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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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1380795 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
6 S1 d% ~# h6 x( d/ n4 d$ h# y( t% BNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
+ q6 j% D' ]4 i5 k9 R$ F, h- t! r, |+ Author Affiliations
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: K  v; d' c. p# j1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ! t2 i( \6 s4 H% v
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 2 L9 J- L  [- X  U* M
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan , {# i3 F* @  \3 p$ i8 u9 h' W4 G
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan $ m$ t4 F) w3 p/ D5 M2 n& V
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
6 v0 r$ B& S2 E  l4 d( d6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan " e2 N) p( o) X  A" _
7Kinki University School of Medicine, Osaka 589-8511, Japan
/ v9 m4 S1 {- K* C# G/ X/ V8Izumi Municipal Hospital, Osaka 594-0071, Japan
  t+ D! l+ ?: ^/ u9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan ' S2 v2 L2 T- }6 x4 ]
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
- C5 f( N$ W9 W1 bAbstractBackground: 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. 5 ?, d9 P! r  X4 j) p4 n% I
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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
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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
$ Y5 Y, k9 I% O4 m5 H4 O* a4 h+ L, O8 ~+ d( Q
Affiliations: 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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9 \. e+ ~1 m/ s1 Y0 P& u' kPublished online on: Thursday, December 1, 2011
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Doi: 10.3892/ol.2011.507
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! y9 l+ r0 p- b( O# `1 Y0 Q5 [Pages: 405-410 " @# G# s- A! T3 ?. l

3 Q: I' g% z3 f' D: {2 NAbstract:
: J8 [% y6 i7 s1 `- H) gS-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." H$ p$ e3 Z; U! ~: u9 i; V4 x* _) u

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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
+ d4 M, p' b2 kF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 1 |- C+ L2 k* k& o
+ Author Affiliations
. Z2 s0 S7 L( g  U% h1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
9 c( @4 u! }( H2 o2Department of Thoracic Surgery, Kyoto University, Kyoto * A6 w: \* Z4 o8 P) v
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan : l7 D! S) f0 S+ Y3 H7 d- j0 Y! `
&#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 7 Q) C3 d1 c, w. l; a
Received September 3, 2010.
) J' P4 \2 J9 k' LRevision received November 11, 2010.
* O) [, H5 ~7 o( W, jAccepted November 17, 2010.
5 F# W1 V* X% x! a# bAbstract1 ?. _" c% o$ i& k$ ?6 {9 R. z( 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. 1 I  N% ?7 C6 \8 s5 h3 Z3 P4 W5 M
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 B& _  U3 b  a" R. F0 H
Results: 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.
+ W" \: m, `& t3 K: X" S1 i8 \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。& y+ l2 U5 J" Q  [' m
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?% b& |+ L  e# D1 k+ W, i. X" 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 Chemotherapy8 p6 F0 O2 _9 ^: F- J0 K
http://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC* J: j: b/ J3 `: O" b  l" f
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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- t2 p8 }- I( W7 C% T9 p- ^) E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。
; _1 A) h+ a8 }9 C: I$ ~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
0 m4 y9 N1 ?7 E% v( D( l: N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。
7 u9 c  e. w( k* i0 u% C3 {2 D至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。: x# v1 V2 r' \! X- o
不错。

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