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A randomised study of oral versus intravenous chemotherapy in poor prognosis small cell lung cancer (SCLC)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN73797340
Enrollment
Unknown
Registered
2001-07-01
Start date
1997-01-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Lung (small cell) Cancer Lung (small cell)

Interventions

1. Regimen A: Chemotherapy, oral etoposide repeated every 3 weeks for six courses. 2. Regimen B: Multi-drug chemotherapy, CAV (cyclophosphamide, adriamycin, vincristine) alternating every 3 weeks with

Sponsors

UK Co-ordinating Committee for Cancer Research (UKCCCR)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Histologically or cytologically proven SCLC 2. Patients with extensive disease and poor prognosis, i.e., Eastern Cooperative Oncology Group (ECOG) performance 2 or 3 or alkaline phosphatase >1.5 upper limit normal range 3. Patients 75 years and over, whatever stage of disease, deemed fit for randomisation 4. No previous malignancy, except non-melanomatous skin cancer in the preceding 3 years 5. No medical contraindications to treatment 6. Adequate renal function

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
Not provided at time of registration

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026