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Melanocytic-Nevi-Counts During Chemotherapy of Children With Malignancies.


N/A
N/A
18 Years
Not Enrolling
Both
Nevus, Pigmented

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Trial Information

Melanocytic-Nevi-Counts During Chemotherapy of Children With Malignancies.


Objectives:

Patients given chemotherapy because of different malignancies have an increased
susceptibility to cutaneous tumours and infection and a change of number of nevi during
treatment is discussed. We investigated wether total nevi count changes in children
undergoing chemotherapy. Therefore 16 (8m, 8f) children suffering from leukaemia (11),
lymphoma (2), adenosarcoma of the kidney (1), Ewing´s sarcoma (1) and neuroblastoma (1) aged
between 2 and 17 years (median:8 years), under chemotherapy at the pediatric department of
oncology, were examined at the beginning and 9-12 months after starting chemotherapy. As
control group age and sex matched children of the local population were used.

Materials and Methods:

At the beginning of chemotherapy the nevi were counted on the total body. All nevi were
larger in diameter than 1mm and as melanocytic lesion identifiable. Clinical and dermoscopic
photographs were taken of every nevus. If the patient had more than 50 nevi, only nevi on
the face, right arm, upper back and the buttocks were documented. Reassessment was repeated
every 3 month.

Conclusion:

In our patients under chemotherapy during one year the development of new nevi is similar to
sex and age matched children of the general population. During this short period development
of nevi seems not to be influenced by chemotherapy.


Inclusion Criteria:



- Patient and/or parents willing to participate in the study

- Age under 18

Study Group Only:

- Patient suffering from a malignancy requiring systemic chemotherapy

Exclusion Criteria:

- Patient and/or parents who decline to participate in the study

Type of Study:

Observational

Study Design:

Observational Model: Case Control, Time Perspective: Prospective

Outcome Measure:

total body nevus count

Outcome Time Frame:

Every three months during a one year period

Safety Issue:

No

Principal Investigator

Barbara Binder, MD

Investigator Role:

Study Chair

Investigator Affiliation:

Department of Dermatology, Medical University of Graz, Austria

Authority:

Austria: Agency for Health and Food Safety

Study ID:

001

NCT ID:

NCT00600431

Start Date:

February 2006

Completion Date:

December 2007

Related Keywords:

  • Nevus, Pigmented
  • nevus count
  • children
  • chemotherapy
  • Nevus
  • Nevus, Pigmented

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