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Current Concepts
  in the Diagnosis of Lung Cancers
                           BY THE
INTERNATIONAL ASSOCIATION FOR THE STUDY OF LUNG CANCER
               ADELAIDE CONVENTION CENTER
             ADELAIDE, SOUTH AUSTRALIA, AUSTRALIA



                FELIPE S TEMPLO JR., MD
PART I: ANATOMICAL PATHOLOGY
            NEEDS
PHC data (1998-2003). Templo FS, Orillaza MA, Tan CD (2003)

๏ƒ˜Correct specific diagnosis in 30% (38% SCC and 23% AdenoCA)

๏ƒ˜NSCLC-NOS is 62% (22.6% SCC and 37.7% AdenoCa)

๏ƒ˜Incorrect specific diagnosis is 7.5% (10% AdenoCA and
                                       4.7% SCC)
LEPIDIC




            ACINAR




PAPILLARY             MICROPAPILLARY




      SOLID WITH MUCIN
PART II: MOLECULAR PATHOLOGY
             NEEDS
Testing for research purposes only
2010


                   NON-SMALL CELL LUNG CARCINOMAS




                                     NON-SQUAMOUS CELL CA*
SQUAMOUS CELL CA




                                               MUTATION TESTING

                                         EGFR :exons 19 &21;
  NO TESTING
                                                exons 18-21
  UNLESS REQUESTED            FISH       KRAS :(exon 2/codon12-13
  BY THE ONCOLOGIST           ALK        (OPTIONAL)
22012
5 unstained sections
5 unstained slides
KRAS MUTATION TESTING
EML-4-ALK TESTING



                    Positive for
                    translocation




                    Negative for
                    translocation
Laser microdissection
GENERAL RECOMMENDATIONS FOR EGFR/KRAS
                 TESTING:
๏ƒ˜ Blocks (formalin-fixed, paraffin-embedded) are highly
  recommended for optimal testing.
๏ƒ˜ Testing can be performed on primary tumor or a site of
  metastasis
  1) FFPE tissue block containing 20% to 25% tumor OR
  2) 3-4 precut unstained slides from paraffin block in 5 micron
  sections and one H&E reference slide (manual microdissection)
       Use special slides for laser microdissection (7 micron)
๏ƒ˜ FFPE blocks from surgical resections, excisional biopsies, fine
  needle aspirates (FNA) and biopsy, core needle biopsies, cell
  blocks (pleural effusions, ascites and FNAs) and bone marrow.
๏ƒ˜ A minimum of 300-500 viable tumor cells are required.
EXPERIENCE AT ST VINCENTโ€™S HOSPITAL
TISSUE COLLECTION/FIXATION

24 HOURS                                          BIOPSY
                 FIXATION/TISSUE PROCESSING



                PATHOLOGISTโ€™S REVIEW AND
 1-2            REPORT                            PATHOLOGY
WORKING
DAYS
EXCEPT     DECISION FOR EGFR MUTATION ANALYSIS,
IHC               TUMOR CONTENT REVIEWED



             TUMOR MICRODISSECTION IF NEEDED      MOLECULAR
                                                  TESTING

  5-7
 WORKING            EGFR MUTATION TESTING
 DAYS
                                                  FINAL
              FINAL REPORT WITH TUMOR HISTOLOGY   REPORT
              AND MUTATION RESULTS
NEW CANDIDATE PREDICTIVE MARKERS

๏ƒ˜ HER2
๏ƒ˜ RAF
๏ƒ˜ PI3KCAโ€“AKTโ€“mTOR pathway
๏ƒ˜ C-MET
๏ƒ˜ Insulin-like growth factor (IGF1R)
๏ƒ˜ Fibroblastic growth factor receptor 1 (FGFR1) and
  discoidin domain receptor family, member 2 (DDR2)
๏ƒ˜ Target molecules for chemotherapeutic agents
Questions?

1. Which Patients Should Be Tested for the Presence
   of These Mutations to Determine Their First-line
   Therapy Options?
๏ƒ˜ First, what is the chance of an activating mutation being
  present?
๏ƒ˜ Second, what is the cost of testing?
๏ƒ˜ How should testing be performed?
๏ƒ˜ Which mutations of the EGFR are clinically significant?

                             2011 by American Society of Clinical Oncology.
Questions?
2. Should Patients with Less than 10 Packs/Year
   Smoking History and Non-squamous Histology Be
   Empirically Treated with Oral EGFR TKIs
   in the Absence of EGFR Testing?

3. Should KRAS Testing Be Used to Deny Patients
   Therapy with Oral EGFR TKI Inhibitors?

4. Is There a Role for EGFR FISH Testing When
   Considering the Use of First-generation Oral EGFR
   TKIs?                  2011 by American Society of Clinical Oncology.
Questions?
5. How Common Is ALK?

6. What Are the Key Clinical Features Associated with
   ALK?

7. Should All Patients with NSCLC Be Tested for ALK?


                        2011 by American Society of Clinical Oncology
Questions?

8. Should Patients with EGFR or KRAS Mutant Lung
   Cancer be Tested for ALK?

9. What Is the Diagnostic Test of Choice for ALK?

10. Are There Other Diagnostic Modalities for ALK?




                  2011 by American Society of Clinical Oncology
Copyright ยฉ 2012 by the
International Association for the Study
of Lung Cancer
ACKNOWLEDGEMENT
1. DR. LINDY CLARKE, FRCPA
   The Prince Charles Hospital
   Brisbane, Queensland, Australia


2. DR. PRUDENCE RUSSELL, FRCPA
   St. Vincentโ€™s Hospital and Peter McCallum Cancer Centre
   Melbourne, Victoria, Australia


3. Ms. KAREN LATHER
   The Australian Lung Foundation
   Adelaide, South Australia, Australia

   Copyright ยฉ 2012 by the International Association for the Study of Lung Cancer

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Current Concepts in the Diagnosis of Lung Cancer

  • 1. Current Concepts in the Diagnosis of Lung Cancers BY THE INTERNATIONAL ASSOCIATION FOR THE STUDY OF LUNG CANCER ADELAIDE CONVENTION CENTER ADELAIDE, SOUTH AUSTRALIA, AUSTRALIA FELIPE S TEMPLO JR., MD
  • 2. PART I: ANATOMICAL PATHOLOGY NEEDS
  • 3.
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10.
  • 11.
  • 12.
  • 13.
  • 14.
  • 15.
  • 16.
  • 17.
  • 18.
  • 19.
  • 20.
  • 21.
  • 22. PHC data (1998-2003). Templo FS, Orillaza MA, Tan CD (2003) ๏ƒ˜Correct specific diagnosis in 30% (38% SCC and 23% AdenoCA) ๏ƒ˜NSCLC-NOS is 62% (22.6% SCC and 37.7% AdenoCa) ๏ƒ˜Incorrect specific diagnosis is 7.5% (10% AdenoCA and 4.7% SCC)
  • 23.
  • 24.
  • 25.
  • 26.
  • 27.
  • 28.
  • 29.
  • 30.
  • 31.
  • 32.
  • 33.
  • 34.
  • 35.
  • 36.
  • 37.
  • 38.
  • 39. LEPIDIC ACINAR PAPILLARY MICROPAPILLARY SOLID WITH MUCIN
  • 40.
  • 41.
  • 42.
  • 43.
  • 44.
  • 45. PART II: MOLECULAR PATHOLOGY NEEDS
  • 46.
  • 47. Testing for research purposes only
  • 48. 2010 NON-SMALL CELL LUNG CARCINOMAS NON-SQUAMOUS CELL CA* SQUAMOUS CELL CA MUTATION TESTING EGFR :exons 19 &21; NO TESTING exons 18-21 UNLESS REQUESTED FISH KRAS :(exon 2/codon12-13 BY THE ONCOLOGIST ALK (OPTIONAL)
  • 49. 22012
  • 51.
  • 54.
  • 55. EML-4-ALK TESTING Positive for translocation Negative for translocation
  • 56.
  • 58. GENERAL RECOMMENDATIONS FOR EGFR/KRAS TESTING: ๏ƒ˜ Blocks (formalin-fixed, paraffin-embedded) are highly recommended for optimal testing. ๏ƒ˜ Testing can be performed on primary tumor or a site of metastasis 1) FFPE tissue block containing 20% to 25% tumor OR 2) 3-4 precut unstained slides from paraffin block in 5 micron sections and one H&E reference slide (manual microdissection) Use special slides for laser microdissection (7 micron) ๏ƒ˜ FFPE blocks from surgical resections, excisional biopsies, fine needle aspirates (FNA) and biopsy, core needle biopsies, cell blocks (pleural effusions, ascites and FNAs) and bone marrow. ๏ƒ˜ A minimum of 300-500 viable tumor cells are required.
  • 59.
  • 60. EXPERIENCE AT ST VINCENTโ€™S HOSPITAL
  • 61. TISSUE COLLECTION/FIXATION 24 HOURS BIOPSY FIXATION/TISSUE PROCESSING PATHOLOGISTโ€™S REVIEW AND 1-2 REPORT PATHOLOGY WORKING DAYS EXCEPT DECISION FOR EGFR MUTATION ANALYSIS, IHC TUMOR CONTENT REVIEWED TUMOR MICRODISSECTION IF NEEDED MOLECULAR TESTING 5-7 WORKING EGFR MUTATION TESTING DAYS FINAL FINAL REPORT WITH TUMOR HISTOLOGY REPORT AND MUTATION RESULTS
  • 62.
  • 63. NEW CANDIDATE PREDICTIVE MARKERS ๏ƒ˜ HER2 ๏ƒ˜ RAF ๏ƒ˜ PI3KCAโ€“AKTโ€“mTOR pathway ๏ƒ˜ C-MET ๏ƒ˜ Insulin-like growth factor (IGF1R) ๏ƒ˜ Fibroblastic growth factor receptor 1 (FGFR1) and discoidin domain receptor family, member 2 (DDR2) ๏ƒ˜ Target molecules for chemotherapeutic agents
  • 64.
  • 65. Questions? 1. Which Patients Should Be Tested for the Presence of These Mutations to Determine Their First-line Therapy Options? ๏ƒ˜ First, what is the chance of an activating mutation being present? ๏ƒ˜ Second, what is the cost of testing? ๏ƒ˜ How should testing be performed? ๏ƒ˜ Which mutations of the EGFR are clinically significant? 2011 by American Society of Clinical Oncology.
  • 66. Questions? 2. Should Patients with Less than 10 Packs/Year Smoking History and Non-squamous Histology Be Empirically Treated with Oral EGFR TKIs in the Absence of EGFR Testing? 3. Should KRAS Testing Be Used to Deny Patients Therapy with Oral EGFR TKI Inhibitors? 4. Is There a Role for EGFR FISH Testing When Considering the Use of First-generation Oral EGFR TKIs? 2011 by American Society of Clinical Oncology.
  • 67. Questions? 5. How Common Is ALK? 6. What Are the Key Clinical Features Associated with ALK? 7. Should All Patients with NSCLC Be Tested for ALK? 2011 by American Society of Clinical Oncology
  • 68. Questions? 8. Should Patients with EGFR or KRAS Mutant Lung Cancer be Tested for ALK? 9. What Is the Diagnostic Test of Choice for ALK? 10. Are There Other Diagnostic Modalities for ALK? 2011 by American Society of Clinical Oncology
  • 69. Copyright ยฉ 2012 by the International Association for the Study of Lung Cancer
  • 70. ACKNOWLEDGEMENT 1. DR. LINDY CLARKE, FRCPA The Prince Charles Hospital Brisbane, Queensland, Australia 2. DR. PRUDENCE RUSSELL, FRCPA St. Vincentโ€™s Hospital and Peter McCallum Cancer Centre Melbourne, Victoria, Australia 3. Ms. KAREN LATHER The Australian Lung Foundation Adelaide, South Australia, Australia Copyright ยฉ 2012 by the International Association for the Study of Lung Cancer