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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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1308230 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/ v# `: W9 z  C8 y8 j% y
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
- X  o# r3 m0 k+ l" |+ Author Affiliations
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' W$ \1 l4 ?" E* }1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
* U  T& |: T/ K0 i1 o, D2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan % W1 q" D9 x. T/ S' o
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ) M$ Q" O7 p/ q# h3 ~  w
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 9 N3 B8 N7 t0 f" l. d
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
/ z0 I+ I* C0 W, d0 W4 B6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 1 {- R3 }( F0 u8 X
7Kinki University School of Medicine, Osaka 589-8511, Japan & i) _. s- @5 ]- o, f1 A
8Izumi Municipal Hospital, Osaka 594-0071, Japan . F* I7 E2 }1 Y( q
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
0 l, G7 J' A: g* M6 p) bCorrespondence 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 # i- M1 M! u' _. Z* s
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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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
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! J' H% k  d3 W  ~% z1 M1 c# XAffiliations: 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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Published online on: Thursday, December 1, 2011
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+ D5 Z, D7 g( d, HDoi: 10.3892/ol.2011.507 6 Y$ g+ }! v/ V5 ~  y. C4 l9 {
8 F3 D+ C; v% y; h. I
Pages: 405-410 * D$ c4 I2 W! @1 J" Y# _

' @' w% i+ m2 J7 aAbstract:
1 Y% `, A; w" ?" F& AS-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 population: L2 @5 O8 l' M
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
8 y( O0 C% B- z) V4 `2 E, I8 M/ C, N+ Author Affiliations
  L! M( d. f- D8 z% A( A0 u- O% Z1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 9 s8 u7 _2 y$ `! F# w- _
2Department of Thoracic Surgery, Kyoto University, Kyoto
: y1 |# \  f. _, w7 ~5 f( m* ]3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
9 f1 U8 q; \" g- |( 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
, _6 c0 e& c1 W# DReceived September 3, 2010. & p. X1 j5 W! m, K5 F8 [+ @# t
Revision received November 11, 2010. 2 A/ j' l: v/ H; c/ w# f" _
Accepted November 17, 2010.
6 ^# m& F# Z! t# kAbstract
" r. z- A5 Q& K: n# x# TBackground: 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 n1 b7 o. i/ _( \# d9 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. 0 m4 e1 K4 t  _) ?7 R- w1 b
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.
! C) c# v, W- V# @3 |& \Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. & \, s: z7 {, U8 f2 T
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。7 q" g7 L* _8 ?* _( b: s: t
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 Chemotherapy7 n& b7 C* i) [: v6 K# D% r8 E
http://clinicaltrials.gov/ct2/show/NCT01523587/ `" `5 h- k, V5 O- \

; {  p, h6 q" F# @- q3 I$ wBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
2 A+ `( T. e* @- I/ J3 ihttp://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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% b  E0 r5 R* V! R4 G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。- L" ]0 P9 E! x2 |6 [
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
2 D0 R/ _+ `- W# g: w# S2 c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。
. ?3 b  p5 n# Q/ h& ~/ L. G' e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。8 S" M, h5 L( J3 L5 k1 \6 D$ [
不错。

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