The
South Florida Bone Marrow Stem Cell Transplant Institute is a 4,000 sq. ft.
facility located in Bethesda
Health City, Boynton Beach, Florida.
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A biopsy is necessary to ensure the patient's bone
marrow is free of cancer cells prior to the transplant.
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The Transplant Team
We recognize that a successful outpatient program
requires a unique and highly motivated team of professionals and supporting
organizations. The South Florida Bone Marrow/Stem Cell Transplant Institute is fully committed to
providing a highly experienced staff trained in the following areas:
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Transplant Physicians.
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Bone Marrow/Stem Cell Laboratory Staff.
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Chemotherapy/Transplant Nurses (clinic and home care).
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Psycho-Social and Nutritional Consultants.
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Administrative Staff.
The expanded transplant team is comprised of a wide array of
professionals which provide the sum total of services required to support the
treatment program. The interior team includes the transplant physician,
clinical coordinator, transplant nurses, chemotherapy pharmacist, nutritionist
and the administrative staff. The exterior team includes the various BMSCTI affiliates which directly support the bone marrow stem cell treatment program.

Within the Bethesda Healthcare System,
particularly Bethesda Memorial Hospital and its Comprehensive Cancer Care
Center, there is an extensive network of medical specialists and ancillary
providers which can support all outpatient needs of the Institute.

Dr. Maharaj is in charge of cryopreservationfor his
patients
Eligibility
Criteria:
Acute Myelogenous
Leukemia
Patients in CR 1 or CR 2,
with standard or intermediate risk based
upon cytogenetics are eligible. Patients
with good (CR 1) or poor risk features are
not considered eligible.
Acute Lymphoblastic
Leukemia
Patients in CR 1 or CR 2 who
do not have a suitable related HLA-matched
donor are eligible.
Chronic Myeloid
Leukemia
Patients in chronic phase who
do not have a suitable HLA-matched donor
are eligible.
Multiple Myeloma
Patients with Durie-Salmon Stage II or
III, newly diagnosed or responsive
disease. This includes those patients with
previously untreated disease, those with
at least partial response to prior
chemotherapy, and those in responsive
relapse.
Hodgkin’s Disease
Lymphoma
Patients with Hodgkin’s
Disease who have failed to achieve a
complete remission with conventional
chemotherapy or relapsed from initial or
later remission; or have high risk disease
(International Prognostic Index) at
initial diagnosis.
Non Hodgkin’s
Lymphoma: Low Grade Stage III, IV
Patients
with recurrent low grade non-Hodgkin’s
lymphoma and one or more adverse
prognostic factors (B symptoms, bulky
tumor mass, more than two relapses, high
LDH, Hb < 10 g/dl).
Non-Hodgkin’s
Lymphoma: Intermediate or High Grade
Intermediate or high grade lymphoma
responding to standard chemotherapy but
failing to achieve complete remission by
completion of 50% of their standard
induction treatment and demonstrating
plateau or progression; or relapsed from
initial or later remission. High risk
disease (International Prognostic Index)
at initial presentation.
Breast Carcinoma:
with 4 or more positive axillary nodes
(TAX 321 BCIRG 002 randomized clinical
trial) Patients with invasive
adenocarcinoma with at least four axillary
lymph nodes (pN1) showing evidence of
tumor among a minimum of six resected
nodes.
Breast Carcinoma: Stage
II and III
Patient should have
undergone a radical, modified radical (MRM),
or breast-sparing procedure plus axillary
dissection. Patient should have a biopsy
proven diagnosis of epithelial carcinoma
of the breast. Greater than or equal to 10
lymph nodes positive for carcinoma or high
risk primary breast carcinoma.
Breast Carcinoma: Stage IV
Histologically
proven diagnosis of adenocarcinoma of the
breast. Bilateral carcinoma is acceptable.
Biopsy proven metastatic breast cancer or
unequivocal evidence of metastasis on
radiographic studies. Patients must
demonstrate chemotherapy-sensitivity and
be in a state of minimal disease or
complete remission. Tumor markers may be
used as support of data; however, they are
not adequate for diagnosis of recurrence.
Ovarian Carcinoma:
Stage III, IV
or high risk Tissue documented epithelial
ovarian cancer with residual disease after
initial response to standard chemotherapy,
or residual disease following standard
induction chemotherapy as demonstrated by
either clinical or radiological evidence
of less than complete response,
persistently elevated CA-125 or residual
disease at second look. Patients with
persistent or recurrent ovarian cancer
must be incurable with available
conventional chemotherapy.
Germ Cell Tumor:
Poor Risk
Patients with relapsed or high risk
(International Germ Cell Consensus
Classification) disease at presentation.
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