Feasibility of sequential adjuvant chemotherapy with a 3-month oxaliplatin-based regimen followed by 3 months of capecitabine in patients with stage III and high-risk stage II colorectal cancer: JS']JSWOG-C2 study

被引:6
作者
Tsuruta, Atsushi [1 ]
Yamashita, Kazuki [2 ]
Tanioka, Hiroaki [3 ]
Tsuji, Akihito [4 ,5 ]
Inukai, Michio [6 ]
Yamakawa, Toshiki [7 ]
Yamatsuji, Tomoki [8 ]
Yoshimitsu, Masanori [9 ]
Toyota, Kazuhiro [10 ]
Yamano, Taketoshi [11 ]
Nagasaka, Takeshi [12 ]
Okajima, Masazumi [13 ]
机构
[1] Kawasaki Med Sch Hosp, Dept Digest Surg, Okayama, Japan
[2] Okayama Rosai Hosp, Dept Surg, Okayama, Japan
[3] Okayama Rosai Hosp, Dept Med Oncol, Okayama, Japan
[4] Gen Hosp, Kobe City Med Ctr, Dept Med Oncol, Kobe, Hyogo, Japan
[5] Kagawa Univ Hosp, Fac Med, Dept Clin Oncol, Takamatsu, Kagawa, Japan
[6] Okayama Saiseikai Gen Hosp, Dept Med, Okayama, Japan
[7] Kagawa Prefectural Cent Hosp, Dept Surg, Takamatsu, Kagawa, Japan
[8] Kawasaki Med Sch, Dept Gen Surg, Okayama, Japan
[9] Hiroshima City Asa Hosp, Dept Surg, Hiroshima, Japan
[10] Natl Hosp Org Higashihirosima, Med Ctr, Dept Surg, Higashihiroshima, Japan
[11] Kurashiki Med Ctr, Dept Surg, Kurashiki, Okayama, Japan
[12] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Surg Gastroenterol, Okayama, Japan
[13] Hiroshima City Hosp, Dept Surg, Hiroshima, Japan
关键词
oxaliplatin; peripheral neurotoxicity; adjuvant chemotherapy; Patient Neurotoxicity Questionnaire; COLON-CANCER; DOUBLE-BLIND; PHASE-III; FLUOROURACIL; LEUCOVORIN; TRIAL; NEUROTOXICITY;
D O I
10.2147/DDDT.S112322
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Six months of oxaliplatin-based chemotherapy is the standard adjuvant chemotherapy for completely resected stage III colorectal cancer (CRC). Also, patients with stage II CRC who are considered to be at high risk of disease recurrence often receive the same adjuvant chemotherapy treatment. We prospectively investigated the extent and degree of neuropathy suffered by stage III and high-risk stage II resectable CRC patients who underwent sequential approach involving 3 months of an oxaliplatin-based regimen followed by 3 months of capecitabine. Patients and methods: Patients with completely resected stage III and high-risk stage II CRC aged >= 20 years were eligible. Patients were treated with folinic acid, fluorouracil, and oxaliplatin (FOLFOX) or capecitabine and oxaliplatin (CAPOX) for 3 months followed by capecitabine (2,500 mg/m(2) on days 1-14 every 3 weeks) for 3 months. Primary end points were frequency and the grade of oxaliplatin-induced neurotoxicity as evaluated using the physician-based Common Terminology Criteria for Adverse Events version 4.0 (CTCAE) grading and the patient-based scale, self-reported Patient Neurotoxicity Questionnaire. Results: Ninety-one patients were enrolled and 86 patients assessed. Eighty-four percent of patients completed the planned oxaliplatin-based therapy for 3 months, and 63% of patients completed all treatments for the full 6 months. Overall incidences of grade 3 or 4 peripheral sensory or motor neuropathy according to the CTCAE were 3.5% and 1.2%, respectively. Regarding the peripheral sensory neuropathy, the proportion of Patient Neurotoxicity Questionnaire (grade C-E) and CTCAE (grade 2-4) at months 1.5/3/6 were 11.3/22.1/29.4% and 5.3/4.4/11.3%, respectively (Spearman correlation coefficient: 0.47). Conclusion: A sequential approach to adjuvant chemotherapy with 3 months of an oxaliplatin-based regimen followed by 3 months of capecitabine was tolerated by patients and associated with a low incidence of neuropathy.
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页码:3827 / 3835
页数:9
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