Paclitaxel/Carboplatin (PC) Followed by Gefitinib Versus PC in Advanced Non-small Cell Lung Cancer (PRIDE)

Asan Medical Center

Status and phase

Completed

Phase 2

Conditions

Non Small Cell Lung Cancer

Treatments

Drug: Paclitaxel/Carboplatin

Drug: Paclitaxel/Carboplatin/Gefitinib

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01196234

AMC 2009-0677

Details and patient eligibility

About

This study compares paclitaxel/carboplatin (PC) to PC chemotherapy followed by gefitinib for 2 weeks in patients with Non-small Cell Lung Cancer (NSCLC) without epidermal growth factor receptor (EGFR) mutations.

Expanded acronym : [P]aclitaxel/Ca[r]boplatin (PC) followed by Gef[i]tinib in A[d]vanc[e]d Non-small Cell Lung Cancer (NSCLC): Randomized phase II study.

Full description

A randomized phase II trial that compares paclitaxel/carboplatin (PC) to PC chemotherapy followed by gefitinib for 2 weeks in patients with NSCLC without EGFR mutations. While previous studies with cytotoxic agents and gefitinib failed to show any benefit, we altered the schedule of administration in hopes to gain synergy between agents.

Enrollment

84 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

More than 18 years of age
Histologically documented non-small cell lung cancer with metastasis (Stage IV) or locally advanced (Stage IIIB) with malignant effusion.
At least 1 measurable lesion as defined by RECIST1.0. All target lesions must have a unidirectional diameter of at least 1cm. Baseline measurements must be compared within 4 weeks prior to enrollment.
ECOG PS 0-2
At least 1 week since the last radiotherapy. Patients must have recovered from all acute toxicities from radiotherapy.
Patients must have adequate hematologic, renal and liver function as defined by Hb > 9g/dL, neutrophils > 1000/mm3, platelets > 50,000/mm3, creatinine < 2mg/dL, and AST (SGOT) and/or ALT (SGPT) < 5 x UNL (upper normal limit).
Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests and other study procedures.
Written and voluntary informed consent understood, signed and dated.

Exclusion criteria

Patients with tumor harboring EGFR mutation.
Prior systemic therapy for NSCLC
Non-smoking patients with adenocarcinoma. But if those patients show wild type EGFR, they are eligible to this study.
Symptomatic brain metastasis. Brain metastases stable < 2 weeks before dosing or requiring concurrent steroid treatment or with clinical symptoms.
Major surgery within 3 weeks prior to study enrollment.
Previous (less than 3 years ago) or current malignancies at sites other than curatively treated in situ carcinoma of cervix, or basal or squamous cell carcinoma of the skin.
Severe medical illness or active infection that would impair the ability to receive gefitinib.
Pregnancy or breast feeding.