Docetaxel/Pemetrexed as 1st Line Treatment in Patients With Non Small Cell Lung Cancer (NSCLC)

Phase 1

Completed

• Conditions: Non Small Cell Lung Cancer
• Interventions: Drug: Docetaxel; Drug: Pemetrexed

• Registration Number: NCT00684099
• Lead Sponsor: Hellenic Oncology Research Group

Brief Summary

This trial will determine the maximum tolerated dose the recommended phase II dose and the efficacy of this combination in locally advanced or metastatic NSCLC patients

Detailed Description

Docetaxel as single-agent therapy (100 mg/m2 and 75 mg/m2, every 3 weeks) produces response rates of 26% to 54%. Docetaxel has proven superior compared to best supportive care (BSC) in chemotherapy-naïve as well as in platinum pretreated patients. In addition, docetaxel is active in cisplatin refractory or resistant patients, producing responses ranging from 18% to 25%, implying a lack of cross-resistance between docetaxel and cisplatin, probably due to their different mechanisms of action. Furthermore, docetaxel is associated with significant prolongation of survival when administered as second line therapy, in pretreated patients with advanced NSCLC. Phase II studies of pemetrexed in previously untreated patients with NSCLC have demonstrated single agent response rates of 17% to 23%. A phase II study of pemetrexed in patients with advanced NSCLC, who had progressed during or within 3 months of completing first-line chemotherapy, demonstrated a response rate of 8.9% and median survival time of 5.7 months. Multivariate analysis established an association between an increased risk of severe pemetrexed toxicity and elevated homocysteine (folate and/or B12 vitamin deficiency marker) levels. Since December 1999, all pemetrexed-treated patients are required to receive folic acid and Vitamin B12. A recently reported phase III study compared pemetrexed with docetaxel as 2nd line therapy in patients with advanced NSCLC. Treatment with pemetrexed resulted in clinically equivalent efficacy outcomes, but with significantly fewer side effects compared with docetaxel.

Study Timeline

• Study Start: 2006-05
• Study First Submitted: 2008-05-22
• Study First Submitted QC: 2008-05-23
• Study First Posted: 2008-05-26
• Primary Completion: 2009-05
• Study Completion: 2009-05
• Status Verified: 2009-12
• Last Update Submitted: 2009-12-14
• Last Update Posted: 2009-12-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

• Histologically confirmed inoperable (stage IIIB-IV) NSCLC. A block of Formaline Fixed Parafine Embedded tissue representative for the primary diagnosis should be available for genomic analysis (phase II part)
• Written informed consent
• Prior chemotherapy with platinum compounds in association with or without taxanes (phase I part)
• Previously untreated with docetaxel and pemetrexed (phase II part)
• Bidimensionally, non-irradiated measurable disease (according to RECIST criteria) (phase II)
• Age ≥18 years
• World Health Organization (WHO) performance status (PS) 0-2
• Life expectancy of at least 12 weeks
• Serum bilirubin less than 1.5 times the upper normal limit (UNL)
• AST and ALT less than 2.5 times the UNL in the absence of demonstrable liver metastases, or less than 5 times the UNL in the presence of liver metastases.
• Serum creatinine less than 1.5 times the UNL
• Neutrophil count more than 1.5x 109 /L
• Platelet count more than 100x 109 /L

Exclusion Criteria

• Other co-existing malignancies or malignancies diagnosed within the last 5 years (with the exception of basal cell carcinoma or cervical cancer in situ)
• Any evidence of severe uncontrolled concomitant disease (in the opinion of the investigator)
• Any unresolved chronic toxicity greater than CTC grade 2 from previous anticancer therapy
• Patients with unstable central nervous system metastases
• Malnutrition (loss of ≥ 20% of the original body weight)
• Performance status: 4
• Psychiatric illness or social situation that would preclude study compliance
• Pregnant or lactating women

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
1	Docetaxel	-
1	Pemetrexed	-

Primary Outcome Measures

Name	Time	Method
Evaluation of Dose Limited Toxicity and Maximum Tolerated Dose for the docetaxel/pemetrexed doublet	2 years

Secondary Outcome Measures

Name	Time	Method
Response rate for the docetaxel/pemetrexed doublet	2 years

Trial Locations

Locations (8)

"Laikon" General Hospital, Medical Oncology Unit, Propedeutic Dep of Internal Medicine; 🇬🇷 Athens, Greece

Air Forces Military Hospital, Dep of Medical Oncology; 🇬🇷 Athens, Greece

Sotiria" General Hospital, 1st Dep of Pulmonary Diseases; 🇬🇷 Athens, Greece

"Diabalkaniko" Hospital of Thessaloniki; 🇬🇷 Thessaloniki, Greece

"Theagenion" Anticancer Hospital of Thessaloniki; 🇬🇷 Thessaloniki, Greece

"IASO" General Hospital of Athnes, Dep of Medical Oncology; 🇬🇷 Athens, Greece

Sismanogleio General Hospital, 1st, 2nd Dep of Pulmonary Diseases; 🇬🇷 Athens, Greece

University General Hospital of Alexandroupolis, Dep of Medical Oncology; 🇬🇷 Alexandroupolis, Greece