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Hydroxychloroquine and Temsirolimus in Treating Patients With Metastatic Solid Tumors That Have Not Responded to Treatment
A Phase I Trial of Hydroxychloroquine in Combination With Temsirolimus in Patients With Refractory Solid Tumors
RATIONALE: Drugs used in chemotherapy, such as hydroxychloroquine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Temsirolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving hydroxychloroquine together with temsirolimus may kill more tumor cells.
PURPOSE: This phase I trial is studying the side effects and best dose of hydroxychloroquine when given together with temsirolimus in treating patients with metastatic solid tumors that have not responded to treatment.
Studie Overzicht
Toestand
Interventie / Behandeling
- Ander: farmacologische studie
- Ander: analyse van biomarkers in het laboratorium
- Ander: hogedrukvloeistofchromatografie
- Ander: massaspectrometrie
- Ander: immunologische techniek
- Geneesmiddel: hydroxychloroquine
- Ander: elektronenmicroscopie
- Geneesmiddel: temsirolimus
- Procedure: autophagy inhibition therapy
Gedetailleerde beschrijving
OBJECTIVES:
Primary
- Determine the maximum tolerated dose of hydroxychloroquine (HCQ) in combination with temsirolimus (TEM) in patients with metastatic refractory solid tumors.
Secondary
- Describe the toxicity of this regimen in these patients.
- Measure the response rate in patients treated with this regimen.
Tertiary
- Establish a population pharmacokinetic (PK) model for HCQ and its metabolites in combination with TEM.
- Use the population PK model to estimate the exposure of HCQ in individual patients.
- Compare PK parameters for this regimen to data from published single agent studies.
- Measure the change in median number of autophagic vesicles/cell in peripheral blood mononuclear cells with TEM alone and with TEM and HCQ and correlate these changes with HCQ exposure.
OUTLINE: This is a dose-escalation study of hydroxychloroquine.
Patients receive temsirolimus IV over 30 minutes once a week beginning in week 1 and oral hydroxychloroquine twice daily beginning in week 2. Courses repeat every 8 weeks in the absence of disease progression or unacceptable toxicity.
Blood samples are collected at baseline and periodically during study for pharmacokinetic and pharmacodynamic studies and measurement of autophagy inhibition. Samples are analyzed via HPLC and tandem mass spectrometry, immunoblotting assays, and electron microscopy.
Studietype
Inschrijving (Verwacht)
Fase
- Fase 1
Contacten en locaties
Studie Locaties
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Pennsylvania
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Philadelphia, Pennsylvania, Verenigde Staten, 19104-4283
- Abramson Cancer Center of the University of Pennsylvania
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
DISEASE CHARACTERISTICS:
Histologically confirmed refractory solid tumor for which no curative standard therapy exists
- Metastatic disease
Treated brain metastases that have been stable ≥ 3 months allowed
- At least 1 week since prior steroids
PATIENT CHARACTERISTICS:
- ECOG performance status of 0-1
- ANC ≥ 1,500/mm^3
- Platelet count ≥ 100,000/mm^3
- Creatinine ≤ 2 times upper limit of normal (ULN)
- ALT and AST ≤ 5 times ULN
- Total bilirubin ≤ 1.5 mg/dL
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- No serious concurrent infection or medical illness that would jeopardize the ability of the patient to receive the treatment outlined in this protocol with reasonable safety
No prior or other concurrent malignancy except for curatively treated carcinoma-in-situ at any site or basal cell carcinoma or squamous cell carcinoma of the skin
- Patients who have been free of disease (any prior malignancy) for ≥ 5 years are eligible
- No porphyria
- No psoriasis, except well controlled psoriasis under the care of a specialist
- No previously documented macular degeneration or diabetic retinopathy
- No HIV positivity
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- Any number and type of prior anticancer therapies allowed
- No prior mTOR inhibitors
- At least 4 weeks since prior immunotherapy (i.e., aldesleukin, interferon, CTLA-4) or chemotherapy and recovered
- At least 2 weeks since prior oral targeted therapy and recovered
- At least 4 weeks since prior and no other concurrent investigational anticancer therapy (except for vaccines)
- No other concurrent therapy
- No concurrent combination antiretroviral therapy for HIV-positive patients
- No concurrent cytochrome P450 enzyme-inducing anticonvulsant drugs (i.e., phenytoin, carbamazepine, phenobarbital, primidone, or oxcarbazepine)
- Concurrent non-enzyme inducing anticonvulsants, including felbamate, valproic acid, gabapentin, lamotrigine, tiagabine, topiramate, zonisamide, or levetiracetam allowed
- Concurrent hematologic growth factors (filgrastim [G-CSF], pegfilgrastim, epoetin alfa) allowed in patients with severe myelosuppression
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
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Maximum tolerated dose of hydroxychloroquine
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Secundaire uitkomstmaten
Uitkomstmaat |
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Responspercentage
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Toxicity rate as assessed by NCI CTCAE v. 3.0
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Pharmacokinetic and pharmacodynamic correlative endpoints
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Medewerkers en onderzoekers
Medewerkers
Onderzoekers
- Hoofdonderzoeker: Ravi Amaravadi, MD, Abramson Cancer Center of the University of Pennsylvania
Studie record data
Bestudeer belangrijke data
Studie start
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Neoplasmata
- Fysiologische effecten van medicijnen
- Moleculaire mechanismen van farmacologische werking
- Anti-infectieuze middelen
- Enzymremmers
- Antireumatische middelen
- Antineoplastische middelen
- Immunosuppressieve middelen
- Immunologische factoren
- Antibacteriële middelen
- Antibiotica, antineoplastiek
- Antischimmelmiddelen
- Antiprotozoaire middelen
- Antiparasitaire middelen
- Antimalariamiddelen
- Sirolimus
- Hydroxychloroquine
Andere studie-ID-nummers
- CDR0000643294
- UPCC-08908
- 807931
- WYETH-C-UPCC-03809
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