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NCT Number: NCT01850303

Maintenance After Induction Chemotherapy in Elderly Patients With Advanced Non-small Cell Lung Cancer

For elderly patient, the treatment of Non Small Cell Lung Cancer was based on monotherapy but IFCT-0501 trial begun in 2006, demonstrated that a bitherapy (carboplatin and paclitaxel) is better than monotherapy in term of overall survival and progression free survival. The current recommendations are now to administer a carboplatin based bitherapy (4 or 6 cycles). After the treatment is stopped until progression and initiation of a second line treatment. The risk of this strategy is to be confronted to a rapid disease progression during the free interval. Indeed, about 1/3 of the patients whose disease was controlled after the chemotherapy do not receive 2nd line. The concept of maintenance is based on a continuous therapeutic pressure in order to preserve the therapeutic profit obtained by the treatment of 1st line (induction chemotherapy).

There is two types of maintenance :

* continuous maintenance therapy which consists in continuing the treatment initially associated with platinum until disease progression. * switch maintenance which consists in introducing a new treatment after the end of induction chemotherapy The two types are validated by several trials. The marketing authorization of pemetrexed was enlarged to maintenance for non squamous carcinoma.

Gemcitabine has a good tolerance profile which make possible the use in a maintenance strategy. Several trials evaluated maintenance with this product and some show benefits in term of progression free survival.

The objective of this trial is to evaluate the switch maintenance in elderly patient with a controlled disease after 4 cycles of chemotherapy carboplatin-paclitaxel.

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Key information

Age range

70 year–89 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Abbeville - CH, Abbeville, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically or cytologically documented Non Small Cell Lung Cancer non resectable or non irradiable stage III or stage IV
  • EGFR wild type or non feasible EGFR
  • 90 >Age ≥ 70
  • ECOG Performance status : 0, 1 or 2
  • Mini-Mental Test Status (MMS) > 23

Exclusion criteria

  • Mixed non-small cell and small cell tumors
  • Patients with EGFR mutated tumor
  • Patient with EML4-ALK translocation
  • Evolutive or symptomatic metastasis of central nervous system
  • Superior vena cava syndrome
  • Calcemia > 2,70 mmol/L

Treatment and study plan

Pemetrexed

Drug

Gemcitabine

Drug

Induction chemotherapy

Drug

4 cycles of carboplatin-paclitaxel

Primary outcomes

  1. Overall survival

    Time frame: Up to 15 months

Secondary outcomes

  1. Feasibility of treatment (number of cycles of maintenance)

    Time frame: 84 days on average

    Number of cycles of maintenance (median)

  2. Progression free survival

    Time frame: up to 7 months

  3. response and stabilisation duration

    Time frame: up to 7 months

  4. Number of patient with at least one adverse event

    Time frame: up to 7 months

  5. Treatment duration

    Time frame: Up to 7 months

  6. 2nd line response rate

    Time frame: Up to 4 months

  7. Number of adverse events

    Time frame: Up to 7 months

  8. 2nd line overall survival

    Time frame: Up to 7 months

  9. 2nd line progression free survival

    Time frame: Up to 4 months

Sponsors and collaborators

Lead sponsor

Intergroupe Francophone de Cancerologie Thoracique

Other

Registry information

Official study title

Phase III Study Comparing Maintenance With Pemetrexed or Gemcitabine to a Surveillance in Elderly Patients (70 Years Old and More) With a Advanced Non Small Cell Lung Cancer Controlled by Induction Chemotherapy.

Acronym: MODEL

Important dates

Study start
2013
Primary completion
2018
Study completion
2020
First posted
May 9, 2013
Registry last updated
Mar 14, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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