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Single Arm Study of Induction Chemoradiotherapy Combined With Surgery in the Treatment of Locally Advanced SNMM

A Prospective Single Arm Clinical Study of Induction Chemoradiotherapy Combined With Surgery in the Treatment of Locally Advanced Sinonasal Malignant Melanoma

Status
UNKNOWN
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05009446
Acronym
SNMM
Enrollment
28
Registered
2021-08-17
Start date
2021-08-10
Completion date
2025-08-10
Last updated
2021-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mucosal Melanoma, Sinonasal Melanoma

Keywords

Sinonasal mucosal melanoma, Inductive radiotherapy, chemotherapy, overall survival

Brief summary

Sinonasal mucosal melanoma (SNMM) is a very rare tumor, and SNMM is highly aggressive in nature, with a 5-year survival rate of about 20\ 30%. Most patients underwent local recurrence and distant metastasis within one or two years of treatment. There is no unified standard for the treatment of SNMM.The principle of treatment for surgically resectable stage T3 and partial T4 SNMM is complete resection of the primary tumor, combined with postoperative radiotherapy. While locally unresectable SNMM has a poorer prognosis, lower incidence, fewer clinical data have been reported. This study will explore the role of preoperative radiotherapy and chemotherapy in improving the 2-year OS rate, loco-regional control rate and distant metastasis rate.

Interventions

PROCEDUREendoscopic surgery

endoscopic surgery or endoscope-assisted surgery open surgery

RADIATIONintensity-modulated radiation therapy or volume of rotating intensity-modulated radiotherapy or Proton or heavy ion radiation therapy

radiotherapy was administrated before surgery

DRUGChemotherapy drug

Chemotherapy was administrated before surgery. Chemotherapy may also be administrated after surgery in selected cases.

Sponsors

Chinese Academy of Medical Sciences
CollaboratorOTHER
Eye & ENT Hospital of Fudan University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age over 18 years old; 2. Pathologically confirmed with sinonasal mucosal melanoma; 3. Eligible for assessment by enhanced contrast computed tomography scan or magnetic Resonance Imaging (MRI); 4. T4N0-1M0 according to the 8th edition American Joint Committee on Cancer (AJCC) staging system, and breaks through the natural anatomical boundaries of orbital fascia or dura mater; or 2) any Tumor stage, with retropharyngeal node metastasis. unresectable tumor after multi-disciplinary team (MDT) discussion. 5. Eastern Cooperative Oncology Group (ECOG) score between 0 to 2; 6. No distant metastasis; 7. Adequate organ function; 8. Sign the informed consent forms.

Exclusion criteria

1. There is evidence or suspicious of distant metastasis on clinical examination or imaging examination; 2. suffered from uncontrolled concurrent diseases that may interfere with treatment; 3. Suffered from another malignant tumor or multiple primary tumors at the same time within 5 years (excluding fully treated basal cell or squamous cell skin cancer, cervical cancer in situ, etc.); 4. With surgical contraindications: severe cardiopulmonary disease, coagulation dysfunction, etc; 5. With and conditions that interfere with patient compliance or safety; 6. With severe mental or neurological diseases; 7. Uncontrolled active infection diseases; 8. Pregnant or breastfeeding women; 9. Patients without personal freedom or independent civil capacity; 10. Other situations that are not suitable.

Design outcomes

Primary

MeasureTime frameDescription
Overall survivalFrom date of first treatment until the date of death from any cause,through study completion,up to 2 years.2 year Overall Survival rate

Secondary

MeasureTime frameDescription
Progression-free survivalFrom date of first treatment until the date of first documented progression or date of death from any cause, whichever came first,through study completion,up to2 yearsthe date of first treatment to the first recording of disease progression or death from any cause.
Local progression free survivalFrom date of first treatment to local failure or date of death from any cause,through study completion,up to 2 yearsthe date of first treatment to local failure or death
Regional progression free survivalFrom date of first treatment to regional failure or date of death from any cause, through study completion,up to 2 yearsthe date of first treatment to regional failure or death
Distant metastasis free survivalFrom date of first treatment to distant metastasis or date of death from any cause, through study completion,up to 2 yearsthe date of first treatment to distant metastasis or death
ORRFrom date of first treatment to the date of best overall response before surgery, assessed up to 6 monthsobjective remission rate

Countries

China

Contacts

Primary ContactXiaole Song, MD
jxfxsxl@163.com15821388769

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026