The document summarizes three cases of patients with colorectal cancer undergoing chemotherapy treatment.
Case I describes a 49-year-old female undergoing FOLFIRI treatment. The pharmacist calculates the doses for her fourth cycle based on her weight and surface area.
Case II describes a 45-year-old male undergoing XELOX treatment who develops severe neuropathy. He is switched to FOLFIRI plus bevacizumab.
Case III describes a 50-year-old female started on FOLFIRINOX who develops side effects and is switched to FOLFOX plus panitumumab. Her doses and management are discussed.
The document summarizes three cases of patients with colorectal cancer undergoing chemotherapy treatment.
Case I describes a 49-year-old female undergoing FOLFIRI treatment. The pharmacist calculates the doses for her fourth cycle based on her weight and surface area.
Case II describes a 45-year-old male undergoing XELOX treatment who develops severe neuropathy. He is switched to FOLFIRI plus bevacizumab.
Case III describes a 50-year-old female started on FOLFIRINOX who develops side effects and is switched to FOLFOX plus panitumumab. Her doses and management are discussed.
The document summarizes three cases of patients with colorectal cancer undergoing chemotherapy treatment.
Case I describes a 49-year-old female undergoing FOLFIRI treatment. The pharmacist calculates the doses for her fourth cycle based on her weight and surface area.
Case II describes a 45-year-old male undergoing XELOX treatment who develops severe neuropathy. He is switched to FOLFIRI plus bevacizumab.
Case III describes a 50-year-old female started on FOLFIRINOX who develops side effects and is switched to FOLFOX plus panitumumab. Her doses and management are discussed.
COLORECTAL CANCER Dr. Soha Said Mohamed, PHD Supervisor of the oncology clinical pharmacy Alexandria Main University Hospital CASE I
AS is 49 old female patient , she was
diagnosed as Stage III metastatic colon cancer, the oncologist decided to start FOLFIRI regimen for 4 cycles and then re asses. Her wt :113 kg, Ht: 155cm. 1.According to the previously mentioned protocol, the dose of irinotecan would be………………….over…………hrs Ca-leucovorin …………..over…………hrs 5-fu IVP………………… 5-fu continuous infusion……………..over………………hrs BSA=√(113 X 155/3600) = 2 Irinotecan= 2 X 180 =360 mg over 1.5 hours Leucovorin= 2 X 400 = 800 mg over 1.5 hours 5-FU IVP= 2 X 400 = 800 mg 5-FU infusion= 2 X 2400 = 4800 mg over 46 hours After 3 cycles the patient come to the chemotherapy clinic c/o diarrhea , her CBC; Hb:11.8, PLT:163, ANC:0.85, Bilirubin:0.8, SGPT, SGOT:22,32 respectively. 2.As a clinical pharmacist, what would be your recommendation for; A.management of late onset diarrhea, and preventive measures B. this cycle and the next one?? A- Irinotecan diarrhea Early onset Late onset Timing During or within 24 hours of > 24 hours of administration, administration median onset of 5 days after cycle Associated Symptoms rhinitis, hypersalivation, miosis, Risk of dehydration and lacrimation, diaphoresis, electrolyte imbalance if not flushing, and abdominal properly managed cramping Mechanism cholinergic syndrome mediated abnormal ion transport in the by increased anticholinesterase injured intestinal mucosa, activity of the irinotecan parent leading to increased secretion compound of water and electrolytes into the intestinal lumen Management 1- Infusion time not less than 90 Loperamide 4 mg immediately, minutes (peak plasma conc.) then 2 mg after each loose 2- Atropine 0.3 – 0.6 mg IV or stool until diarrhea-free for 12 SC as needed, repeated up to a hours, maximum 16 mg/ day for maximum dose of 1.2 mg a total of 48 hours B- Cycle decision (Pt CBC and protocol requirement) 3.dose of irinotecan would be…………………. Ca-leucovorin ………….. 5-fu IVP………………… 5-fu continuous infusion……………..
Irinotecan= 2 X 150 = 300 mg
Leucovorin= 2 X 400 = 800 mg 5-FU IVP= 2 X 320 = 640 mg 5-FU infusion = 2X 2000 = 4000 mg • 4.After the forth cycle the patient came to the consultant clinic for re assessment, and after doing PET CT, the decision was to continue more two cycles Case II AA is a 45 years old male patient diagnosed with metastatic rectal cancer, the oncologist decided to give him XELOX regimen. Wt:82 kg, Ht:170 cm 1.According to the protocol , the oxaliplatin dose ……………over….hrs 2.Capcitabine dose…………………….BID , from Day…to Day………, and what is your patient education tips??? After two cycles , the patient was c/o of sever neuropathy grade IV. So he was shifted to another regimen FOLFIRI+ 3.Bevacizumab, was it a right decision???/ 4.The dose would be of Bevacizumab…………….mg 5.The most characteristic side effects of bevacizumab are……………………….. 6.According to the previously mentioned protocol, the dose of irinotecan would be………………….over…………hrs, Ca-leucovorin …………..over…………hrs 5-fu IVP………………… 5-fu continuous infusion……………..over………………hrs 7.The …………………….enzyme is responsible for fluorouracil metabolism 8.This regimen should be repeated every……………….. Case III
A 50 years old female was diagnosed with metastatic colon
cancer(moderately differentiated adenocarcinoma), and she would start FOLFORINOX protocol on 28/11/2022. her weight :88kg. Hieght:166cm 1.What would be the doses for each drug ?? Oxaliplatin Irinotecan Ca leucovorin and 5-fu After two cycles the patient was re- assessed, showing poor tolerance, abdominal colic and persistent nausea and vomiting so she was shifted to FOLFOX- PANITUMAB regimen 2.What would be the doses of the previous regimen??
3.The most characteristic side effects of vectibex??
4.The most important patient education tips for vectibex are……………
5.After two cycles the patient come with peripheral
tingling and numbness sensation ,what is the cause of such adverse effect and how to manage??? 6.What is the preventive measures of skin toxicity of panitumab??? 7.This protocol repeated every………….days , for maximum……………cycles.
8.After three cycles , CBC of the patient was Hb:12,
WBC:2.6, ANC:0.43, what would be the dose of this patient for current and next cycle, if you know that her weight was decreased by 15kg???