Chordoma Family Study
| Status: | Completed |
|---|---|
| Conditions: | Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 4 - 75 |
| Updated: | 3/31/2019 |
| Start Date: | August 1, 2003 |
| End Date: | December 29, 2017 |
The Chordoma Family Study: A Pilot Collaboration Between NCI and Massachusetts General Hospital (MGH) to Identify Chordoma Families
This pilot study, conducted by the National Cancer Institute and the Massachusetts General
Hospital, will investigate genetic factors that contribute to the development of chordoma in
people from some families. Chordoma is a very rare, potentially fatal, slow-growing bone
tumor derived from remnants of embryonic material. This study will determine the feasibility
of conducting a larger study aimed at identifying new families with multiple members affected
by chordoma to study the genetic basis of the disease.
English-speaking persons diagnosed with chordoma when they were 18 years of age or younger
and who were treated at the Massachusetts General Hospital Department of Radiation Oncology
between 1988 and the end of the study period may be eligible for this protocol. The age range
of these patients is currently from about 5 months to 33 years.
Patients (or parents of minor patients) will be mailed a packet with instructions for
completing the following procedures at home:
- Provide permission for researchers to obtain medical records relating to the patient's
chordoma and any other serious medical conditions he or she has had, and to obtain a
piece of the patient's stored tumor tissue.
- Complete a questionnaire about the patient's close blood relatives, including parents,
brothers, sisters, and any more distant relatives who have had chordoma or a cancer or
tumor which started in the brain or spine. The questionnaire will also include
demographic information, such as education, marital status, ethnicity, religion, and
household income.
- Collect two samples of cheek cells (only from patients 6 years and older). Patients'
packets include instructions and materials for collecting the cells. Parents of children
6 to 9 years old will collect cells from the child's mouth using a sterile soft-bristled
brush contained in a tube. They will brush the inside of the child's cheek with the
brush for about 30 seconds and then place the brush back in the tube. They will repeat
this procedure with a second brush. Patients 10 years of age and older will rinse their
mouth for about 45 seconds with a mouthwash provided in their packets and then spit the
mouthwash into a collection container. They will repeat the procedure several hours
later.
All participants will return the signed permission forms, questionnaires, and cheek cell
samples to the researchers in a pre-addressed stamped envelope, which is also provided in the
packet.
Hospital, will investigate genetic factors that contribute to the development of chordoma in
people from some families. Chordoma is a very rare, potentially fatal, slow-growing bone
tumor derived from remnants of embryonic material. This study will determine the feasibility
of conducting a larger study aimed at identifying new families with multiple members affected
by chordoma to study the genetic basis of the disease.
English-speaking persons diagnosed with chordoma when they were 18 years of age or younger
and who were treated at the Massachusetts General Hospital Department of Radiation Oncology
between 1988 and the end of the study period may be eligible for this protocol. The age range
of these patients is currently from about 5 months to 33 years.
Patients (or parents of minor patients) will be mailed a packet with instructions for
completing the following procedures at home:
- Provide permission for researchers to obtain medical records relating to the patient's
chordoma and any other serious medical conditions he or she has had, and to obtain a
piece of the patient's stored tumor tissue.
- Complete a questionnaire about the patient's close blood relatives, including parents,
brothers, sisters, and any more distant relatives who have had chordoma or a cancer or
tumor which started in the brain or spine. The questionnaire will also include
demographic information, such as education, marital status, ethnicity, religion, and
household income.
- Collect two samples of cheek cells (only from patients 6 years and older). Patients'
packets include instructions and materials for collecting the cells. Parents of children
6 to 9 years old will collect cells from the child's mouth using a sterile soft-bristled
brush contained in a tube. They will brush the inside of the child's cheek with the
brush for about 30 seconds and then place the brush back in the tube. They will repeat
this procedure with a second brush. Patients 10 years of age and older will rinse their
mouth for about 45 seconds with a mouthwash provided in their packets and then spit the
mouthwash into a collection container. They will repeat the procedure several hours
later.
All participants will return the signed permission forms, questionnaires, and cheek cell
samples to the researchers in a pre-addressed stamped envelope, which is also provided in the
packet.
Chordoma is a rare, slow growing, potentially fatal bone tumor derived from remnants of
vestigial or ectopic notochord. It occurs almost exclusively in the axial skeleton (skull
base, vertebrae, sacrum and coccyx), is somewhat more frequent in males than females, and has
a median age at diagnosis of 58.5 years, with a range from early childhood to over 70 years.
This typically sporadic tumor usually presents at an advanced stage and the associated
mortality is high due to local destruction or distant metastases.
Recently, we identified several families with chordoma in multiple relatives in a pattern
consistent with transmission of an autosomal dominant trait. Using clinical and genotyping
information from three such families, we mapped a familial chordoma gene to chromosome 7q33.
Now, we need to identify more multiplex chordoma families to participate in studies to fine
map and clone this gene. To do this, we established collaboration with Dr. Norbert Liebsch,
Department of Radiation Oncology (DRO), Massachusetts General Hospital (MGH), Boston. Since
1975, this department has treated ~500 patients with chordoma of the skull base or cervical
spine from all over the world; about 400 of these patients speak English.
The proposed study is a pilot study based on up to 80 English-speaking MGH chordoma patients
diagnosed age 18 years for whom Dr. Liebsch is the physician of record. We chose this group
because of Dr. Liebsch's personal knowledge of the patients and the fact that young age at
diagnosis may indicate increased genetic susceptibility to chordoma. A major purpose of the
pilot study is to determine the feasibility of conducting a larger study encompassing the
remaining (~320) English-speaking MGH chordoma patients. The major goal of the full study
would be to identify new multiplex chordoma families to participate in clinical and gene
mapping studies.
The data collection components of the pilot study include 1) a family medical history
questionnaire completed by each patient/parent or next of kin in person or over the
telephone, 2) collecting buccal cells from each patient ~ age 6 years via a mailed buccal
cell collection kit, 3) abstracting information about each patient's past medical history
from the DRO/MGH medical records, and 4) obtaining paraffin blocks or slides on each
chordoma/other primary cancer from the MGH Pathology Department or relevant outside
institutions. DNA from buccal cells and tumor will be used for molecular studies.
We will re-contact any family from the pilot study who reports chordoma or astrocytoma in at
least one blood relative of the MGH patient. If we confirm these diagnoses we will invite
selected family members to participate in clinical and gene mapping studies conducted under a
separate NIH approved protocol. We will consider the pilot study to be a success if up to 30-
35 of the 80 chordoma patients/parents/next of kin participate in it, OR if we identify a new
multiplex chordoma family that is willing to participate in clinical and gene mapping
studies.
vestigial or ectopic notochord. It occurs almost exclusively in the axial skeleton (skull
base, vertebrae, sacrum and coccyx), is somewhat more frequent in males than females, and has
a median age at diagnosis of 58.5 years, with a range from early childhood to over 70 years.
This typically sporadic tumor usually presents at an advanced stage and the associated
mortality is high due to local destruction or distant metastases.
Recently, we identified several families with chordoma in multiple relatives in a pattern
consistent with transmission of an autosomal dominant trait. Using clinical and genotyping
information from three such families, we mapped a familial chordoma gene to chromosome 7q33.
Now, we need to identify more multiplex chordoma families to participate in studies to fine
map and clone this gene. To do this, we established collaboration with Dr. Norbert Liebsch,
Department of Radiation Oncology (DRO), Massachusetts General Hospital (MGH), Boston. Since
1975, this department has treated ~500 patients with chordoma of the skull base or cervical
spine from all over the world; about 400 of these patients speak English.
The proposed study is a pilot study based on up to 80 English-speaking MGH chordoma patients
diagnosed age 18 years for whom Dr. Liebsch is the physician of record. We chose this group
because of Dr. Liebsch's personal knowledge of the patients and the fact that young age at
diagnosis may indicate increased genetic susceptibility to chordoma. A major purpose of the
pilot study is to determine the feasibility of conducting a larger study encompassing the
remaining (~320) English-speaking MGH chordoma patients. The major goal of the full study
would be to identify new multiplex chordoma families to participate in clinical and gene
mapping studies.
The data collection components of the pilot study include 1) a family medical history
questionnaire completed by each patient/parent or next of kin in person or over the
telephone, 2) collecting buccal cells from each patient ~ age 6 years via a mailed buccal
cell collection kit, 3) abstracting information about each patient's past medical history
from the DRO/MGH medical records, and 4) obtaining paraffin blocks or slides on each
chordoma/other primary cancer from the MGH Pathology Department or relevant outside
institutions. DNA from buccal cells and tumor will be used for molecular studies.
We will re-contact any family from the pilot study who reports chordoma or astrocytoma in at
least one blood relative of the MGH patient. If we confirm these diagnoses we will invite
selected family members to participate in clinical and gene mapping studies conducted under a
separate NIH approved protocol. We will consider the pilot study to be a success if up to 30-
35 of the 80 chordoma patients/parents/next of kin participate in it, OR if we identify a new
multiplex chordoma family that is willing to participate in clinical and gene mapping
studies.
- INCLUSION/EXCLUSION CRITERIA:
All English-speaking persons diagnosed with chordoma at age 18 years or less either at MGH
or elsewhere, and treated by DRO, MGH between 1988 and the end of the study period (n
=100). Ages will range from 5 months - 33 years. There is no age limit fo the
self-administered questionnaire or the telephone interview because a parent can complete it
on behalf of any case who is less than 18 years, but collection of buccal cells will be
limited to cases older than or equal to age 6 years.
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