Dentures and Dental Implants in Treating Patients Undergoing Surgery for Mouth Cancer
Status: | Completed |
---|---|
Conditions: | Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 35 - 80 |
Updated: | 4/21/2016 |
Start Date: | June 1997 |
End Date: | May 2003 |
Efficacy of Implant-Supported Maxillofacial Prostheses
RATIONALE: The use of dentures and dental implants may help maintain chewing and speaking
ability following surgery to remove tumors in the mouth.
PURPOSE: Phase II trial to study the effectiveness of dentures and dental implants in
maintaining the ability to chew and speak in patients undergoing surgery for mouth cancer.
ability following surgery to remove tumors in the mouth.
PURPOSE: Phase II trial to study the effectiveness of dentures and dental implants in
maintaining the ability to chew and speak in patients undergoing surgery for mouth cancer.
OBJECTIVES:
- Determine whether conventional or implant supported dental prostheses and current
surgical reconstructive procedures restore oral function and quality of life to
pre-cancer surgery levels in patients with early oral cancer.
OUTLINE: Patients complete a series of objective and subjective functional tests,
questionnaires, and baseline examinations. Within 1-5 days, patients undergo the composite
resection, including reconstructive surgery for the mandibulectomy group. Patients in the
maxillectomy group receive an immediate maxillary surgical obturator. Approximately 6 weeks
after ablative surgery, some patients receive radiotherapy for 5-7 weeks.
Patients receive 2-4 implants at 12-16 weeks after completion of radiotherapy or 8-16 weeks
after ablative surgery. Patients then receive conventional dentures at 4-22 weeks after
implant surgery. Implants are exposed during 27-48 weeks after placement and abutments
connected for fabricating dental prostheses. Approximately 8 weeks are needed to fabricate
the implant supported prosthesis.
Patients complete quality of life and other questionnaires prior to and at 8-21 weeks after
surgery, 16 weeks after conventional denture insertion, and then 16 weeks after implant
supported prosthesis insertion.
Patients are followed every 6 months for at least 3 years.
PROJECTED ACCRUAL: A total of 62 patients (22 requiring maxillectomy and 40 requiring
mandibulectomy) will be accrued for this study within 42 months.
- Determine whether conventional or implant supported dental prostheses and current
surgical reconstructive procedures restore oral function and quality of life to
pre-cancer surgery levels in patients with early oral cancer.
OUTLINE: Patients complete a series of objective and subjective functional tests,
questionnaires, and baseline examinations. Within 1-5 days, patients undergo the composite
resection, including reconstructive surgery for the mandibulectomy group. Patients in the
maxillectomy group receive an immediate maxillary surgical obturator. Approximately 6 weeks
after ablative surgery, some patients receive radiotherapy for 5-7 weeks.
Patients receive 2-4 implants at 12-16 weeks after completion of radiotherapy or 8-16 weeks
after ablative surgery. Patients then receive conventional dentures at 4-22 weeks after
implant surgery. Implants are exposed during 27-48 weeks after placement and abutments
connected for fabricating dental prostheses. Approximately 8 weeks are needed to fabricate
the implant supported prosthesis.
Patients complete quality of life and other questionnaires prior to and at 8-21 weeks after
surgery, 16 weeks after conventional denture insertion, and then 16 weeks after implant
supported prosthesis insertion.
Patients are followed every 6 months for at least 3 years.
PROJECTED ACCRUAL: A total of 62 patients (22 requiring maxillectomy and 40 requiring
mandibulectomy) will be accrued for this study within 42 months.
DISEASE CHARACTERISTICS:
- Diagnosis of early oral cancer lesions requiring one of the following:
- Partial or total unilateral maxillectomy OR
- Partial lateral mandibulectomy with or without partial glossectomy
- Edentulous or edentulous in the maxillary arch prior to or after ablative surgery
(maxillectomy group)
- Partial mandibulectomy leaving the condyles intact bilaterally (mandibulectomy group)
- Must have sufficient bone in the selected implant sites to accommodate 2-4 implants
of at least 10 mm in length
- No temporomandibular dysfunction and/or functionally restrictive opening
- No requirement for total glossectomy, reconstructive maxillary surgery, or maxillary
sinus lift
- No requirement for radiotherapy after mandibular reconstructive surgery
PATIENT CHARACTERISTICS:
Age:
- 35 to 80
Performance status:
- Not specified
Life expectancy:
- Not specified
Hematopoietic:
- Not specified
Hepatic:
- Not specified
Renal:
- Not specified
Other:
- No oral discomfort that would preclude study
- No complications after ablative or reconstructive surgery that would preclude dental
rehabilitation with implants
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- Not specified
Chemotherapy:
- Not specified
Endocrine therapy:
- Not specified
Radiotherapy:
- See Disease Characteristics
- No prior or concurrent radiotherapy of greater than 5,500 cGY to potential implant
site
Surgery:
- See Disease Characteristics
We found this trial at
1
site
10833 Le Conte Avenue # 8-950
Los Angeles, California 90095
Los Angeles, California 90095
(310) 825-5268
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Jonsson Comprehensive Cancer Center at UCLA In the late 1960s, a group of scientists and...
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