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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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1280999 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 Type4 x  s+ t: X; t; G& f
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 0 j! Y  N/ x/ P
+ Author Affiliations, |5 z5 l9 l( L; r

) u) L" Z5 g- J& Z# b( c1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
" ~) c  K: S7 i0 Q1 A4 q: m' Z2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
( y' Z1 T3 M/ V5 s- K5 s3 u3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan / B! ]/ W2 W8 B
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
8 V3 g5 T2 @( A" `) @; q5 G) K5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan " m8 ^9 l# J; [/ @$ F+ R
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
9 e+ U; w4 s& b$ {; H7Kinki University School of Medicine, Osaka 589-8511, Japan 9 c0 w" [+ c7 @1 J# T
8Izumi Municipal Hospital, Osaka 594-0071, Japan : g& h* a* b2 P8 _8 l
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 6 ]7 K$ G' g5 Y8 g$ p7 C1 c4 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 2 y8 w$ g# L& {; b, n' W$ Z
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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, _1 I4 b  e. J" H1 @# M9 QAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 8 i2 |, x  e. c6 m) r8 s
/ [& m/ d7 d3 Y' O$ S$ 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  2 h' ~' b3 ?& L
  Y2 N- Z- Z! g; J( [- |  a
Published online on: Thursday, December 1, 2011 5 H/ G) V& P& ^

' F4 y* X2 ?( X! _Doi: 10.3892/ol.2011.507
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9 W3 ]8 ?7 i, c4 R& t0 d5 J% Z2 F, gPages: 405-410
) y- s) z* U9 H% ?: i/ B6 u+ F9 ?. R; R+ N  t9 I. ?. x$ i6 |! P* I
Abstract:
: X# i+ {, ?# F. i( _3 ?! BS-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.- A9 u' K) |9 z$ w1 v1 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( @: @+ x' ?" f6 N
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
- H/ L: k, G, g: c+ Author Affiliations2 f: N# N2 j5 @
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
* S% Z- v' f. I* x( ~" M0 p2Department of Thoracic Surgery, Kyoto University, Kyoto - O& R; D9 _% |" E* f
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
7 A- J/ H8 V1 Z! L7 @3 {" W&#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 0 c' N6 |( h- R0 e7 t
Received September 3, 2010. 6 ]5 g. f3 V  O+ ?5 t
Revision received November 11, 2010. ! f/ g3 d3 e5 i4 d* ]. \2 n8 C7 M
Accepted November 17, 2010. # y. W9 `4 D3 n. B, m# h
Abstract
3 w( |' ^- w8 y" b- }" \- \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. 9 B% @, t' i8 u+ c8 F6 g8 i
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.
, b, Z( M# \5 Y9 F$ P- c* sResults: 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.
; {2 c& D8 {! C+ p) zConclusion: 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。9 U+ [1 o! E/ N
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( I* d' s5 T9 P: D' j
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% [5 v9 D' e; R: p6 z0 [
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 7 Q) L- S2 E4 z# v& X
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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。
6 `% P# M/ L& q7 J  X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
7 a+ i8 I  ^% a( J0 O: h- r( F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。
! T: O6 m0 i; }, ?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。- Y$ ~0 b/ S1 c4 X7 x
不错。

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