Safety Study of Nelfinavir + Cisplatin + Pelvic Radiation Therapy to Treat Cervical Cancer
- Conditions
- Cervical Cancer
- Interventions
- Radiation: Pelvic External Beam Radiation TherapyRadiation: BrachytherapyProcedure: Pharmacokinetic SamplingProcedure: Cervical BiopsyProcedure: Pelvic ExaminationProcedure: Pap SmearProcedure: AudiogramProcedure: ProctoscopyProcedure: CytoscopyProcedure: Renal UltrasoundProcedure: CT ScanProcedure: Whole Body PET/CT Scan
- Registration Number
- NCT01485731
- Lead Sponsor
- University of Miami
- Brief Summary
Nelfinavir will increase the efficacy of Cisplatin based chemo- radiation therapy for locally advanced cervical cancer.
- Detailed Description
Despite cisplatin chemoradiation, 40-50% of women with locally advanced cervical cancer will die from their disease. The evaluation of new chemoradiation regimens have since included cisplatin to further build on its current success. In one year, Nelfinavir will be off patent and become a potential cost effective therapy. HIV Protease inhibitors are now being explored as potential therapies in oncology. The repositioning of HIV protease inhibitors, specifically nelfinavir in cancer therapeutics, is based on three facts. First, recent studies show that HIV protease inhibitors are established broad-spectrum anti-cancer agents that work through pleiotropic mechanisms such as by down-regulating activated mitogenic signaling pathways, and activating the immune response with Nelfinavir being the most potent \[7\]. Second, HIV protease inhibitors including nelfinavir can target specific viral antigens. Nelfinavir has been shown to target Human Papilloma Virus (HPV)-transformed cervical carcinoma cells via inhibition of E6-mediated proteosomal degradation of mutant p53 \[8\]. Thirdly, Nelfinavir has radiosensitizing properties through inhibiting the PI3K/Akt signaling pathway as demonstrated in vivo and in vitro in head and neck and pancreatic cancers models \[9\].
Nelfinavir is currently being evaluated as a radiosensitizer in head and neck and pancreatic cancers in phase I/II clinical trials. Brunner et al. (2008) recently completed the first phase I trial of nelfinavir added to chemoradiation for locally advanced pancreatic cancer \[16\]. Investigators treated 12 patients with advanced pancreatic carcinoma with Nelfinavir 1250 mg orally twice daily starting 3 days before radiation therapy and continued until the last day of radiation. They found no significant toxicity attributable to nelfinavir and observed a response rate of 50% versus 30% in historical controls. There were 5 of 12 patients with grade 3 hematologic toxicities (4 with leukopenia and 2 with thrombocytopenia). There were 3 of 12 patients with grade 3 GI toxicity (including abdominal pain, nausea, vomiting). There were no grade 4 drug related toxicities \[16\]. There were grade 1/ 2 toxicities including hematologic (thrombocytopenia, anemia, neutropenia), gastrointestinal toxicities (nausea, vomiting, diarrhea, abdominal pain), and elevated transaminases which were approximately 70%. Ten of 12 patients completed therapy. Complete responses were observed in 5 patients and partial responses were observed in 5 of 10 patients. Overall, the addition of Nelfinavir added minimal additional toxicity. Determination of a dose for biologic activity was not performed \[14\].
In summary, HIV protease inhibitors have a very broad spectrum of anti-tumor activity and can inhibit proliferation and/or cause death in the majority of cancer cell lines tested in a dose-dependent manner \[7\]. Nelfinavir has been found to be the most potent anti-tumor agent among the HIV protease inhibitors. As a result, several clinical trials are investigating Nelfinavir as a chemotherapeutic agent with and without concurrent radiation therapy in varied disease sites including rectal, head \& neck, glioblastomas, pancreas, renal cell, non-small cell lung cancer, liposarcoma, and gliomas. The NCI is also investigating Nelfinavir as single agent chemotherapy in advanced and recurrent solid tumors \[15\].
As Nelfinavir has both cytotoxic and radiation sensitizing effects, it is an ideal agent to use in combination with cisplatin-based chemoradiation in locally advanced cervical cancers.
In this study, patients with clinical stages IIA, IIB, IIIA, IIIB, IVA cervical carcinoma limited to the pelvis will receive twice daily oral Nelfinavir (NFV) and weekly IV cisplatin in combination as radiosensitizers with daily whole pelvic external beam (Mon-Fri) followed by intracavitary radiation brachytherapy.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 8
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All patients with primary, previously untreated, histologically confirmed invasive carcinoma of the uterine cervix (any cell type). Clinical stages IIA, IIB, IIIA, IIIB, IVA.
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Patients must have adequate bone marrow, renal and hepatic function:
- ANC ≥ 1,500/μL;
- Platelet count ≥ 100,000/μL;
- Creatinine < 2.0 mg/dL;
- Total Bilirubin ≤ 1.5 times normal;
- SGOT ≤ 3 times normal.
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Patients with a GOG Performance Status of 0, 1, or 2.
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Patients with ureteral obstruction must be treated with stent or nephrostomy tube.
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Patients must be entered within eight weeks of diagnosis.
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Patients of childbearing potential must use an effective form of birth control."Patients receiving oral contraceptives should be instructed that alternate or additional contraceptive measures should be used during therapy with VIRACEPT. "
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Seronegative HIV status.
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Patients must be at least 18 years of age.
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Patients must have signed an approved informed consent and authorization permitting release of personal health information.
- Patients with Stage IA, IB or IVB disease.
- Patients who have known metastases to other organs outside the radiation field at the time of the original clinical and surgical staging.
- Patients who have received previous pelvic or abdominal radiation, cytotoxic chemotherapy, or previous therapy of any kind for this malignancy.
- Patients with septicemia or severe infection.
- Patients who have circumstances that will not permit completion of this study or the required follow-up.
- Patients who are pregnant at the time of diagnosis and do not wish pregnancy termination prior to initiation of treatment.
- Patients with renal abnormalities, such as pelvic kidney, horseshoe kidney, or renal transplantation, that would require modification of radiation fields.
- Patients with other concomitant malignancies (with the exception of non-melanoma skin cancer), who had (or have) any evidence of other cancer present within the last 5 years.
- Patients with GI tract disease resulting in an inability to take oral medication, malabsorption syndrome, a requirement for IV alimentation, prior surgical procedures affecting absorption, uncontrolled inflammatory GI disease (e.g., Crohn's, ulcerative colitis).
- Patients with poorly controlled diabetes mellitus despite medication.
- Patients taking anti-arrhythmic agents such as amiodarone, quinidine, rifampin, ergot derivatives such as ergotamine, St Johs Wort, HMG-CoA reductase inhibitors such as lovastatin, neuroleptic such as pimozide, sedatives such as midazolam and triazolam among other CYP3A4 and CYP2C19 substrates.
- Patients with Phenylketonuria.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Nelfinavir + Cisplatin + Pelvic Radiation Therapy Cervical Biopsy Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy Pelvic Examination Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy Cytoscopy Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy CT Scan Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy Pelvic External Beam Radiation Therapy Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy Pharmacokinetic Sampling Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy Whole Body PET/CT Scan Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy Brachytherapy Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy Proctoscopy Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy Pap Smear Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy Audiogram Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy Renal Ultrasound Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy Nelfinavir Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy Nelfinavir + Cisplatin + Pelvic Radiation Therapy Cisplatin Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy
- Primary Outcome Measures
Name Time Method Number of Patients with Adverse Events in Phase 1 Study of Nelfinavir + Cisplatin + Pelvic Radiation Therapy 3 Years Number of Patients with Adverse Events in Phase 1 Study of Nelfinavir + Cisplatin + Pelvic Radiation Therapy
The proportion of enrolled patients for whom Nelfinavir dose can be successfully administered in combination with Cisplatin and Pelvic Radiation Therapy. 3 Years Maximum tolerable Phase II dose of Nelfinavir in combination with Cisplatin and Pelvic Radiation Therapy.
- Secondary Outcome Measures
Name Time Method Serum Levels of Nelfinavir and other Biomarker Activity 3 Years To determine the levels of Akt activity (and downstream effectors such as pGSK3, pEBP1) and p16INK4A in addition to the presence of Human Papilloma Virus (HPV) 16 and18,and E6/E7 RNA in cervical biopsy specimens of patients at three different time points (1. pre-nelfinavir, pre-radiation, 2. while on nelfinavir, pre-radiation, 3. at completion of radiation therapy), and correlate the levels of these markers to serum Nelfinavir levels from blood drawn at the day of the biopsy.
Response to protocol therapy 3 years Tumor response to protocol therapy will be measured using Response Evaluation Criteria In Solid Tumors (RECIST) criteria.
Progression-free Survival 3 years Progression-Free Survival is the period from start of treatment until documented disease progression or death from any cause. For surviving patients without progression, progression-free survival will be censored at the last date of documented progression-free status.
Overall Survival 3 years Survival is the observed length of life from start of treatment to death. For surviving patients, follow-up will be censored at the date of last contact.
Trial Locations
- Locations (1)
University of Miami
🇺🇸Miami, Florida, United States