1.A Case of Capecitabine and Cisplatin-induced Cutaneous Hyperpigmentation.
Sang Hyeon HWANG ; Ji Hye PARK ; Chong Won CHOI ; Ga Young LEE ; Won Serk KIM
Korean Journal of Dermatology 2014;52(3):210-212
No abstract available.
Cisplatin
;
Hyperpigmentation*
;
Capecitabine
2.Nasolacrimal Duct Stenosis after Oral Capecitabine Administration
Yeonji JANG ; Namju KIM ; Keun Wook LEE ; Ho Kyung CHOUNG ; Sang In KHWARG
Korean Journal of Ophthalmology 2019;33(1):95-96
No abstract available.
Capecitabine
;
Constriction, Pathologic
;
Nasolacrimal Duct
3.Cessation or dose reduction of Capecitabine due to Complications in Patients with Colon Cancer.
Journal of the Korean Society of Coloproctology 2010;26(4):240-240
No abstract available.
Capecitabine
;
Colon
;
Colonic Neoplasms
;
Deoxycytidine
;
Fluorouracil
;
Humans
4.Metronomic chemotherapy with capecitabine for metastatic colorectal cancer in very elderly patients.
Yun Hwa JUNG ; Won Jik LEE ; Jae Ho BYEON ; In Kyu LEE ; Chi Wha HAN ; In Sook WOO
The Korean Journal of Internal Medicine 2017;32(5):926-929
No abstract available.
Administration, Metronomic
;
Aged*
;
Capecitabine*
;
Colorectal Neoplasms*
;
Drug Therapy*
;
Humans
5.Hand-foot Syndrome Due to Capecitabine.
Chong Won CHOI ; Chang Hun HUH
Korean Journal of Dermatology 2005;43(7):965-968
Hand-foot syndrome, also known as acral erythema, is a distinctive and relatively common toxic reaction due to some anticancer drugs. It is characterized by a painful erythema on the palms and soles during chemotherapy, which is often preceeded by paresthesia. We report two cases of hand-foot syndrome induced by capecitabine, which is a relatively brand-new oral anticancer agent. Hand-foot syndrome is one of the most common complications of capecitabine, and is on the increase. Therefore, dermatologists should be aware of it.
Drug Therapy
;
Erythema
;
Hand-Foot Syndrome*
;
Paresthesia
;
Capecitabine
6.XELOX ± Bevacizumab compared to FOLFOX4 ± Bevacizumab in first line metastatic colorectal cancer in a non-reimbursed health care system: A cost analysis.
Tan Jerry Y. ; Yacat Andrew A ; Sacdalan Dennis L.
Acta Medica Philippina 2015;49(2):64-67
INTRODUCTION: XELOX is non-inferior to FOLFOX-4 as a first-line treatment for metastatic colorectal cancer. This study compares the costs associated with XEL0X+/-bevacizumab versus FOLFOX4+/-bevacizumab in a non-reimbursed, out of pocket Philippine health care system.
METHODS: This is a cost-minimization analysis using Philippine General Hospital as base case and a typical Filipino patient of 60 kg with BSA 1.66. The outcome data were derived from the N016966 trial. These included the drugs capecitabine, 5-fluorouracil, oxaliplatin, and bevacizumab (BEV); chemotherapy cycles and corresponding hospital admission for each regimen; resources associated with treatment of adverse events such hospital days, ambulatory consultations, concomitant
medication, and central venous line insertion/removal, with costs and charges based on the local setting.
RESULTS: Highest cost (direct and/or indirect) was for FOLFOX4+BEV, followed by XEL0X+BEV, FOLFOX4, and then XELOX. The use of XELOX resulted in a cost saving of PhP 158,642 per patient compared with FOLFOX4. The use of XEL0X+BEV resulted in a cost saving of PhP 186,144 per patient compared with FOLFOX4+BEV.
CONCLUSION: XEL0X+/-BEV is less costly than FOLFOX4-F/-BEV in an out-of-pocket Philippine tertiary hospital setting from the patient's perspective.
Xelox ; Folfox ; Colorectal Neoplasms ; Capecitabine ; Fluorouracil ; Oxaliplatin ; Bevacizumab
7.Overview of Radiation Therapy for Treating Rectal Cancer.
Bong Hyeon KYE ; Hyeon Min CHO
Annals of Coloproctology 2014;30(4):165-174
A major outcome of importance for rectal cancer is local control. Parallel to improvements in surgical technique, adjuvant therapy regimens have been tested in clinical trials in an effort to reduce the local recurrence rate. Nowadays, the local recurrence rate has been reduced because of both good surgical techniques and the addition of radiotherapy. Based on recent reports in the literature, preoperative chemoradiotherapy is now considered the standard of care for patients with stages II and III rectal cancer. Also, short-course radiotherapy appears to provide effective local control and the same overall survival as more long-course chemoradiotherapy schedules and, therefore, may be an appropriate choice in some situations. Capecitabine is an acceptable alternative to infusion fluorouracil in those patients who are able to manage the responsibilities inherent in self-administered, oral chemotherapy. However, concurrent administration of oxaliplatin and radiotherapy is not recommended at this time. Radiation therapy has long been considered an important adjunct in the treatment of rectal cancer. Although no prospective data exist for several issues, we hope that in the near future, patients with rectal cancer can be treated by using the best combination of surgery, radiation therapy, and chemotherapy in near future.
Appointments and Schedules
;
Chemoradiotherapy
;
Drug Therapy
;
Fluorouracil
;
Hope
;
Humans
;
Radiotherapy
;
Rectal Neoplasms*
;
Recurrence
;
Standard of Care
;
Capecitabine
8.Long-term oncologic outcomes of neoadjuvant concurrent chemoradiotherapy with capecitabine and radical surgery in locally advanced rectal cancer: 10-year experiences at a single institution.
Kyung Ha LEE ; Jin Soo KIM ; Ji Yeon KIM
Annals of Surgical Treatment and Research 2016;91(4):178-186
PURPOSE: Oral capecitabine has demonstrated to be safe and efficient as neoadjuvant concurrent chemoradiotherapy (NCRT) for locally advanced rectal cancers. The aim of this study was to evaluate the long-term oncologic outcomes of NCRT with capecitabine and radical surgery. METHODS: From January 2000 to June 2010, 238 patients were treated at our center for locally advanced rectal cancers using conventional NCRT with capecitabine and radical surgery. Univariate and multivariate analyses were used to evaluate the factors associated with oncologic outcomes with log rank and Cox regression tests. RESULTS: The incidence of grade >3 capecitabine-related toxicity was found to be 4.6%. A pathologic complete response was observed in 14.7% of patients. The 5-year overall and 5-year disease-free survival rate, local and systemic recurrence rate were 82.8%, 75.1%, 4.8%, and 20.3%. Abdominoperineal resection and node-positive disease were independent prognostic factors of 5-year overall survival, 5-year disease-free survival, and systemic recurrence. CONCLUSION: NCRT with capecitabine and radical surgery showed favorable long-term oncologic outcomes with benefits of acceptable toxicity and convenience. We suggest that capecitabine can be one of the favorable therapeutic options for NCRT in rectal cancer.
Capecitabine*
;
Chemoradiotherapy*
;
Disease-Free Survival
;
Humans
;
Incidence
;
Multivariate Analysis
;
Neoadjuvant Therapy
;
Prognosis
;
Rectal Neoplasms*
;
Recurrence
9.A New Option for Advanced Gastric Cancer: Docetaxel and Novel Oral Fluoropyrimidine Combination Chemotherapy.
Journal of the Korean Medical Association 2007;50(6):556-560
Although gastric cancer is the most common cancer and the second leading cause of cancer deaths in Korea, the prognosis for advanced gastric cancer remains poor, and there is no established standard front-line chemotherapy for advanced stage. However, many clinical trials have been developed to improve the response rate and survival in patients with advanced gastric cancer. Novel oral fluoropyrimidines, capecitabine and S-1, are substituting inconvenient 5-FU continuous infusions. These oral fluoropyrimidines combined with docetaxel (1-hour infusion) lead to improve anticancer efficacy and convenience. Capecitabine and docetaxel combination regimens showed response rates 39~60% with median survival 9.5~12 months, and major adverse reactions were hand-foot syndrome and neutropenia. Also, S-1 and docetaxel combination regimens showed response rates 46~56% with median survival 14~14.9 months, and major adverse reaction was neutropenia. The combination of docetaxel and novel oral fluoropyrimidine is highly active and well tolerated in patients with advanced gastric cancer. Large randomized clinical trials are warranted to confirm the efficacy of those regimens. Also, we are looking forward to having the results from studies of new chemotherapeutic agents and modalities.
Capecitabine
;
Drug Therapy
;
Drug Therapy, Combination*
;
Fluorouracil
;
Hand-Foot Syndrome
;
Humans
;
Korea
;
Neutropenia
;
Prognosis
;
Stomach Neoplasms*
10.Hand-foot Syndrome Following Capecitabine (Xeloda(R)) Monotherapy for Colorectal Cancer.
Soon Do PARK ; Kil Yeon LEE ; Sun Jin PARK ; Suk Hwan LEE ; Sang Mok LEE
Journal of the Korean Society of Coloproctology 2009;25(4):227-233
PURPOSE: Capecitabine (Xeloda(R)), which is a systemic prodrug of 5-fluorouracil, can be used in oral formulation for treatment of advanced colorectal cancer as a 1st line or an alternative modality to I.V. 5-fluorouracil-based chemotherapy. One of the most common side effects of this drug is hand-foot syndrome (HFS), palmar-plantar erythrodysesthesia syndrome. We planned this study to clarify the incidence and the clinical course of severe hand-foot syndrome (WHO classification, grade 3 or 4) following capecitabine monotherapy for adjuvant treatment of colorectal cancer. METHODS: From August 2006 to August 2008, 45 colorectal cancer patients were treated with capecitabine, 1,250 mg/m2, orally administered twice daily for 2 wk, followed by 1 wk of rest, given as 3-wk cycles. Seven of them discontinued the drug within 3rd cycle due to poor performance status, gastrointestinal troubles, or other causes. We retrospectively analyzed the remaining 38 patients' medical records and defined the incidence and the clinical course of HFS. RESULTS: Of the 38 patients, 17 (44.7%) suffered severe HFS after capecitabine monotherapy. Of those 17, 5 (29.4%) had severe symptoms after the 1st chemotherapy cycle, and 14 patients (82.4%) had severe symptoms within the 4th cycle. Three of the 14 female and 14 of the 24 male patients complained of severe HFS, showing a statistical male predominance (P=0.043). Eventually, we had to decrease capecitabine to 75% of the daily dose in 12 patients and to 50% in one patient, and to discontinue its use in 4 patients. CONCLUSION: Capecitabine monotherapy very frequently provokes severe HFS, especially in the early cycles of chemotherapy and in males.
Capecitabine
;
Colorectal Neoplasms
;
Deoxycytidine
;
Female
;
Fluorouracil
;
Hand-Foot Syndrome
;
Humans
;
Incidence
;
Male
;
Medical Records
;
Retrospective Studies