitfenster: Change from baseline to 1.5, 2, 2.5 and 3 years
Change from baseline to 1.5, 2, 2.5 and 3 years

Mitarbeiter und Ermittler

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

Sponsor

Ermittler

  • Hauptermittler: Jun Zhang, M.D., Baylor College of Medicine

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Allgemeine Veröffentlichungen

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

1. Juni 2014

Primärer Abschluss (Tatsächlich)

1. August 2016

Studienabschluss (Tatsächlich)

1. August 2016

Studienanmeldedaten

Zuerst eingereicht

17. Dezember 2013

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

17. Dezember 2013

Zuerst gepostet (Schätzen)

23. Dezember 2013

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

18. Januar 2018

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

16. Januar 2018

Zuletzt verifiziert

1. Januar 2018

Mehr Informationen

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