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Chemotherapy Sequencing Guide – For therapies given on the same day
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Vi
B1, P2
Bleomycin
Carboplatin
Cisplatin
No Effect
F1, C2
No Effect
No Effect
F1, C2
G1, C2
T
C1, I2
E
No Effect
T1, C2
T
P1, C2
T
T1, C2
T
C1, P2
T
Cyclophosphamide
F1, C2
E
Cytarabine
D1, G2
Dacarbazine
No Effect
Docetaxel
No Effect
Doxo1,
Doce2
T
No Effect
Doxo1,
Doce2
T
Doxorubicin
D1, F2
G1, D2
No Effect
G1, D2
No Effect
Epirubicin
I1, D2
T
I1, D2
LD1, D2
T
D1, O2
P1, D2
No Effect
D1, V2
T
D1, T2
T, PK
D1, P2
T, PK
G1, E2
E1, P2
PK, T
E1, M2
Etoposide
No Effect
T1, E2
E1, V2
F1, C2
E
Fludarabine
Fluorouracil
Gemcitabine
F1, C2
F1, C2
No Effect
G1, C2
T
D1, G2
D1, F2
No Effect
G1, D2
G1, D2
G1, F2
G1,E2
I1, F2
T
G1, F2
L1, F2
E
O1, D2
G1, I2
F1, M2
E
P1, F2
G1, O2
P1, G2
E, T
I1, D2
T
Ifosfamide
I1, B2
C1, I2
E
I1, D2
I1, F2
T
L1, F2
E
P1, I2
No Effect
G1, I2
M1, L2
T
No Effect
LD1, D2
T
Liposomal
Doxorubicin
D1, O2
Oxaliplatin
O1, D2
No Effect
Methotrexate
V1, G2
P1, G2
E, T
I1, P2
Leucovorin
G1, O2
No Effect
F1, M2
E
LD1, V2
PK, T
P1, O2
M1, L2
T
E1,M2
Mitomycin
Paclitaxel
Pr
ala
te
xa
tre
I1,B2
Bevacizumab
Irinotecan
Pe
m
e
d
xe
tre
B1, P2
No Effect
P1, C2
T
C1, P2
T
D1, P2
T, PK
E1, P2
PK, T
No Effect
P1, D2
Pemetrexed
P1, G2
E, T
I1, P2
P1, I2
P1, O2
PEM1,
PAC2
P1, G2
E, T
PEM1,
PAC2
P1, G2
Pralatrexate
Topotecan
P1, F2
T1, C2
T
T1, C2
T
D1, T2
T, PK
D1, V2
T
Vinorelbine
1. Match chemotherapy agents from either the top or side columns.
3. Determine the order of “optimal sequence” as demonstrated in the
following example:
> G1, F2 = Gemcitabine given first, followed by Fluorouracil given
second.
2. First initial(s) of each agent used to explain sequence
> Example: M + methotrexate, 1 = administer first
4. Letter(s) under optimal sequence, T, E, or PK refers to an
interaction. Refer to INTERACTION LEGEND at right.
(valid only for therapies given on the same day)
No Effect
E1,V2
Vincristine
“OPTIMAL SEQUENCE” DIRECTIONS FOR USE
T1,E2
V1, G2
LD1, V2
PK, T
INTERACTION LETTERS
If a letter is present under the “optimal sequence” symbols, an interaction has been
noted in published data. Data is limited to a human, in-vivo interaction with a clear
benefit for the “optimal sequence” administration order. The letter and sequence
benefit interaction are summarized at right:
No Effect
T = a TOXICITY related interaction can be avoided
The literature supported no difference in order sequencing with respect to outcome or toxicity.
E = EFFICACY related interaction happens
X1, Y2
E
See OPTIMAL SEQUENCE directions on how to read the sequence order and Interaction letters.
PK = a PHARMACOKINETIC related interaction
X1, Y2
The literature noted no clinical effect from sequence order.
Empty Box = denotes a lack of evidence in the literature.
© October 2011 McKesson Specialty Health. All rights reserved.
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Chemotherapy Sequencing Chart
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