Prophylactic Cranial Irradiation (PCI) Cognitive Tests in Non-small Cell Lung Cancer (NSCLC) Patients

NCT ID: NCT01290809

Last Updated: 2015-10-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

170 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-01-31

Study Completion Date

2015-10-31

Brief Summary

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Stage III non-small cell lung cancer (NSCLC) patients constitute a significant proportion of the lung cancer population. The prognosis of these patients has improved over the years due the introduction of combined modality treatment, including high-dose chemo-radiotherapy. The brain, however, remains one of the major sites of failure. Patients with brain metastasis suffer from a variety of neurological, cognitive and emotional difficulties that are known to adversely affect the health-related quality of life. Prophylactic Cranial Irradiation (PCI) can prevent or delay the development of brain metastasis, and as such can improve neurological disease-free survival and consequently health-related quality of life. But survival is short, and toxicities are real, as PCI in itself can also induce adverse effects. The cognitive adverse effects of PCI are not sufficiently illuminated and documented, due to the lack of formal and systematic evaluation in patient populations expected to have short survival. Also, recent attempts to reduce cognitive side effects of PCI by the application of hippocampal-avoidance PCI in order to prevent memory deficits have not been fully evaluated yet.

Before PCI can be offered routinely to stage III NSCLC patients in daily practice, the costs and benefits of this therapy should be investigated properly, to allow for well-informed treatment choices.

Detailed Description

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Conditions

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NSCLC

Study Design

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Observational Model Type

CASE_CROSSOVER

Study Time Perspective

PROSPECTIVE

Study Groups

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Prophylactic Cranial Irradiation

NSCLC patients treated with whole brain PCI: cognitive functioning as assessed by neuropsychological tests?

No interventions assigned to this group

no Prophylactic Cranial Irradiation

NSCLC patients not treated with whole brain PCI: cognitive functioning as assessed by neuropsychological tests?

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* UICC stage III A or III B (without malignant pleural or pericardial effusion) non-small cell lung cancer
* Whole body PDG-PET scan before the start of therapy available: no distant metastasis.
* CT or preferably MRI of the brain before the start of radical therapy available; no brain metastasis.
* Platinum-based chemotherapy is mandatory.
* Radical local therapy: concurrent or sequential chemotherapy and radiotherapy with or without surgery.
* Radiotherapy dose without surgery to at least biological equivalent of 60 Gy.
* No prior cranial irradiation.sufficient proficiency in Dutch language
* sufficient proficiency in Dutch language
* MRI (and not CT scan) pre-PCI

Exclusion Criteria

* none
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The Netherlands Cancer Institute

OTHER

Sponsor Role collaborator

Amsterdam UMC, location VUmc

OTHER

Sponsor Role collaborator

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

OTHER

Sponsor Role collaborator

Maastricht University Medical Center

OTHER

Sponsor Role collaborator

University Medical Center Groningen

OTHER

Sponsor Role collaborator

Maastricht Radiation Oncology

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Dirk deruysscher

Role: PRINCIPAL_INVESTIGATOR

Maastro Clinic, The Netherlands

Locations

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Academic Medical Center

Amsterdam, , Netherlands

Site Status

NKI

Amsterdam, , Netherlands

Site Status

VU University Medical Center

Amsterdam, , Netherlands

Site Status

University Medical Center Groningen

Groningen, , Netherlands

Site Status

Countries

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Netherlands

Other Identifiers

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093074

Identifier Type: -

Identifier Source: org_study_id

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