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

16 januari 2018 bijgewerkt door: 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.

Studie Overzicht

Toestand

Beëindigd

Interventie / Behandeling

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

7

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Texas
      • Houston, Texas, Verenigde Staten, 77030
        • Baylor College of Medicine

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

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.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Lenalidomide
Oral lenalidomide 10 mg daily until disease progression
lenalidomide 10mg/day orally until disease progression
Andere namen:
  • Revlimid

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Progression free survival
Tijdsspanne: 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

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Number of participants with adverse events
Tijdsspanne: 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
Tijdsspanne: Change from baseline at 1 week
Change from baseline at 1 week
Change in circulating immune cells
Tijdsspanne: Change from baseline at 5 weeks
Change from baseline at 5 weeks
Change in circulating immune cells
Tijdsspanne: Change from baseline at 9 weeks
Change from baseline at 9 weeks
Change in circulating immune cells
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: Change from baseline to 1.5, 2, 2.5 and 3 years
Change from baseline to 1.5, 2, 2.5 and 3 years

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Onderzoekers

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

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Algemene publicaties

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 juni 2014

Primaire voltooiing (Werkelijk)

1 augustus 2016

Studie voltooiing (Werkelijk)

1 augustus 2016

Studieregistratiedata

Eerst ingediend

17 december 2013

Eerst ingediend dat voldeed aan de QC-criteria

17 december 2013

Eerst geplaatst (Schatting)

23 december 2013

Updates van studierecords

Laatste update geplaatst (Werkelijk)

18 januari 2018

Laatste update ingediend die voldeed aan QC-criteria

16 januari 2018

Laatst geverifieerd

1 januari 2018

Meer informatie

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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