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A Phase II Trial of Cisplatin-Docetaxel Induction Plus Concurrent 3-D Conformal Radiotherapy and Weekly Chemotherapy (TAXCIS)

12 december 2017 uppdaterad av: Centre Antoine Lacassagne

Cisplatin-Docetaxel Induction Plus Concurrent 3-D Conformal Radiotherapy and Weekly Chemotherapy for Locally Advanced Non-Small Cell Lung Cancer Patients: A Phase II Trial

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.

Studieöversikt

Detaljerad beskrivning

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.

Studietyp

Interventionell

Inskrivning (Faktisk)

44

Fas

  • Fas 2

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 75 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

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.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Radiochemotherapy
Induction chemotherapy with docetaxel and cisplatine and concomitant radiotherapy
Induction chemotherapy
Pulmonary and mediastinal radiotherapy
Induction chemotherapy

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
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
Tidsram: 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).
up to 3 years

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Overall survival and at 12 months
Tidsram: up to 3 years
To evaluate the overall survival at 12 months between the first day of treatment to the death
up to 3 years
Response delay
Tidsram: 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
up to 3 years
Progression Free Survival
Tidsram: up to 3 years
To evaluate Progression free survival according to RECIST criteria
up to 3 years
Tolerance profile of the association in terms of immediate and delayed toxicity
Tidsram: up to 3 years
To evaluate early and late toxicity according to the NCI-CTC
up to 3 years
Quality of Life evaluation (EORTC QLQ-C30 and QLQ-LC13)
Tidsram: 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
up to 3 years

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

5 augusti 2004

Primärt slutförande (Faktisk)

31 oktober 2010

Avslutad studie (Faktisk)

31 oktober 2011

Studieregistreringsdatum

Först inskickad

30 november 2017

Först inskickad som uppfyllde QC-kriterierna

12 december 2017

Första postat (Faktisk)

13 december 2017

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

13 december 2017

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

12 december 2017

Senast verifierad

1 november 2017

Mer information

Termer relaterade till denna studie

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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