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Guidelines on Diagnosis and Treatment of Malignant Lymphomas

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Haematopoietic Recombinant<br />

Growth Factor Support<br />

Erythropoietin<br />

Erythropoietin may be used to reduce transfusi<strong>on</strong> requirements in<br />

selected patients with lymphoma undergoing chemotherapy.<br />

Granulocyte col<strong>on</strong>y stimulating factors<br />

Haematopoietic growth factors currently in use include:<br />

Filgrastim - r-met HuG – CSF Neupogen<br />

Lenograstim - r-HuG – CSF Granocyte<br />

Pegylated Filgrastim<br />

Neulasta<br />

Indicati<strong>on</strong>s<br />

Haematopoietic growth factors may be indicated in the following<br />

circumstances <strong>and</strong> are particularly important for maintaining dose<br />

intenstity when chemotherapy is being given with curative intent:<br />

1. Chemotherapy support<br />

2. Peripheral blood stem cell harvest /<br />

progenitor cell mobilisati<strong>on</strong><br />

3. Post peripheral blood stem cell infusi<strong>on</strong><br />

4. Neutropenic sepsis<br />

5. Invasive fungal infecti<strong>on</strong><br />

Chemotherapy Support<br />

Primary prophylaxis<br />

May be used in ‘at risk patients’ or those who have had a<br />

previous episode <strong>of</strong> febrile neutropenia receiving curative<br />

chemotherapy, as recommended below.<br />

At risk patients<br />

■ Patients receiving chemotherapy who are at ‘high risk’<br />

(e.g. ≥ 40% likelihood) <strong>of</strong> developing febrile neutropenia or<br />

infecti<strong>on</strong> e.g.<br />

■<br />

■<br />

■<br />

■<br />

■<br />

Pre-existing neutropenia due to disease<br />

Extensive prior chemotherapy<br />

Previous irradiati<strong>on</strong> to the pelvis or other areas c<strong>on</strong>taining<br />

large amounts <strong>of</strong> b<strong>on</strong>e marrow<br />

History <strong>of</strong> recurrent febrile neutropenia while receiving earlier<br />

chemotherapy <strong>of</strong> similar or lesser dose-intensity<br />

C<strong>on</strong>diti<strong>on</strong>s potentially enhancing the risk <strong>of</strong> serious infecti<strong>on</strong><br />

e.g. poor performance status, decreased immune functi<strong>on</strong>,<br />

open wounds or already active tissue infecti<strong>on</strong><br />

Sec<strong>on</strong>dary prophylaxis –<br />

Previous episode <strong>of</strong> febrile neutropenia<br />

The use <strong>of</strong> GCSF should be c<strong>on</strong>sidered in patients receiving<br />

curative chemotherapy who have had a previous episode <strong>of</strong><br />

febrile neutropenia.<br />

Peripheral blood stem cell harvest<br />

Both Filgrastim <strong>and</strong> Lenograstim may be used for priming (either<br />

al<strong>on</strong>e or in combinati<strong>on</strong> with chemotherapy). The choice <strong>and</strong><br />

dose used depends <strong>on</strong> the protocol for harvesting. Plerixifor<br />

with G-CSF may be used for patients who have failed to achieved<br />

successful mobilisati<strong>on</strong> with c<strong>on</strong>venti<strong>on</strong>al approaches.<br />

70

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