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临床试验/NCT00515970
NCT00515970暂停不适用

Prospective Randomized Trial: Curettage Versus Excision in Nodular and Superficial Basal Cell Carcinomas

University Hospital Tuebingen2 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2007年12月最近更新:
适应症

试验速览

阶段
不适用
状态
暂停
入组人数
400
试验地点
2
主要终点
Recurrence of BCC, confirmed by biopsy

研究概览

简要总结

Basal cell carcinoma (BCC) is the most frequent skin cancer. Uncontrolled growth destroys local anatomic structures. There are various treatment alternatives with different recurrence rates and expenses. After surgical excision, the recurrence rate is in between 3 and 4% and the procedure is relatively expensive. Photodynamic therapy as well as imiquimod 5% are expensive therapies with high recurrence rates, that lack histologic evidence of BCC. Cryosurgery and curettage are inexpensive, although the recurrence rates are higher than after surgical excision.

This prospective, randomized trial compares recurrence rates, cosmetic outcome, and surgery-related complications after curettage versus surgical excision in nodular and superficial BCC. About 600 tumors will be included. One half is treated by curettage, the other half by surgical excision. The follow-up period is four years. If the difference between recurrence rates is ≤7% and the cosmetic outcome as well as the surgery-related complications are not worse after curettage, surgical excision must be considered an overtreatment.

详细描述

  1. First presentation of a patient with clinical or histopathological diagnosis of BCC

  2. Study patient number, first and surname, date of birth and gender are listed in a distinct file.

  3. Informed consent

  4. Whole body screening for skin cancer

  5. In- or exclusion of the patient. If the patient is excluded, no more data are obtained.

  6. Recording of the following features in an electronic file:

  7. Number of BCCs

  8. Anatomic location

  • Lip
  • Eyelid
  • Ear
  • Nose
  • Other parts of the face
  • Scalp or neck
  • Trunk
  • Arm, hand, or shoulder
  • Leg, foot, or hip
  1. Position
  • Ventral or dorsal. If the tumor is located at the lateral margin of ventral and dorsal, it is considered ventral.
  • Right, left, midline
  • Distinct BCCs are numbered. To ensure future distinction of different tumors, numbering starts with the most up-right-ventral tumor and ends with the most down-left-dorsal one. Numbering continues with BCCs that appear later during the period of recruitment.
  1. Diameter in mm

  2. In- or exclusion of the tumor

  3. Photographs of the included BCCs

  4. Randomization is performed by the Department of Biostatistics (distance to the Department of Dermatology = 1.7 km) with envelopes containing the assigned study arm. The study physician calls one of four staff members of the Department of Biostatistics and asks for randomization. The envelopes are not opened unless the electronic data file is completed by the study physician.

  5. Disinfection

  6. Local anesthesia

  7. Surgery

  8. Dressing

  9. If histopathology discovers another BCC type than nodular or superficial or even another tumor than BCC, then the tumor is excluded.

  10. Follow-up visit 3 and 6 months (+/- 30 days) after the operation. In BCCs that had to be operated in >1 step, the day of the follow-up visit refers to the initial operation.

  11. In case of clinical suspicion of recurrence of BCC a punch biopsy is taken. If the biopsy confirms recurrence, the endpoint is achieved.

  12. If BCCs must be added to a patient during the recruitment period, follow-up visits always refer to the latest BCC.

  13. If the patient visits our department not within the defined follow-up period, the appointment is not recorded (except confirmation of recurrence).

  14. Patients who provide no feedback receive phone calls.

  15. If a patient or a private practitioner suspect a recurrence of BCC beyond a defined follow-up period, of course, the patient is invited as early as possible to our department, where a biopsy will be taken.

  16. The patient receives a letter containing a list of the BCCs treated within the study. The private practitioner is to be visited with the list after 12, 24, and 36 months (+/- 30 days) referring to the last operation within the recruitment period. The letter contains a questionnaire about scar size and suspicion of recurrence of BCC. The practitioner or the patient return the questionnaire with the answers to our department. If recurrence is suspected we take a biopsy.

  17. When follow-up is closed for an individual patient, the reason is recorded:

  18. Planned end of follow-up after 48 months.

  19. Patient has moved.

  20. Death (date of death).

  21. Consent withdrawn.

  22. Patient has become meanwhile so ill or high-maintenance that no more follow-up visits can be planned.

  23. Recurrence of all of the patient's BCCs.

  24. Statistic evaluation is based on an intention-to-treat-analysis.

  25. The trial is designed to prove the equivalence of treatment modalities. A statistic test is used for evaluation, including the Kaplan-Meier-method. When all 4 study arms contain 116 BCCs, a 2-group-test on the equivalence of ratios with a 1-sided significance level of 0.05 will have a power of 80% to disprove the null hypothesis. The null hypothesis is that standard and test method are not equivalent (ratio difference delta T - delta S ≥ 0.15). Then the alternative hypothesis is more probable, meaning that the ratios in both groups are equivalent supposed that the expected ratio difference is 0.07 and the ratio within the standard group is 0.03 (according to an expected recurrence rate of 3% in the surgical excision study arm).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Clinical or histologic diagnosis of BCC
  • Patient Dependent

排除标准

  • > 5 BCCs at presentation
  • Immunosuppressive drugs
  • Pregnancy
  • Disability to give informed consent
  • Synchronous participation in other studies
  • Progeroid syndromes
  • Other malignant tumors, except for BCC and squamous cell carcinoma, or monoclonal neoplasms of the hematopoietic or immune system
  • Critical illness precluding sufficient follow-up visits
  • Tumor Exclusion Criteria:
  • Recurrent BCC
  • Nodular BCC with an exophytic part of > 1.5 mm above skin level
  • Nodular BCC with a diameter of > 10 mm
  • Superficial BCC with a diameter of > 20 mm
  • Ulceration
  • Blurred margins
  • Histopathologic evidence of a tumor type different from nodular or superficial BCC

结局指标

主要结局

Recurrence of BCC, confirmed by biopsy

时间窗: 4 years after surgery

次要结局

  • Secondary hemorrhage as remembered by the patient(3 months (plus or minus 30 days) after surgery)
  • Wound infection as remembered by the patient(3 months (plus or minus 30 days) after surgery)
  • Hypesthesia after surgery(3 months (plus or minus 30 days) after surgery)
  • Keloid(3 months (plus or minus 30 days) after surgery)
  • Functional impairment or disfigurement by the scar. Keloid is always a disfiguring scar. If the scar is recognized as keloid, the measure "disfigurement" cannot be used here.(3 months (plus or minus 30 days) after surgery)
  • Subjective assessment of the esthetic outcome of the scar on a scale of excellent, good, satisfying, moderate, unfavorable; done by the patient(3, 6, 12, 24, 36, and 48 months (plus or minus 30 days) after surgery)
  • Subjective assessment of the esthetic outcome of the scar on a scale of excellent, good, satisfying, moderate, unfavorable; done by the study physician(3, 6, 12, and 48 months (plus or minus 30 days) after surgery)
  • Subjective assessment of the esthetic outcome of the scar on a scale of excellent, good, satisfying, moderate, unfavorable; done by a private practitioner(12, 24, and 36 months (plus or minus 30 days) after surgery)
  • Scar length in mm(6 and 48 months (plus or minus 30 days) after surgery)
  • Scar width in mm, perpendicular to its length(6 and 48 months (plus or minus 30 days) after surgery)
  • Color of the scar: hyperpigmented, hypopigmented, or erythematous(6 and 48 months (plus or minus 30 days) after surgery)
  • Level of the scar: atrophic, skin level, hypertrophic, or keloid(6 and 48 months (plus or minus 30 days) after surgery)

研究者

申办方类型
Other

研究点 (2)

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