Lymphoma Flashcards

1
Q

VIPD: components

A

etoposide, ifosfamide, cisplatin, dexamethasone

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2
Q

FLIPI score components

A

LNASH

LDH elevated

Nodal areas > 4

Age > 60

stage III-IV

Hgb < 12

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3
Q

stage III/IV HL: poor prognostic factors

A

MASHAWL

male

age>45

stage IV

Hgb<10.5

albumin<4

WBC>15

lymphocyte<0.6

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4
Q

solitary plasmacytoma: likelihood of transformation to multiple myeloma

A

osseous: 60%
extraosseous: 40%

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5
Q

relapsed/refractory DLBCL: treatment paradigm

A

(ILROG guidelines)

CR (Deauville 1-3) to salvage chemo:

30-36 Gy / 1.5-2.0 Gy per fx pre- or post-transplant

30 Gy / 1.5 Gy BID is an option for urgency pre-transplant

Post-transplant is done within 4-12 wks after

Pre-transplant is done ASAP, within 4 weeks after chemo

Volume: ISRT. Can consider including adjacent nodes that responded to first line chemo

PR (Deauville 4-5) residual focus after salvage chemo:

36 Gy / 1.8-2 Gy per fx with boost to 40-45 Gy / 1.8-2.2 Gy per fx to PR site

Volume and timing as above

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6
Q

FLIPI 5yr OS by score

A

5yr OS:

0-1 points 90%

2 points 80%

3-5 points 50%

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7
Q

FLIPI-2 score components

A

BBLAH

B2 microglobin elevated

bone marrow positive

ymph node > 6cm

age > 60

Hgb < 12

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8
Q

Early stage unfavorable HL: treatment paradigm

A

chemo, then post-chemo PET. If Deauville 1-3, treat with RT. If Deauville 4, consider another 2 cycles of chemo

Varous regimens:

30Gy/15fxs after ABVD x4 per HD11

20Gy/10fxs after escBEACOPP x 4 per HD11

30Gy/15fxs after escBEACOPPx2 + ABVDx2 per HD14 (best results)

36Gy/18fxs for bulky

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9
Q

NK T-cell lymphoma: outcomes

A

3yr OS 85%

3yr LC 60%

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10
Q

intraocular DLBCL: treatment paradigm

A

vitreous biosy

36Gy to globe and optic nerve extending to chiasm

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11
Q

Testicular DLBCL: 5yr OS

A

5yr OS 85%

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12
Q

cutaneous T-cell lymphoma: doses

A

Localized: electrons to 20-24 Gy with at least 2 cm margin. Some treat up to 36 Gy.

Generalized: TSEBT to 10-12 Gy (1 Gy per day, 4 days per week, for 3 weeks) per guidelines. With this regimen retreatment is allowed

Palliation: 2x2 Gy repeated until good response or single dose 8 Gy. Margin 1-2 cm

(ILROG guidelines)

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13
Q

gastric MALT: indications for xrt

A

H. pylori positive after failure with antibiotics

H. pylori negative

t(11;18) positive more likely to fail antibiotics but still try

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14
Q

stage III/IV HL: indications for radiation

A

partial response, bulky disease, or bone involvement

typically 30Gy/15fxs, maybe higher if bone involvement

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15
Q

Lugano staging tips for HL and DLBCL

A
  • PET is adequate to assess bone marrow involvement and can be highly suggestive for extralymphatic involvement
  • Routine bone marrow biopsy no longer indicated for HL and DLBCL.
  • Consider bone marrow biopsy in HL if cytopopenias present and consider in DLBCL if suspecting a different histology
  • BM biopsy still required in follicular, MZL, burkitt’s
  • Use A and B status only for Hodgkin, not NHL
  • For bulky, add the word “bulky” to the stage, not letter X
  • Bulky disease in HL is >10 cm or >1/3 the transthoracic diameter. CT is appropriate (CXR not required)
  • For extranodal, use letter E modifier. Extranodal is only applicable for Stage I-II per Lugano. No such thing as Stage IIIE or IVE. Just Stage III and IV.
  • Splenomegaly is defined as size >13 cm. PET avidity is not relevant when determining splenomegaly
  • Hepatomegaly is focal or disseminated PET avidity
  • Bulky in NHL is definted as ≥7.5 cm per NCCN and DSHNHL RICOVER (not defined in Lugano)
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16
Q

relapsed/refractory HL: criteria for transplant

A

General indications:

Localized relapse

Bulky disease

Persistent FDG uptake after ICE or ASCT

Critical for LC (nerve compression, SVC compression, airway compression, lymphedema, hydronephrosis)

Desseminated disease may be all treated with RT of toxicity profile is reasonable

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17
Q

Lymphoma: NCCN unfavorable factors

A

≥4 nodal sites

bulky disease >10 cm or mediastinal mass ratio >1/3

ANY B symptoms

Not counted: extranodal disease

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18
Q

lymphocyte predominant HL: characteristics

A

A HL. Markers similar to PMBCL except CD30. CD20+, CD15-, CD30-(very rarely CD30+).

Path: popcorn cells (large cells with multilobulated or round nuclei) and nodularity and replacement of nodal architecture.

80% present as early stage. Usually peripheral adenopathy with central sparing. Often extranodal. Some will relapse but relapse survival still better than HL.

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19
Q

BEACOPP: components

A

Bleomycin

Etoposide

Doxorubicin

Cyclophosphamide

Vincristine

Procarbazine

Prednisone

Q3w

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20
Q

NK T-cell lymphoma: workup

A

Include evaluation of nasopharynx with flexible scope, testicular exam, skin exam, CSF analysis, EBV viral load, MRI nasopharynx

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21
Q

total skin electron beam therapy: side effects

A

desquamation, hair loss, lymphedema, nail loss, loss of sweating, second malignancy

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22
Q

Lymphoma: follow up

A

Year 1-2 q 3 mo, Year 3-5 q 6mo: H&P, CBC/plt/ESR

imaging at 6, 12, and 24 mos

Annual flu shot, TSH, CXR, counseling on fertility, psychosocial, reproduction, cardiovascular, breast self exam, skin cancer risk

After 5 years - annual BP check, echo/stress test/carotid US screening q10 yrs, mammogram at 8 yr or age 40 (MRI if age 10-30 at treatment), CBC/chem/TSH/lipids, CXR

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23
Q

cutaneous B-cell lymphoma: treatment options aside from xrt

A

intralesional steroids, R,topicals, other systemic therapy such as is used for follicular lymphoma

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24
Q

mantle cell lymphoma: treatment paradigm for stage I-III

A

induction hyper-CVAD

30Gy ISRT

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25
Early stage favorable HL: treatment paradigm
ABVD x 2 cycles then obtain post-chemo PET. Deauville ≤3 give 20 Gy/ 10 fx Deauville 4 give two more cycles and reassess Deauville 5, biopsy first, and if positive see refractory pathway
26
follicular lymphoma: workup
In follicular lymphoma, excisional biopsy still recommended as in all lymphomas. If excisional bx not feasible, can do core needle bx with immunohistochem, flow cytometry, FISH. FISH testing: if 1p36 translocation positive, disease will be localized and no staging studies are needed Labs: Hep B, B2 microglobin plus standard BM bx (still required in follicular with Lugano)
27
NK T-cell lymphoma: treatment paradigm
stage I: radiation alone (50Gy + boost) stage II-IV: chemoradiation VIPD then 45Gy 40Gy with concurrent cisplatin then VIPD x3 cycles (Korea)
28
MZL/MALT: general approach
PET. BM bx is required per Lugano. An Indolent lymphoma per ILROG extranodal guidelines RT alone to 24 Gy (20-30 Gy) Per NCCN surgery alone is allowed for parotid, breast, lung, thyroid
29
SMILE: components
steroid dex, MTX, ifosphamide, pegaspargase, etoposide
30
NK T-cell lymphoma: xrt fields
Always include bilateral nasal cavity, bilateral anterior ethmoid, hard palate and ipsilateral maxillary sinus. Bilateral maxillary sinus tumor of bilateral or posterior nasal cavity. Include adjacent structures or nodes only if these are involved No elective neck radiation, even if nodes involved. Use ISRT. Waldeyers ring location: cover entire ring.
31
Lymphoma: GHSG unfavorable factors
≥3 nodal sites bulky ≥1/3 chest extranodal involvement ESR ≥30 with B and ≥50 without B
32
gastric MALT: sim
supine, wingboard, 4DCT, optional 10 cc oral contrast, empty stomach (treat in AM or NPO for 3 hours).
33
solitary plasmacytoma: dose and field
40-50Gy Osseous: involved lesion plus margin Extraosseous: involved lesion, and consider adding regional lymph nodes Conservative: Give 2-3 cm to block edge. If vertebral body, treat that entire vertebra, 1 level only Other strategy: Treat whole bone. Treat one vertebral body above and below
34
lymphocyte predominant HL: treatment paradigm for IA/IIA nonbulky
30 Gy if \<5 cm, 36 Gy if \>5 cm treatment is RABVD or RCHOP +/- xrt for IB/IIB or bulky disease
35
Early stage favorable HL: 10yr OS and PFS on HD10
10yr OS 94% 10yr PFS 87%
36
Lymphoma nodal sites
37
total skin electron beam therapy: narrative
I would position the patient at 3 m SSD with beam spoiler 1 cm thick placed in front of the patient. I would treat 3, out of total 6, positions per day for 4 days per week, delivering 1 Gy per day, ensuring to boost areas of possible underdosage including soles, perineum, scalp, under breasts and pannus. I would place TLDs to confirm adequate dosage. The beam would be moved + and – 20 degrees.";;Treat in 6 positions to cover total skin, 3 positions per day, 4 days per week. Boost to soles, perineum, and scalp. Also need to boost "shadow areas" under breast, pannus, etc. Can shield eyes. Can intermittently shield nail beds and tops of feet to reduce risk of edema. Put TLDs on areas at risk of underdosage such as scalp vertex, axilla, inframmary folds, perineum, intergluteal cleft, medial thighs, soles of feet, palms (patient usually is supported by handles).;;A beam spoiler 1 cm thick is placed in front of patient to increase large angle scatter and improve dose homogeneity. The beam is positioned 3 m SSD and moved +/- 20 degrees (angles reduce photon contamination to less than 1%). Goal is to achieve dose homogeneity in the coronal plane. Rx and Dmax are at skin surface, and 80% dose is at 0.7-1.0 cm depth
38
DLBCL: workup
H&P, family history, B symptoms (fever, weight loss, nightsweats) performane status, complete LN exam, Waldeyer's ring, palpation of abd/spleen/liver Excisional biopsy of node. IHC. Karyotype or FISH for double hit (BCL2, BCL6, myc) Labs: CBC w/ diff, LFTs, CMP, **uric acid**, LDH, beta-HCG, HIV test, Hepatitis B Studies: CXR, CT C/A/P, PET. BM bx if PET negative and cytopenias present (always do BMbx for follicular, MZL, and Burkitts) Pre chemo assessment: Echo/MUGA, PFTs dental eval if treating neck fertility counseling LP in DLBCL for testicular, paranasal sinus, epidural, or HIV assoc lymphoma, or if more than 2 extranodal sites and elevated LDH (NCCN)
39
IPI score: 5yr OS by score (rituximab era)
5yr OS: score 0: 95% score 1-2: 80% score 3-5: 55%
40
R-CHOP: components and dose
Rituximab 375 mg/m2, d1 Cyclophophamide 750 mg/m2, d1 Doxorubicin 50 mg/m2, d1 Vincristine 1.4 mg/m2 (max 2 mg), d1 Prednisone 100 mg po qd d1-5 Q3w x 6-8 cycles
41
Lymphoma: sim for head/neck, chest, abdomen, pelvis
H&N: do dental eval first. Use bite block to divert tongue away from field if possible. Mask. Chest: 4DCT, vac loc. Breath hold increasing in use to spare heart and lung Abdomen: 4DCT. Empty stomach and treat at same time each day. If using oral contrast also sim without contrast. Daily CBCT. Pelvis: If young age, do pregnancy testing and fertility testing. Consider sperm banking, egg banking, ovarian transposition, testicular clamshell
42
follicular lymphoma: treatment paradigm
stage I-II, grade 1-2: xrt alone (24Gy) stage I-II, grade 3: treated like DLBCL (R-CHOP + xrt)
43
TBI treatment fields
Treat AP/PA - Treat at 400 cm SSD - I would first measure the patient to create compensators for appropriate dose distribution. I would give zofran for nausea prophylaxis - Patient standing - Treat at extended SSD with beam spoiler - Treat with 12 Gy, BID dosing, 5-10 cGy/min, lung dose \<10 Gy for ablative with fludarabine/cyclophosphamide
44
Early stage DLBCL: radiation doses
36Gy for bulky tumor or bony disease 40Gy for partial response on PET
45
mantle cell lymphoma: workup
Standard workup Examine H&N area including waldeyer ring, size of liver and spleen EGD to look for MALT is optional PET BM bx in all Extremely rare to see localized disease
46
Testicular DLBCL: workup
Standard workup and PET plus: LP and CSF MRI brain skin exam (bilateral involvement is still stage I)
47
H. pylori+ gastric MALT: antibiotic regimens
1st line triple therapy: PPI, clarithromycin, amoxicillin. ("CAP") 2nd line quadruple therapy: PPI, bismuth, metronidazole, tetracycline. ("P BMT");
48
relapsed/refractory HL: treatment paradigm
(ILROG guidelines) ISRT is appropriate with autologous SCT and can be given before or after SCT. **CR after salvage chemo (often ICE):** CR Deauville 1-3: consider 30 Gy, or 36 Gy for Deauvile 3 CR on PET (D score 1-3) but \>2.5 cm on CT: 36 Gy Previously irradiated: ≥18 Gy as dosimetry allows Prior to ASCT or 4-12 weeks after **PR (Deauville 4) after salvage chemo:** PR sites to 36-40 Gy and CR sites to 30-36 Gy May treat only PR sites if volume is large TLI: 18 Gy in 1.8 Gy BID over 1-2 weeks to refractory disease followed by 18 Gy in same fx to TLI Give RT prior to ASCT with goal of minimal residual disease May also consider further chemo **Deauville 5 after salvage chemo:** If limited refractory, consider RT as above RT not rec for disseminated disease RT before ASCT is favored consider 40-45 Gy
49
primary mediastinal B-cell lymphoma: treatment paradigm and outcome
(DA) R-EPOCH x6 is often used (NIH), then assess response with PET. Consider RT 30-36 Gy for Deauville 4-5 Consider RT to 36 Gy for bulky 5yr OS 95%
50
gastric malt: dose and fields
30Gy/20fxs CTV: EGD to duodenal bulb, also including any positive nodes ITV: add another 1-2 cm per extranodal guidelines PTV: add another 1 cm Might be able to reduce margins with daily CBCT IMRT or 4-field
51
gastric MALT: follow up after antibiotics
Endoscopy with bx in 3 mos. General guide: if still H pylori+ give 2nd line abx, if lymph+ give RT: pylori/lymph- ---\> no further therapy H pylori+/lymph- ---\> 2nd line abx (PBMT) H pylori-/lymph+ ---\> RT lymph+/H pylori+ ---\> 2nd line abx PBMT if stable. If symptoms or progessive dz give RT + 2nd ABX PBMT
52
Orbital DLBCL: treatment paradigm
30 Gy for CR if after chemo. For residual disease consider 40-45 Gy. Include entire orbit. May boost to gross disease
53
gastric MALT: outcomes
MALT 5-yr OS 95% 90% MALT are H pylori +
54
cutaneous B-cell lymphoma: workup
(marginal zone or follicular) Standard H&P with attention to full skin exam. Biopsy (punch, excisional, or incisional). For T cell get peripheral smear for Sezary cells (necessary for staging) CT C/A/P and/or PET. BM Bx useful for select cases 5-10% present with sezary syndrome: \>1000 cells/uL usually with generalized erythroderma
55
Deauville scoring
1. No uptake 2. Uptake ≤mediastinum 3. Uptake \>mediastinum but ≤liver 4. Uptake moderately \>liver 5. Uptake markedly \>\>liver Score of 4 and 5 are always positive. In some situations, 3 is considered positive.
56
TBI narrative
I would position the patient at 4 m SSD standing, treating AP/PA. I would have measured the patient to create compensators and I would place a beam spoiler in front of the patient for appropriate dose distribution. Lead would be used to protect the lungs. (ablative) I would deliver 1.5 Gy BID for four days total to total 12 Gy, 5-10 cGy/min for ablation, with fludarabine and cyclophosphamide chemotherapy and nausea prophylaxis. I would keep the lung dose \<10 Gy.
57
gastric MALT: workup
H&P, family history, B symptoms (fever, weight loss, nightsweats) performane status, complete LN exam, H&N exam noting Waldeyer's ring, eyes, and salivary glands, palpation of abd/spleen/liver Labs: CBC, LDH, CMP. Consider BHCG Imaging: CT C/A/P. Upper endoscopy, EUS and biopsy. FISH for t(11;18). Look for H pylori on path (use modified Geimsa stain). If negative, get blood Ab test, urea breath test, or stool Ab test. Staging imaging: CT C/A/P and PET (PET is now rec on NCCN, but caution: often not FDG avid)
58
solitary plasmacytoma: workup
CT and MRI of affected area. Consider MRI spine H&P, CBC, CMP (Calcium, albumin), LDH, beta-2 microglobulin, SPEP, UPEP, serum and urine immunofixation, skeletal survey, bone marrow bx with IHC + flow, cytogenetics, FISH analysis, serum free light chain, 24 hr urine protein For multiple myeloma need all of: - BM plasma cells \>10% OR plasmacytoma - serum or urine monoclonal protein - CRAB: one of calcium, renal insufficiency, anemia, osteolytic bone lesions Multiple skeletal lesions also diagnoses MM
59
cutaneous T-cell lymphoma: treatment options aside from xrt
Localized options: topical corticosteroids, nitrogen mustard, imiquinod, retinoids, phototherapy Systemic options (localized or diffuse): retinoids, interferon, HDAC inhibitors (vorinistat), electrocorporeal photophoresis, methotrexate
60
cutaneous B-cell lymphoma: doses
Generally only local RT for B cell; never total skin. 1.0-1.5 cm margin Low grade: 24-40 Gy Int grade: RCHOP x3 + RT up to 36 Gy Palliative: 2x2 Gy gives CR in 70%
61
ABVD: components and dose
Doxorubicin 25 mg/m2, d1 and 15 Bleomycin 10 U/m2, d1 and 15 Vinblastine 6 mg/m2, d1 and 15 Dacarbazine375 mg/m2, d1 and 15 Q4w
62
characteristics of primary mediastinal B-cell lymphoma
An NHL. Distinct from DLBCL by CD markers, often CD20+. CD15- and CD30 weakly + or -. BCL6 positive. Path: fibrosis, necrosis, and thymic cells. No nodularity (nodularity is seen in classical HL and NLPHL). Sheets or irregular clusters of large cells, may resemble R-S cells. Arises in thymus (extranodal), common in women, usually stage I-II. Arises in anterior MS, sometimes also with cervical and SCV nodes. More common in females 2:1, usually age 30s
63
Ocular lymphoma: workup
For MALT: upper and lower endoscopy CT C/A/P Consider PET
64
Testicular DLBCL: treatment paradigm
orchiectomy -\> 6 cycles RCHOP + 4 cycles intrathecal MTX -\> RT to contralateral testicle, scrotum 25-30 Gy in 1.5-2 Gy per fx, use electrons. Include nodes only if involved
65
Early stage unfavorable HL: 5yr OS and PFS on HD11
5yr OS 94% 5yr PFS 87%
66
HL: workup
H&P, family history, B symptoms (fever, weight loss, nightsweats) performane status, complete LN exam, Waldeyer's ring, palpation of abd/spleen/liver Excisional biopsy of node. IHC. May require FISH and cytogenetics Labs: CBC w/ diff, LFTs, CMP, ESR, LDH, beta-HCG, HIV test, Hepatitis B Studies: CXR, CT C/A/P, PET. BM bx if PET negative and cytopenias present Pre chemo assessment: Echo/MUGA, PFTs dental eval if treating neck fertility counseling
67
Early stage DLBCL: treatment paradigm
R-CHOP x 3-6 cycles. Some give 6 if IPI score ≥2 or bulky. 3 cycles with RT if Deaville 1-3
68
(DA) R-EPOCH: components
Dose Adjusted based on ANC and platelet counts rituximab etoposide prednisone vincristine cyclophosphamide doxorubicin
69
IPI score
age\>60 PS\>1 LDH\>1.5x nl extranodal dx in more than one site stage III/IV