LYCHOP Protocol 1aug2014

BCCA Protocol Summary for Treatment of Lymphoma with
DOXOrubicin, Cyclophosphamide, vinCRIStine and predniSONE

(CHOP)
Protocol Code
LYCHOP
Tumour Group
Lymphoma
Dr. Laurie Sehn
Contact Physician
ELIGIBILITY:
Special: Patients with previously untreated, advanced stage diffuse large B-cell lymphoma should be
treated with LYCHOP-R. This protocol, LYCHOP, is for use for all other patients being treated with CHOP
for aggressive histology lymphoma.
Histology:
Diffuse large B-cell
Mantle cell
Peripheral T-cell, all aggressive varieties
Discordant with one of the above histologies present
EXCLUSIONS:
Congestive cardiac failure requiring current treatment (LYCHOP may be used but DOXOrubicin
should be omitted, see cardiotoxicity below)
TESTS:
Baseline (required before first treatment): CBC and diff, platelets, bilirubin, AST, ALT
Baseline (required, but results do not have to be available to proceed with first treatment; results must
be checked before proceeding with cycle 2): LDH, HBsAg, HBcoreAb
Before each treatment: CBC and diff, platelets, (and bilirubin if elevated at baseline)
For all patients planned to receive CHOP x 6-8 cycles, reassess all sites of disease after cycles 4 and
6 to determine duration of treatment
PREMEDICATIONS:
Antiemetic protocol for highly emetogenic chemotherapy (see protocol SCNAUSEA)
SUPPORTIVE MEDICATIONS:
If HBsAg or HBcoreAb positive, start lamiVUDine 100 mg/day PO for the duration of chemotherapy and for
six months afterwards.
TREATMENT:
Drug
DOXOrubicin
vinCRIStine
Dose
2
50 mg/m on day 1
2
1.4 mg/m * on day 1
(*no cap on dose)
2
cyclophosphamide
750 mg/m on day 1
predniSONE
45 mg/m **on days 1 to 5

(**round off dose to nearest 25mg)
BCCA Administration Guideline

IV push
IV in 50 mL NS over 15 mins
IV in 100 to 250* mL NS over 20 min to 1 hour
(*use 250 mL for doses greater than 1000 mg)
BC Cancer Agency Protocol Summary LYCHOP
PO in am with food
Page 1 of 3
Warning: The information contained in these documents are a statement of consensus of BC Cancer Agency professionals regarding their views of currently accepted approaches to treatment. Any clinician
seeking to apply or consult these documents is expected to use independent medical judgement in the context of individual clinical circumstances to determine any patient's care or treatment. Use of these
documents is at your own risk and is subject to BC Cancer Agency's terms of use available at www.bccancer.bc.ca/legal.htm
Stage IA or IIA, bulk less than 10 cm, radio-encompassable: Repeat every 21 days or when the
neutrophil and platelet counts have recovered sufficiently to allow 100% dosing if that is determined
sooner than every 21 days, x 3 cycles then proceed with planned radiation.
All other stages: Repeat every 21 days or when the neutrophil and platelet counts have recovered
sufficiently to allow 100% dosing if that is determined sooner than every 21 days, x 6 to 8 cycles (2 cycles
post maximum response, minimum 6)
Discontinue if no response after 2 cycles.
CNS Prophylaxis:
Patients with initial sinus involvement with large cell lymphoma who have a complete response at the
completion of their chemotherapy should receive intrathecal methotrexate 12 mg alternating with
intrathecal cytarabine 50 mg twice weekly x 6 doses (3 doses of each over 3 weeks) starting in week 18.
(See protocol LYIT for details)
DOSE MODIFICATIONS:
1. Elderly Patients (age greater than 75 years):
Cycle 1 doses of cyclophosphamide and DOXOrubicin should be administered at 75% doses. Further
treatment should be given at the maximum dose tolerated by the patient, trying to escalate up to full 100%
doses, but using the baseline experience with the 75% doses to guide these decisions.
2. Hematological: DOXOrubicin, cyclophosphamide and etoposide, if used, see below:
9
ANC (x10 /L)

greater than or equal to 0.8
less than 0.8
Dose Modification
100%
100% plus filgrastim 300 mcg daily x 5 days, starting
7 days after each IV chemotherapy
The patient should be treated with Filgrastim (G-CSF) in doses sufficient to allow full dose treatment on a
21 day schedule using the above dose modifications. Note: this guideline applies only if the treatment is
potentially curative and after experience with one or more cycles of treatment indicate Filgrastim (G-CSF)
is required. (See Pharmacare guidelines)
9
Transfuse as needed to keep hemoglobin greater than 90 g/L, platelets greater than 20 x 10 /L.
3. Neurotoxicity: vinCRIStine only:
Toxicity
Dysesthesias, areflexia only
Abnormal buttoning, writing
Motor neuropathy, moderate
Motor neuropathy, severe
Dose Modification
100 %
67%
50%
Omit
4. Hepatotoxicity: DOXOrubicin only:

Bilirubin (micromol/L)
Dose Modification
2 to 35
35 to 85
Greater than 85
100%
50%
Omit DOXOrubicin. ADD cyclophosphamide
2
350 mg/m to the dose already planned.
Page 2 of 3
Note: This adjustment is only necessary for the initial treatment. After the hyperbilirubinemia has
resolved, adjustment is only necessary if overt jaundice re-occurs. Serum bilirubin does not need to be
requested before each treatment.
5. Cardiotoxicity: DOXOrubicin only:

When DOXOrubicin cannot be used due to proven cardiac dysfunction, it can be replaced by etoposide
2
2
50 mg/m IV on day 1, 100 mg/m PO on day 2 and 3. (Use non-DEHP equipment with in-line filter)
PRECAUTIONS:
1. Neutropenia: Fever or other evidence of infection must be assessed promptly and treated
aggressively.
2. Cardiac Toxicity: DOXOrubicin is cardiotoxic and must be used with caution, if at all, in patients with
severe hypertension or cardiac dysfunction. Cardiac assessment is recommended if lifelong dose of
2
450 mg/m to be exceeded. (BCCA Cancer Drug Manual)
3. Extravasation: DOXOrubicin and vinCRIStine cause pain and tissue necrosis if extravasated. Refer
to BCCA Extravasation Guidelines.
4. Hypersensitivity: If applicable, monitor etoposide infusion for the first 15 minutes for signs of
hypotension. Refer to BCCA Hypersensitivity Guidelines.
5. Hepatitis B Reactivation: All lymphoma patients should be tested for both HBsAg and HBcoreAb. If
either test is positive, such patients should be treated with lamiVUDine during chemotherapy and for
six months afterwards. Such patients should also be monitored with frequent liver function tests and
hepatitis B virus DNA at least every two months. If the hepatitis B virus DNA level rises during this
monitoring, management should be reviewed with an appropriate specialist with experience managing
hepatitis and consideration given to halting chemotherapy.
Call Dr. Laurie Sehn or tumour group delegate at (604) 877-6000 or 1-800-663-3333 with any
problems or questions regarding this treatment program.
Date activated:
01 Aug 2000
Date revised:
1 Aug 2014 (non-PVC changed to non-DEHP, in-line filter added)
References:
1. Fisher RI, Gaynor ER, Dahlberg S, Oken MM, et al. Comparison of a standard regimen (CHOP) with
three intensive chemotherapy regimens for advanced non-Hodgkins lymphoma. N Engl J Med
1993;328:1002-6.
2. McKelvey EM, Gottlieb JA, Wilson HE, Haut A, et al. Hydroxyldaunomycin (Adriamycin) combination
therapy in malignant lymphoma. Cancer 1976;38:484-93.
Page 3 of 3

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BCCA Protocol Summary for Treatment of Lymphoma with

DOXOrubicin, Cyclophosphamide, vinCRIStine and predniSONE

750 mg/m on day 1

45 mg/m **on days 1 to 5

BCCA Administration Guideline

BC Cancer Agency Protocol Summary LYCHOP

ANC (x10 /L)

4. Hepatotoxicity: DOXOrubicin only:

BC Cancer Agency Protocol Summary LYCHOP

5. Cardiotoxicity: DOXOrubicin only:

1 Aug 2014 (non-PVC changed to non-DEHP, in-line filter added)

BC Cancer Agency Protocol Summary LYCHOP

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