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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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1236755 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 u; J0 p# F1 WNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
; b( m7 c* c9 i+ Author Affiliations- u* f" t6 `& l4 g) \  B7 h, V" B0 J

( m/ u, q) \% D, |1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
8 Q6 u7 ~' M; f8 I: Y# a2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 5 ?% }7 R9 T+ }; x( }" C6 s; [
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
$ z  m' J9 B4 X" j/ [4 F4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
. R3 b: Y& z9 s% j5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
6 s% l5 h% u: F# s; M% {6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
/ K7 S  @5 Z! I4 F( H7Kinki University School of Medicine, Osaka 589-8511, Japan " L1 D+ m  M" S
8Izumi Municipal Hospital, Osaka 594-0071, Japan
& @  D" ^$ ^8 g3 [( l' |8 M9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 5 z2 c& i  Z5 H9 r
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 - d$ L/ y) |  m) B0 A6 [/ o; \: W
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. 2 I) I5 W, V9 r+ x' ^

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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 & t; b8 i% d, ?8 V0 x+ w3 g
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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
: G' [7 }: A) G8 Q4 l5 D+ B8 M- Z/ `8 I* n* V* ?) Y2 f6 s
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  + Y7 l3 @& q: @4 ?; p% |! P: k( w
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Published online on: Thursday, December 1, 2011 : W  ], G) Y$ ^' Z$ {! D7 q

3 S1 n9 w; m" a9 k/ d. N0 V/ Q& k# hDoi: 10.3892/ol.2011.507 ( R" V9 U' S& N) R: U) [

6 G* W& ]2 t& }) e% y$ |' ?Pages: 405-410
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+ h# t# P' S* {* N) w1 @/ u) X7 D3 QAbstract:
& h0 W; J& N6 x/ r1 sS-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 n" z' u. 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# `6 N: ~, U! d3 M# T7 E* L6 g5 M
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
( j9 }6 y$ Z; a. g+ Author Affiliations
7 v5 ?( m' d! ~+ t& Z1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
7 @8 K8 l; }) w3 V- h2Department of Thoracic Surgery, Kyoto University, Kyoto $ r4 s. q% o5 S
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 2 r+ r: A8 ]) X
&#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
: {  v1 _% V7 \1 K0 mReceived September 3, 2010.
. k1 P% f9 H" H$ `0 @. Q4 KRevision received November 11, 2010. $ m4 _; m. p; ]: e
Accepted November 17, 2010. ) D5 v9 [6 p, v# O8 H
Abstract
$ z. Q0 b0 L' V8 w  J; D" KBackground: 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.
$ A: y: v# }/ s+ {1 y8 rPatients 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.
) P5 j* O, D# d8 |3 B( c% ~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.
" |. H# U! l) B! yConclusion: 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。
; g3 T5 h/ |2 i- [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) S% O' H  j- Z5 p  h; {
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$ n) E. h, K1 Q2 e
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。$ J. A" a3 a, q6 `# H9 P; N4 E
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
) e* {8 O4 z8 y% I/ {; U, `& Z- P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。( q# A6 H, Z  [4 \
至今为止,未出 ...

2 k) t3 H9 q* S  h! j4 L没有副作用是第一追求,效果显著是第二追求。, p" ^( {% g4 U, V4 j
不错。

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