Pulmonary Neoplasms Flashcards

Objectives

1
Q

Describe the incidence, risk factors, percentage of lung cancer related to tobacco use

A
  • Worldwide— #1 cause of cancer death is lung cancer
  • Lung cancers have been linked to a metabolite of tobacco smoke, benzo(a)pyrene, which is abnormal in 60% of primary lung neoplasms.
    • 90% is found in smokers
  • 2nd hand exposure does increase the overall risk of lung cancer for non-smokers, but not as much as active smoking does.
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2
Q

signs and symptoms of local and metastatic lung cancer

A
  • only 5% are asymptomatic and extra-pulmonary sx are 1st clue to diagnosing
    • Dyspnea
    • Cough, usually non-productive
    • When it is productive, usually thin mucoid secretions in large amts
    • Hemoptysis
    • Chest pain
    • Hoarseness
    • Pleural effusion(s)
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3
Q

Describe the diagnostic tests that should be ordered for suspected lung cancer

A
  • Imaging:
    • CXR- Pa/Lat- for screening purposes
      • 1st choice- cheap/available
    • CT scan with contrast
      • 2nd study performed to evaluate lymphadenopathy
        • look for: speculated, irregular, non-calcified
    • PET for metastases (likes highly metabolic areas)
  • Invasive studies:
    • Bronchoscopy
    • Mediastinoscopy
    • EBUS- for mediastinal lymphadenopathy
    • FNA- when masses cant be reached with bronchoscopy
      • CT guided, needs to be greater than 2 cm
    • Thoracentesis- for therapeutic and to determine if pleural effusion is malignant or not
    • Open biopsy- last resort choice
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4
Q

small cell lung cancer

A
  • Aggressive and presents in advanced stage
  • From neuroendocrine cells
  • Central of lungs
  • Smokers
    • Can lead to:
      • Hypercalcemia
      • SIADH
      • ACTH production
    • Sensitive to chemo and radiation
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5
Q

Non-small cell carcinoma

A

*80% of cases

  • Adenocarcinoma
  • Squamous cell carcinoma
  • Large cell carcinoma
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6
Q

Non-small cell carcinoma: Adenocarcinoma

A
  • MC type of NSCS = HYPERCALCEMIA
    • From bronchial mucosal gland
    • Develops peripherally
    • Not associated with smoking normally
    • Bronchioalveolar carcinoma:
      • Subset of adenocarcinoma
        • Found in alveolar walls, slow growing
        • MC in non-smokers
      • On imaging: ground-glass opacities or pneumonia on imaging
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7
Q

Non-small cell carcinoma: Squamous cell carcinoma

A
  • 2nd most common
    • Found centrally normally within major bronchi
    • Develops in squamous cells
      • Can cause hemoptysis and post-obstructive pneumonia
    • MC associated with hypercalcemia and tobacco abuse
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8
Q

Non-small cell carcinoma: Large cell carcinoma

A
  • Tobacco abuse
  • Any part of lung and associated with friable tissue and hemoptysis
  • Wet TP
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9
Q

Pancoast tumor

A
  • Superior sulcus tumors
    • Extrapulmonary lung cancer
    • Defined by location in lung apex
    • Majority are NSCLS- squamous
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10
Q

Pancoast tumor signs and symptoms

A
  • Shoulder pain on affected side; more painful than others due to invasion of brachial plexus
  • Horner’s Syndrome: involvement of sympathetic chain and inferior cervical ganglion
  • Weakness and muscle atrophy, wt loss
  • SVC syndrome (less common)
    • Restriction of SVC so it cuts off blood supply from arms and head of patients causing edema of head and arms
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11
Q

Pancoast etiology

A
  • can be caused by lesions other than lung cancer
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12
Q

Identify the pulmonary complications of lung cancer

A
  • Reduced FEV1 and associated dyspnea
  • Acute Hypoxemia vs. acute on chronic hypoxemia
  • Recurrent pneumonias, often post-obstructive
  • MC: Chronic cough and hemoptysis
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13
Q

Paraneoplastic Syndrome

A

Paraneoplastic Syndrome

  • A constellation of symptoms, neurologic & otherwise, not caused by a primary disorder in that system.
    • Exact cause is unknown, but thought to relate to immune response to neoplastic process.
  • General
    • Anorexia, cachexia, and weight loss
  • Cutaneous
    • Itching, Flushing, Pigmented skin lesions
  • Endocrine
    • SIADH >hyponatremia; Ectopic production of ACTH>hyperglycemia, hypokalemia, hypertension, central obesity, moon facies; Insulin like growth factors>Hypoglycemia; parathyroid hormone-related peptide (PTHRP) >hypercalcemia
  • Neurologic
  • Peripheral neuropathy
  • Hematologic
  • RBC aplasia, anemia of chronic disease, leukocytosis, thrombocytosis, eosinophilia, basophilia, and disseminated intravascular coagulation.
  • Hypercoaguable states, and thromboembolic events
  • GI
  • Watery diarrhea with subsequent dehydration and electrolyte imbalances
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14
Q

Metastatic Disease

A
  • body.
  • Common sites for primary pulmonary carcinoma to metastasize to:
    • Liver, adrenal glands, bone, and brain
    • Liver metastases are uncommon early in the disease process. Autopsy results show liver mets in >50% of patients with both NSCLC & SCLC
    • Adrenal metastases show often, but usually are asymptomatic. Approximately 2.5% of these mets are malignant in NSCLC, with up to 17% in SCLC
  • Bone metastases appear often & are typically symptomatic, with back pain a frequent symptom. Other signs include hypercalcemia as a result of bone invasion. Appear in 20% of NSCLC & 30-40% of SCLC.
  • Brain metastases can include paraneoplastic phenomena and tumors. Symptoms also include HA, seizures, & visual field loss. With NSCLC, is most prevalent with adenocarcinoma. With SCLC, appears in 20-30% of patients at presentation.
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15
Q

Staging of Lung Cancers

A
  • Difference between NSCLC & SCLC is important in multiple regards:
    • Affects the staging of the respective cancer
    • Affects the treatment options
  • Once the diagnosis of lung cancer has been confirmed via pathology, staging begins.
    • PET scan confirms any hypermetabolic areas in the body.
    • Look for lymph node enlargement via imaging studies: CT with contrast, if imaging confirms lymphadenopathy, may need biopsy to confirm.
    • Search for any metastases via imaging studies: CT & MRI.
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16
Q

Staging of lung cancers - NSCLC

A
  • Resectability = staging
  • TNM International Staging System
    • T = Tumor 6th Edition 2002 (proposed 7th edition pending)
    • N = Node
    • M = Metastasis
  • Stages I, II, IIIA – Surgery
  • Stage IIIB or IV – non-resectable

Stage IV – Surgery for isolated brain or adrenal mets

17
Q

TNM Staging System

A
  • AJCC TNM staging system for lung cancer (7th edition, January 1, 2010)
  • Much revised system devised for clarification of tumors
    • Tumor
    • Nodal involvement
    • Metastases
18
Q

TNM Staging System: Primary tumor (T)

A
  • T1 - Tumor <3 cm diameter without invasion more proximal than lobar bronchus
  • T2 - Tumor >3 cm diameter OR tumor of any size with any of the following: Invades visceral pleura. Proximal extent at least 2 cm from carina. Atelectasis/obstructive pneumonitis of less than entire lung.
  • T3 – Tumor >7 cm OR tumor of any size with any of the following: Invasion of chest wall. Involvement of diaphragm, mediastinal pleura, or pericardium. Atelectasis involving entire lung. Proximal extent within 2 cm of carina without carinal invasion. Satellite tumor nodule(s) within same lobe as primary tumor.
  • T4 - Tumor of any size with any of the following: Invasion of mediastinum. Invasion of heart or great vessels. Invasion of trachea or esophagus. Invasion of vertebral body or carina. Presence of malignant pleural or pericardial effusion. Satellite tumor nodule(s) in different lobe on ipsilateral side.
19
Q

TNM Staging System: Nodal involvement (N)

A
  • N0 - No regional node involvement
  • N1 - Metastasis to ipsilateral hilar and/or ipsilateral peribronchial nodes
  • N2 - Metastasis to ipsilateral mediastinal and/or subcarinal nodes
  • N3 - Metastasis to contralateral mediastinal or hilar nodes OR ipsilateral or contralateral scalene or supraclavicular nodes
20
Q

TNM Staging System: Metastasis (M)

A
  • M0 - Distant metastasis absent
  • M1 - Distant metastasis present
    • M1A – Malignant pleural/percardial effusion, pleural nodules, or contralateral pulmonary nodules
    • M1B – Any other distant metastasis
21
Q

NSCLC Staging

A

Stage groupings of TNM subsets

  • Stage 0 — TisN0M0
  • Stage IA — T1a-1bN0M0
  • Stage IB — T2aN0M0
  • Stage IIA — T1a-2aN1M0 or T2bN0M0
  • Stage IIB — T2bN1M0 or T3N0M0
  • Stage IIIA — T3N1M0 or T1a-3N2M0 or T4N0-1M0
  • Stage IIIB — T4N2M0 or T1a-4N3M0
  • Stage IV — Any T Any N M1a-1b
22
Q

SCLC Staging

A

Staging is much simpler for SCLC 2° to the more rapid doubling time of small cell

  • Limited – disease confined to single hemithorax or 1 radiation port
  • Extensive – any disease spread beyond the ipsilateral hemithorax

At presentation, approximately 60-70% have extensive stage disease.

  • This is important with regards to treatment options.
23
Q

Tx regimens

A
  • Treatment is dependent on cancer staging results
24
Q

NSCLC Stage IA & IB Tx

A

The main treatment modality for tx at this stage is surgical resection. Chemotherapy is not recommended at this stage.

  • Lobectomy is the gold standard option & is preferred.
  • VATS resection is an option if the patient cannot tolerate a full lobar resection.

Non-surgical options exist for those patients with multiple medical comorbidities

  • Radio Frequency (RF) ablation – radiowaves from a probe in the tumor burn the tumor cells.
  • Cryoablation – a cryoprobe placed in the tumor freezes the cells
  • Radiation therapy – multiple radioactive modalities exist including sterotactic, daily definitive, & hyperfractonation.

Poor surgical candidates include – bad COPD’ers, previous CABG, ESRD/HD

25
Q

NSCLC Stage IIA & IIB Tx

A
  • Surgery is still the 1st line treatment modality, with adjuvant chemotherapeutic agents used in conjunction.
  • The thought process behind adding adjuvant tx at this point is that the most likely reason for failure of potentially curative surgery is distant metastases.
  • The key chemotherapeutic agent at this stage is cisplatin, a platinum based pharmaceutical.
  • Can be used in conjunction with vinorelbine.
  • Another option is carboplatin with paclitaxel
26
Q

Surgery Stage IIIA & B Tx

A
  • Stage III is the most debated stage for tx options.
  • Surgery is not considered definitive tx & is only recommended to debulk T3 tumors. Once it progresses to T4 status, it is considered a part of tx, but not curative in and of itself.
  • Chemotherapy is also not considered definitively curative. The agents used are platinum-based (cisplatin and carboplatin) with etoposide or docetaxel.
  • Radiation is the lone “curative” tx and can be used as a paliative option as well.
  • Definitive XRT, with no other tx, has a median survival rate of 10 months and a 5-year survival rate of 5%.
  • Take home point – at this stage, multiple modalities are needed.
27
Q

NSCLC Stage IV Tx

A
  • At this stage, no treatment is considered curative as the spread is too far. Treatment options consist of chemo and XRT, but only in a palliative situation.
  • Surgical options are present only for isolated brain & adrenal mets.
  • Palliative options should be presented to patients once staged at this level.
  • Yes, this includes hospice…
28
Q

SCLC Treatment

A

Again, treatment is based on staging results. And its highly responsive to chemotherapeutic agents.

Limited stage SCLC – Chemotherapy with radiation

  • Most popular regimens include platinum based therapies in conjunction with thoracic XRT. These chemo options have the best response rate.
    • Cisplatin plus etoposide, or carboplatin plus etoposide
  • Extensive stage SCLC – Chemotherapy
  • Carboplatin plus etoposide is the preferred combo regimen, 2° to a more favorable toxicity profile.
  • Cisplatin plus irinotecan is showing promise in studies, but is not statistically significant with overall survival rates of 9.9% compared with carboplatin plus etoposide at 9.1%.
29
Q

Lung Cancer Mortality

A

Statistics even with treatment – Dismal!!

Overall 5-year survival > 16%

  • Colon (65%), Breast (89%), Prostate (99%)

Progress with treatment minimal

  • 2007 – 5 year survival 16%
  • 1974 - 5 year survival 13%
  • 1960 - 5 year survival 8%
30
Q

Survival Rates - SCLC

A
  • 60-70% of patients with small cell lung cancer (SCLC) have clinically disseminated or extensive disease at presentation. Extensive-stage SCLC is incurable.
  • When given combination chemotherapy, patients with extensive-stage disease have a complete response rate of more than 20% and a median survival longer than 7 months; however, only 2% are alive at 5 years.
  • With limited-stage dz treated with combo chemo plus chest radiation, a complete response rate of 80% and survival of 17 months have been reported; 12-15% of patients are alive at 5 years
31
Q

Survival Rates - NSCLC

A
  • NSCLC 5-year rates are much better when caught early.
  • Untreated Stage IV NSCLC
  • Median Survival 4 to 5 months
  • Survival Rate at 1 year = 10%