Carcinoma, Non-Small-Cell Lung Clinical Trial
Official title:
Phase I Study of Sequential Depsipeptide/Flavopiridol Infusion for Malignancies Involving Lungs, Esophagus, Pleura, Thymus or Mediastinum
Verified date | May 20, 2013 |
Source | National Institutes of Health Clinical Center (CC) |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will test the safety and effectiveness of two experimental medicines -
depsipeptide and flavopiridol - given together to treat cancers of the lung, esophagus, and
pleura. It will determine the highest dose that these drugs can safely be given together and
will test whether giving them together works better at shrinking tumors than giving either
one alone.
Patients 18 years of age and older with cancer of the lung, esophagus, or pleura, or other
cancers that have spread to the lungs or pleura may be eligible for this study. Candidates
are screened with a medical history and physical examination, blood tests, electrocardiogram
(EKG), x-rays and scans, pulmonary function tests, and a tumor biopsy (removal of a small
piece of tumor tissue for microscopic examination).
Participants are admitted to the hospital for treatment for approximately 10 days during each
28-day treatment cycle. Depsipeptide is infused through an arm vein or central venous
catheter (tube placed in a large vein in the neck or chest) for 4 hours. When this infusion
is complete, flavopiridol is infused over 72 hours. The dose of depsipeptide is increased
four times over the period of the study with successive groups of patients, and flavopiridol
is increased once to determine the maximum safe dose of giving these drugs together.
Blood tests are done before and after each depsipeptide infusion and 3 more times for the
next 24 hours, and at various times over 4 days during the flavopiridol infusion to evaluate
the effects of the medicines. Samples are also drawn periodically throughout the treatment
cycle to evaluate safety. Heart function is monitored with several EKGs before and during the
depsipeptide doses. The drug has shown effects on EKG tracings, but does not appear to injure
the heart muscle.
Tumor biopsies are done before treatment begins and on the fifth day of the first treatment
cycle. The biopsies may be done either in the operating room by passing a tube (bronchoscope)
down the throat and into the lungs or in the Radiology Department using a thin needle put
through the chest wall into the tumor. For the bronchoscopy, numbing medicine is sprayed into
the back of the throat to reduce discomfort, and for the needle biopsy, the skin over the
biopsy area is numbed. Optional repeat biopsies may be requested before the start of the
second treatment cycle and on day 5 of that cycle. (The repeat biopsies are not required for
participation in the study.) At the time of each tumor biopsy, a buccal mucosal biopsy is
also done. This involves scraping a tongue depressor along the inside of the mouth to collect
cells for examination.
At the end of the first treatment cycle, patients return to NIH for evaluation with a
physical examination, blood work, x-rays, and scans of the chest, abdomen, pelvis, and brain.
Patients who are not experiencing significant drug side effects are offered a second cycle,
exactly like the first. The two cycles complete one course of treatment, after which patients
once again return to NIH for evaluation. Additional treatment cycles may be offered to
patients whose tumors have shrunk or remained stable with therapy. Patients whose tumors have
not responded to therapy or who have developed severe drug side effects are taken off the
study.
Status | Terminated |
Enrollment | 23 |
Est. completion date | May 20, 2013 |
Est. primary completion date | May 20, 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
- INCLUSION CRITERIA: 1. Patients with histologically or cytologically proven small cell or non-small cell lung cancers, esophageal cancers, malignant pleural mesotheliomas chest wall sarcoma, or epithelial thymomas are eligible for evaluation. In addition, patients with cancers of nonthoracic origin with metastases to the lungs, pleura or germ cell tumors refractory to standard therapy are eligible for evaluation. 2. Chemo naive patients with inoperable lung and esophageal cancers, pleural mesotheliomas, sarcoma, thymomas, as well as tumors of non-thoracic origin with metastasis within the thorax may be eligible for study provided they have been apprised of, and refused potentially effective first line chemotherapy. 3. Patients with intracranial metastases which have been treated by surgery or radiation therapy may be eligible for study provided there is no evidence of active disease and no requirement for anticonvulsant therapy or steroids. 4. Patients with prior Depsipeptide or Flavopiridol exposure are eligible for study provided they have not experienced dose limiting toxicity at the dose of DP or FLA that they are scheduled to receive. 5. Patients must have had no chemotherapy, biologic therapy, or radiation therapy for their malignancy for at least 30 days prior to treatment. At least six weeks must elapse between mitomycin C or nitrosourea treatment and DP/FLA therapy. Patients may have received localized radiation therapy to non-target lesions provided that the radiotherapy is completed 14 days prior to commencing therapy, and the patient has recovered from any toxicity. 6. Patients must have an ECOG performance status of 0 - 2. 7. Patients must have adequate pulmonary reserve evidenced by FEV1 and DLCO greater than the 30% predicted, and pCO2 less than 50 mm Hg and pO2 greater than 60 mm Hg on room air ABG. 8. Patients must be 18 years of age or older due to the unknown effects of HDAC inhibitors and cdk inhibitors during childhood and adolescent development. 9. Patients must have a platelet count greater than 100,000, an ANC equal to or greater than 1500 without transfusion or cytokine support, a normal PT, and adequate hepatic function as evidenced by a total bilirubin of less than 1.5 x upper limits of normal, and AST/ALT less than or equal to 1.5 times upper limit of normal. Serum creatinine less than or equal to 1.6 mg/ml or the creatinine clearance must be greater than 70 ml/min/1.73m(2). 10. Patients must be aware of the neoplastic nature of his/her illness, the experimental nature of the therapy, alternative treatments, potential benefits, and risks. The patient must be willing to sign an informed consent. EXCLUSION CRITERIA: 1. Patients with limited stage SCLC and operable NSCLC or operable esophageal cancer will be excluded. 2. Patients with potentially treatable pulmonary metastases from lymphomas or germ cell tumors will be excluded. 3. Patients who have received three or more systemic cytotoxic treatment regimens will be excluded due to possible cumulative marrow suppression. 4. Cardiac exclusion criteria, patients with known cardiac abnormalities such as: Uncontrolled arrhythmias - History of serious ventricular arrhythmias not controlled by coronary artery bypass surgery. - Patients with a history of sustained VT, VF, Toursades de Pointes, or cardiac arrest who do not have an automatic implantable cardioverter defibrillator in place. - Congenital Long QT syndrome or QTc greater than 480 msec. - Patients with Mobitz II second degree block who do not have a pacemaker. - Patients with any cardiac arrhythmia requiring anti-arrhythmic medication other than a beta blocker or calcium channel blocker. - Patients in whom digitalis cannot be discontinued. Decompensated heart failure (NYHA Class II or IV). LVEF less than 50% by MUGA scan or echocardiogram. Hypertrophic or restrictive cardiomyopathy from prior treatment of other causes and patients with left ventricular hypertrophy. Uncontrolled hypertension (i.e. greater than or equal to160/95). Myocardial infarction within one year of study. Clinically significant active myocardial ischemia on the basis of nuclear imaging or angiography. History of coronary artery disease (e.g. angina Canadian Class II-IV or positive stress imaging study). Patients with other cardiac disease may be excluded at the discretion of the PI following consultation with cardiology. 5. Co-medication causing QTc prolongation (information at Appendix A and http://georgetowncert.org/gqdrugs_torsades.asp) unless a 5 half-life washout period has elapsed between discontinuing the drug and entering this study. 6. Patients with active intracranial and leptomeningeal metastases, as well as those requiring anticonvulsant medications or steroids to control cerebral edema will be excluded. 7. Patients with life expectancy less than three months will be excluded. 8. Patients with pulmonary embolism or deep venous thrombosis requiring anticoagulation within six months of protocol entry will be excluded. 9. Pregnant patients and nursing mothers will be excluded due to the unknown, potentially harmful effects of HDAC inhibitors and cdk inhibitors on fetal and early childhood development. 10. Patients with active infections will be excluded. 11. Patients with HIV infection will be excluded due to the potential risk of opportunistic infection during DP/FLA-induced myelosuppression and potentially deleterious activation of viral gene expression. 12. Patients will have a screening 12 lead EKG and those patients with left ventricular hypertrophy will not be eligible. 13. Patients who are taking hydrochlorothiazide (HCTZ) will have this agent stopped or switched to a potassium-conserving combination (e.g. Maxide or Dyazide) or other antihypertensive agent. Patients, who cannot have the agent stopped or switched to a potassium-conserving combination or other antihypertensive agent, will not be eligible. |
Country | Name | City | State |
---|---|---|---|
United States | National Institutes of Health Clinical Center, 9000 Rockville Pike | Bethesda | Maryland |
Lead Sponsor | Collaborator |
---|---|
National Cancer Institute (NCI) |
United States,
Baylin SB, Esteller M, Rountree MR, Bachman KE, Schuebel K, Herman JG. Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer. Hum Mol Genet. 2001 Apr;10(7):687-92. Review. — View Citation
Otterson GA, Khleif SN, Chen W, Coxon AB, Kaye FJ. CDKN2 gene silencing in lung cancer by DNA hypermethylation and kinetics of p16INK4 protein induction by 5-aza 2'deoxycytidine. Oncogene. 1995 Sep 21;11(6):1211-6. — View Citation
Wang C, Fu M, Mani S, Wadler S, Senderowicz AM, Pestell RG. Histone acetylation and the cell-cycle in cancer. Front Biosci. 2001 Apr 1;6:D610-29. Review. — View Citation
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04879849 -
A Study of TAK-676 With Pembrolizumab After Radiation Therapy to Treat a Number of Cancers
|
Phase 1 | |
Completed |
NCT04426825 -
A Study of Atezolizumab in Combination With Bevacizumab in Patients With EGFR Mutation Positive Stage IIIB-IV Non-Squamous Non-Small Cell Lung Cancer
|
Phase 2 | |
Terminated |
NCT03166631 -
A Trial to Find the Safe Dose for BI 891065 Alone and in Combination With BI 754091 in Patients With Incurable Tumours or Tumours That Have Spread
|
Phase 1 | |
Completed |
NCT02864394 -
Study of Pembrolizumab Versus Docetaxel in Participants Previously Treated for Non-Small Cell Lung Cancer (MK-3475-033/KEYNOTE-033)
|
Phase 3 | |
Completed |
NCT02810457 -
Evaluation of FKB238 and Avastin in Patients With Advanced/Recurrent Non-squamous Non-small Cell Lung Cancer
|
Phase 3 | |
Recruiting |
NCT04592523 -
A Study of Usage of Brigatinib in the Treatment of Adult Participants for Approved Indications In South Korea
|
||
Recruiting |
NCT04838548 -
A Study to Evaluate the Efficacy and Safety of MRG003 in Patients With EGFR-Positive Advanced Non-Small Cell Lung Cancer
|
Phase 2 | |
Recruiting |
NCT04077463 -
A Study of Lazertinib as Monotherapy or in Combination With Amivantamab in Participants With Advanced Non-small Cell Lung Cancer
|
Phase 1 | |
Recruiting |
NCT05167604 -
Clinical Value of MRD Monitoring for Adjuvant Therapy in Postoperative NSCLC
|
||
Recruiting |
NCT04603807 -
A Study to Compare the Efficacy and Safety of Entrectinib and Crizotinib in Participants With Advanced or Metastatic ROS1 Non-small Cell Lung Cancer (NSCLC) With and Without Central Nervous System (CNS) Metastases
|
Phase 3 | |
Completed |
NCT04948411 -
Durvalumab as Maintenance in Patients Who Received Chemoradiotherapy for Unresectable Stage III NSCLC: Real World Data From an Expanded Access Program in Brazil
|
||
Active, not recruiting |
NCT04487080 -
A Study of Amivantamab and Lazertinib Combination Therapy Versus Osimertinib in Locally Advanced or Metastatic Non-Small Cell Lung Cancer
|
Phase 3 | |
Not yet recruiting |
NCT04255836 -
Durvalumab Combined With Chemotherapy and Stereotactic Body Radiotherapy (SBRT) in Patients With Oligometastatic Non-small Cell Lung Cancer (NSCLC)
|
Phase 2 | |
Completed |
NCT01953913 -
Afatinib (BIBW 2992) in Advanced Non-Small Cell Lung Cancer Patients With EGFR Mutation
|
Phase 3 | |
Recruiting |
NCT05715229 -
Immune Profile Selection By Fraction of ctDNA in Patients With Advanced NSCLC Treated With Immunotherapy
|
Phase 2 | |
Recruiting |
NCT04931654 -
A Study to Assess the Safety and Efficacy of AZD7789 in Participants With Advanced or Metastatic Solid Cancer
|
Phase 1/Phase 2 | |
Suspended |
NCT05421936 -
Osimertinib for NSCLC With Uncommon EGFR Mutations
|
||
Completed |
NCT02847377 -
A Positron Emission Tomography (PET) Imaging Agent [18F]-ODS2004436 as a Marker of EGFR Mutation in Subjects With NSCLC
|
N/A | |
Completed |
NCT04427072 -
Study of Capmatinib Efficacy in Comparison With Docetaxel in Previously Treated Participants With Non-small Cell Lung Cancer Harboring MET Exon 14 Skipping Mutation
|
Phase 3 | |
Recruiting |
NCT04823377 -
Impact of a Process Optimizing the Decision to Continue or Stop Cancer Treatments in Patients With Advanced Non-small Cell Lung Cancer.
|
N/A |