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APPROVED INDICATIONS
Multiple Myeloma
Mantle cell lymphoma
ELIGIBILITY CRITERIA
EXCLUSION CRITERIA
ASSESSMENT OF RESPONSE
Paraprotein (serum/urine) every 2 cycles in myeloma patients. Assess symptoms.
REVIEW BY CLINICIAN
Prior to each cycle, unless being reviewed by a Nurse Specialist or Pharmacist under
a locally agreed framework. Minimum consultant review annually.
TOXICITIES
Common: Myelosuppression (moderate risk), Nausea/Vomiting, Fatigue,
Immunosuppression
Less Common: Flushing, Rash, Allergic Reaction, Pulmonary Toxicity, Cardiac
Toxicity, SiADH, Haemorrhagic Cystitis
Haematological Toxicity:
(Note: where haematological disease is affecting bone marrow function, lower
treatment parameters may be acceptable. This should be clearly documented for the
specific patient.)
Delay treatment on Day 1 and Day 22 if ANC < 1.53 x 109cells/l or PLT < 75 x
109cells/l. (Some clinicians use ANC <1.3.) If patients recurrently have low counts
consider switching to C-Weekly Regimen in myeloma patients.
Renal Function:
TREATMENT LOCATION
Suitable for administration in chemotherapy day units, under the supervision of
haematology teams from Level 1 – 4 Haematology Services.
Document Control
Document Title: ABCM NECN protocol CRP08 H020
Current
Document No: CRP08 H020 1.1
Version:
Calum Polwart, Network Pharmacist Approval
Author:
NECN Signature*
Date
Approved by: Diane Plews / Ann Lenard 20/03/2012
Approved:
Due for Review: April 2014
Summary of
1.0a ‘Final Version’ Approved
Changes
Protocol reviewed. Cyclophosphamide dose adjustments in renal impairment
1.1
added.