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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.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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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.

A. Hessels, MD PhD contact

06-25648774

a.c.hessels@umcg.nl

Netherlands1 site, 1 recruiting
  • UMCG

    Groningen

    Recruiting

Other trials in Netherlands

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.
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 groups in NCT06484491
Study groupRoleWhat they receive
Arm 1 Intervention groupExperimentalDose-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.

  1. 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)
  1. 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

  2. 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

  3. 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

  4. Overall survival

    Measured: Data for assessing overall survival will be recorded up to 2 years after chemoradiotherapy

  5. 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

  6. 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

  7. 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

  8. 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

  9. 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

  10. 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.

  1. First posted3 Jul 2024
  2. Study start1 Sep 2025
  3. Primary completion1 Oct 2027 (estimated)
  4. Study completion1 Oct 2028 (estimated)

Resources

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)
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

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.

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