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Systemic anti-cancer therapy (SACT) 

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  • Chapter 07: Oncology I. Systemic anti-cancer therapy (SACT)
  • Systemic anti-cancer therapy (SACT) 

Systemic anti-cancer therapy (SACT) 

Systemic anti-cancer therapy (SACT) 

on 16 Jan, 2025
  • Date16 Jan, 2025

Systemic anti-cancer therapy (SACT) 

 

Cytotoxic chemotherapy 

 

  • They work by interfering with the processes involved in cell division. 
  • Side effects of treatment are largely a result of their antiproliferative actions in normal tissues such as the bone marrow, skin and gut; other organs, such as the heart, kidney and peripheral nervous system, may also be affected.
  • The dosing schedule is determined by the choice of treatments and recovery of normal tissues, usually the bone marrow. 
  • Adverse effects:
  1. Nausea and vomiting: combination of dexamethasone & ondansetron
  2. Myelosuppression: The risk of neutropenia can be reduced with the use of specific growth factors (G–CSF) 

 

Hormone therapy 

 

  • Hormones are important cell-signaling molecules and, in some cancers, may be key drivers of tumor growth.  
  • Example:
  1. ER-positive breast cancer: 
  • adjuvant hormone therapy 
  1. Prostate cancer: hormonal therapy 
  • luteinising hormone releasing hormone (LHRH) analogue: goserelin 
  • anti-androgen: bicalutamide

 

Targeted therapies 

 

  • They target specific genes & proteins that are involved in the growth and survival of cancer cells.
  • Two groups: 
  1. monoclonal antibodies (-mab): target molecules are overexpressed on the outside of the cancer cell.
  2. small molecule inhibitors (-ib): they target processes within the cell, such as the cytoplasmic tyrosine kinase, and are designed to be small enough to enter the cell. 
  • Example: 
  1. Epidermal growth factor receptor (EGFR) inhibitor: 
  • for lung adenocarcinomas (EGO): erlotinib, gefitinib or osimertinib. 
  1. HER2 (member of the  EGFR family): 
  • found in breast, gastric, pancreatic, lung cancer; poor prognosis factor
  • trastuzumab, pertuzumab. 
  1. Vascular endothelial growth factor receptor (VEGFR) inhibitors: 
  • for renal cell carcinoma:  sunitinib, pazopanib and cabozantinib 
  • hepatocellular carcinoma: sunitinib 
  • thyroid cancer: 
  1. VEGF-A antibody for ovarian, colorectal and breast: 
  • Bevacizumab
  • Colorectal cancer: 
  • cetuximab, panitumumab

 

Immunotherapy

 

  • anti-cancer therapies that work by harnessing the immune system to attack cancer cells. 
  • Example:
  1. Cytokines therapy  (interferon alpha and interleukin-2): 
  • melanoma, RCC
  1. Immune checkpoint inhibitor: 
  • melanoma, RCC, lung, bladder, head and neck etc. 
  • Nivolumab, pembrolizumab
  1. Cellular immunotherapy: (modified cell therapy)
  • hematological malignancies. 
  • TIL therapy, TCR therapy, CART therapy  
  • Cancer treatment vaccines 

SAQ. Role of immunotherapy in oncology. How will you assess and manage Immune Related Adverse Effects (IRAE)

 

Immune-related adverse events 

 

  • Side-effects of checkpoint inhibitor immunotherapy agents occur when the immune system is stimulated to attack healthy cells and tissues in the body. 
  • These immune-related adverse events (IRAEs) are increasingly being recognized as oncological emergencies. 

 

Clinical features: 

  • Almost any body system may be affected,
  • colon, endocrine organs (thyroid, adrenal and pituitary glands) , lungs, liver, skin, nervous system

 

Investigatigation:

  • multidisciplinary approach including oncologists and relevant system specialists. 
  • Specialist investigations may be required depending on the body system affected. 

 

Treatment:

  • Dampening the immune response: high-dose steroids. 
  • Additional immunosuppressive therapies
  • In case of endocrine organ inflammation: replacement of deficient hormones
  • Checkpoint inhibitor immunotherapy treatment: permanently discontinued. 
  • In other cases, and in patients with endocrine IRAEs who commence replacement hormone therapy, it may be possible to reintroduce checkpoint inhibitor immunotherapy treatment. 

 

SAQ. A 60 year old female patient with stage 3 adenocarcinoma of lung presented with fatigue and constipation. She is taking durvalumab for his cancer. On examination pulse: 48 beats/min, BP: 130/100 mmHg. On investigation S.TSH 13 mIU/l, FT4 normal.

 

  1. Write down the complete diagnosis. 
  • Stage 3 adenocarcinoma of lung with durvalumab induced immune related adverse events causing hypothyroidism.

 

  1. Name 5 other organs that may be affected in this case.
  1. Lung, Liver, Skin
  2. Nervous system
  3. Endocrine organs( adrenal, thyroid, pituitary)

 

  1. Enumerate 3 management options
  • Multidisciplinary approach 
  • High dose steroids
  • Additional immunosuppressants 
  • Replacement of thyroid hormone
  • Discontinuation of immunotherapy ( checkpoint inhibitor)

 

SAQ. Mention the role of molecular targeted therapies in the management of cancer patients with their examples.

Ans to the Q.N- 2(C)

 

Moleculare the moleculare different in di targeted therapy patients with taregeted therapy can cere. is the new ho Now a day widely use cancarco 10

 

Target of the Specific therapy: Treatment molecules Spread of cancere involved Cells. in is targeled growth the

 

Types of targeted therapy:

 

Monoclonal anlibodies.

 

II Small molecules inhibitores.

 

Some con cere common targeted therrapy used in patients:

Biraast receptore Cancerc: Those who have Trastuzumab. positive HER 2

 

0 Chronic myeloid leukaemia Philadelphia kinase chromosome. inhibitores Those positive who Tyrosine Imatinib. arce

 

D Renal cell carcinoma

 

TKI Sunitinib s Pazopanib

 

  • MTOR Temsircolimus severcolimus.

 

Lymphoma : Anti-CD20 monoclonal antibody Rituximab

 

  • Anti-CD 30 Breentuximab (fore Hodgkin’s disense)

 

Lung Cancerc

 

Tk1

 

Erlotinib

 

  • Monoclonal antibody to EGFR

 

Bevacizumab.

 

Myeloma : Anti- 27 (Refractory cases) CD 38 monoclonal antibody eg Dara tumumab.

26

  • They target specific genes & proteins that are involved in the growth and survival of cancer cells.
  • Two groups: 
  1. monoclonal antibodies (-mab): target molecules are overexpressed on the outside of the cancer cell.
  2. small molecule inhibitors (-ib): they target processes within the cell, such as the cytoplasmic tyrosine kinase, and are designed to be small enough to enter the cell. 
  • Example: 
  1. Epidermal growth factor receptor (EGFR) inhibitor: 
  • for lung adenocarcinomas (EGO): erlotinib, gefitinib or osimertinib. 
  1. HER2 (member of the  EGFR family): 
  • found in breast, gastric, pancreatic, lung cancer; poor prognosis factor
  • trastuzumab, pertuzumab. 
  1. Vascular endothelial growth factor receptor (VEGFR) inhibitors: 
  • for renal cell carcinoma:  sunitinib, pazopanib and cabozantinib 
  • hepatocellular carcinoma: sunitinib 
  • thyroid cancer: 
  1. VEGF-A antibody for ovarian, colorectal and breast: 
  • Bevacizumab
  • Colorectal cancer: 
  • cetuximab, panitumumab

 

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Topics

  • Chapter 04: Clinical Immunology (4)
    • Cryoglobulin (1)
    • Hereditary angioedema (1)
    • Monoclonal antibody (Mab) (1)
    • Primary Immune Deficiency (1)
  • Chapter 05: Population health & Epidemiology (2)
    • Case control Vs Cohort study (1)
    • Screening tools / test (1)
  • Chapter 06: Principles of Infectious Diseases (1)
    • Antimicrobial stewardship (AMS) (1)
  • Chapter 07: Oncology (9)
    • A. Breaking Bad News (1)
    • B. Investigation in cancer patient (1)
    • C. CUP / MUO (1)
    • D. Neutropenic fever (1)
    • E. Hypercalcemia in malignancy (1)
    • F. Immune-related adverse events (IRAE) (1)
    • G. Tumor lysis syndrome (1)
    • H. Malignant pleural effusion (1)
    • I. Systemic anti-cancer therapy (SACT) (1)
  • Chapter 08: Palliative - ethical issue (4)
    • Informed written consent (1)
    • Non medical issue (1)
    • Pain management (1)
    • Palliative care (1)
  • Chapter 09: Acute Medicine (8)
    • ARDS (1)
    • Coma (1)
    • How to write an ICU discharge summary (1)
    • ICU-acquired weakness (1)
    • OSPE/IOE (1)
    • Rhabdomyolysis (1)
    • Sepsis (1)
    • Ventilator-induced lung injury (VILI) (1)
  • Chapter 10: Poisoning (6)
    • A. Poisoning by pharmaceutical agent (0)
    • B. drugs of misuse. (0)
    • C. Poisoning by chemical and pesticides (6)
      • 1. Carbon monoxide (CO) poisoning (1)
      • 2. OPC Poisoning (1)
      • 3. Paraquat Poisoning (1)
      • 4. Ethanol intoxication (acute alcohol consumption) (1)
      • 5. Chronic Lead poisoning (1)
      • 6. Gas tablet poisoning (1)
    • D. Environmental poisoning (0)
    • E. Food related poisoning (0)
  • Chapter 11: Envenomation (0)
  • Chapter 12: Environmental Medicine (6)
    • Drowning (1)
    • Frostbite (1)
    • Heat stroke (1)
    • High Altitude illness (1)
    • Hypothermia (1)
    • Immersion (1)
  • Chapter 18: Nephrology (6)
    • 01. Investigation (1)
    • 02. Clinical Presentation (3)
      • (A). Polyuria (1)
      • (B). Haematuria (1)
      • (C). Proteinuria (1)
    • 03. Glomerular Disease (2)
      • IgA Nephropathy (1)
      • RPGN (1)
    • 10. Infection of Urinary Tract (0)
    • 4. Tubulo-interstitial Diseases (0)
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    • 7. Acute Kidney Injury (AKI) (0)
    • 8. Chronic Kidney Disease (CKD) (0)
    • 9. Renal Replacement Therapy (RRT) (0)
  • Chapter 19: Clinical Biochemistry and Metabolic medicine (1)
    • Potassium Homeostasis (1)
      • Hyperkalaemia (0)
      • Hypokalaemia (1)
  • Chapter 20: Endocrinology (19)
    • Adrenal Gland Diseases (6)
      • Adrenal insufficiency (1)
      • Congenital Adrenal Hyperplasia (CAH) (1)
      • Cushing Syndrome (1)
      • Pheochromocytoma (1)
      • Primary hyperaldosteronism (1)
      • Steroid withdrawal or tapering (1)
    • Autoimmune Polyendocrine Syndrome(APS) (0)
    • Endocrine Pancreas (0)
    • Hypothalamo-pituitary Disease (0)
    • Multiple Endocrine Neoplasia (MEN) (0)
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      • Hyperparathyroidism (1)
      • Pseudohypoparathyroidism (1)
    • Reproductive Endocrinology (6)
      • Delayed puberty / Hypogonadism (1)
      • Hirsutism (1)
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      • Hypothyroidism (0)
      • Subclinical Hypothyroidism (1)
      • Subclinical Thyrotoxicosis (1)
      • Thyroid Lump or Swelling (1)
      • Thyrotoxicosis (1)
  • Chapter 22: Nutritional factors in disease (4)
    • Intestinal Failure (1)
    • Refeeding Syndrome (1)
    • Vitamin deficiency or excess (2)
      • Scurvy (1)
      • Vit B3 (Niacin) deficiency: Plegra (1)
  • Chapter 23: Gastroenterology (15)
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    • Esophagus (3)
      • Achalasia of the esophagus (1)
      • Dysphagia (1)
      • GERD (1)
    • Pancreas (0)
    • Small Gut (9)
      • A. Coeliac disease (1)
      • B. Small intestinal bacterial overgrowth (SIBO) (1)
      • C. Whipple disease (1)
      • D. Bile acid diarrhea (1)
      • E. Radiation enteropathy (1)
      • F. Protein-losing enteropathy (1)
      • G. Eosinophilic gastroenteritis (1)
      • H. Lactose intolerance (0)
      • I. IPSID (1)
      • J. IBS (1)
    • Stomch (3)
      • Gastric carcinoma (1)
      • Peptic ulcer disease - PUD (1)
      • Zollinger Ellison syndrome (ZES) (1)
  • Chapter 24: Hepatology (2)
    • Inherited Liver Disease (2)
      • Hemochromatosis (1)
      • Wilson disease (1)
  • Chapter 25: Hematology (1)
    • Anemia (1)
      • Microcytic Hypochromic Anemia (MHA) (1)
        • Iron Deficiency Anemia (IDA) (1)
  • Chapter 26: Rheumatology (3)
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      • Polymyositis & Dermatomyositis (0)
    • Disease of Bone (2)
      • Hypertropic Osteoarthropathy (1)
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  • Chapter 27: Dermatology (1)
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      • Hyperthyroidism in Pregnancy (1)
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  • Chapter 34: Ageing (7)
    • Delirium (1)
    • Fall (1)
    • Frailty (1)
    • Geriatric giants (1)
    • MDT (1)
    • Prescribing & deprescribing (1)
    • Urinary Incontinence (1)
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    • Obstetrics (0)
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