G uidelines fo r the treatment of advanced colon and rectal cancers 1 NCCN Clinical Practice Guideline in Oncology Rectal Cancer Version 12020 2 NCCN Clinical Practice Guideline in Oncology Colon Cancer ID: 911782
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Slide1
CRC: treatment guidelines
Guidelines for the treatment of advanced colon and rectal cancers
1. NCCN Clinical Practice Guideline in Oncology. Rectal Cancer
, Version 1.2020;
2. NCCN Clinical Practice Guideline in Oncology. Colon Cancer
, Version 1.2020;
3
. Van
Cutsem
E, et al. Ann
Oncol
2016;27(8):
1386–422.
Slide2IntroductionThis slide deck summarises the recommended treatment pathways provided by
ESMO and NCCN for locally advanced or metastatic CRC, which includes
rectal and colon cancers1–3Please refer to the full guidelines for more information on:Diagnostic work-up and follow-upTreatment of early- and intermediate-stage diseaseDetails of specific treatment regimens1. NCCN Clinical Practice Guideline in Oncology. Rectal Cancer, Version 1.2020; 2. NCCN Clinical Practice Guideline in Oncology. Colon Cancer, Version 1.2020; 3. Van Cutsem E, et al. Ann Oncol
2016;27(8):1386–422.
CRC, colorectal cancer; ESMO, European Society for Medical Oncology; NCCN, National Comprehensive Cancer Network.
Slide3ESMO consensus guidelines
Summary of management guidelines for patients with metastatic colorectal cancer
1. Van Cutsem E, et al. Ann Oncol 2016;27(8):1386–422.
Slide4Zurich treatment algorithm
ChT, chemotherapy; EGFR, epidermal growth factor receptor; FP, fluoropyrimidine; mt, mutant; OMD, oligometastatic disease; VEGF, vascular endothelial growth factor; WT, wild-type.
1. Van Cutsem E, et al. Ann Oncol 2016;27(8):1386–422.
Slide5Systematic therapy choices for patients with unresectable metastatic disease
*If not previously given. Based on the Zurich treatment algorithm; excluding patients with OMD. Treatment decisions at each stage should consider patient suitability, tolerability, and prior exposure to targeted agents.ChT, chemotherapy;
EGFR, epidermal growth factor receptor; FC, 5-fluorouracil and cisplatin; FOLFIRI, folinic acid, fluorouracil, irinotecan; FOLFOXIRI, folinic acid, fluorouracil, oxaliplatin, irinotecan; FP, fluoropyrimidine; mt, mutant; OMD, oligometastatic disease; VEGF, vascular endothelial growth factor; VEGFR, vascular endothelial growth factor receptor; WT, wild-type.1. Van Cutsem E, et al. Ann Oncol 2016;27(8):1386–422.
Slide6Systematic therapy choices for patients with unresectable metastatic disease
*If not previously given. Based on the Zurich treatment algorithm; excluding patients with OMD. Treatment decisions at each stage should consider patient suitability, tolerability, and prior exposure to targeted agents. ChT, chemotherapy; EGFR, epidermal growth factor receptor; FC, 5-fluorouracil and cisplatin; FOLFIRI, folinic acid,
fluorouracil, irinotecan; FOLFOXIRI, folinic acid, fluorouracil, oxaliplatin, irinotecan; FP, fluoropyrimidine; mt, mutant; OMD, oligometastatic disease; VEGF, vascular endothelial growth factor; VEGFR, vascular endothelial growth factor receptor; WT, wild-type.1. Van Cutsem E, et al. Ann Oncol 2016;27(8):1386–422.
Slide7NCCN Clinical Practice Guidelines
Treatment considerations for advanced colon and rectal cancers
1. NCCN Clinical Practice Guideline in Oncology. Rectal Cancer, Version 1.2020; 2. NCCN Clinical Practice Guideline in Oncology. Colon Cancer, Version 1.2020.
Slide8Subsequent treatment considerations for advanced colon and rectal cancers1. NCCN Clinical Practice Guideline in Oncology. Rectal Cancer, Version 1.2020; 2. NCCN Clinical Practice Guideline in Oncology. Colon Cancer, Version 1.2020.
Please refer to the
NCCN treatment guidelines for full details of the decision-making pathway and treatment options at each stage.BRAF, B rapidly accelerated fibrosarcoma; dMMR, deficient mismatch repair; FP, fluoropyrimidine; KRAS, Kirsten rat sarcoma; MSI-H, high levels of microsatellite instability; NCCN, National Comprehensive Cancer Network; NRAS, neuroblastoma rat sarcoma; RAS, rat sarcoma.Treatment of advanced CRC should be considered as a continuum of care. Decision-making at each stage of therapy should account for patient suitability and tolerability, tumour biomarkers, and prior exposure to chemotherapies and/or targeted agentsConsider the patient’s prior treatments. Have they received a previous:Oxaliplatin-based chemotherapy?Irinotecan-based chemotherapy?Oxaliplatin
- and irinotecan-based regimen?FP without oxaliplatin/irinotecan?Consider the results of molecular testing. Is the patient’s tumour:- KRAS/NRAS/BRAF wild-type? - HER2-amplified, RAS wild-type?- BRAF
V600E-positive?
-
dMMR
/MSI-H
?
Initial systemic therapy:
Is
the patient
considered appropriate for intensive therapy?
Slide9Summary
Slide10SummaryESMO and NCCN guidelines aim to provide guidelines for the diagnosis, treatment and follow-up of CRC based on the
findings of evidence-based medicineBoth sets of guidelines provide specific treatment recommendations for patients with defined molecular markers (including RAS,
BRAF, MSI and HER2)Management of CRC can be considered a ‘continuum of care’, and treatment decisions at each stage should take into account the patient’s clinical status and treatment goals1. Van Cutsem E, et al. Ann Oncol 2016;27(8):1386–422.CRC, colorectal cancer; ESMO, European Society for Medical Oncology; HER2, human epidermal growth factor receptor 2; MSI, microsatellite instability; NCCN, National Comprehensive Cancer Network.