Bendamustine With Irinotecan Followed by Etoposide/Carboplatin for Patients With Extensive Stage Small Cell Lung Cancer

The University of Alabama at Birmingham logo

The University of Alabama at Birmingham

Status and phase

Completed
Phase 2
Phase 1

Conditions

Chemonaive
Extensive Stage Lung Cancer
Small Cell Lung Cancer

Treatments

Drug: Novel Drug Combination

Study type

Interventional

Funder types

Other
NETWORK

Identifiers

NCT00856830
F080929010
UAB 0818 (Other Identifier)

Details and patient eligibility

About

Small cell lung cancer, or SCLC, constitutes approximately 15% of the 170,000 new cases of lung cancer diagnosed annually in the United States. Extensive-stage SCLC comprises two thirds of new cases and is generally considered sensitive to chemotherapy, despite a median time to progression of 4 months. SCLC is one of the most aggressive and lethal types of cancer, with a median survival of 9 months (range 7-11 months) in patients diagnosed with extensive disease. Overall, the majority of patients with SCLC die in less than 2 years (2-year survival rates generally less than 10%), and the 5-year survival rate is 2.3% for patients with extensive disease. The regimen of etoposide in combination with a platinum (cisplatin or carboplatin) is generally considered the "standard of care" although a recent Phase III trial suggests improved survival with the combination of cisplatin/irinotecan. Further evaluation of new agents in combination regimens attempting to overcome the intrinsic drug resistance seen in extensive-stage SCLC is warranted attempting to improve survival and achieve palliation of disease-related symptoms.

Full description

We are proposing a novel combination of bendamustine plus irinotecan followed by the standard regimen of etoposide with carboplatin. This will allow the investigation of response to the novel combination as well as any improvement in outcomes compared to historical controls.

Enrollment

30 patients

Sex

All

Ages

18 to 79 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Histologic or cytologic diagnosis of extensive stage SCLC.
  • Measurable or assessable tumor parameters.
  • ECOG Performance Status 0-2.
  • Age between 18 and 79 years (in the State of Alabama > 18).
  • Adequate bone marrow, liver and renal function, defined as:
  • Absolute neutrophil count (ANC) ≥ 1500/µL
  • Hemoglobin ≥ 8g/dl
  • Platelet count ≥ 100,000/µL
  • SGOT/SGPT ≤ 2 x upper limit of normal or ≤ 5 x upper limit of normal when liver metastases are present.
  • Total bilirubin value ≤ 2 x upper limit of normal.
  • Serum creatinine value ≤ 2 x upper limit of normal.
  • Fully recovered from any previous surgery (at least 4 weeks since major surgery)
  • Must have recovered from prior radiation therapy (at least 3 weeks)
  • All subjects must agree to practice approved methods of birth control (if applicable). A negative pregnancy test must be documented during the screening period for women of childbearing potential.
  • Must provide written informed consent and authorization to use and disclose health information (HIPAA).
  • Extensive-stage SCLC as defined as disease not confined to one hemithorax, including ipsilateral pleural effusion or pericardial effusion.
  • No prior chemotherapy.

Exclusion criteria

  • Concurrent cancer chemotherapy, biologic therapy or radiotherapy.
  • Administration of any investigational drug within 28 days prior to administration of the current therapy.
  • Symptomatic brain metastases; those patients should be treated first with either whole brain radiation therapy or radiosurgery.
  • Concurrent serious infection.
  • Concomitant severe or uncontrolled underlying medical disease unrelated to the tumor, which is likely to compromise patient safety and affect the outcome of the study.
  • History of other malignancy (except non-melanoma skin cancer or carcinoma in situ of the cervix), unless in complete remission and off all therapy for a minimum of 2 years.
  • Neuropathy at baseline ≥ Grade 2.
  • Any evidence or history of hypersensitivity or other contraindications for the drugs used in this trial.
  • History of chronic diarrhea; or diarrhea (excess of 2-3 stools/day above normal frequency) in the past 2 weeks.
  • History of a positive serology for human immunodeficiency virus (HIV).
  • Psychiatric disorder that prevents patients from providing informed consent or following protocol instructions.
  • Pregnant or lactating women.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Novel Drug Combination
Experimental group
Description:
This novel drug combination includes: Bendamustine, Irinotecan, and Etoposide/Carboplatin. This study has only one arm but it incorporates two phases. Phase I utilizes a combination of bendamustine and irinotecan for Regimen A followed by etoposide and carboplatin for Regimen B.
Treatment:
Drug: Novel Drug Combination

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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