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Heated chemo after surgery shows promise for rare chest cancer spread

NCT ID NCT07328074

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looks at whether combining a special surgery (electrocautery) with heated chemotherapy given directly into the chest can help people with thymic tumors that have spread to the chest lining. About 70 participants will receive the treatment and be followed for up to 3 years to see if it delays the cancer's return and improves quality of life. The approach aims to destroy remaining cancer cells with heat and drugs, but it is still experimental and carries risks from both surgery and chemotherapy.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
cisplatin and doxorubicin (heated chemotherapy)
What this could lead to
If this works, it could offer a more effective way to control thymic tumors that have spread to the chest lining, potentially delaying recurrence and improving survival.
What could go wrong
This is a small, early observational study with no comparison group, so results may not be definitive. The heated chemotherapy can cause serious side effects, and the surgery carries risks like infection or bleeding.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 70 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Feb 2026

An estimate. Start dates often move.

Expected to finish

Feb 2031

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adults aged 16-80 years with pathologically confirmed thymic epithelial tumors (thymoma or thymic carcinoma) with pleural dissemination or recurrence, suitable for electrocautery resection and hyperthermic intrathoracic chemotherapy as determined by multidisciplinary team.

Ages

16 to 80 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Pathologically confirmed thymic epithelial tumor (TET) * Imaging evidence of thymic epithelial tumor with pleural dissemination or recurrence, deemed suitable for HITHOC by multidisciplinary thoracic team * Age ≥16 years and ≤80 years * American Society of Anesthesiologists (ASA) physical status classification I-II * Normal major organ function * No history of other malignancies * Prior chemotherapy completed \>4 weeks, radiotherapy \>6 weeks, immunotherapy \>6 weeks before enrollment * No allergy to cisplatin or doxorubicin * Able to understand the study content and provide informed consent Exclusion Criteria: * Evidence of extrathoracic metastasis on imaging or pathological examination * Myasthenia gravis in unstable phase or acute exacerbation * Severe systemic comorbidities, such as active infection, poorly controlled diabetes, coagulopathy, bleeding tendency, or ongoing thrombolytic/anticoagulation therapy * Positive serum pregnancy test or lactation (females) * History of organ transplantation (including autologous bone marrow transplantation and peripheral blood stem cell transplantation) * History of peripheral nervous system disease, significant psychiatric disorder, or central nervous system disease * Currently participating in other clinical trials

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

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  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Shanghai General Hospital, Department of Thoracic Surgery

    Shanghai, Shanghai Municipality, 200080, China

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