Lymphoma Flashcards

1
Q

What are the risk factors for developing lymphoma? (3)

A

Immunosuppression: transplant, immunosuppressants, HIV, congenital immune deficiency

Virus & bacteria: HIV, EBV, HTLV-1 (T-cell lymphoma), H.pylori (GALT)

FH of Lymphoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Lymphoma - common presentations? (P; 3)

A

Peripheral lymphadenopathy (i.e. palpable lumps)

Intravacity lymphadenopathy (mediastinal widening, intra-abdominal LN in scan performed for other reasons)

B- symptoms (weight loss, fever, night sweats)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What investigations would you like to review for this patient with Lymphoma? (4)

A

LN biopsy (not FNAB, the definitive dx should be made on excision biopsy) - to confirm the dx (e.g. RS cells in HL) and identify the subtype

BM aspirate/biopsy - to exclude BM involvement

CT Neck+CAP (ask for CXR first - look for hilar lymphadenopathy) & PET scan for staging (combined scan is readily available)

Bloods: FBC (cytopaenia -?BM involvement), LDH, ESR - (disease activity)

Ask if patient had LP (important in high-grade lymphoma)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Lymphoma staging?

A

Ann-Arbor classificaiton (I-IV + A/B).

I: single LN region or a single extra-lymphatic site

II: ≥2 LN regions on the same side of diaphragm - with/without spleen (IIs)

III: both sides of diaphragm - with/without spleen involvement (IIIs)

IV: extra-lymphoid tissues (e.g. bone/lung) in addition to lymphoid tissue

A = No constitutional symptoms

B = B symptoms present

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the long-term management issues in patients with Lymphoma and how would you manage them? (this is essentially the same questions as “Non-pharmacological Mx of Lymphoma patients”

(7 key elements, 4 minimum)

A

Monitoring for relapse & complications. Key issues to discuss are - Cancer, Cardiac, Endocrine, Neuropsychiatric.

1. Monitoring for Relapse

  • 3-6 monthly first few years (depends on subtypes). History & Examination (important as relapses are usually symptomatic and rarely identified on imaging alone) and FBC, LDH and electrolytes.

2. Malignancy surveillance (risk continues at least 30y or more)

  • Educate/counsel yearly to improve Risk awareness, encouraging them to report symptoms
  • Breast***: surveillance from 40y or 8y from irradiation. Annual Mammogram + consider annual MRI (if irradiated 10-35yo).
  • Lung Ca: annual CXR, smoking cessation
  • Skin Ca: annual complete skin exam, sun-screen advice
  • Annual FBC (Leukaemia, MDS), Routine age-appropriate cancer surveillance: exception. Consider early colonoscopy.

3. Cardiovascular +Respiratory health

  • Risk comes from Adriamycin, -Rubicins & RTx (usually 10y after)
  • Minimise CV risk factors: exercise, w.loss, Mediterranean diet, smoking cessation), manage HTN and Dyslipidaemia
  • Refer to Cardiology for baseline evaluation
  • Resting + stress TTE: frequency based on baseline finding + CV risk factors.
  • If patient had RTx to lung fields, do annual spirometry/PFT.

4. Fertility

  • Offer counselling and referal for sperm/ovum banking
  • Refer to reproductive endocrinologist
  • Consider HRT in premature ovarian failure + DEXA screen

5. Thyroid

  • Monitor for Hypothyroidism for those who had RTx to the neck or WBI - annual thyroid examination + TSH

6. Psychiatric/cognitive/Neuro evaluation

  • Monitor for depression, PTSD and neurocognitive impairment, especially those at increased risk (Cranial irradiation, intrathecal therapy)
  • Prompt referral to AH if developing cognitive impairment.
  • Vinblastine/Vincristine: painful PN with loss of deep tendon reflexes.

7. Written information & support

  • All of these issues can be overwheling and may cause a great deal of anxiety
  • Support them, provide them with written documentation of treatment summary, surveillance…etc.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are pharmacological options for Hodgkin’s Lymphoma?

A

Based on staging: I-II (RTx or abbreviated chemo), III-IV (full chemo + consolidation RTx)

Field RTx +

a) 4-6 cycles of ABVD (Adriamycin, Bleomycin, Vinblastine, Dacarbazine) - less BM toxicity, less infertility
b) BEACOPP (bleomycin, etoposide, Adriamycin, Cyclophosphamide, Oncovin (vincristine), prednisolone, procarbazine - more toxic, more infertility, but MORE effective.

Hence if patient had HL - must mention Cardiovascular + Pulmonary + PN + Osteoporosis (if BEACOPP) surveillance.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Do you know of any pharmacological therapies that could be used in patients with Hodgkin’s Lymphoma who failed ABVD or BEACOPP? (2)

A

PD-1 blockade (Nivolumab): since RS cells expresses PDL1. Recent study demonstrated good response rate with complete remission.

Brentuximab (anti-CD30) in relapse/refractory Hodgkin’s.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Risk of secondary Cancers in Hodgkin’s lymphoma:

AML: what are the risk factors? (3)

A

Risk is about 2-10% at 10y

Risk factors: alkylating/etoposide chemo, age of treatment, combined modality therapy. (basically +++ chemo burden + young age)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What 2 solid tumours are patients at most risk following tx for Hodgkin’s lymphoma involving radiation?

A

Depends on Radiation dose + Field size.

Breast: RR upto 75

Thyroid: RR upto 30.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Lymphoma - PRIC MCP?

A

P: lymphadenopathy, B-symptoms, incidental from imagings

R: immunosuppression, FH, micro (EBV, HTLV-1, HIV, H.pylori)

I: LN biopsy, CT, PET, BM biopsy, LP

C: disease = relapse? therapy = secondary Ca? cardio/resp toxicity? thyroid? PN? depression/PTSD? fertility?

M: which chemo, how many, radiation - where? dose? WBI?

Is patient on appropriate malignancy surveillance? annual blood test, mamogram, CXR, cardiac investigations. Has patient has had banking done (if younger patient)

C: remission or refractory?

P: insights into the survivorship issues relating to Lymphoma. Does the patient have a good understanding?

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the treatment options for Relapsed Hodgkin’s lymphoma? (3)

A

If relapsed >1y after → retreatment with original regime

If <1y → second line therapy

Can consider Autologous SCT after high-dose chemotherapy.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are the risk factors for poor outcome in patients with Lymphoma? (5)

A

Age > 60

Raised LDH

Low ECOG

Ann-Arbor stage III-IV

More than 1 extra-nodal site

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are indications to treating SLL/CLL (mature B-cell neoplasm)?

A

These are most common: 75% of NHL.

Observe if only BM inovlvement + lymphocytosis (survival >10y).

If liver or spleen involved, especially if BM failure present, treatment usually indicated.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Pharmacological options for NHL: mature-B cell neoplasma (CLL/SLL - chronic lymphocytic leukaemia, small lymphocytic lymphoma - 4)?

A

Options are;

  • Oral Chlorambucil (4)
  • IV Fludarabine (more potent) + Rituximab
  • BM transplant in young.
  • Newer anti-CD20 in elderly with multiple comorbidities (e.g. obinutuzumab or ofatumumab)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Treatment (4) and prognosis of MALT-Lymphoma?

A

8% of NHL.

Curable when localised

Eradication of H.pylori will induce remission in 75%.

Otherwise RTx.

For more widespread disease/resistant disease: Rituximab.

Treat Hepatitis C.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Pharmacological Mx for Follicular (22%) and Diffuse Large B-cell Lymphoma (33%)? 5y survival for treated patients?

A

Usually R-CHOP (cyclophosphamide, HyroxyDaunorubicin, Oncovin/Vincristine, Prednisolone) +/- maintenance Rituximab.

Follicular: 75% remission rate, 5y survival rate 50-90% (Based on risk factors)

DLBCL: cure upto 70%, 5y survival rate 50-90% (Based on risk factors)

17
Q

So which Lymphomas are more difficult to treat and aggressive? (3)

A

HIV related NHL

Mantle cell lymphoma

Burkitt’s lymphoma (aggressive but curable)