Principle of Oncology Flashcards

1
Q

ALL is diagnosed by

A

Bone marrow evaluation that demonstrates >25% of the bone marrow cells as a homogeneous population of lymphoblasts.

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2
Q

An agent specifically designed to inhibit the BCR-ABL kinase resulting from the translocation

A

Imatinib

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3
Q

An agent specifically designed to inhibit the BCR-ABL kinase resulting from the translocation

A

Imatinib

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4
Q

Initial therapy, termed remission induction is designed to

A

Eradicate the leukemic cells from the bone marrow. During this phase, therapy is given for 4 wk and consists of vincristine weekly, a corticosteroid such as dexamethasone or prednisone, and usually a single dose of a long-acting, pegylated asparaginase preparation.

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5
Q

Initial therapy, termed remission induction is designed to

A

Eradicate the leukemic cells from the bone marrow. During this phase, therapy is given for 4 wk and consists of vincristine weekly, a corticosteroid such as dexamethasone or prednisone, and usually a single dose of a long-acting, pegylated asparaginase preparation.

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6
Q

Second phase of treatment in ALL is

A

Consolidation; focuses on intensive CNS therapy in combination with continued intensive systemic therapy in an effort to prevent later CNS relapses.

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7
Q

Second phase of treatment in ALL is

A

Consolidation; focuses on intensive CNS therapy in combination with continued intensive systemic therapy in an effort to prevent later CNS relapses.

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8
Q

Many regimens provide 14-28 wk of therapy, with the drugs and schedules used varying depending on the risk group of the patient this period of treatment is often termed as

A

intensification and includes phases of aggressive treatment (delayed intensification) as well as relatively nontoxic phases of treatment (interim maintenance)

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9
Q

Many regimens provide 14-28 wk of therapy, with the drugs and schedules used varying depending on the risk group of the patient this period of treatment is often termed as

A

intensification and includes phases of aggressive treatment (delayed intensification) as well as relatively nontoxic phases of treatment (interim maintenance)

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10
Q

Finally, patients enter the maintenance phase of therapy, which lastsfor 2-3 yr, depending on the protocol used patients are given

A

Daily mercaptopurine and weekly oral methotrexate, usually with intermittent doses of vincristine and a corticosteroid.

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11
Q

Cellular classification of AML

A

> 20% of bone marrow cells on bone marrow aspiration or biopsy touch preparations constitute a fairly homogeneous population of blast cells, with features similar to those that characterize early differentiation states of the myeloidmonocyte-megakaryocyte series of blood cells.

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12
Q

Diagnosis confirmation of CML

A

It is confirmed by cytogenetic and molecular studies that demonstrate the presence of the characteristic Philadelphia chromosome and the BCR-ABL gene rearrangement

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13
Q

Diagnosis confirmation of CML

A

It is confirmed by cytogenetic and molecular studies that demonstrate the presence of the characteristic Philadelphia chromosome and the BCR-ABL gene rearrangement

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14
Q

Pathognomonic features of Hodgkin Lyphoma

A

Reed Sternberg Cells

-A large cell (15-45 µm in diameter) with multiple or multilobulated nuclei.
-The RS cell is clonal in origin and arises from the germinal center B cells but typically has lost most B-cell gene expression and function.

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15
Q

Hodgkin Lyphoma - B symptoms

A

Considered important in staging are unexplained fever >38°C (100.4°F), weight loss >10% total body weight over 6 mo, and drenching night sweats

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16
Q

The genetic changes that contribute to cancer tend to affect three main types of genes:

A
  1. Proto-oncogenes.- involved in normal cell growth and division. They become cancer-causing genes (or oncogenes) allowing cells to grow and survive.
  2. Tumor suppressor genes - involved in controlling cell growth and division.
  3. DNA repalr genes.- involved in fixing damaged DNA
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17
Q

Risk Factors: Lifestyle and environmental risk factors

A
  • Tobacco
  • Alcohol
  • Diet
  • Sunlight
  • Radiation
    -Industrial agents and chemicals
  • Hormones
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18
Q

An increase in the number of cells in an organ or tissue, leading to an increase in size. It is often a response to a stimulus and is usually reversible.

A

Hyperplasia

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19
Q

An increase in the size of individual cells, leading to the enlargement of a tissue or organ without an increase in cell number

A

Hypertrophy

20
Q

Abnormal development or growth of cells within a tissue or organ.

The cells appear disordered and may vary in size and shape and is often considered a precancerous condition and may progress to cancer if not treated.

21
Q

The loss of differentiation and structure in cells, often seen in malignant tumors. These cells have an irregular appearance and lack the normal features of mature, specialized cells.

22
Q

A reversible change where one differentiated cell type is replaced by another. It is often an adaptive response to chronic irritation or stress.

A

Metaplasia

23
Q

A reversible change where one differentiated cell type is replaced by another. It is often an adaptive response to chronic irritation or stress.

A

Metaplasia

24
Q

The formation of a new, abnormal growth of tissue, which can be benign (non-cancerous) or malignant (cancerous)

25
10 Acquired Capabilities of Cancer
1. Sustaining proliferative signaling 2. Evading growth suppressors 3. Avoiding immune destruction 4. Enabling replicative immortality 5. Tumor promoting inflammation 6. Activating invasion and metastasis 7. Inducing angiogenesis 8. Genome instability and mutation 9. Resisting cell death 10. Deregulating cellular energetics
26
Warning SIgns of Cancer: Needed for immediate follow up
C - Change in bowel or bladder habits A - A sore that does not heal U - Unusual bleeding or discharge T - Thickening or lump in breast or elsewhere I - Indigestion or difficulty in swallowing O - Obvious change in wart or mole N - Nagging cough or hoarseness
27
Lesions can invade and destroy adjacent structures and spread to distant sites (metastasize) to cause death. Collectively referred to as cancers
Malignant neoplasm
28
its microscopic and gross characteristics are considered to be relatively innocent, implying that it will remain localized and is amenable to local surgical removal and produce more than localized lumps, and sometimes they produce significant morbidity or are even lethal.
Benign tumor
29
Malignant neoplasms arising in “solid” mesenchymal tissues or its derivatives
Sarcomas
30
Malignant neoplasms of epithelial cells, regardless of the tissue of origin
Carcinomas
31
All tumors, benign and malignant, have two basic components:
1. The parenchyma, made up of transformed or neoplastic cells 2. The supporting, host-derived, non-neoplastic stroma, made up of connective tissue, blood vessels, and host-derived inflammatory cells
32
Local invasion
The growth of cancers is accompanied by progressive infiltration, invasion, and destruction of surrounding tissues, whereas most benign tumors grow as cohesive expansile masses that remain localized to their sites of origin
33
Benign tumors characteristics
Because benign tumors grow and expand slowly, they usually develop a rim of compressed fibrous tissue -This capsule consists largely of extracellular matrix that is deposited by stromal cells such as fibroblasts -Encapsulation creates a tissue plane that makes the tumor discrete, moveable (non-fixed), and readily excisable by surgical enucleation
34
Metastasis
● Metastasis is defined by the spread of a tumor to sites that are physically discontinuous with the primary tumor and unequivocally marks a tumor as malignant by definition benign neoplasms do not metastasize ● The invasiveness of cancers permits them to penetrate into blood vessels, lymphatics, and body cavities, providing opportunities for spread
35
Malignant neoplasms disseminate by one of three pathways:
1. Seeding within body cavities 2. Lymphatic spread 3. Hematogenous spread
36
Is a neoplasm characterized by infiltration of the blood, bone marrow, and other tissues by proliferative, clonal, poorly differentiated cells of the hematopoietic system and is the most common acute leukemia in older patients, with a median age at diagnosis of 67 years
Acute Myeloid Leukemia
37
Anemia characcteristics in AML
- Normocytic normochromic - Reduced reticulocyte count - Red blood cell (RBC) survival is decreased by accelerated destruction - Active blood loss may rarely contribute to the anemia.
38
Anemia characcteristics in AML
- Normocytic normochromic - Reduced reticulocyte count - Red blood cell (RBC) survival is decreased by accelerated destruction - Active blood loss may rarely contribute to the anemia.
39
Abnormal rod-shaped granules called _______ are not uniformly present, but when they are, AML is virtually certain
Auer rods
40
is a cell cycle S-phase–specific antimetabolite that becomes phosphorylated intracellularly to an active triphosphate form that interferes with DNA synthesis
Cytarabine
41
are DNA intercalators. Their primary mode of action is thought to be inhibition of topoisomerase II, leading to DNA breaks
Anthracyclines
42
Is the most frequent neoplastic disease in children with an early peak at the age of 3–4 years
Acute Lymphoblastic Leukemia
43
ALL Characteristics
● Malignant clone arises from hematopoietic progenitors in the bone marrow or lymphatic system resulting in an increase of immature nonfunctioning leukemic cells ● Infiltration of bone marrow leads to anemia, granulocytopenia, and thrombocytopenia with the clinical manifestations of fatigue, weakness, infection, and hemorrhages. ● Lymph node enlargement, hepatosplenomegaly
44
ALL Bone marrow examination
● Bone marrow aspirates are important for immunological, cytogenetic, and genomic markers ● Direct smears from the bone marrow are essential to confirm the diagnosis of acute leukemia and to distinguish between AML and ALL ● The bone marrow is usually heavily packed with leukemic blast cells comprising >90% of the nucleated cells
45
ALL Peripheral blood
● WBC in about 40% of ALL patients is reduced or normal ● Leukemic blast cells (LBC) in the peripheral blood are largely responsible for the rise in white blood cell count ● 8% of the ALL patients, no circulating leukemic blast cells are observed. ● Anemia, thrombocytopenia, and neutropenia
46
ALL Peripheral blood
● WBC in about 40% of ALL patients is reduced or normal ● Leukemic blast cells (LBC) in the peripheral blood are largely responsible for the rise in white blood cell count ● 8% of the ALL patients, no circulating leukemic blast cells are observed. ● Anemia, thrombocytopenia, and neutropenia