Lung Cancer Clinical Trial

ADI-PEG 20 in Combination With Gemcitabine and Docetaxel After Progression on Frontline Therapy in Non-small Cell and Small Cell Lung Cancers

Summary

In this study, patients with small cell or non-small cell lung cancer will receive ADI-PEG 20, gemcitabine, and docetaxel after demonstrated progression on frontline therapy. In phase I of the study, up to 6 dose levels will be tested to find the recommended phase II dose (RP2D), after which patients enrolling to phase II will be treated at that dose level to assess efficacy. Although safety and tolerability has been previously determined in the sarcoma population, dose de-escalations of the chemotherapies in that patient population were required. Therefore, a phase I portion will be incorporated to determine the RP2D of the triplet in this population.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Histologically or cytologically confirmed extensive stage small cell or metastatic non-small cell lung cancer that has progressed on frontline therapy. Phase II enrollment will occur separately to the SCLC and NSCLC cohorts, with up to 36 enrolled in each cohort.
Measurable disease defined as lesions that can be accurately measured in at least one dimension (longest diameter to be recorded) as ≥ 10 mm with CT scan, as ≥ 20 mm by chest x-ray, or ≥ 10 mm with calipers by clinical exam.
Treated with at least one previous line of systemic therapy. The allowable window between treatments is 21 days for chemotherapy or a TKI or 5 half-lives for a TKI (whichever is shorter), 21 days and progression by CT for immunotherapy, 21 days for RT, 21 days for surgery, or 28 days for an investigational agent.
At least 18 years of age.
ECOG performance status ≤ 1.

Normal bone marrow and organ function as defined below:

Leukocytes ≥ 3,000/mcL
Absolute neutrophil count ≥ 1,500/mcL
Platelets ≥ 100,000/mcL
Total bilirubin ≤ 2 x IULN, patients with Gilberts must be below 3xIULN
AST(SGOT)/ALT(SGPT) ≤ 3 x IULN (or ≤ 5 x IULN if liver metastases are present)
Creatinine clearance > 60 mL/min by MDRD or by 24 hour urine
Serum uric acid ≤ 8 mg/dL (with or without medication control)
The effects of ADI-PEG 20 on the developing human fetus are unknown. For this reason and because chemotherapeutics are known to be teratogenic, women of childbearing potential must agree to use adequate contraception (hormonal or barrier method of birth control, abstinence) prior to study entry, for the duration of study participation, and for one month after completion of study treatment. Should a woman become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately. Men treated or enrolled on this protocol must also agree to use adequate contraception prior to the study, for the duration of the study, and for one month after completion of study treatment.
Ability to understand and willingness to sign an IRB approved written informed consent document (or that of legally authorized representative, if applicable).

Exclusion Criteria:

A history of other malignancy with the exception of:

Malignancies for which all treatment was completed at least 2 years before registration and the patient has no evidence of disease
Basal cell or squamous cell carcinoma of the skin which was treated with local resection only
Carcinoma in situ of the cervix
Other tumors discussed with the study PI
Currently receiving any other investigational agents.
Prior treatment with ADI-PEG 20 or gemcitabine (prior docetaxel is allowed).
Presence of untreated or unstable brain metastases. Patients with treated/stable brain metastases, defined as patients who have received prior therapy for their brain metastases and whose CNS disease is radiographically stable at study entry, are eligible.
A history of allergic reactions attributed to compounds of similar chemical or biologic composition to ADI-PEG 20, gemcitabine, pegylated compounds, or other agents used in the study.
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia.
History of seizure disorder not related to underlying cancer.
Grade 2 or higher neuropathy
Pregnant and/or breastfeeding. Women of childbearing potential must have a negative pregnancy test within 14 days of study entry.
Patients with HIV are eligible unless their CD4+ T-cell counts are < 350 cells/mcL or they have a history of AIDS-defining opportunistic infection within the 12 months prior to registration. Concurrent treatment with effective ART according to DHHS treatment guidelines is recommended.

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

108

Study ID:

NCT05616624

Recruitment Status:

Not yet recruiting

Sponsor:

Washington University School of Medicine

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There is 1 Location for this study

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Washington University School of Medicine
Saint Louis Missouri, 63110, United States More Info
Brian A Van Tine, M.D., Ph.D.
Contact
314-362-8903
[email protected]
Brian A Van Tine, M.D., Ph.D.
Principal Investigator
Jared Cohen, M.D.
Sub-Investigator
Ramaswamy Govindan, M.D.
Sub-Investigator
Siddhartha Devarakonda, MBBS
Sub-Investigator
Daniel Morgensztern, M.D.
Sub-Investigator
Saiama Waqar, MBBS
Sub-Investigator
Mia Weiss, M.D.
Sub-Investigator
Esther Lu, Ph.D.
Sub-Investigator
Sasha Harberg, PharmD, BCOP
Sub-Investigator

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

108

Study ID:

NCT05616624

Recruitment Status:

Not yet recruiting

Sponsor:


Washington University School of Medicine

How clear is this clinincal trial information?

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