390 likes | 411 Views
Explore the evolution and complexity of colorectal cancer treatment options, including new chemotherapeutic agents, biologicals, surgery, and imaging advances. Discover the benefits of systemic treatments and the latest research in CRC management. Learn about neoadjuvant and adjuvant therapies, metastatic CRC, and key issues in liver metastases treatment. Dive into neoadjuvant chemotherapy advantages, target therapy, and the impact of KRAS mutations on treatment efficacy.
E N D
1. THERAPEVTIC PUZZLE IN SYSTEMIC TREATMENT OF COLO-RECTAL CANCER Rado Janša
University Clinical centre Ljubljana, Slovenia
DPT of gastroenterology
2. Epidemiology of colorectal cancer (CRC)
3. CRC: an evolution of treatment options and complexity Common cancer – advanced disease
Introduction of new chemotherapeutic agents
Introduction of new biologicals
Improved surgical/imaging techniques
Continuum of care approach
Improved understanding of tumour biology
4. COMBINATION !!!
5. OPTIONS FOR TREATMENT OF CRC
OPERATION
RADIOTHERAPHY
ADJUVANT THERAPHY
NEOADJUVANT THERAPHY
SYSTEMIC TREATMENT OF PROGRESSIVE DISEASE
6. What is New in the Systemic Treatment of Colorectal Cancer?
7. Major Advances New chemotherapy
Irinotecan
Oxaliplatin
Capecitabine
Antibodies
VEGF antibodies (bevacizumab)
EGFR antibodies (cetuximab, panitumumab)
8. Advances in the Treatment of Metastatic Colorectal Cancer
9. Adjuvant Chemotherapy Stage III colon cancer (T1-4, N1-2, M0)
Increase 5-y survival rate for 15%
XELODA 5y survival 81%
5-FU/LV 5y survival 78%
FOLFOX 4 (2006) 5y survival 84%
Stage II T3,4, N0, M0
5-y survival rate 70-80%
Treatment in clinical trials
Perforation of GIT, ileus, large tumor, T4, vascular and perinevral invasion, CEA very high befor operation
10. X-ACT Capecitabin (Xeloda)- standard adjuvant treatment of CRC
11. Xeloda = 5-FULV
13. ADJUVANT THREATMENT OF RECTAL CANCER Tumor – 12 cm upper of anus
Stage II and stage III
Standard theraphy = a combination of radiation and chemotheraphy
Preoperative or postoperative radiotherapy (5 weeks, TD 45-50-54) + Capecitabine
14. METASTATIC COLORECTAL CANCER
15. What are the key issues in the management of CRC liver metastases? Agree on resectability
Which metastases, considered initially not resectable, can become resectable after response to chemotherapy?
Which chemotherapy regimen?
Chemotherapy
Preoperative?
Postoperative?
Perioperative?
16. Colon cancer metastases:Treatment profile
17. Secondary resection of CRC liver metastases
18. Neoadjuvant chemotherapy for resectable liver metastases Rationale
Eliminate micrometastatic disease and allow eradication of dormant cancer cells
Increase rate of complete resection and of less extended liver resections, upon tumor shrinkage1
Response to neoadjuvant therapy is an important prognostic factor2,3
Can serve as a test for chemoresponsiveness
19. Neoadjuvant chemotherapy for resectable liver metastases Potential disadvantages
May induce hepatic damage and affect postoperative outcome
Disappearance of liver metastases on imaging with neoadjuvant therapy can complicate the next therapeutic steps
Progression during perioperative chemotherapy
20. Liver damage
21. Vascular lesions: Oxaliplatin
(Rubbia-Brandt et al, 2004)
Steatosis: 5FU, irinotecan?
(Parikh et al, 2003)
Steatohepatitis: irinotecan
(Vauthey et al, 2006) Liver damage induced by chemotherapy
22. NEOADJUVANT CHEMOTHERAPY
TARGET AGENTS
COMBINATION
23. TARGET THERAPY
24. VEGF is a key mediator of angiogenesis
IGF = insulin-like growth factor; PDGF = platelet-derived growth factor; EGF = epidermal growth factor; IL = interleukin; bFGF = basic fibroblast growth factor; VEGF = vascular endothelial growth factor; TGF = transforming growth factor; HER2 = human epidermal growth factor-2
Ferrara N, Davis-Smyth T. The biology of vascular endothelial growth factor. Endocr Rev 1997;18:4–25.
Kerbel R, Folkman J. Clinical translation of angiogenesis inhibitors. Nat Rev Cancer 2002;2:727–39.
IGF = insulin-like growth factor; PDGF = platelet-derived growth factor; EGF = epidermal growth factor; IL = interleukin; bFGF = basic fibroblast growth factor; VEGF = vascular endothelial growth factor; TGF = transforming growth factor; HER2 = human epidermal growth factor-2
Ferrara N, Davis-Smyth T. The biology of vascular endothelial growth factor. Endocr Rev 1997;18:4–25.
Kerbel R, Folkman J. Clinical translation of angiogenesis inhibitors. Nat Rev Cancer 2002;2:727–39.
25. Avastin prevents angiogenesis through a novel mechanism of action Avastin
prevents the binding of VEGF to its receptors
recognises all major isoforms of human VEGF
26. Avastin adds strong benefit to all regimens: OS
27. BRiTE*: Continuation of Avastin post-first progression significantly increases OS (time from initiation of first-line treatment to death)
28. Avastin has a well-established safety profile in phase III trials and clinical practice
29. CETUKSIMAB
block EGFR receptor
Antitumor activity
30. KRAS analysis: Objective and methodology To retrospectively investigate the impact of the KRAS mutation status of tumors on PFS and RR in the first-line treatment of mCRC with FOLFIRI ± ERBITUX
Efficacy analyses repeated on KRAS evaluable population
Genomic DNA isolated from archived tumor material
Paraffin-embedded, formalin-fixed tissue
KRAS mutation status of codons 12/13 determined using quantitative PCR-based assay
31. Relating KRAS status to efficacySecondary endpoint: Response
32. ERBITUX + CT in KRAS wild-type: Consistent results
33. Avastin demonstrates OS benefit regardless of KRAS mutation status
34. KRAS testing
35. SURGICAL THERAPY OF METASTATIC CRC
36. SUBSTRATS on CYP system(kompetition) ANTICANCER AGENTS:kapecitabin, ciklofosfamid, docetaxel, erlotinib, gefitinib, imatinib, doxorubicin, hexamethylmelanine, dacarbazine, irinotekan, fulvestrant, exemestane(aromazin), anastrozole(arimidex)
NSAR, PARACETAMOL
ETANOL
PPI: omeprazol
ANTIEPILEPTIKI
STATINI, ANTIKOAGULANTI, BLOKATORJI Ca KANALCKOV
ANTIBIOTIKI
37. INHIBITION on CYP system:
- amiodaron
- antifungics
- omeprazol
- cimetidin
- eritromicin
- klaritromicin
- ciprofloksacin
- inhiitors of HIV
- verapamil
- disulfiram
- grapefruit
38. Chemotherapy: What we know Downsizing with systemic chemotherapy provides response rates of 40–60% and allows ~10% ofnon-resectable patients to become resectable
5-year survival rates similar to that of patients with primarily resectable metastases
Chemotherapy is associated with hepatic toxicity
39. Biomarkers
The KRAS biomarker is predictive for efficacy and will allow for tailored therapy, improving outcomes for patients with mCRC
CRYSTAL – OPUS - BRITE
Multidisciplinary team
Greater emphasis on a multidisciplinary approach is required to achieve optimal results
40. CONCLUSIONS