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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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1265522 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
* B4 t& S% K& b( ]! X% BNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 1 ^* i' l; F) b  `# |! ~7 i2 D
+ Author Affiliations& A1 l7 E5 B# U: t7 S
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 7 v8 J0 z) K( [- q7 m# x
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
& ^: ^8 b4 B+ \! X" H3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ( K' q3 c9 O8 Z& F
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
- y2 U& a! t3 O! o! M) Q$ {$ C, I5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan & w6 c' |% m3 e3 ?$ m
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan % o7 F/ Y" K+ F8 \
7Kinki University School of Medicine, Osaka 589-8511, Japan ; Y) X  @! w* b3 u) C
8Izumi Municipal Hospital, Osaka 594-0071, Japan ) p/ f! X  O. ^& k
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
7 E2 u* y9 a$ K5 V7 _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 3 n5 f0 p& Q5 l. h* x
AbstractBackground: 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
% U( a$ L: a0 {, Z; u* B( ~# `4 A7 m' O/ y' i3 d- }# N" B/ Y; `
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato . M+ R& m  a* I1 x

6 d, v! \# u6 R( K, KAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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, N; @* |* W# Y/ l6 ^Published online on: Thursday, December 1, 2011
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3 \+ ]/ _. j) ?7 g0 e' BDoi: 10.3892/ol.2011.507
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Pages: 405-410 / Y1 F( S" q2 {3 `& [

7 l5 E4 ~, k0 m: y4 r7 rAbstract:
8 `, P  n+ p( W: s2 F% n# \# y& \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.' @7 \) z8 F! x8 @

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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( Y+ G/ z9 y0 W4 K0 m1 b- j
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 " D  p; Y' {8 N2 h# M# t
+ Author Affiliations
, Z+ L" I+ b* N- ~5 c* f9 X) N1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 0 W, x! d  e/ t# K3 t& u+ p
2Department of Thoracic Surgery, Kyoto University, Kyoto
8 b. e2 ?3 f! W4 `- F- R. T1 X3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 5 j2 l( O" B$ g, S
&#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 3 N$ v6 S4 R; `1 W, [
Received September 3, 2010.
3 i8 A  r) B9 m( y& f# WRevision received November 11, 2010.
6 G: x1 e$ F, g% s- b. n. ?Accepted November 17, 2010. " g# N, a" |$ n
Abstract# [8 b5 |* }& ~& W- r
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. . K$ B- K0 ~; E! ]
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.
  a' M$ [3 j" iResults: 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.
0 Z  d. f$ b3 NConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 3 A0 u2 v. w& ^8 r0 I0 N; }: [
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。& _  b6 @  K/ F! N5 A! y
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?
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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" U! U1 I1 e# B" Y! R! Z
http://clinicaltrials.gov/ct2/show/NCT01523587+ a3 f4 g' y# r7 d; I8 X

& e' Y- X$ E6 |; b2 \+ @) I' s. |BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC- c; p+ \* ~' V; O& Z6 B' H
http://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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( p* W& Q$ V. v4 l! J  m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。' c9 w' @8 }$ X7 }' U
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

9 t; F+ t- B/ U+ X( S& J没有副作用是第一追求,效果显著是第二追求。
' ?& N5 B. w$ P6 p& ^不错。

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