Topotecan in Combination With Pemetrexed in Patients With Advanced Malignancies

SCRI Development Innovations

Status and phase: Completed; Phase 1

Conditions: Endometrial Cancer; Lung Cancer; Ovarian Cancer; Cervical Cancer

Treatments: Drug: pemetrexed; Drug: topotecan

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT00315861

SCRI REFMAL 72

105114

H3E-US-I013 LILLY

Details and patient eligibility

About

Currently, no data exists regarding the safety and tolerability of a combination regimen utilizing weekly topotecan in combination with pemetrexed. Although both drugs are associated with myelosuppression, it is hoped that the utilization of the weekly topotecan dosing schedule will allow the drugs to be easily combined. This phase I trial will evaluate the safety and tolerability of weekly topotecan in combination with pemetrexed in patients with advanced solid tumors.

Full description

Three patients will be accrued at each of 5 dose levels. Dose escalation will only proceed if none of the additional 3 patients experience DLT. The highest dose level that generates DLT in 0/3 or 1/6 patients will be the maximum tolerated dose (MTD) or the doses recommended for subsequent studies. A total of 10 patients will be treated at the MTD to further assess the toxicity of the dosing regimen and its suitability for use in subsequent trials. Patients may continue to receive treatment until unacceptable toxicity or disease progression is encountered. Treatment cycles will be repeated every 21 days. The protocol is also designed to enroll an additional 10 patients at the maximum tolerated dose to increase the confidence in the safety and suitability of the doses that are chosen for subsequent studies.

• Topotecan Day 1 and 8
• Pemetrexed Day 1

Enrollment: 15 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Histologically proven advanced solid tumors
• Measurable or evaluable disease
• Age ≥ 18 years
• Karnofsky performance status ≥ 80% (ECOG 0 or 1)
• Adequate liver, bone marrow and kidney function

Exclusion criteria

• More than 3 prior chemotherapy regimens in the metastatic setting
• Prior treatment with topotecan or pemetrexed
• Clinically significant third space fluid present at the time of treatment
• Unable to interrupt aspirin, other non-steroidal anti-inflammatory drugs
• Inability to take steroid premedications or vitamin supplementation
• The presence of active brain metastases
• Prior radiotherapy within 4 weeks prior to the first day of treatment
• Prior surgery within 3 weeks prior to the first day of treatment
• Prior chemotherapy within 3 weeks prior to the first day of treatment

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)