Introduction Flashcards

Staging systems prophylatic pinning chemotherapy Radiation therapy

1
Q

What does the prognosis of bone cancer depend on?

A
  • Overall Stage
  • Presence of Metastasis
  • Skip ( discontinuous) lesion within the same bone
  • Histologic grade
  • tumour size
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2
Q

Name a staging system?

A
  • Enneking
  • the musculoskeletal tumour society system
  • Most popular for orthopaedic surgeons
  • Two systems- one for benign & one for malignant
  • Malignant lesion used Roman numerials I,II III
  • Benign lesions use Arabic numbers 1,2,3
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3
Q

Dsecribe the enneking staging system for malignant tumours?

A

Stage IA

  • Low grade
  • T1 intracompartmental
  • Mo no mets

Stage IB

  • Low grade
  • T2- Extracompartmental
  • Mo - no mets

Stage IIA

  • High grade
  • T1- Intracompartmental
  • Mo- no mets

Stage IIB

  • High grade
  • T2- Extracompartmental
  • Mo- no mets

Stage IIIA

  • Metastatic
  • T1- _intracompartmental _
  • M1- regional or distant mets

Stage III B

  • Metastatic
  • T2- extracompartmental
  • M1- mets distant or regional
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4
Q

What are difference between tumour compartments?

A
  • Intracompartmental
    • bone tumours confined within cortex of the bone
  • Extracompartmental
    • Bone tumours extend beyond the bone cortex
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5
Q

What are the differences between high and low grade tumours?

A
  • Histologically , tumours graded based on percentagee of cellular atypia
  • Low grade tumours
    • ​Low metastatic potential
  • High grade tumours
    • _Greater metastatic potential _
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6
Q

Can you describe the numbering for benign tumours?

A
  1. Latent lesion - non osssifying fibroma
  2. Active lesion- ABC, chondroblastoma
  3. Agressive lesion- GCT of bone
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7
Q

What is the criteria to predict the risk of pathological fx?

A
  • the presence of significant functional pain
  • >50% destruction of cortical bone
  • Formal staging systems
    • Mirel criteria
    • Harington criteria
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8
Q

Why is prophylatic fixation of fx preferred to fixation of pathological fx?

A
  • Shorter operation time
  • Decreased Morbidity
  • Quicker recovery
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9
Q

Describe the Harington criteria?

A
  • >50% destruction of diaphyseal cortices
  • >50-75% destruction of metaphysis (>2.5cm)
  • Permeative destruction of subtrochanteric femoral region
  • Persistent pain following irradiation
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10
Q

Describe the Mirel criteria?

A
  • Score >8 = prophylatix pinning
  • score divided into
    • Site
      • Upper limb (1), Lower lImb (2), Peritrochanteric (3)
    • Pain
      • Mild (1), Moderate (2), severe (3)
    • Lesion
      • Blastic (1), Mixed (2) , Lytic (3)
    • Size
      • <1/3 (1), 1/3-2/3 (2), >2/3 (3)
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11
Q

What is the tx logarthim for a Path fx ?

A
  • Obtain tissue diagnosis
    • Unless pt has known primary neoplasm w bone biopsy proven skeletal mets, the treating surgeon should biopsy lesion in question
    • biopsy may require separate incision used for im nailing of bone
    • if biopsy suggests primary neoplasm ( like sarcoma) may benefit from neoadjuvant chemo/radiotx then close wound & refer to local sarcoma centre prior to stabilisation- as surgical tx will contaminate entire bone w sarcoma and affect ability to preform limb salvage
  • Surgical Fixation
    • ​don’t proceed unless primary neoplasm ruled out.
    • goals of fixation
      • maximise ability to immediate mobilistion & WB.
      • Protect entire bone in setting of systemic /met disease
      • Optimise implant choice in content of pt;s overall prognosis
      • Type of fixation depends on site of lesion
        • ​hemi for femoral neck/im nail for peritrochanteric
  • ​​​Post op radiation
    • **​refer to oncologist for post op radiotx to **
      • ​decrease pain
      • slow progression
      • tx remaining burden not removed in surgery
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12
Q

What cancers have the worse life expectancy?

A
  • Lung cancer
  • **Melanoma **
  • < 6months and <5% 5 yr survival when bone mets are present
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13
Q

Where is the common site for all boney mets?

A
  • The spine
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14
Q

Where is the common site for pathological fracture secondary to metastasis in bone?

A
  • Proximal femur
  • femur is most common long bone assoc with mets disease
  • the stress risers around the proximal femur make it vunerable to fx
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15
Q

What is the mechanism of chemotherapy?

A
  • It induces Apoptosis
    • ​= programmed cell death
  • may target specific proteins over expressed in cancer cells
    • e.g. tyrosine kinase inhibitors block tyrosine kinase receptos overexpressed in neoplastic cancer cells - herceptin in breast cancer
  • elimates micrometastasis in lungs
  • >98% necrosis with chemotherapy is good prognostic sign
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16
Q

Describe the important of resistance to chemotherapy

A
  • Expression of multi- drug resistant (MDR) gene portends very poor prognosis
    • cells can pump out chemotherapy out of cell
    • present in 25% of Primary lesion and 50% metastatic lesion
17
Q

What are the indications to use chemotherapy?

A
  • Integral component of tx along with surgical resection in
    • Osteosarcoma ( Intramedullary /periosteal)
    • **Ewing’s sarcoma **
    • Primary neuroectodermal tumour
    • Malignant fibrous histocytoma
    • Dedefferentiated chondrosarcoma
    • Chemotherapy for soft tissue sarcoma is contraversial
18
Q

What is the administration of chemotherapy ?

A
  • Preoperative- neoadjuvant- given for 8-12 weeks
  • Post operative given for 6-12 months
19
Q

Can you name a chemotherapy agent and its side effects?

A
  • Doxorubicin
    • is an anthracylcine antibiotic commonly used in oncological protocols- tx osteosarcoma
    • Inhibits DNA/RNA synthesis and blocks topoisomerase II=> apoptosis
    • functions as a cytostatic agent
  • Side effct
    • cardiac toxicity-> cardiomyopathy
    • dexrazone- drug protective against cardiac effects of doxorubicin
  • ​Cyclophospphamide- SE = myelosuppression/ urotoxicity

***chemo targets rapidly dividing cells - so also lining the gut, bone marrow, hair and skin

20
Q

What is radiotherapy’s mode of action?

A
  • Production of free radicals
  • direct genetic chnage
21
Q

What are the indications for radiotherapy?

A
  • Definitive control of primary malignant bone tumours
    • Ewing’s sarcoma
    • Primary neuroectodermal toumour
    • Hemangioendoelioma
    • solitary plasmacytoma of bone
  • Adjuvant to surgical excision
    • soft tissue sarcoma
    • given pre/post surgical excision
  • Palliative care & impending fracture fixation
    • mets bone disease
    • require to reduce overall tumour burden
    • prostate cancer are very radiosensitive
    • breast cancer is 70% sensitive, 30% Resistant
    • Gi and renal are not radiosensitive
22
Q

What is the typical dose of radiotherapy?

A
  • I rad= IcentiGray
  • Typical dose = 180-200 cGy/day
  • radiation is given in fractions as radiotherapy is accumulative
  • the total dose is summuation of all the separate fractions given during tx
  • <45 gray => uncomplicated tissue healing
  • 45-55= usually heals with no problems
  • >60 Gray= tissue not likely to heal
23
Q

What are the complications of radiotherapy?

A
  • Early effects
    • delayed wound healing
    • infection
    • desquamation
  • Late effects
    • fibrosis
    • joint stiffness
    • secondary sarcoma
    • fractures
24
Q

Describe the epidemiology of post radiation sarcoma?

A
  • defined by the development of sarcoma in a region previosuly radiated for malignancy
  • inicidence 13%
  • more frequent in pts prior to chemotherapy
  • overall pt prognosis is poor
25
Q

Describe the epidemiology of post radiation fx?

A
  • Approx 25% incidence following soft tissue sarcoma resection and external beam irradiation
  • risk factors
    • female
    • anterior femoral compartment resection
    • age >50 yrs
    • periosteal stripping
    • radiation dose >60 Gy
    • osteoporosis