Concurrent and Non-concurrent Chemo-radiotherapy or Radiotherapy Alone for Patients With Oligo-metastatic Stage IV Non-small Cell Lung Cancer (NSCLC)

Sponsor
Maastricht Radiation Oncology (Other)
Overall Status
Completed
CT.gov ID
NCT01282450
Collaborator
(none)
60
1
1
62
1

Study Details

Study Description

Brief Summary

In recent years, it has become clear, that also in non-small cell lung cancer (NSCLC), a group of patients with less than 5 distant metastases may experience long-term survival when treated radically to all macroscopic cancer sites. Thus has mostly been established for individuals with so-called solitary brain metastases and to a lesser extend in solitary adrenal gland metastases, but in other metastatic subgroups, the same may be applicable. In a prospective survey in the region of the Integral Cancercentre (IKL), we could identify on a yearly base 30 patients with NSCLC who could theoretically be amendable for radical treatment of all oligo-metastatic locations. We therefore want to perform a prospective study in which patients with less than 4 oligo-metastatic sites from a primary NSCLC will be treated radically with the aim to improve long-term survival. As many discussion points remain, even after thorough discussions with chest physicians, pulmonary surgeons and colleagues from diagnostic disciplines, we decided to go for a pragmatic approach, implying that all macroscopic disease sites should be treated radically, being defined as surgery with a R0 resection or in case of an unforeseen R1 resection, followed by radiotherapy, or radiotherapy to a biological equivalent of at least 60 Gy in 30 daily fractions. In the same patient, one metastatic site may be treated with surgery and another with radical radiotherapy. Systemic treatment was not made mandatory, because it was felt that it's role is unclear in patients with early stage local cancer and with oligo-metastatic disease.

Condition or Disease Intervention/Treatment Phase
  • Radiation: Radiotherapy
Phase 2

Detailed Description

Eligible patients (see below) will receive radical radiotherapy to the primary tumor and the initially involved mediastinal lymph nodes to an MLD (Mean Lung Dose) of 20 +/- 1Gy, irrespective of lung function and/or to all metastatic sites to a minimal biological equivalent of 60Gy in 30 daily fractions. This may be delivered with hypofractionated stereotactic techniques or with other more protracted fractionation regimen.

Both the primary tumor, the regional N1 lymph nodes and the oligo-metastatic site(s) may be treated with surgery, as long as an R0 resection is deemed possible. Systemic treatment is not required, but should be given according to the local extend of the tumor.

Local radiotherapy will be delivered according to the protocol of MAASTRO clinic for that anatomical site.

Other dose-constraints: spinal cord max: 54Gy, brachial plexus (Dmax): 66Gy The radiation doses will be specified according to ICRU 50. Lung density corrections will be applied, as well as all standard QA procedures. Technical requirements are the same as in standard practice at MAASTRO clinic.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Official Title:
Concurrent and Non-concurrent Chemo-radiotherapy or Radiotherapy Alone for Patients With Oligo-metastatic Stage IV Non-small Cell Lung Cancer (NSCLC).
Study Start Date :
May 1, 2006
Actual Primary Completion Date :
Jul 1, 2011
Actual Study Completion Date :
Jul 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Experimental: Single arm

Eligible patients

Radiation: Radiotherapy
Radiotherapy
Other Names:
  • Radiotherapy with or without surgery or chemotherapy
  • Outcome Measures

    Primary Outcome Measures

    1. Overall survival [2 years]

      The survival of participating patient two years after entering the study

    2. Overall survival [3 years]

      The survival of participating patients, three years after entering the study.

    Secondary Outcome Measures

    1. Progression free survival [2 years]

    2. Dyspnea (CTC4.0) [2 years]

    3. Dysphagia (CTC 4.0) [2 years]

    4. Patterns of recurrence [2 years]

    5. Progression free survival [3 years]

    6. Dyspnea (CTC4.0) [3 years]

    7. Dysphagia (CTC4.0) [3 years]

    8. Patterns of recurrence [3 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Histological or cytological proven NSCLC

    • UICC stage IV, or solitary metastases (< 5), which are amendable for radical local treatment

    • Performance status 0-2

    • Other malignancy is allowed if controlled at the point of diagnosis

    Exclusion Criteria:
    • Not NSCLC or mixed NSCLC and other histologies (e.g. small cell carcinoma)

    • Stage I-III, except for T4 because of pleural metastases

    • Performance status 3 or more

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 MAASTRO clinic Maastricht Limburg Netherlands 6229 ET

    Sponsors and Collaborators

    • Maastricht Radiation Oncology

    Investigators

    • Principal Investigator: Dirk De Ruysscher, MD, PhD, MAASTRO clinic, Maastricht Radiation Oncology

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT01282450
    Other Study ID Numbers:
    • Oligometa's
    First Posted:
    Jan 25, 2011
    Last Update Posted:
    Jul 19, 2011
    Last Verified:
    Jul 1, 2011
    Keywords provided by , ,
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 19, 2011