Lec 1: Supportive Care Flashcards

1
Q

Myelosuppression? Talk about it

A

Myelosuppression from chemotherapy can lead to neutropenia, anemia and thrombocytopenia

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2
Q

Thrombocytopenia

A
  • Can be a limiting factor for patients who require venous
    thromboembolism (VTE) prophylaxis (i.e. hospitalized patients)
  • Can limit ability to continue therapeutic anticoagulation for patients who have an indication for anticoagulation
  • Typically managed with platelet transfusions
  • Important to keep in mind platelet count before administering any IM injections (sometimes patient’s require transfusions before IM injections, or other procedures)
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3
Q

Anemia

A
  • Typically, asymptomatic patients without significant comorbidities are just being observed (Just monitor them)
  • For other patients who require treatment RBC transfusions should be considered (safer than ESA -ESA is for a specific population)
  • Use of erythropoiesis stimulating agents (ESAs) can considered for specific patient populations
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4
Q

Anemia - Use of erythropoiesis stimulating agents (ESAs)
…should be avoided in what patient group? can be used in what patient group? BBW?

A
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5
Q

Neutropenia… and it’s category

A
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6
Q

Neutropenia and Granulocyte-colony stimulating factor (G-CSF)

A

Duration and severity of neutropenia is improved with the use of granulocyte-colony stimulating factor (G-CSF) aka Neupogen.
.
NOTE: The use of Neupogen has improved neutropenia by decreasing the duration and severity

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7
Q

G-CSF can be used to prevent or reduce
neutropenia… Risk assessment considerations when considering adding G-CSF

A

Risk assessment considerations when considering adding G-CSF
- Disease/ what type of cancer
- Chemotherapy regimen (high dose, dose-dense, standard dose)
- Patient risk factors
- Treatment intent (curative vs. Palliative)
-IMPORTANT: If overall risk of febrile neutropenia is >20% (high-risk) G-CSF is generally used!

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8
Q

Neutropenia
G-CSF considerations (the OG stuff)

A
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9
Q

Neutropenia
Pegylated G-CSF

A
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10
Q

Neutropenia
Adverse reactions with G-CSF and pegylated G-CSF

A
  • Allergic reactions
  • Injection site reactions
  • Bone pain (10-30% of patients)
    ——- Preferred management: loratadine 10 mg daily for 5-7 days after G-CSF (why should we NOT opt for NSAID in patient with thrombocytopenia? it can increase risk of bleeding!)
  • Other: Splenic rupture, secondary malignancy (AML and MDS), fever, rash
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11
Q

Febrile Neutropenia (FN) and it’s requirements

A

NOTE: If the MASCC score is < 21 the patient is considered high risk!!!!

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12
Q

Outpatient management for Febrile Neutropenia (FN) in low-risk patients

A

Oral antibiotic regimens (pick one of the 3):
- Ciprofloxacin plus amoxicillin/clavulanate (Augmentin)
- Levofloxacin
- Moxifloxacin
.
Continue to monitor patient daily for response and toxicity

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13
Q

Inpatient management for Febrile Neutropenia (FN) in high-risk patients

A

Empiric antibiotic therapy: monotherapy antipseudomonal beta-lactam
— Cefepime (2 grams q8h IV)
— Meropenem
— Piperacillin/tazobactam
.
MRSA coverage is not typically added empirically unless there is a history or indication
.
Concern for abdominal infection: favor piperacillin/tazobactam (Zosyn) empirically for anaerobe
coverage
.
Consider fungal coverage if patient is persistently febrile after 4 days
.
Consider history of previous antimicrobial prophylaxis regimens is applicable

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14
Q

Potential outcomes of treatment for Febrile Neutropenia (FN)

A
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15
Q

Which of the following is the biggest limiting factor which can impact a patient’s ability to receive anticoagulation while on active chemotherapy?
A. Thrombocytopenia
B. Anemia
C. Bleeding
D. Neutropenia
E. Infection

A
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16
Q

K.N. is a 70 YOM with newly diagnosed testicular cancer who is starting Cycle 1 of chemotherapy with VIP (etoposide, ifosfamide, and cisplatin, chemo on days 1-5, 21-day cycle) which has a high risk of febrile neutropenia (≥ 20%). The patient’s last standing weight was 81 kg on
C1D1. Which option for primary prophylaxis would be best for this patient?
A. Zarxio 300 mcg SubQ daily starting on day 5 until ANC recovery
B. Tbo-filgrastim 480 mcg SubQ daily starting on day 6 until ANC recovery
C. Udneyca 6 mg SubQ once on day 5
D. Neupogen 300 mcg IV daily starting on Day 6 until ANC recovery

A
17
Q

K.L. is a 72 YOM with Non-Hodgkins Lymphoma on treatment with HyperCVAD. The patient presented to the ED overnight with a fever of 38.9°C and ANC of 400 cell/m3. Blood cultures were drawn before starting antibiotics and the results are still pending. The patient weight’s is 96 kg and his last CrCl was 65 mL/min. The
ER provider started the patient on empiric cefepime 1 gm q8h IV. The patient has now been admitted and transferred to the oncology unit. Would you like to make
any changes at this time?
A. Yes
B. No
C. Maybe?

A

A. Yes!!! Why?
empiric cefepime should be 2gm Q8h IV! Need highest dose possible!

18
Q

Immune checkpoint-related toxicities and the timeline? Just know general

A
19
Q

Principles of management of Immune checkpt toxicity

A
  • Refer to guidelines for specific management of each toxicity (NCCN, ESMO)
    .
    Steroids
  • Lower grades (1-2): Prednisone 1-2 mg/kg
  • Higher grades (3-4) or serious toxicities: Methylprednisolone 1-2 mg/kg
    .
    These patients with serious toxicities must continue a long steroid taper
    .
    For some toxicities infliximab can be used