Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03274414
Other study ID # 17-442
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date September 1, 2017
Est. completion date January 13, 2023

Study information

Verified date January 2023
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is being done to test a new treatment plan for large tumors in the sinus or nasal cavity that will include endoscopic surgery plus chemotherapy and proton-beam radiation therapy.


Recruitment information / eligibility

Status Completed
Enrollment 3
Est. completion date January 13, 2023
Est. primary completion date January 13, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age greater than or equal to 18 years. - Histopathologically confirmed diagnosis of one the following cancer types: - Squamous cell carcinoma - Esthesioneuroblastoma - Adenoid cystic carcinoma - Adenocarcinoma - Paranasal sinus/nasal cavity malignancy is considered unresectable with negative margins surgery or resection would be considered excessively morbid. This could include lesions with: - Carotid involvement - Cavernous sinus invasion - Brain invasion - Orbital apex - Intraconal space - Pterygoid musculature involvement - Invasion of the clivus - Resection of at least 80% of the volume of the tumor is feasible. Resectability will be determined by the surgeon and radiologist after discussion among the multidisciplinary team. For patients who have had surgery at an outside institution, the same parameters will be thoroughly screened to ensure the patient met the same inclusion criteria and resection standards. - Patients must be a candidate for surgery (as per treating surgeon) and be able to tolerate proton radiation and chemotherapy (as per treating radiation oncologist and medical oncologist). - Karnofsky performance statue >/= 70 - The subject has organ and marrow function and laboratory values rendering safe administration of Cisplatin: - The ANC >/= 1000/mm3 without colony stimulating factor support - Platelets >/= 100,000/mm3 - Hemoglobin >/= 9 g/dL - Bilirubin </= 1.5 mg/dL the ULM. For subjects with Gilbert's disease, bilirubin </= 3.0 mg/dL - Serum albumin >/= 2.8 g/dl - Creatinine clearance (CrCl) >/= 60 mL/min. For creatinine clearance estimation, the Cockcroft and Gault equation should be used: - Male: CrCl (mL/min) = (140 = age) x wt (kg) / (serum creatinine x 72) - Female: Multiply above result by 0.85 - ALT and AST </= 3.0 ULN - Serum phosphorus, calcium, magnesium and potassium >/= LLN - No evidence of intercurrent infection - Negative pregnancy test for women of childbearing potential (<51 years of age) as per institutional policy. - Patients with distant metastatic disease may not be included. - Patient must be able to read and write in English. - Patients who intitially meet the histopathological inclusion criteria but surgical pathology report shows Sinonasal Undifferentiated Carcinoma. Exclusion Criteria: - Tumor is deemed to be resectable with negative margins by conventional surgical standards. - Patients not able to receive standard-dose cisplatin based on the judgement of the treating medical oncologist. - Patients with chronic kidney disease (GFR <60), uncontrolled hypertension, congestive heart failure, pre-existing bone marrow dysfunction, or cytopenias. ° Congestive heart failure (CHF): New York Heart Association (NYHA) Class II-IV at the time of screening - Concurrent uncontrolled hypertension defined as sustained blood pressure > 150 mm Hg systolic or > 100 mm Hg diastolic despite optimal antihypertensive treatment within 7 days of the first dose of study treatment; If severe hearing impairment is measured or if significant neuropathy is reported at baseline the treating physician will discuss the risks for further permanent hearing loss and neuropathy with the patient. - Patients not able to have a MRI (due to pacemaker, claustrophobia, etc.). - Inability to return to MSKCC for frequent scheduled hydration sessions post-chemotherapy. - Inability to comply with requirements for cisplatin administration anti-emetic regimens post-treatment. - Patients not able or unwilling to travel for proton therapy.

Study Design


Intervention

Drug:
Cisplatin
Cisplatin should be administered on day 1 (+/- 3 days) of the start of radiotherapy and then every 3 weeks (unless there is a delay for safety concerns such as neutropenia) for a total of 3 cycles. 100 mg/m^2 (dose reductions after the first cycle allowed for toxicity)
Radiation:
Adjuvant Proton Radiotherapy
Proton therapy treatment will follow the National Cancer Institute's "Guidelines for the Use of Proton Radiation Therapy in NCI-Sponsored Cooperative Group Trials". Proton therapy techniques may include passively scattered or scanning or pencil beam technology.
Procedure:
Endoscopic Resection
In brief, an endoscope is used and two surgeons perform the intervention in a binostril manner. Tumor is generally resected with an emphasis on identification of the attachments in the paranasal sinuses, nasal cavity, or skull base.
Drug:
cisplatin and etoposide
If the final surgical pathology report shows SNUC, at the discretion of the treating medical oncologist, the patient will receive an addition of etoposide chemotherapy to cisplatin chemotherapy. The dose of cisplatin will be decresed from 100 mg/m2 to 60 mg/m2. Cisplatin should be administered on days 1-2, 21-22 and 42-43 at a dose of 60 mg/m2 and Etoposide should be administered at days 1-3, 21-23, and 42-44 at a dose of 120 mg/m2.

Locations

Country Name City State
United States Memoral Sloan Kettering Basking Ridge Basking Ridge New Jersey
United States Memoral Sloan Kettering Westchester Harrison New York
United States Memoral Sloan Kettering Monmouth Middletown New Jersey
United States Memorial Sloan Kettering Bergen Montvale New Jersey
United States Memorial Sloan Kettering Cancer Center New York New York

Sponsors (1)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Local Control Assessment of Unresectable Paranasal Sinus and Nasal Cavity Tumors Assessment of local control after near-total endoscopic resection (NTR) followed by concurrent chemotherapy with proton-beam radiation in unresectable tumors (which we define as expected inability to perform negative margin surgery) of the paranasal sinuses and nasal cavity. 1 year
See also
  Status Clinical Trial Phase
Recruiting NCT02012699 - Integrated Cancer Repository for Cancer Research
Completed NCT03096808 - Adaptive Radiotherapy for Head and Neck Cancer Phase 2
Recruiting NCT05614375 - Endoscopic Surgery in the Treatment of Soft Tissue Sarcoma in Nasal and Paranasal Sinus
Recruiting NCT05114707 - Camrelizumab Plus Chemoradiotherapy for Patients With Locoregional Cancer of Nasal Cavity and Paranasal Sinuses Phase 2