Clinical trial · Interventional
Hypoxia-guided Radiotherapy With Cisplatin-etoposide in Stage I-III : Small Cell Lung Cancer(SCLC)
Individualized Hypoxia-guided Radiotherapy Combined With Standard Cisplatin-etoposide in Stage I-III SCLC
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Small Cell Lung Cancer (SCLC) | Lung Small Cell Carcinoma | ALIAS | 0.85 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| [18F]HX4 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- [18F]HX4
- interventionNames
- Drug: [18F]HX4
Primary outcomes (1)
- measure
- Cumulative local progression 18 months post-treatment as evaluated in a chest FDG-PET-CT scan
- timeFrame
- 2 years
Secondary outcomes (1)
- measure
- Overall survival
- timeFrame
- 2 years
- description
- Overall survival at two years
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available