Lymphoma Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

Chemotherapy for DLBCL

A

R-CHOP
rituximab, cyclophosphamide, doxorubicin
vincristine
prednisone

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2
Q

DLBLC IPI prognostic score

AND DLBCL Risk Factors

A

“PLEAS” (pleaing to live bc this is an aggressive cancer):
- Performance status: ECOG ≥2
- LDH > ULN
- Extranodal sites: ≥1
- Age: over 60
- Stage III/IV (for stage modified early treatment, this is a point for Stage II)

Risk Factors: (PMH) BLEAS
IPI factors:
- bulk (tumor size > 7cm)
- LDG abnormal
- Extranodal: testes, stomach, breast, bone
- Age > 60
- Stage II

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3
Q

Follicular lymphoma prognosis score (FLIPI-2)

A

Follicular lymphoma IPI: (BASH’D with a 2x2 board)

B:bone marrow involvement
A: Age > 60
S: Serum beta-2-microglobulin elevated
H: Hg < 120
D: Diameter of largest LN > 6cm

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4
Q

Hodgkin Lymphoma IPS prognosis

A

HALSWAM: think lake HALstat SWAM: 45M swimming tired by anemia buoyant because albumin <40 causing edematous legs
- Hg <105,
- Albumin < 40g/l
- lymphopenia,
- stage 4 disease by Ann arbor classification
- WBC >15
- Age ≥45
- male

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5
Q

Most common chemotherapy for HL

A

ABVD:
- Adriamycin, bleomycin, vinblastine, DTIC (dacarbazine)

BEACOPP: now used for high-risk patients:
- Bleomycin, Etoposide, ADRIAMYCIN (DOXOrubicin), Cyclophosphamide, ONCOVIN ®
(VinCRIStine), Procarbazine, Prednisone

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6
Q

Lymphoma Staging

A

Stage I = single LN region or extra-lymphatic site/lymphoid structure (ex: basically only the spleen, thymus, and waldeyer’s ring)

Stage II = ≥2 LN regions or lymphoid structures on the same side of the diaphragm (ex: hilum and mediastinum are two different LN regions)

Stage III = LN regions or lymphoid structures on both side of the diaphragm

Stage IV = diffuse involvement of ≥1 extra-lymphatic organ or site (liver, lung, bone marrow, CSF) Ex: axillary LN with erosion into the bone: this is NOT stage 4. This would be 2E because it is local. If locoregional involvement and not in the liver then chances are it is not stage 4.

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7
Q

HL risk factors (affect treatment)

A

Think: almost stage III if rules of 3’s:
- 3 areas involved
- ESR ≥30 w/ B symptoms otherwise ≥50
- Greater than 1/3 thoracic diameter
-Extranodal disease

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8
Q

Treatment HL Stage I/II

A

Favourable (no risk factors);
- ABVD x 2 + 20Gy/10 ISRT
- OR ABVD x 2 then PET, if CR additional 2x (otherwise, 6 cycles total ABVD)

Unfavourable:
- ABVD x 4 (can give x6 if bulky disease) + 30Gy/20 ISRT
- OR ABVD x 2 then PET, additional 2-4 if CR (not for bulky disease).

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9
Q

Treatment DLBCL early stage and advanced stage

A

No RF: RCHOP x 4. If PET negative, observe. If positive, ISRT 36Gy/20#

If RF: RCHOP x 6. If PET negative, observe. If bulk, then give 30Gy/20# if CMR. If PR, give 40Gy/20#.

Advanced stage (III-IV):
- RCHOP x 6

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10
Q

Treatment double hit B cell lymphoma and what does this entail?

A

C-MYC and BCL2 and/or BCL6 translocation by FISH

Treat with Dose adjusted (DA) - R - EPOCH x 6. No XRT afterwards. Give MTX for CNS prophylaxis.

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11
Q

Treatment of primary mediastinal B cell lymphoma (think: monique ray)

A

RCHOP x 6 -> ISRT 30Gy/20 if CMR, 36Gy if otherwise. We usually always give rads!!! Alternative: DA-R-EPOCH x 6 with no rads afterwards.

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12
Q

Management Follicular Lymphoma:

A

24Gy/12 ISRT for localized disease. No chemo.
Advanced: treat if GELF criteria (Bendamustine + Rituxumab x 6)

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13
Q

Subtypes of DLBCL :

A
  • Germinal Center B cell (most common)
  • Activated B cell (second most prominent); worse prog
  • Primary mediastinal B cell lymphoma
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14
Q

PMH guidelines for Risk factors in DLBCL

A

IPI factors: age> 60, abnromal LDH, Stage II, Tumor size > 7cm, Extranodal involvement

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15
Q

Treatment high grade B cell lymphoma and what characterizes this

A

double hit: C-MYC and BCL2 or BCL6: DA-R-EPOCH x 6 , MTX for CNS prophylaxis

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16
Q

Primary mediastinal B cell lymphoma treatment

A

RCHOP x 6 -> ISRT 30-36/20. Alternative: DA-EPOCH x 6, no rads afterwards

17
Q

Indication for TBI

A

Mantle cell lymphoma: advanced stage <65. RCHOP alternating with R-DHAP x 6 -> ASVT (TBI 12Gy/6 BID then cytarabine/melphalan) then ASCT followed by maintenance ritux

18
Q

GELF criteria

A

1) involvement of 3 nodal sites each with diamter of 3cm
2) any nodal or extra-nodal mass 7cm in diameter
3) B symptoms
4) splenomegaly
5) pleural effusion or ascites
6) cytopenias: WBC < 1.0 or plt < 100
7) leukemic phase of disease with >5.0x10^9

19
Q

FLIPI-1: know this as well!

A

Four nodal areas or more
Ldh greater than normal
Age >60
Stage III or IV
Hb> 120

20
Q

1) Prognosis for HL/NHL

2) prognosis pre rituximab

A

for simplicity, will say:
0-1 RF points: 90%
2-3: 80%
4-5: 60%

2: subtract

21
Q

What to do for refractory HL?

A

High dose chemo with autologous BMT

22
Q

What percent does adding RT to HL, DLBCL offer

A

decreases LR by 60%, absolute OS benefit like 5%

23
Q

Criteria for diagnosis of MM, SP

A

Criteria for Dx of MM:
o Clonal plasma cells of ≥10% (on either BM Bx or a Bx from other tissue)
o Monoclonal protein in Serum protein electrophoresis (SPEP) or urine protein electrophoresis (UPEP)
o Evidence of end-organ damage that can be attributed to the underlying plasma cell proliferative disorder, specifically: Hypercalcemia, Renal insufficiency, Anemia,Bone lesions, Clonal bone marrow plasma cell percentage ≥60%, involved:uninvolved serum free light chain ratio ≥100, >1 focal lesions on MRI studies

Criteria necessary for the Dx of SP:
o Solitary bone lesion on skeletal survey
o Histologic evidence of plasmacytoma by bx
o <5% plasma cells on marrow aspirate
o No other end organ damage attributable to plasma cell dyscrasia

24
Q

INvestigations to order: do not forget to test for:

A

MUGA
Pregnancy/fertility banking