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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1307025 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
2 i7 N) p# r$ W$ r: Q  F1 SNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
' r- D7 ?: s5 P& F3 h. ^$ k7 N+ Author Affiliations
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. z9 A, m) {9 p1 j2 Z( J' Y6 r1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
6 m6 U- w0 i1 I0 }, T' b/ f% M" w2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan / w8 ~( a- ^$ S5 A, a
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan . l' S/ c1 s" X5 d9 l
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
7 q7 v" T, `6 V4 I. _5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ! u  \4 t9 N( C# a) I
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
. [, `2 {5 g. g) G6 g! F4 M2 ^$ P7Kinki University School of Medicine, Osaka 589-8511, Japan % \" i6 ~" w7 k  e
8Izumi Municipal Hospital, Osaka 594-0071, Japan
! e/ `: K8 I0 ~" h5 u; Z) o9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
! i! O& x" s7 g6 L. w1 q" `Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
$ `- }) T6 j7 _. s3 u6 QAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type ; y% E5 n! K( [9 a8 Y/ y/ ^4 B3 d
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato : Y6 m! [6 F+ k

% i* ]& o1 K/ N/ a# P: N- UAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  / a" c: c. x. t

1 F; B% f, G+ }0 y7 DPublished online on: Thursday, December 1, 2011
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Doi: 10.3892/ol.2011.507
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# N6 |% I3 k: BPages: 405-410 : U3 X# e$ M7 L: S1 G
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Abstract:9 |) j) z  w. F1 D: {3 _/ C0 y  U) K
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population
) r1 G, r( v- J' h% N; u6 }F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
4 D* u* X& i0 h* ~- y8 F. H+ Author Affiliations/ O& T% E: X. d6 `3 s2 q3 P
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu , v6 _4 P' m7 [1 o$ u
2Department of Thoracic Surgery, Kyoto University, Kyoto
* b2 H, v9 V5 ~1 N, b9 A* ~! \8 A3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 8 G  ]4 o5 _# k8 f
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
# h! _! \5 T4 N& [, G0 |/ @Received September 3, 2010. 6 o& A4 q& L8 ]" c$ V% I, y
Revision received November 11, 2010. 8 e( n* m/ F- M" @0 o2 J
Accepted November 17, 2010. / N9 W/ Z6 N; J! \& I* G( v
Abstract7 e( b" e" I7 t# ]! y# m1 U  f
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. - y# B& ~0 `& H
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
2 V. X  w/ x' V3 w6 _& jResults: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. ) g/ t. p- `# z
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
  k) W: V' K8 s) `/ ~5 q+ S8 u今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?9 m# Z/ X* E7 U/ v. C8 Q6 k$ w
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy$ A2 K  |7 d; o7 B+ a9 D- f: D4 H
http://clinicaltrials.gov/ct2/show/NCT01523587
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  X9 T- B# \7 M0 b& P$ E4 r. w& M4 XBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
7 f8 P+ S# j9 Z. {* ~) r( whttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
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1 e# k# d  P" \7 T1 l4 h从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
4 W2 F3 o# q5 K& [至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
2 n$ {! `# x' E, R* N4 J& X! t3 D, c从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。9 d* M; c; i6 S' Y3 ^
至今为止,未出 ...

4 T. g2 o1 F7 p4 n; E" ]没有副作用是第一追求,效果显著是第二追求。) y9 t* e( B4 N; B
不错。

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