A Trial of Amrubicin and Carboplatin With Pegfilgrastim in Patients With Extensive-Stage Small Cell Lung Cancer
This proposed trial will investigate the combination of amrubicin and carboplatin in the first-line treatment of patients with extensive-stage small cell lung cancer (ES- SCLC). Since myelosuppression is the most common toxicity produced by this drug combination, pegfilgrastim will be administered with each treatment cycle. This trial will be the first clinical trial to evaluate a combination of amrubicin and carboplatin in the first-line treatment of ES SCLC in a U.S. population.
Ask AI to explain this studyKey things to know
This describes the study’s primary purpose.
Plus 1 other study approaches.
These are broad labels—not an eligibility decision.
Checked against the public recordLast updated May 5, 2016 · Source: ClinicalTrials.gov
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Interventional
Locations may change over time.
Study sponsor
What this study is about
- Purpose
- Treatment
- Study type
- Interventional
- Phase
- Phase 2
- Sponsor
- SCRI Development Innovations, LLC
- Interventions being studied
- Drug: Amrubicin; Drug: Carboplatin; Drug: Pegfilgrastim
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.
- 1. Cytologically and/or histologically confirmed small-cell lung cancer with extensive stage disease. 2. Measurable or evaluable disease per RECIST criteria version 1.1. 3. Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0-1. 4. Left ventricular ejection fraction (LVEF) ≥50% by echocardiogram (ECHO) or multiple gated acquisition scan (MUGA). 5. QTc interval of ≤450 msec. on ECG. 6. Adequate organ function, including the following:
- ANC ≥1500 cells/micro liter
- Platelet count ≥100,000 cells/micro liter
- Hemoglobin ≥9 g/dL
- Total bilirubin ≤1.5 x ULN; AST/ALT ≤2.5 x ULN, (except if due to hepatic metastases, then ≤5 x ULN)
- Serum creatinine ≤1.5 x ULN 7. Patients must be able to receive growth factors (G-CSF). 8. Women of childbearing potential must have a negative serum or urine pregnancy test performed ≤ 7 days prior to start of treatment. Women of childbearing potential or men with partners of childbearing potential must use effective birth control measures during treatment. If a woman becomes pregnant or suspects she is pregnant while participating in this study, she must agree to inform her treating physician immediately. 9. Patients ≥18 years of age. 10. Patients must be accessible for treatment and follow-up. 11. Patients must be able to understand the investigational nature of this study and give written informed consent prior to study entry.
- 1. Previous treatment for limited-stage SCLC. 2. Previous chemotherapy or radiation therapy for SCLC (unless radiation was administered for brain metastases). 3. Active brain metastases. Patients with treated brain metastases are eligible, if (1) radiation therapy was completed ≥ 21 days prior to first dose of amrubicin; (2) follow-up scan shows no disease progression; an absence of neurologic symptoms and (3) patient does not require steroids. 4. Mixed small cell/non-small cell tumors or other neuroendocrine lung cancers. 5. Women who are pregnant or breastfeeding. 6. Suspected, diffuse idiopathic interstitial lung disease or pulmonary fibrosis. 7. Patients with New York Heart Association (NYHA) class II or greater congestive heart failure (CHF). 8. Any of the following ≤6 months prior to starting study treatment:
- myocardial infarction;
- severe unstable angina;
- ongoing cardiac dysrhythmia. 9. Family history of idiopathic cardiomyopathy or uncontrolled heart arrhythmia. 10. Treatment for other invasive cancers during the previous 5 years, or the presence of any active invasive cancer of any type (with the exception of non-melanoma skin cancers). 11. Uncontrolled hypertension (i.e., blood pressure \>150/90 mmHg that cannot be controlled with standard anti-hypertensive agents). 12. Major surgical procedure or significant traumatic injury ≤ 28 days of study initiation. 13. History of seropositive HIV or patients who are receiving immunosuppressive medications that would in the opinion of the investigator increase the risk of the serious neutropenic complications. 14. Concurrent severe, intercurrent illness including, but not limited to, ongoing or active infection, or psychiatric illness/social situations that would limit compliance with study requirements. 15. Any condition that would prevent patient comprehension of the nature of, and risk associated with, the study. 16. Use of any non-approved or investigational agent ≤30 days prior to administration of the first dose of study drug. Patients may not receive any other investigational or anti-cancer treatments while participating in this study.
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- Northeast Arkansas ClinicJonesboro, Arkansas
- Florida Cancer SpecialistsFort Myers, Florida
- Watson Clinic Center for Cancer Care and ResearchLakeland, Florida
- Florida Hospital Cancer InstituteOrlando, Florida
- Medical Oncology Associates of AugustaAugusta, Georgia
- Baptist Hospital EastLouisville, Kentucky
- Norton Cancer InstituteLouisville, Kentucky
- Hematology Oncology Clinic, LLPBaton Rouge, Louisiana
- Center for Cancer and Blood DisordersBethesda, Maryland
- National Capital Clinical Research ConsortiumBethesda, Maryland
- Grand Rapids Clinical Oncology ProgramGrand Rapids, Michigan
- Research Medical CenterKansas City, Missouri
Source and freshness
Processed from ClinicalTrials.gov. Last public update: May 5, 2016. Always confirm current availability with the study team.