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Topotecan for Irinotecan-Refractory SCLC

Salvage Treatment With Topotecan in Patients With Irinotecan-Refractory Small Cell Lung Cancer

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00502762
Enrollment
Unknown
Registered
2007-07-18
Start date
2004-09-30
Completion date
2007-08-31
Last updated
2008-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer, Refractory to Chemotherapy

Keywords

small-cell lung cancer, refractory, topotecan

Brief summary

Although the efficacy of topotecan as second-line chemotherapy for SCLC has been consistently demonstrated in phase II/III clinical trials, the choice of irinotecan as first-line therapy prevented use of the evidence-based option. This pilot study will be conducted to determine the activity and safety of topotecan in SCLC patients refractory to first-line therapy with irinotecan and platinum.

Detailed description

Current commonly used second-line approaches for SCLC include re-induction with first-line therapy for chemosensitive disease, or single-agent topotecan. Although the efficacy of topotecan as second-line chemotherapy for SCLC has been consistently demonstrated in a number of clinical studies, the choice of irinotecan as first-line therapy prevented use of the evidence-based option such as topotecan. Topotecan and irinotecan are cytotoxic agents that inhibit same intracellular pathway, namely topoisomerase I, which is an enzyme involved in DNA replication and RNA transcription. Although their mechanism of action is similar, the preclinical and clinical data of these two drugs have some notable differences. Topotecan and irinotecan have different spectra of antitumor activity in various models of human cancer. Clinical data support that these agents may have different spectra of activity. The differences in antitumor activities may also reflect different mechanisms of resistance. Furthermore, topotecan and irinotecan have different limiting toxicities (myelosuppression and diarrhea, respectively).

Interventions

DRUGtopotecan

Sponsors

Gachon University Gil Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* histologically or cytologically proven SCLC * refractory to prior irinotecan-based chemotherapy * Eastern Cooperative Oncology Group (ECOG) performance status ≤2 * age between 18 and 75 years * no active brain or leptomeningeal metastases * adequate hematologic, hepatic and renal functions * at least one measurable lesion(s)

Exclusion criteria

* pregnant or lactating women * patients with active infection * extensive radiotherapy within the previous 4 weeks * previous other malignancies with the exception of adequately treated non-melanoma skin cancer or in situ cervical cancer * any severe comorbid illness * a known history of anaphylaxis of any origin * history of severe adverse events to the drug used in this study

Design outcomes

Primary

MeasureTime frame
Response rate

Secondary

MeasureTime frame
Safety

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026