scholarly journals Plasma exosomal microRNA‑125b as a monitoring biomarker of resistance to mFOLFOX6‑based chemotherapy in advanced and recurrent colorectal cancer patients

Author(s):  
Takahiro Yagi ◽  
Hisae Iinuma ◽  
Tamuro Hayama ◽  
Keiji Matsuda ◽  
Keijirou Nozawa ◽  
...  
2003 ◽  
Vol 105 (4) ◽  
pp. 491-493 ◽  
Author(s):  
Hiroshi Nakayama ◽  
Kenji Hibi ◽  
Tsunenobu Takase ◽  
Taiji Yamazaki ◽  
Yasushi Kasai ◽  
...  

2013 ◽  
Vol 31 (4_suppl) ◽  
pp. 562-562
Author(s):  
Yoichiro Yoshida ◽  
Seiichiro Hoshino ◽  
Naoya Aisu ◽  
Masayasu Naito ◽  
Syu Tanimura ◽  
...  

562 Background: Neutropenia is a major factor affecting the continuation of chemotherapy for colorectal cancer. In many clinical trials, a neutrophil count of more than 1500 is targeted for the continuation of chemotherapy; for a count of less than 1500, medication is commonly discontinued. However, there is no definite evidence for setting the targeted neutrophil count at 1500. In our department, chemotherapy is discontinued when the neutrophil count is less than 1000 (Grade 3); for a count of 1000 to 1500 (Grade 2), chemotherapy is continued. We examined the neutrophil count during continuation of chemotherapy in patients with a count of 1000 to 1500, and verified whether these neutrophil counts warrant discontinuation of medication. Moreover, we examined the neutrophil count during the previous course of chemotherapy when it fell below 1000. Methods: The study included 104 patients who received XELOX + bevacizumab (BV) therapy, XELOX therapy, and XELIRI + BV therapy for advanced or recurrent colorectal cancer. Results: The patients with a neutrophil count of 1000 to 1500 were 26 (23.1%) of the total. Two (7.7%) of 26 patients had a neutrophil count of less than 1000 during the following course of chemotherapy. Moreover, among the patients with a neutrophil count of less than 1000, 25% had a count of 1000 to 1500 during the previous course of chemotherapy and 75% had a count of more than 1500. Conclusions: According to these results, Grade 2 neutropenia cannot predict the risk of the Grade 3 neutropenia. Continuation of chemotherapy in patients with a neutrophil count of 1000 to 1500 may be appropriate, and discontinuation of therapy is not always required.


2021 ◽  
Vol 6 (11) ◽  

Fluoropyrimidine is commonly used to treat unresectable cases of metastatic colorectal cancer or as an adjuvant therapy for colorectal cancer. Dihydropyrimidine dehydrogenase (DPD) is an enzyme encoded by the DPYD gene, which is responsible for the rate-limiting step in pyrimidine catabolism and breaks down >80% of standard doses of 5-fluorouracil (5-FU). Reductions in DPD activity increase the half-life of 5-FU, resulting in excess 5-FU accumulation and toxicity, which can lead to life-threatening side effects. There have been several published case reports about DPD deficiency in colorectal cancer patients from Western countries. However, case reports of DPD deficiency in Japanese colorectal cancer patients are rare because the measurement of DPD activity is not covered by the public medical insurance system in Japan, and DPD activity is not currently measured in daily clinical practice. Furthermore, there have not been any reports about anticancer drug therapy for Japanese patients with DPD deficiency. In this report, we describe a case in which a Japanese patient with colorectal cancer was diagnosed with DPD deficiency. The DPD deficiency arose as a severe adverse effect of mFOLFOX6/CapOX treatment for recurrent colorectal cancer, and the patient was subsequently treated with TAS-102, without experiencing any severe adverse effects. We report this case along with a review of the literature.


2003 ◽  
Vol 10 (1) ◽  
pp. 59-64 ◽  
Author(s):  
Darius C. Desai ◽  
Emanuel E. Zervos ◽  
Mark W. Arnold ◽  
William E. Burak ◽  
Joseph Mantil ◽  
...  

2008 ◽  
Vol 55 (3) ◽  
pp. 25-29
Author(s):  
R.W.Jr Beart

Justification for the management of recurrent colorectal cancer begins with proof that the ultimate outcome measured by survival can be influenced. To do this, we must prove there is value to follow up of colorectal cancer patients. Without follow up, the management of recurrent cancer is limited.


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