Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT05808790

Colorectal Pulmonary Metastases: Pulmonary Metastasectomy Versus Stereotactic Ablative Radiotherapy

COPPER is an international, multicenter, parallel-arm, phase III randomized controlled trial comparing two local treatment strategies (SABR or metastasectomy) for patients with an indication for local treatment for limited (max. three) colorectal pulmonary metastases

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Amsterdam University Medical Center (AUMC)

Amsterdam, 1081 HZ, Netherlands

About this study

The study is formally endorsed by the Dutch Society of Lung Surgery (NVvL), the Dutch Society of Cardiothoracic Surgery (NVT), the Dutch Society of Radiation Oncology (NVRO). The main objective of the proposed randomized trial is to compare efficacy of SABR to the efficacy of metastasectomy with regards to the primary endpoint (local recurrence free survival at 5 years) in patients with limited colorectal pulmonary metastases. This will determine the most effective local treatment modality. The investigators hypothesize that patients with limited colorectal pulmonary metastases will have non-inferior overall survival after pulmonary metastasectomy compared to SABR, however metastasectomy will result in superior local recurrence free survival at five years when compared to SABR. In addition, the investigators hypothesize that SABR is associated with lower morbidity, comparable quality of life and comparable health care costs compared to metastasectomy. Recurrent metastases are preferably treated by the index treatment to which the patient was randomized, local recurrent metastases are preferably treated by means of cross-over between both arms. Comparing metastasectomy to SABR for patients with colorectal pulmonary metastases will present the international community the evidence needed to better select patients for local radical treatment, while diminishing uncertainty for patients and care givers.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years
  • Eastern Cooperative Oncology Group (ECOG)-Performance status 0 - 2
  • Willing to provide informed consent
  • Patients with 1 to 3 lung metastases from colorectal cancer eligible for both a minimally invasive surgical resection and SABR, as assessed by the multidisciplinary tumor board (MDT)
  • Radically treated primary colorectal cancer
  • Patient is able and willing to complete the quality-of-life questionnaires
  • Previous liver metastases are radically treated with curative intent
  • Histologically confirmed malignancy with metastatic disease detected on imaging. Biopsy of metastasis is preferred, but not required.

Exclusion criteria

  • Previous or present metastases outside liver or lungs
  • Concurrent malignant cancer, or history of other malignant cancers within the past 5 years (excluding prespecified low-risk cancers)
  • Hilar or mediastinal lymph node metastases
  • Poor cardiopulmonary function test
  • Inability to treat all colorectal metastases
  • Surgical resection by means of a bilobectomy or pneumonectomy

Treatment and study plan

Minimally invasive pulmonary metastasectomy

Procedure

Surgical margin is equal to tumor size, if possible The goal is a parenchymal-sparing resection

Other names: Lung metastasectomy

stereotactic ablative radiotherapy

Radiation

Depending on tumor location, 54 Gy in 3 fractions, 55 Gy in 5 fractions, 60 Gy in 8 fractions.

Other names: SABR, Stereotactic body radiation therapy (SBRT)

Primary outcomes

  1. Local recurrence-free survival

    Time frame: From date of randomization through study completion, up to 10 years

    Time from randomization to local recurrence or death from any cause

Secondary outcomes

  1. Overall survival (OS)

    Time frame: 5 years

    Time from randomization to death from any cause

  2. Progression-free survival (PFS)

    Time frame: 5 years

    Time from randomization to disease progression at any site or death

  3. Local recurrence rate (LRR) per tumor

    Time frame: 5 years

    Proportion of treated metastases with local recurrence

  4. Quality of life (QoL) assessment - EuroQoL (EQ-5D-5L)

    Time frame: 5 years

    [0-5 for 5 dimensions, higher score = worse QoL]

  5. Quality of life assessment - Functional Assessment of Cancer Therapy: General (FACT-G)

    Time frame: 5 years

    [27 questions in 4 subscales, higher score = better QoL]

  6. Health economic evaluation - Institute for Medical Technology Assessment (iMTA) - iMTA Medical Cost Questionnaire (iMCQ)

    Time frame: 5 years

    Medical costs [Euro]

  7. Health economic evaluation - iMTA Productivity Cost Questionnaire (iPCQ)

    Time frame: 5 years

    Productivity costs [Euro]

  8. Tumor patterns of failure

    Time frame: 5 years

    Local, regional and distant disease control based on surveillance imaging

  9. Rate of adverse events

    Time frame: 2 years

    Frequency of adverse events and serious adverse events

  10. Multiparameter flow cytometric analyses (FACS)

    Time frame: 1 months

    Peripheral blood mononuclear cell (PBMC) concentration

Study contacts

Contact information is provided by the study sponsor or research team.

Martijn van Dorp, MD

CONTACT

[email protected]

+31 20 444 4444 ext. 61647

Simone Gooijer, MD

CONTACT

[email protected]

+31 20 444 4782

Sponsors and collaborators

Lead sponsor

Amsterdam UMC, location VUmc

Other

Collaborators

  • Dutch Cancer Society

Registry information

Official study title

Colorectal Pulmonary Metastases: Pulmonary Metastasectomy Versus Stereotactic Ablative Radiotherapy: a Phase III Multicenter Randomized Controlled Trial

Acronym: COPPER

Important dates

Study start
2024
Primary completion
2030
Study completion
2030
First posted
Apr 11, 2023
Registry last updated
Apr 11, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.