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About
The clinical trial is a phase 1, single-arm trial that will evaluate the safety of the investigational treatment on metastatic cancer in patients who have a deleterious or suspected deleterious BRCA1, BRCA2, or PALB2 genetic alteration. The investigational treatment will involve 2 cycles of a combination of intravenous melphalan, BCNU, low-dose I.V. ethanol, vitamin B12b, and vitamin C in association with autologous hematopoietic stem cell infusion. A dose-escalation schedule will be employed for vitamin C.
Full description
In the current clinical trial, subjects with BRCA-related or PALB2-related metastatic pancreatic or breast cancer will receive a combination of melphalan, BCNU, low-dose ethanol, vitamin B12b, and vitamin C in conjunction with autologous stem cell infusion. The drug combination is designed to address multiple mechanisms of melphalan resistance. The purpose of the ethanol is the protection of RBC catalase activity.
Investigational Treatment Description:
Hematopoietic Stem Cell Collection
Investigational Drug Therapy and Stem Cell Infusion
All subjects will receive two cycles of investigational drug therapy with stem cell infusion unless precluded by adverse reactions.
Subjects will receive on day -2:
On day 0, at least 2 × 10^6 CD34+ cells/kg will be infused as per the institution's standard procedures.
Subjects will receive supportive care as per the institution's standard procedures before, during, and after the investigational drug therapy and stem cell infusion.
Additional Cycles a. Subjects will receive a second cycle of the investigational treatment described immediately above in "Investigational Drug Therapy and Stem Cell Infusion," with an interval of approximately 6 weeks between cycles.
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
Inclusion Criteria
Age ≥ 18 years.
Pancreatic or breast cancer, as described below.
Stage IV (based on AJCC staging guidelines) at the time of enrollment.
a. Note that potential subjects with stage IV cancer that have had a complete response from prior chemotherapy are still potentially eligible.
Expected survival time ≥ 6 months, as determined by the investigator.
Life expectancy not severely limited by diseases other than malignancy, as determined by the investigator.
Karnofsky score ≥ 60%.
No chemotherapy within 2 weeks of enrollment.
Prior surgical resection or ablation of the primary tumor is allowed but not required.
If post-surgical, the subject must be at least 28 days post-op with the surgical wounds healed and significant complications resolved.
Potential subjects who have received previous chemotherapy and/or PARP inhibitors may be enrolled.
Measurable or non-measurable disease by the revised response evaluation criteria in solid tumors (RECIST) v.1.1.
A germline or somatic BRCA1, BRCA2, or PALB2 mutation.
For potential subjects with a germline mutation:
a. The mutation must be known to be deleterious or suspected to cause functional impairment as assessed by a CLIA-certified laboratory according to the variant classification criteria described in the study protocol.
For potential subjects with somatic mutations:
For potential subjects with pancreatic cancer:
For potential subjects with breast cancer:
Histological or cytological confirmation of the primary cancer diagnosis is required.
Metastatic disease must be histologically or cytologically confirmed unless in the clinical judgment of the investigator a biopsy is not needed for diagnostic purposes.
Female participants of childbearing potential must agree to do one of the following from the time of signing of the informed consent through 6 months after the last dose of melphalan:
Male participants:
Unless the male is in a monogamous relationship with a female that does not have child-bearing potential, male subjects (even if surgically sterilized) must agree to do one of the following from the time of signing of the informed consent through 6 months after the last dose of melphalan:
Exclusion Criteria
Biliary tract obstruction.
Current cholangitis. A biliary stent in situ does not otherwise exclude protocol participation.
A history of only one episode of cholangitis and fewer than 30 days have passed since discontinuation of antibiotic treatment.
A history of multiple episodes of cholangitis and after discussion between the site study team and sponsor medical monitor and careful evaluation for suitability the patient is deemed to be unsuitable for the trial due to risk of recurring cholangitis.
Portal hypertension.
Sinistral portal hypertension.
Clinically significant malignant ascites or malignant pleural effusion, as determined by the investigator.
Metastatic lesion to the heart or eye.
Chemotherapy for an indication other than treatment of the current cancer within the past 1 year with a more than 30% risk of recurrence as determined by the investigator.
Known or suspected metastatic involvement of the central nervous system.
Left ventricular ejection fraction less than 45% by Multigated Acquisition Scan or echocardiogram (or significantly below the lower limit of normal for the specific test).
Clinically significant structural heart disease or vascular disease.
Myocardial infarction within 6 months prior to enrollment; New York Heart Association (NYHA) Class III or IV heart failure; angina; uncontrolled ventricular arrhythmias; or electrocardiographic evidence of acute ischemia or active conduction system abnormalities.
Clinically significant prolongation of QTc (Bazett formula) on EKG, defined as > 0.45 s in males and > 0.47 s in females.
Severe hypertension, which is defined as the presence of any of the following:
Other clinically significant cardiovascular disease.
NOTE:
History or evidence of interstitial lung disease (e.g., pneumonitis or pulmonary fibrosis).
If a smoker, refusal to stop smoking for the duration of the trial.
FEV1 or DLCO (adjusted for hemoglobin) < 50% of predicted.
Total bilirubin > 2x upper normal limit, except that potential subjects with Gilbert's Disease are permitted to exceed 2x upper normal limit.
ALT or AST > 2.5x upper normal limit.
Alkaline phosphatase > 2.5x upper normal limit, in conjunction with elevated GGT.
Albumin < 3.0 g/dl.
Clinical evidence of sinusoidal obstruction syndrome.
Corrected creatinine clearance consistently < 50 ml/min/1.73 m^2.
Clinically significant renal disease.
Hemolytic anemia.
Catalase deficiency.
Evidence of bone marrow insufficiency or failure, in the judgment of the investigator.
A hemoglobin < 9 g/dL.
G6PD deficiency as measured by quantitative enzyme levels below the normal reference range in blood.
Pre-existing bleeding diathesis or coagulopathy.
Potential subject is pregnant.
Breast feeding and unwilling to stop.
Wilson's disease.
Primary or secondary hemochromatosis.
Hgb A1c > 9%.
Hyperuricemia that is not responsive to therapy.
Plasma oxalate greater than 10 µM, which is not responsive to measures to reduce the level below 10 µM.
a. Subjects must be off vitamin C for at least 48 hours prior to the oxalic acid measurements and have fasted overnight.
Prior or current hepatitis B or C.
HIV infection or seropositivity for HIV.
Active, clinically significant bacterial, viral, or fungal infection.
History of colonization with a multidrug-resistant "superbug" that poses a high risk of an untreatable infection in the setting of neutropenia.
Uncontrolled seizure disorder.
If a potential subject has received radiation, then any of the following:
History of significant allergy or other contraindication to BCNU, melphalan, vitamin B12b, vitamin C, pegfilgrastim, or Neupogen, or to any excipient in those drugs.
Use of any of the following cytochrome P450 2b6 (CYP2b6) inducers within 21 days of the planned date of BCNU treatment: phenobarbital, carbamazepam, rifampicin, phenytoin, sulfinpyrazone, or verapamil.
Disulfiram (Antabuse) use within 30 days of the planned ethanol administration.
Current chronic use of immunosuppressive agents (e.g., methotrexate, cyclosporine, corticosteroids).
Prior bone marrow stem cell transplant.
Except for adjuvant therapy for breast cancer or pancreatic cancer, prior radiation therapy to the brain, kidneys, pelvis, or GI tract or treatment with yttrium-90.
Prior treatment with bleomycin or BCNU.
Prior treatment, within 30 days of enrollment, with a drug that has not been FDA-approved for any indication (cancer or otherwise).
Subject has not fully recovered (i.e., there remain toxicities > Grade 1) from the reversible effects of prior chemotherapy, with the exception of chemotherapy-induced alopecia and grade 2 peripheral neuropathy, unless in the opinion of the principal investigator the effects are not of clinical significance.
Any concurrent anticancer treatment.
Serious underlying medical or psychiatric illness or another condition that in the clinical judgment of the principal investigator is likely to interfere with the potential subject completing participation in the trial, based on safety concerns or otherwise.
Inability or unwillingness to adhere to the study protocol.
Unwillingness to receive ethanol.
Primary purpose
Allocation
Interventional model
Masking
10 participants in 1 patient group
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Central trial contact
General Oncology (study sponsor)
Data sourced from clinicaltrials.gov
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