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在一例转移性乳腺癌患者中,S-1(替吉奥)维持完全缓解约10年。

S-1 (TS-1) maintained complete response for approximately 10 years in a case of metastatic breast cancer.

作者信息

Taira Naruto, Aogi Kenjiro, Ohsumi Shozo, Takashima Shigemitsu, Nishimura Rieko, Doihara Hiroyoshi, Saeki Toshiaki

机构信息

Department of Surgery, National Hospital Organization, National Shikoku Cancer Center, Matsuyama-city, Ehime, Japan.

出版信息

Breast Cancer. 2006;13(2):220-4. doi: 10.2325/jbcs.13.220.

Abstract

We present a patient with pulmonary metastasis from breast cancer who received S-1 (TS-1) and maintained complete response for approximately 10 years after recurrence. A 51-year-old woman underwent modified radical mastectomy for left breast cancer in November 1991. Her cancer was postoperatively classified as pT2 pN0 M0 Stage IIA. As postoperative adjunctive treatment, tamoxifen and hexylcarbamoyl 1-5-FU (HCFU) were given. During the administration period (30 months after surgery), a solitary pulmonary metastasis occurred. Three months after the start of S-1 (100 mg/body/day), the tumor disappeared on images. Thereafter she took S-1 orally for approximately 10 years, and the pulmonary metastatic focus maintained complete response. In addition, no recurrent focus was observed. The adverse events observed during S-1 treatment were nausea, low-grade neutropenia and pigmentation of fingers. All were mild, and S-1 could be continued. Our case illustrates two important characteristics of S-1. First, S-1 was effective even though this patient had a lung metastasis during adjuvant treatment with HCFU. S-1 is a combined formulation containing 5-chloro-2, 4-dihydroxypyrimidine (CDHP; gimestat), which inhibits an enzyme that metabolites 5-FU, dihydropyrimidine dehydrogenase (DPD). Therefore, high 5-FU concentrations are maintained with S-1, and S-1 may be effective in the patients who do not respond to other fluoropyrimidine agents. Second, since S-1 toxicity was mild, long-term treatment for approximately 10 years was possible. Since S-1 contains potassium oxonate (OXO; otastat), gastrointestinal toxicities, the main adverse events of 5-FU agents, could be reduced. The purpose of treatments for metastatic breast cancer is to maintain favorable quality of life (QOL), as well as to improve survival. S-1 could be a valuable agent for breast cancer treatments, since it showed clinical efficacy and mild toxicity, and can be given orally.

摘要

我们报告一例乳腺癌肺转移患者,其接受S-1(替吉奥)治疗,复发后维持完全缓解约10年。一名51岁女性于1991年11月因左乳腺癌接受改良根治术。其癌症术后分期为pT2 pN0 M0 ⅡA期。作为术后辅助治疗,给予他莫昔芬和己基氨甲酰基-1-5-氟尿嘧啶(HCFU)。在给药期间(术后30个月),出现孤立性肺转移。开始服用S-1(100mg/体/天)3个月后,影像学上肿瘤消失。此后她口服S-1约10年,肺转移灶维持完全缓解。此外,未观察到复发灶。S-1治疗期间观察到的不良事件为恶心、轻度中性粒细胞减少和手指色素沉着。均为轻度,S-1可继续使用。我们的病例说明了S-1的两个重要特征。第一,尽管该患者在HCFU辅助治疗期间发生了肺转移,但S-1仍有效。S-1是一种复方制剂,含有5-氯-2,4-二羟基嘧啶(CDHP;吉美嘧啶),它可抑制代谢5-氟尿嘧啶的酶——二氢嘧啶脱氢酶(DPD)。因此,S-1可维持较高的5-氟尿嘧啶浓度,对于对其他氟嘧啶类药物无反应的患者,S-1可能有效。第二,由于S-1毒性较轻,可进行约10年的长期治疗。由于S-1含有奥替拉西钾(OXO;奥替拉西),可减少5-氟尿嘧啶类药物的主要不良事件——胃肠道毒性。转移性乳腺癌治疗的目的是维持良好的生活质量(QOL)以及提高生存率。S-1可能是乳腺癌治疗的一种有价值的药物,因为它显示出临床疗效且毒性较轻,并且可以口服给药。

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