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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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1253980 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 Type5 `; B- g" J- m4 c) B1 |0 T- d, x
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
( @5 k: d/ i6 N: w% G4 M9 {+ Author Affiliations# I2 B2 \; _# s3 N

: ]- j' k* P% F) Z1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
+ P3 [' \4 @  J2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ) U4 L: z" ]: l5 ^0 e' y  E, P: s
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 5 S  L! |" b+ C3 D6 f$ p
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
" o- j1 H' U1 M1 b5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan / S) _$ A- y0 Q! h1 C! ?& S
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 7 H' e$ _2 ?( [3 J% P1 M1 {
7Kinki University School of Medicine, Osaka 589-8511, Japan 3 C3 _) j' H$ n0 O, I
8Izumi Municipal Hospital, Osaka 594-0071, Japan
' Z7 r7 Z$ p9 M9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
5 U( |5 K# y$ }7 Q0 X3 `, l( `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 ^8 A  t0 ~! A5 Y: r7 f
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
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7 z( o, U5 g- e" p6 GAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
. K5 l0 X% |, J( {# U/ M
. O/ T/ z  e0 `* @* d& {$ d+ CAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan    l% N1 r& f( C( ~; j2 Q
4 A3 k( E$ _3 h# G
Published online on: Thursday, December 1, 2011 7 k! F1 q, f3 d- Z, i' ~

) Z/ C8 c. `+ ^Doi: 10.3892/ol.2011.507
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) v! R4 D# @! q/ ~Pages: 405-410 6 y7 l- r  D0 B
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Abstract:
1 G, A) M- N6 ]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 population1 l) g+ Z9 ?2 f0 @+ P& h8 B
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
9 L5 T8 K/ }, \/ w/ o% z+ Author Affiliations
7 W* o; S6 |  P# o1 O/ ]2 N1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
  I' Y5 ?  H8 T2Department of Thoracic Surgery, Kyoto University, Kyoto 1 V% F( Z$ i% B3 A4 V3 Y9 `
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan " K* {. {' `* _; Q! Z- g' 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
4 [$ C$ D: d$ q1 t) a% Z$ FReceived September 3, 2010.
& k5 W% w8 W0 Q' ?3 A" a' A& C6 R' kRevision received November 11, 2010. . Y1 g1 x9 C% X, O3 N# ^, r
Accepted November 17, 2010.
# S5 q7 M, y+ O( d% e% L' X- y! hAbstract
  B1 S2 W6 J& m  s1 T5 x- [( ~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. & g0 m: Q, U! X/ s0 x" r- J
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.
7 m* V6 i; B: `4 vResults: 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. $ s& i; B# R7 N, W, u* {
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 2 L5 d& G8 h8 w4 |) X- _; ]3 }
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。. E8 K7 l; _0 y) v0 Z
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?% h* _5 t( S" R
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
0 C# u9 v* C' m: a. @6 [% Ohttp://clinicaltrials.gov/ct2/show/NCT015235872 j8 R! f" s; m

, a- u( l/ m; o' d" X" {4 v* @' {BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC2 p9 j3 b& H' D/ Q
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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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。
- {7 Y& ^4 _8 A$ s/ v  @# O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
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没有副作用是第一追求,效果显著是第二追求。5 e1 t& b9 L6 P. o' {" U& z. ~
不错。

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