Carcinoma, Non-Small-Cell LungHyDoseNCT06484491
IMPT Dose Escalation for NSCLC (HyDose)
A study testing Dose-escalated intensity-modulated proton therapy (IMPT-74), Cisplatin or carboplatin + pemetrexed for induction chemotherapy, cisplatin + docetaxel for concurrent chemotherapy and Immunotherapy: adjuvant durvalumab in people with Carcinoma, Non-Small-Cell Lung, run by University Medical Center Groningen at 1 site in Netherlands.
Trial summary
The goal of this clinical pilot trial is to learn if dose to the tumor in the lung can be safely increased using proton therapy in stage III non-small-cell lung cancer patients receiving combined chemotherapy and radiotherapy. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Carcinoma, Non-Small-Cell Lung
- What is being tested?
- Dose-escalated intensity-modulated proton therapy (IMPT-74), Cisplatin or carboplatin + pemetrexed for induction chemotherapy, cisplatin + docetaxel for concurrent chemotherapy and Immunotherapy: adjuvant durvalumab
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 87 participants
- Where
- 1 siteNetherlands
- Study dates
- 1 Sep 2025to 1 Oct 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age ≥18 years
- WHO performance score 0-2
- Histologically proven stage III NSCLC
- Planned for CCRT and adjuvant immunotherapy (intention to treat)
- Primary tumour volume outside of mediastinal PRV (i.e., mediastinal envelope + 5 mm) ≥60% of total primary tumour volume (true for 75% of patients in preliminary analysis), for sufficient dose escalation
Who cannot join
- Chemotherapy not given concurrently with radiotherapy
- Upfront decision that adjuvant immunotherapy is not possible
- Primary tumour overlapping ≥40% with mediastinal PRV
- Unable or unwilling to understand the information on trial-related topics, to give informed consent or to fill out quality-of-life questionnaires
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Radiotherapy Dose Escalation Using Intensity-modulated Proton Therapy for Non-small-cell Lung Cancer Patients
The goal of this clinical pilot trial is to learn if dose to the tumor in the lung can be safely increased using proton therapy in stage III non-small-cell lung cancer patients receiving combined chemotherapy and radiotherapy. The main questions it aims to answer are:
- Is the risk of severe radiotherapy toxicities (requiring hospital admission) within acceptable margins ?
- What is a rough estimate of the effect of the treatment under study?
Read more
Compared to standard care in our clinic, all participants in this pilot trial will
- Receive a higher dose of proton therapy to the tumor in the lung albeit with the same number of radiotherapy visits as the current standard treatment.
- Receive two additional follow-up visits at the clinic after treatment, namely 4 and 6 weeks after finishing radiotherapy.
- Two additional blood withdrawals at the last week of radiotherapy and 4 weeks after finishing radiotherapy, to measure a type of white blood cells.
- Receive an extra quality of life questionnaire at the last week of radiotherapy.
- Conditions
- Carcinoma, Non-Small-Cell Lung
- Being tested
- Dose-escalated intensity-modulated proton therapy (IMPT-74), Cisplatin or carboplatin + pemetrexed for induction chemotherapy, cisplatin + docetaxel for concurrent chemotherapy, Immunotherapy: adjuvant durvalumab
- Keywords
- Lung Neoplasms, Proton Therapy, Radiotherapy
- Medical subject headings
- Carcinoma, Non-Small-Cell Lung, Lung Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Dose-escalated intensity-modulated proton therapy (IMPT-74)Radiation
Heterogeneous simultaneous integrated boost of 74.0 Gy (RBE) to primary tumor >15mm away form mediastinal envelope, and 64.0 Gy (RBE) to primary tumor =< 15mm away from mediastinal envelope. The rest of the clinical target volume, including affected lymph nodes, receives 60.0 Gy (RBE).
Cisplatin or carboplatin + pemetrexed for induction chemotherapy, cisplatin + docetaxel for concurrent chemotherapyDrug
Induction course:
-Cisplatin (75 mg/m2) or carboplatin (AUC 6) + pemetrexed (500mg/m2).
Concurrent chemoradiotherapy:
- Weekly cisplatin (20mg/m2) + docetaxel (20mg/m2) on Mondays.
- Radiotherapy will be given for 5x5 days.
Immunotherapy: adjuvant durvalumabDrug
Adjuvant treatment will be given starting 1-6 weeks after chemoradiotherapy if no progression, good performance (PS 0-1), no other contra-indication for immunotherapy.
Doses:
- Start durvalumab 10 mg/kg 1x/14 days.
- If possible after 2 courses switch to 1500 mg flat dose 1x/4 wk.
- Continue for 12 months in total.
| Study group | Role | What they receive |
|---|---|---|
| Arm 1 Intervention group | Experimental | Dose-escalated IMPT Receives: Radiation: Dose-escalated intensity-modulated proton therapy (IMPT-74); Drug: Cisplatin or carboplatin + pemetrexed for induction chemotherapy, cisplatin + docetaxel for concurrent chemotherapy; Drug: Immunotherapy: adjuvant durvalumab |
What is being measured
The primary outcome is the main question the study is designed to answer.
Severe (grade 3+) adverse effects up to six months after radiotherapy
Measured: Data for assesing safety will be recorded from day 1 to 365
Secondary outcomes (10)
Local control of the lung tumour assessed by the treating physician and radiologist according to Response Evaluation Criteria in Solid Tumors (RECIST 1.1)
Local control was defined as the time from randomization until the date of objective disease progression in the lungs (RECIST 1.1). Local progression was defined using RECIST 1.1 as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions. Local control was calculated using the Kaplan-Meier technique.
Measured: Data for assessing local control will be recorded up to 2 years after chemoradiotherapy
Progression-free survival based on review by the treating physician and radiologist according to Response Evaluation Criteria in Solid Tumors (RECIST 1.1)
PFS was defined as the time from randomization until the date of objective disease progression (RECIST 1.1) or death (by any cause in the absence of progression). Progression was defined using RECIST 1.1 as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions. PFS was calculated using the Kaplan-Meier technique.
Measured: Data for assessing progression-free survival will be recorded up to 2 years after chemoradiotherapy
Distant metastasis control based on review by the treating physician and radiologist according to Response Evaluation Criteria in Solid Tumors (RECIST 1.1)
Time to distant metastasis was defined as the time from the date of randomization until the first date of distant metastasis. Distant metastasis was defined as any new lesion that was outside of the radiation field according to RECIST 1.1 or proven by biopsy. Time to distant metastasis was calculated using the Kaplan-Meier technique.
Measured: Data for assessing distant metastasis will be recorded up to 2 years after chemoradiotherapy
Overall survival
Measured: Data for assessing overall survival will be recorded up to 2 years after chemoradiotherapy
Grade 2+ adverse effects (i.e., requiring medication), both acute and late
Measured: Data for assesing safety will be recorded from day 1 to 365
Qualifying for adjuvant immunotherapy after finishing chemoradiotherapy yes/no
Measured: Data on qualifying for adjuvant immunotherapy will be recorded up to 6 weeks after finishing chemoradiotherapy
European Organization for Research and Treatment of Cancer Quality of Life Questionnaires Core-30 item (EORTC QLQ-C30)
The EORTC QLQ-C30 is a disease specific measurement instrument for use in patients with or cured from cancer. It measures a number of aspects of quality of life, namely: physical functioning; role functioning; emotional functioning; cognitive functioning; social functioning. It also evaluates symptoms, such as pain, nausea, sleep, dyspnea, cancer related fatigue, and constipation, diahorrea, and fincancial problems, as well as two questionas about overall quality of life.
The questionnaire consists of a total of 30 items, divided over 9 subscales. The items are on Likert scales. The scores for each subscale can be calculated on a 0-100 scale, as well as the total score. A high score for a functional scale represents a high/healthy level of functioning. A high score for global health status / QoL represents a high QoL. By contrast, a high score for a symptom scale/item represents a high level of symptomatology/problems.
Measured: Data for assesing quality of life will be recorded up to day 730
European Organization for Research and Treatment of Cancer Quality of Life Questionnaires Lung Cancer 13-item (EORTC-QLQ-LC13)
The EORTC QLQ-LC13 is a 13-item lung cancer-specific questionnaire module meant as a disease-specific extension to the EORTC QLC-C30. It contains both multi-item (dyspnea) and single-item (all others) measures of lung cancer-associated symptoms (i.e. coughing, haemoptysis, dyspea and pain) and side-effects from conventional chemo- and radiotherapy (i.e. hair loss, neuropathy, sore mouth and dysphagia). The items are scored on likert scales, and can be converted to a 0-100 scale for each symptom and side effect. A high score represents a high level of symptomatology or problems.
Measured: Data for assesing quality of life will be recorded up to day 730
3 EuroQoL-5D three-level version (EQ-5D-3L)
This questionnaire consists of two pages: the EQ-5D descriptive system and the EQ-5D visual analogue scale (EQ VAS):
- The descriptive system comprises five dimensions, each describing a different aspect of health: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has three levels: no problems, some problems, extreme problems (labelled 1-3). The respondent indicates their health by checking the box against the most appropriate statement in each of the five dimensions.
- The EQ VAS redords the respondent's self-rated health on a vertical VAS where the endpoints are labelled 'The best health you can imagine' and 'The worst health you can imagine'. This information can be used as a quantitative measure of health outcome as judged by the individual respondents.
Measured: Data for assesing quality of life will be recorded up to day 730
Lymphocyte counts after finishing chemoradiotherapy
Measured: Data for assessing lymphocyte counts will be assessed between 4 and 6 weeks after chemoradiotherapy
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Jul 2024
- Study start1 Sep 2025
- Primary completion1 Oct 2027 (estimated)
- Study completion1 Oct 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Carcinoma, Non-Small-Cell LungStudies of the same condition, open and under way.
- More trials run by University Medical Center GroningenThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 87 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University Medical Center Groningen
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- R. Wijsman, MD PhD, Principal investigator, University Medical Center GroningenA. Van der Wekken, MD PhD, Principal investigator, University Medical Center GroningenE. Korevaar, dr ir (PhD), Principal investigator, University Medical Center Groningen
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06484491
- Sponsor's protocol ID
- PNM16745
- Other IDs
- NL86435.042.24
- Acronym
- HyDose
- Status last verified
- Dec 2025
- First submitted
- 17 Jun 2024
- Last updated
- 30 Jan 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 30 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Radiotherapy Dose Escalation Using Intensity-modulated Proton Therapy for Non-small-cell Lung Cancer Patients
- ClinicalTrials.gov ID
- NCT06484491
- Acronym / sponsor ID
- HyDose / PNM16745
- Conditions
- Carcinoma, Non-Small-Cell Lung
- Keywords
- Lung Neoplasms, Proton Therapy, Radiotherapy
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 87 participants (estimated)
- Lead sponsor
- University Medical Center GroningenUniversity, hospital or other
- Study start
- 1 Sep 2025 (actual)
- Primary completion
- 1 Oct 2027 (estimated)
- Study completion
- 1 Oct 2028 (estimated)
- First posted
- 3 Jul 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this clinical pilot trial is to learn if dose to the tumor in the lung can be safely increased using proton therapy in stage III non-small-cell lung cancer patients receiving combined chemotherapy and radiotherapy. The main questions it aims to answer are:
- Is the risk of severe radiotherapy toxicities (requiring hospital admission) within acceptable margins ?
- What is a rough estimate of the effect of the treatment under study?
Compared to standard care in our clinic, all participants in this pilot trial will
- Receive a higher dose of proton therapy to the tumor in the lung albeit with the same number of radiotherapy visits as the current standard treatment.
- Receive two additional follow-up visits at the clinic after treatment, namely 4 and 6 weeks after finishing radiotherapy.
- Two additional blood withdrawals at the last week of radiotherapy and 4 weeks after finishing radiotherapy, to measure a type of white blood cells.
- Receive an extra quality of life questionnaire at the last week of radiotherapy.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Arm 1 Intervention group | Experimental | Radiation: Dose-escalated intensity-modulated proton therapy (IMPT-74), Drug: Cisplatin or carboplatin + pemetrexed for induction chemotherapy, cisplatin + docetaxel for concurrent chemotherapy, Drug: Immunotherapy: adjuvant durvalumabDose-escalated IMPT |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Age ≥18 years
- WHO performance score 0-2
- Histologically proven stage III NSCLC
- Planned for CCRT and adjuvant immunotherapy (intention to treat)
- Primary tumour volume outside of mediastinal PRV (i.e., mediastinal envelope + 5 mm) ≥60% of total primary tumour volume (true for 75% of patients in preliminary analysis), for sufficient dose escalation
Key exclusion criteria (4 listed)
- Chemotherapy not given concurrently with radiotherapy
- Upfront decision that adjuvant immunotherapy is not possible
- Primary tumour overlapping ≥40% with mediastinal PRV
- Unable or unwilling to understand the information on trial-related topics, to give informed consent or to fill out quality-of-life questionnaires
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Dose-escalated intensity-modulated proton therapy (IMPT-74)Heterogeneous simultaneous integrated boost of 74.0 Gy (RBE) to primary tumor >15mm away form mediastinal envelope, and 64.0 Gy (RBE) to primary tumor =< 15mm away from mediastinal envelope. The rest of the clinical target volume, including affected lymph nodes, receives 60.0 Gy (RBE). | Radiation | Arm 1 Intervention group |
| Cisplatin or carboplatin + pemetrexed for induction chemotherapy, cisplatin + docetaxel for concurrent chemotherapyInduction course: -Cisplatin (75 mg/m2) or carboplatin (AUC 6) + pemetrexed (500mg/m2). Concurrent chemoradiotherapy: * Weekly cisplatin (20mg/m2) + docetaxel (20mg/m2) on Mondays. * Radiotherapy will be given for 5x5 days. | Drug | Arm 1 Intervention group |
| Immunotherapy: adjuvant durvalumabAdjuvant treatment will be given starting 1-6 weeks after chemoradiotherapy if no progression, good performance (PS 0-1), no other contra-indication for immunotherapy. Doses: * Start durvalumab 10 mg/kg 1x/14 days. * If possible after 2 courses switch to 1500 mg flat dose 1x/4 wk. * Continue for 12 months in total. | Drug | Arm 1 Intervention group |
Primary outcome
Severe (grade 3+) adverse effects up to six months after radiotherapy
Time frame: Data for assesing safety will be recorded from day 1 to 365
10 secondary outcomes
Local control of the lung tumour assessed by the treating physician and radiologist according to Response Evaluation Criteria in Solid Tumors (RECIST 1.1)
Time frame: Data for assessing local control will be recorded up to 2 years after chemoradiotherapy
Progression-free survival based on review by the treating physician and radiologist according to Response Evaluation Criteria in Solid Tumors (RECIST 1.1)
Time frame: Data for assessing progression-free survival will be recorded up to 2 years after chemoradiotherapy
Distant metastasis control based on review by the treating physician and radiologist according to Response Evaluation Criteria in Solid Tumors (RECIST 1.1)
Time frame: Data for assessing distant metastasis will be recorded up to 2 years after chemoradiotherapy
Overall survival
Time frame: Data for assessing overall survival will be recorded up to 2 years after chemoradiotherapy
Grade 2+ adverse effects (i.e., requiring medication), both acute and late
Time frame: Data for assesing safety will be recorded from day 1 to 365
Qualifying for adjuvant immunotherapy after finishing chemoradiotherapy yes/no
Time frame: Data on qualifying for adjuvant immunotherapy will be recorded up to 6 weeks after finishing chemoradiotherapy
European Organization for Research and Treatment of Cancer Quality of Life Questionnaires Core-30 item (EORTC QLQ-C30)
Time frame: Data for assesing quality of life will be recorded up to day 730
European Organization for Research and Treatment of Cancer Quality of Life Questionnaires Lung Cancer 13-item (EORTC-QLQ-LC13)
Time frame: Data for assesing quality of life will be recorded up to day 730
3 EuroQoL-5D three-level version (EQ-5D-3L)
Time frame: Data for assesing quality of life will be recorded up to day 730
Lymphocyte counts after finishing chemoradiotherapy
Time frame: Data for assessing lymphocyte counts will be assessed between 4 and 6 weeks after chemoradiotherapy
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Jan 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
R. Wijsman, MD PhD principal investigator
University Medical Center Groningen
A. Van der Wekken, MD PhD principal investigator
University Medical Center Groningen
E. Korevaar, dr ir (PhD) principal investigator
University Medical Center Groningen
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Dose-escalated intensity-modulated proton therapy (IMPT-74), Cisplatin or carboplatin + pemetrexed for induction chemotherapy, cisplatin + docetaxel for concurrent chemotherapy and Immunotherapy: adjuvant durvalumab in people with Carcinoma, Non-Small-Cell Lung, run by University Medical Center Groningen at 1 site in Netherlands.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 30 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact A. Hessels, MD PhD (06-25648774, a.c.hessels@umcg.nl), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Severe (grade 3+) adverse effects up to six months after radiotherapy (time frame: Data for assesing safety will be recorded from day 1 to 365). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Jan 2026.