Locally Advanced Non-small Cell Lung Cancer
Conditions
Keywords
Concurrent 3-D chemoradiotherapy,Docetaxel,Cisplatin,Chemotherapy ·
Brief summary
Concurrent chemoradiotherapy (CHRT) is the standard of care for unresectable locally advanced stage III non-small cell lung cancer. However, the optimal combination remains unclear. The aim of this study is to evaluate the efficacy of 2 induction chemotherapy cycles (days 1 and 22) with docetaxel 75 mg/m2 and cisplatin 75 mg/m2 followed by concurrent chemotherapy (weekly docetaxel-cisplatin, 20 mg/m2) and 3-D conformal radiotherapy for 6 weeks (66 Gy/5 fractions per week/2 Gy per fraction). ). The primary endpoint is the response rate. Secondary objectives are toxicity, time to progression, and overall survival.
Detailed description
Lung cancer is the most common malignancy among men in most countries and constitutes the leading cause of cancer death worldwide. Non-small cell histology represents roughly 80% of lung cancer cases comprising one third of patients with stage III, locally-advanced disease at diagnosis. Some stage IIIA cancers are considered resectable but many stage IIIA (with bulky N2) and stage IIIB (T4 any N M0, any T N3M0) cancers are considered unsuitable for surgery. However, some authors have shown that surgery after chemoradiotherapy (CHRT) is beneficial for at least progression-free survival (PFS). Since the 90s, CHRT has become the cornerstone of inoperable locally advanced non-small cell lung cancer (NSCLC). A meta-analysis of 52 randomized studies showed a survival improvement of 3% at 2 years and 2% at 5 years for patients treated with CHRT versus radiotherapy alone \[6\]. Concomitant chemoradiation was demonstrated to be better than sequential administration in terms of overall survival (OS) in 3 out of 4 randomized studies with esophagitis as the dose-limiting toxicity. Nevertheless, the median survival was around 16 months and improvement is needed. To better control micrometastatic disease and reduce distant relapses, one possibility is to increase radiosensitization with higher doses of chemotherapy.The aim of this phase II study is to evaluate the anti-tumoral activity of a weekly docetaxel-cisplatin combination administered concurrently with radiotherapy after 2 induction cycles with the same drugs.
Interventions
DRUGDocetaxel
Induction chemotherapy
RADIATIONconcomitant radiotherapy
Pulmonary and mediastinal radiotherapy
DRUGCisplatin
Induction chemotherapy
Sponsors
Centre Antoine Lacassagne
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
This was a prospective, open-label, multicentric, phase II study.
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* histologically or cytologically confirmed NSCLC, * stage IIIB (excluding malignant pleural or pericardial effusions, tumoral volume exceeding one radiation field, * N3 supraclavicular, and contralateral hilar nodal involvement) or inoperable stage IIIA defined by the new International Staging System \[21\], * 18 ≤ age ≤ 75 years, * Eastern Cooperative Oncology Group Performance Status (ECOG PS) ≤2, * weight loss \<10%, * at least one measurable lesion according to RECIST 1.0 criteria, * adequate hematopoietic function (absolute neutrophil count ≥2 × 109/l, platelets ≥100 × 109/l, and hemoglobin level ≥10g/dl), adequate hepatic function \[total serum bilirubin less than or equal to the institutional upper limit of normal (ULN), aspartate aminotransferase ≤1.5× ULN, and alkaline phosphatase ≤5× ULN\], and adequate renal function (serum creatinine ≤1.5× ULN).
Exclusion criteria
* patients previously treated with radiotherapy or chemotherapy for NSCLC, * previous cancer except basocellular carcinoma and in situ carcinoma of the cervix curatively treated and other cancers curatively treated for at least 5 years, * peripheral neuropathy NCI-CTC grade ≥2, * noncontroled severe disease, * pregnant or breast-feeding women.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| To evaluate the antitumor activity of Docetaxel - Cisplatin and concomitant thoracic radiotherapy after Docetaxel - Cisplatin induction chemotherapy in patients with locally advanced non-operable NSCLC by tumor response rate | up to 3 years | Tumor Response rate between 6 and 8 weeks according to RECIST 1.0 criteria after the end of radiotherapy (except in the case of early progression) that patients: * having received at least 4 weekly injections of Docetaxel and Cisplatin, * who have received the full radiotherapy treatment (except in case of cessation for toxicity, in which case the patients will be evaluable). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Overall survival and at 12 months | up to 3 years | To evaluate the overall survival at 12 months between the first day of treatment to the death |
| Response delay | up to 3 years | Complete response delay evaluated between the day of the complete response to the progression and partial response between the first day of the treatment and the progression |
| Progression Free Survival | up to 3 years | To evaluate Progression free survival according to RECIST criteria |
| Tolerance profile of the association in terms of immediate and delayed toxicity | up to 3 years | To evaluate early and late toxicity according to the NCI-CTC |
| Quality of Life evaluation (EORTC QLQ-C30 and QLQ-LC13) | up to 3 years | To evaluate the quality of life at inclusion, at the end oh chemotherapy, 2 months after the radiotherapy and every 3 months until end of study |
Outcome results
None listed