Lymphoma Flashcards

1
Q

what is lymphoma

A

malignant disease of MATURE lymphocytes, which divide uncontrollably and dont die

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2
Q

where does it accumulate

A

in the LN and the extranodal tissue/organs
can arise anywhere in the body/brain/lung/skin/ GI tract
can spontaneously wax and wane [grow and shrink without trt]

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3
Q

how do people present

A

swollen lymph glands
pain
can deteriorate quickly:
- dehydration
- anaemia
- hypercalcemia: release of osteoclasts
- infection
- critical organ damage

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4
Q

how are they diagnosed

A

FBC: WBC
chest x-ray: involvement in the mediastinum accumulation in the thymus could lead to an SVCO
BM aspiration: ONLY NHL
biopsy
PET/CT: lymphatic involvement/spread NOT for NHL

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5
Q

why is a biopsy needed

A

to find out if it is a HL or NHL due to its presence of reed-steinberg cells

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6
Q

risks of HL

A

EPV
smoking
HIV
incidence has risen 37% since 1990s
links with deprivation

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7
Q

presentation of HL

A

enlarged neck nodes: 60%
axilla: 20%
groin: 15%
enlarged spleen: 10%

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8
Q

what do HL have

A

reed-sternerg cells

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9
Q

what is a variant of RS cell in HL

A

nodular predominant HL

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10
Q

what is stage 1 of a HL

A

1 LN region or 1 extranodal site or organ

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11
Q

what is stage 2 of a HL

A

2 or more LN regions on the same side of diaphragm alone or with involvement limited contiguous

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12
Q

what is stage 3 of a HL

A

LN on both sides of the diaphragm including one organ or area near the LN or spleen

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13
Q

what is stage 4 of a HL

A

dissemination to one or more extra lymphatic organs or tissues with/without involvement of nearby LN

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14
Q

what is an A for modifying features

A

assymptomatic

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15
Q

what is a B for modifying features

A

unexplained fever (>38), night sweats, loss of more than 10% of body weight in 6 mths

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16
Q

what is a E for modifying features

A

involvement of a single, contiguous or proximal extranodal site

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17
Q

what is an X for modifying features

A

bulky disease (mass > 10cm)

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18
Q

what is INRT

A

involved node RT = CTV (node only) + no margin

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19
Q

what is ISRT

A

involved site RT = CTV (node + margin) + only involved nodes included

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20
Q

what is IFRT

A

involved field RT = CTV (entire nodal region)

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21
Q

what is EFRT

A

extended field RT = no longer seen

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22
Q

what used to be the RT technique

A

extended field: mantel + inverted Y + chemo

23
Q

why was the old technique for HL stopped

A

patients were developing AML, secondary cancer. cardiac issues, greater risk of death than relapse in survivors

24
Q

what is RT based on now

A

age, site, size of RT field

25
Q

what chemo is given

A

low dose for children
ABVD [doxorubicin, bleomycin, vinblastine, dacarbazine]

26
Q

what is the trt for stage IA/IIA

A

2-4 cycles of ABVD + RT

27
Q

what is the trt for the other stages

A

6-8 cycles of ABVD +/- RT

28
Q

what are the hodgkin RT sites

A

whole brain (meninges involvement: field extends to C2/3)
breast
bone (A/P) to cover whole bone
thyroid: cervical lymphatics (also in trt field)
orbit: single applied or angled parallel to avoid contralateral eye

29
Q

early HL trt

A

favourable: 2 cycles of ABVD + 20Gy in 10 over 2 weeks
unfavourable: 4 cycles of ABVD + 30Gy in 15 over 3 weeks

30
Q

advanced HL trt

A

RT for residual disease is indicated after partial response chemo
30-36Gy in 15-20 over 3-4 weeks

31
Q

what is given if relapse for HL occurs

A

high dose chemo is given
single site relapse not previously irradiated has 30-34Gy
after chemo 30Gy in 15 over 3 weeks
persistent disease after chemo is 36-40Gy in 18-20 fractions over 3-4 weeks

32
Q

what is given to younger pt who have HL relapse

33
Q

what indicates high chance of relapse after SC transplant

A

high PET uptake

34
Q

what are the palliative recommendations for HL

A

no definitive ones however
30Gy in 10
20Gy in 5
8Gy in 1

35
Q

stats for NHL

A

6th most common in the UK
lower in asian and black ethnic groups
1/39 males
1/51 females

36
Q

what are the risks of NHL

A

age
HEP C [26%]
occupational exposure
- 40% organochlorine
- 22% organophosphate
- 26% field crop
autoimmune conditions
- coeliac
- rheumatoid arthritis

37
Q

how are NHL categorised

A

how fast they grow
what type they originate from (T or B cell)

38
Q

what are NHL classified as

A

low or high grade

39
Q

what is the most common NHL

A

diffuse large B cell

40
Q

what is treatment for NHL dependent on

A

fitness, age, disease subtype

41
Q

what chemo is given for NHL

A

R-CHOP [rituximab, cyclophosphamide, doxorubicin, vincristine, prednisolone]

intrathecal: methotrexate and cytarabine

42
Q

what treatment can be given for NHL

A

chemo
RT
immunotherapy

43
Q

why is RT given

A

if the disease is bulky or aggressive
pt not responding/tolerating chemo

44
Q

RT for NHL, early DLBCL

A

early DLBCL: 30Gy in 15

45
Q

RT for NHL, CMR

A

CMR patients receiving consolidation RT: 30Gy in 15

46
Q

RT for NHL with incomplete response to chemo

A

36-40Gy in 18-20 fractions in 3-4 weeks

47
Q

what is the RT for bridging over for CAR-T therapy for NHL

A

30Gy in 10-15 over 2-3 wks
20Gy in 5

48
Q

what is common in pregnancy

A

HL
RT in the first trimester is avoided
pt in 2nd or 3rd can be avoided

49
Q

how long should pt wait to not get pregnant for after trt

A

2 years to avoid relapse

50
Q

information on HL

A

more often localised to single axial group of nodes (cervical, media, para-aortic)
orderly spread by contiguity
mesenteric nodes + waldeyers ring rarely involved
extranodal involvement uncommon

51
Q

information on NHL

A

more frequent involvement of multiple peripheral nodes
non contiguous spread
mesenteric nodes + waldeyers ring commonly involved
extranodal involvement is common

52
Q

mycosis fungoides

A

T cell lymphoma - skin invasion
superficial or electrons
10Gy in 5
sometimes TBE: 8Gy in 2 or 12Gy in 3

53
Q

what does CNS lymphoma RT impact

A

cognitive function therefore 40-45Gy in 20-25 is given

54
Q

how is RT controversial for

A

paediatrics