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

Hellenic Oncology Research Group

Status and phase

Completed

Phase 2

Phase 1

Conditions

Non Small Cell Lung Cancer

Treatments

Drug: Pemetrexed

Drug: Docetaxel

Study type

Interventional

Funder types

Other

Identifiers

NCT00684099

CT/05.18

Details and patient eligibility

About

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

Full 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.

Enrollment

70 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

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