Small Cell Lung Cancer (SCLC)
Conditions
Keywords
Toxicity, Progression, Survival, SCLC
Brief summary
Since radiation dose escalation to a large volume of tumour inevitably will induce higher toxicity than is currently the case, efforts must be made to limit the volume of tissue irradiated. Moreover, the irradiation of larger tumour volumes leads to a lower achievable tumour dose when keeping the normal tissue doses constant. Central is thus the question whether it would be possible to limit the volume of tumour to be boosted by selectively escalating the radiation dose to specific disease sites which are theoretically more prone to relapse.
Detailed description
Hypoxic imaging with PET scans seems attractive for this purpose as hypoxia is associated with resistance for radiotherapy and approximately 70 % of SCLC are severely hypoxic at diagnosis\[2\]. We hypothesize that it might be possible to use a selective boost in these patients to tumor areas which are still hypoxic at the end of the standard chemo-radiotherapy to a dose of 45 Gy in 30 fractions in 3 weeks. This way all SCLC (small cell lung cancer) patients can receive a safe, but higher dose of radiotherapy to the whole tumor volume, while the most resistant areas receive the highest possible dose. This is a hypothesis generating trial designed to deliver at least the current standard treatment to malignant tissue while defining patient selection criteria for future study.
Interventions
DRUG[18F]HX4
Intravenous injection
Sponsors
Maastricht University Medical Center
Maastricht Radiation Oncology
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Histologically or cytologically confirmed stage I-III small cell lung cancer. WHO performance status 0-2 * Absolute neutrophil count at least 1800/µl and platelets at least 100000/µl and hemoglobin at least 6.2 mmol/l. * Adequate renal function: calculated creatinine clearance at least 40 ml/min * Adequate hepatic function: Total bilirubin ≤ 1.5 x upper limit of normal (ULN) for the institution; ALT, AST, and alkaline phosphatase ≤ 2.5 x ULN for the institution (in case of liver metastases ≤ 5 x ULN for the institution) * No previous platinum chemotherapy or topo-isomerase-inhibitors for SCLC. * Lung function: FEV1 at least 30 % and DLCO at least 30 % of the age predicted value * No history of prior chest radiotherapy * Life expectancy more than 6 months * Willing and able to comply with the study prescriptions * 18 years or older * Not pregnant or breast feeding and willing to take adequate contraceptive measures during the study * Ability to give and having given written informed consent before patient registration * No mixed pathology, e.g. non-small cell plus small cell cancer * No recent (\< 3 months) severe cardiac disease (NYHA class \>1) (congestive heart failure, infarction) * No uncontrolled infectious disease * No other active malignancy * No major surgery (excluding diagnostic procedures like e.g. mediastinoscopy) in previous 4 weeks * No treatment with investigational drugs in 4 weeks prior to or during this study
Exclusion criteria
* The opposite of the above
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cumulative local progression 18 months post-treatment as evaluated in a chest FDG-PET-CT scan | 2 years |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Overall survival | 2 years | Overall survival at two years |
Outcome results
None listed