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{{WBRQuestion
{{WBRQuestion
|QuestionAuthor=William J Gibson
|QuestionAuthor=William J Gibson (Reviewed by {{YD}})
|ExamType=USMLE Step 1
|ExamType=USMLE Step 1
|MainCategory=Pharmacology
|MainCategory=Pharmacology
Line 21: Line 21:
|MainCategory=Pharmacology
|MainCategory=Pharmacology
|SubCategory=Hematology, Oncology
|SubCategory=Hematology, Oncology
|Prompt=A 45 year old man presents to his primary care physician for fatigue and weight loss of 10 pounds over the past month. On physical exam, the spleen is palpable 7 cm below the costal margin and several bruises are observed across the body. Laboratory testing is significant for an elevated white blood cell count and reduced platelet count. Bone marrow biopsy demonstrates hyperplastic granulocytes which are positive for a t(9;22) translocation. The patient is started on an inhibitor to the fusion gene produced by this translocation.  This drug would be expected to have activity in which of the following tumors?
|Prompt=A 45-year-old man presents to his primary care physician for fatigue and weight loss of 10 pounds over the past month. On physical examination, the spleen is palpable 7 cm below the costal margin, and several bruises are observed across the body. Laboratory testing is significant for an elevated white blood cell count and reduced platelet count. Bone marrow biopsy demonstrates hyperplastic granulocytes which are positive for a t(9;22) translocation. The patient is started on an inhibitor of the fusion gene produced by this translocation.  The administered drug is most likely also effective to treat which of the following conditions?
|Explanation=The patient in this vignette has [[chronic myelogenous leukemia]], caused by the BCR-ABL translocation between chromosomes 9 and 22.  This translocation causes a novel tyrosine kinase to be formed that can constitutively transmit cell growth signals in affected cells. [[Imatinib]] blocks the action of this new gene product and thereby starves the tumor cells of the mitogenic signals upon which they rely to survive. Imatinib can also be used to treat [[gastrointestinal stromal tumors]] (GISTs) as its kinase blocking activity is not entirely specific to the BCR-ABL gene product. 85% of GISTs have activating mutations of the c-kit gene, which can be inhibited by imatinib.
|Explanation=The patient in this vignette has [[chronic myelogenous leukemia]], a disorder of the hematopoietic stem cells that is caused by the juxtaposition of the ''ABL'' gene (chromosome 9) and the ''BCR'' gene (chromosome 22), resulting in ''BCR-ABL'' fusion gene, known as the Philadelphia chromosome.  This translocation causes a novel tyrosine kinase that can constitutively transmit cell growth signals in affected cells. Although the pathogenesis of the disease is well-described, the mechanism that causes the translocation is poorly delineated. The diagnosis of CML is often suspected by the presence of excessive granulocytosis with left shift and confirmed by the identification of the Philadelphia chromosome in peripheral blood and bone marrow cells. [[Imatinib]] is a targeted pharmacologic therapy that inhibits the BCR-ABL tyrosine kinase via competitive binding at the ATP-binding site. It has demonstrated significant efficacy for patients with CML.
 
Gastrointestinal stromal tumor (GIST) is a rare non-epithelial neoplasm of the GI tract, the mesentary, or the omentum. The majority of GIST tumors are spindle cell tumors that may be either malignant or benign. Most stromal tumors stain positively for CD117 (>90%), CD34, muscle-specific actin, smooth muscle actin, S-100, and desmin. Patients with GIST may be asymptomatic or have non-specific GI symptoms. On biopsy, GIST often appears as a friable unencapsulated mass that does not arise from the epithelium, but from the muscular layer. Characteristically, the pathogenesis of GIST tumors involves a gain-of-function mutation in the ''KIT'' proto-oncogene, which encodes a transmembrane receptor for stem cell factor that includes a tyrosine kinase component in its intracytoplasmic region. Similar to CML, imatinib has demonstrated efficacy in GIST, whereby it similarly inhibits the tyrosine kinase receptor KIT in a similar fashion to its inhibition of the tyrosine kinase receptor BCR-ABL fusion protein.
|AnswerA=Breast cancer
|AnswerA=Breast cancer
|AnswerAExp=Breast cancer is not currently treated with tyrosine kinase inhibitors. HER2 positive breast cancers can be treated with trastuzamab.
|AnswerAExp=Breast cancer is not currently treated with tyrosine kinase inhibitors. HER2-positive breast cancers may be treated with trastuzamab.
|AnswerB=Gastrointestinal stromal tumor
|AnswerB=Gastrointestinal stromal tumor
|AnswerBExp=Gastrointestinal stromal tumors commonly have mutations in the c-Kit tyrosine kinase. Imatnib is also able to block the kinase activity of the mutated c-Kit.
|AnswerBExp=The pathogenesis of GIST tumors involves a gain-of-function mutation in the ''KIT'' proto-oncogene, which encodes a transmembrane receptor for stem cell factor that includes a tyrosine kinase component in its intracytoplasmic region. Similar to CML, imatinib has demonstrated efficacy in GIST, whereby it similarly inhibits the tyrosine kinase receptor KIT in a similar fashion to its inhibition of the tyrosine kinase receptor BCR-ABL fusion protein.
|AnswerC=Hepatocellular carcinoma
|AnswerC=Hepatocellular carcinoma
|AnswerCExp=Hepatocellular carcinoma is not treated with imatinib. HCC is often secondary to viral hepatitis or cirrhosis and may be treated with surgery or other interventional techniques.
|AnswerCExp=HCC may be secondary to chronic viral hepatitis and/or cirrhosis. Hepatocellular carcinoma (HCC) is not treated with imatinib.
|AnswerD=Mantle cell lymphoma
|AnswerD=Mantle cell lymphoma
|AnswerDExp=Mantle cell lymphoma is a rare non-Hodgkin’s lymphoma that affects elderly males. It is not susceptible to imatinib therapy.
|AnswerDExp=Mantle cell lymphoma is a rare non-Hodgkin’s lymphoma that affects elderly males. Imatinib is not used to treat Mantle cell lymphoma.
|AnswerE=MALT Lymphoma
|AnswerE=Mucosa-associated lymphoid tissue (MALT) lymphoma
|AnswerEExp=MALT Lymphoma is associated with H Pylori infection and is not susceptible to imatinib therapy. For localized MALT Lymphoma, treatment of underlying H. Pylori infection is often sufficient to induce tumor regression.
|AnswerEExp=MALT Lymphoma is associated with ''H. pylori'' infection and is not susceptible to imatinib therapy. For early and localized MALT lymphoma, treatment of underlying ''H. pylori'' infection by antibiotics is often sufficient to induce tumor regression.
|EducationalObjectives=Imatinib, a tyrosine kinase inhibitor, can be used to treat both CML and GISTs.
|EducationalObjectives=Imatinib, a tyrosine kinase inhibitor, may be used to treat both CML and GIST.
|References=First Aid 2014 page 406
|References=Din OS, Woll PJ. Treatment of gastrointestinal stromal tumor: focus on imatinib mesylate. Ther Clin Risk Manag. 2008;4(1):149-62.<br>
First Aid 2014 page 406
|RightAnswer=B
|RightAnswer=B
|WBRKeyword=Cancer, Chemotherapy, Leukemia, Imatinib, CML, Chronic myelogenous leukemia, GIST, Gastrointestinal stromal tumor
|WBRKeyword=Cancer, Chemotherapy, Leukemia, Imatinib, CML, Chronic myelogenous leukemia, GIST, Gastrointestinal stromal tumor
|Approved=Yes
|Approved=Yes
}}
}}

Revision as of 23:02, 20 October 2014

 
Author [[PageAuthor::William J Gibson (Reviewed by Yazan Daaboul, M.D.)]]
Exam Type ExamType::USMLE Step 1
Main Category MainCategory::Pharmacology
Sub Category SubCategory::Hematology, SubCategory::Oncology
Prompt [[Prompt::A 45-year-old man presents to his primary care physician for fatigue and weight loss of 10 pounds over the past month. On physical examination, the spleen is palpable 7 cm below the costal margin, and several bruises are observed across the body. Laboratory testing is significant for an elevated white blood cell count and reduced platelet count. Bone marrow biopsy demonstrates hyperplastic granulocytes which are positive for a t(9;22) translocation. The patient is started on an inhibitor of the fusion gene produced by this translocation. The administered drug is most likely also effective to treat which of the following conditions?]]
Answer A AnswerA::Breast cancer
Answer A Explanation AnswerAExp::Breast cancer is not currently treated with tyrosine kinase inhibitors. HER2-positive breast cancers may be treated with trastuzamab.
Answer B AnswerB::Gastrointestinal stromal tumor
Answer B Explanation [[AnswerBExp::The pathogenesis of GIST tumors involves a gain-of-function mutation in the KIT proto-oncogene, which encodes a transmembrane receptor for stem cell factor that includes a tyrosine kinase component in its intracytoplasmic region. Similar to CML, imatinib has demonstrated efficacy in GIST, whereby it similarly inhibits the tyrosine kinase receptor KIT in a similar fashion to its inhibition of the tyrosine kinase receptor BCR-ABL fusion protein.]]
Answer C AnswerC::Hepatocellular carcinoma
Answer C Explanation AnswerCExp::HCC may be secondary to chronic viral hepatitis and/or cirrhosis. Hepatocellular carcinoma (HCC) is not treated with imatinib.
Answer D AnswerD::Mantle cell lymphoma
Answer D Explanation AnswerDExp::Mantle cell lymphoma is a rare non-Hodgkin’s lymphoma that affects elderly males. Imatinib is not used to treat Mantle cell lymphoma.
Answer E AnswerE::Mucosa-associated lymphoid tissue (MALT) lymphoma
Answer E Explanation [[AnswerEExp::MALT Lymphoma is associated with H. pylori infection and is not susceptible to imatinib therapy. For early and localized MALT lymphoma, treatment of underlying H. pylori infection by antibiotics is often sufficient to induce tumor regression.]]
Right Answer RightAnswer::B
Explanation [[Explanation::The patient in this vignette has chronic myelogenous leukemia, a disorder of the hematopoietic stem cells that is caused by the juxtaposition of the ABL gene (chromosome 9) and the BCR gene (chromosome 22), resulting in BCR-ABL fusion gene, known as the Philadelphia chromosome. This translocation causes a novel tyrosine kinase that can constitutively transmit cell growth signals in affected cells. Although the pathogenesis of the disease is well-described, the mechanism that causes the translocation is poorly delineated. The diagnosis of CML is often suspected by the presence of excessive granulocytosis with left shift and confirmed by the identification of the Philadelphia chromosome in peripheral blood and bone marrow cells. Imatinib is a targeted pharmacologic therapy that inhibits the BCR-ABL tyrosine kinase via competitive binding at the ATP-binding site. It has demonstrated significant efficacy for patients with CML.

Gastrointestinal stromal tumor (GIST) is a rare non-epithelial neoplasm of the GI tract, the mesentary, or the omentum. The majority of GIST tumors are spindle cell tumors that may be either malignant or benign. Most stromal tumors stain positively for CD117 (>90%), CD34, muscle-specific actin, smooth muscle actin, S-100, and desmin. Patients with GIST may be asymptomatic or have non-specific GI symptoms. On biopsy, GIST often appears as a friable unencapsulated mass that does not arise from the epithelium, but from the muscular layer. Characteristically, the pathogenesis of GIST tumors involves a gain-of-function mutation in the KIT proto-oncogene, which encodes a transmembrane receptor for stem cell factor that includes a tyrosine kinase component in its intracytoplasmic region. Similar to CML, imatinib has demonstrated efficacy in GIST, whereby it similarly inhibits the tyrosine kinase receptor KIT in a similar fashion to its inhibition of the tyrosine kinase receptor BCR-ABL fusion protein.
Educational Objective: Imatinib, a tyrosine kinase inhibitor, may be used to treat both CML and GIST.
References: Din OS, Woll PJ. Treatment of gastrointestinal stromal tumor: focus on imatinib mesylate. Ther Clin Risk Manag. 2008;4(1):149-62.
First Aid 2014 page 406]]

Approved Approved::Yes
Keyword WBRKeyword::Cancer, WBRKeyword::Chemotherapy, WBRKeyword::Leukemia, WBRKeyword::Imatinib, WBRKeyword::CML, WBRKeyword::Chronic myelogenous leukemia, WBRKeyword::GIST, WBRKeyword::Gastrointestinal stromal tumor
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