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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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1172327 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" q7 d6 [3 a9 C' w! r9 |$ q
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 7 `7 D8 T- a4 r4 M3 T& A  O* @, g  k, b
+ Author Affiliations
; C, p8 i1 H" w  R5 M# G# B- X# B! v. J/ F/ s" p! ?9 _! b. J! o
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
  @) \* i0 _) n" N6 O* k6 g- {. c2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan - {( a) a8 s3 D* G7 l$ _3 R
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan # X( U% B) E3 b! P% }5 b
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
% S- U* E" w: U) c- r4 D5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
' V0 Z" ~  J1 V: Z6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 6 ~) B& B$ r3 G
7Kinki University School of Medicine, Osaka 589-8511, Japan 9 t; @4 I! Z/ x# ^/ o2 B3 \
8Izumi Municipal Hospital, Osaka 594-0071, Japan
3 |' A! a2 E% t9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan / f6 m+ A$ K8 e! ?
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 ( [. t4 q: W% W+ v
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. & {" p+ H, _$ d4 N

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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 1 f( ~6 u( L* ]' B* z3 m' i1 i

# u  Y$ a5 ^" t1 K6 fAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  3 n3 [5 ?' {) {
' W7 ^: o  |2 n5 F. N! B2 j1 q
Published online on: Thursday, December 1, 2011 8 g' S, G" n( H7 _% b. z# q4 V6 G- |
1 E7 J# ?, }, n8 T, g
Doi: 10.3892/ol.2011.507 4 z0 R/ I! U( @( W
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Pages: 405-410 9 H, V) ?- R( m: W) U! t6 W

+ ^+ c- z# R( a# MAbstract:5 X5 ]; v3 f7 r7 ?! g5 v
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.$ U) k+ D5 m( p* a+ `7 Z

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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
7 n5 P/ I. l% B% l+ W0 KF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3   U  P# m/ X. X2 L; P% h
+ Author Affiliations
8 C8 `* G: b3 @1 d+ d! q  }$ O1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 4 r% ^$ P/ x7 a8 q1 f5 y; V
2Department of Thoracic Surgery, Kyoto University, Kyoto
3 x1 p2 H* J! ?3 J# K' C! ^" r- J3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
3 H" ^9 Y5 g# `$ `" w" G6 P&#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
% s/ X7 @% C( h8 L/ [" E+ g. q; l5 JReceived September 3, 2010.
$ `! F! i( U" J7 ]8 mRevision received November 11, 2010.
3 U" G. O6 |5 t' ?! ~Accepted November 17, 2010. 8 }6 O. ?+ s6 u0 g& b2 f* G
Abstract4 h. N6 T' P& k1 j7 c
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" C  t$ r4 D( _1 n
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. % M6 S3 T6 v! H2 ?: g5 p$ G
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.
) I% ?, C$ q# P9 a, ]$ ~Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ( D: |) }, K6 n* j
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。; j! Y& c: K% U/ t# X! u2 f
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?# ?$ Y+ h: E' o4 f
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
9 d8 k  J" A' s+ c) `' Ahttp://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
' D' [; I0 Z' S; _" ~5 ohttp://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。0 [3 e$ d9 [$ N% X9 x& X/ i8 H
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 |7 G, S) I% o9 h1 U
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。  U  g- T# g- E2 x  C/ F
至今为止,未出 ...

! c6 m  H# Z$ R8 T没有副作用是第一追求,效果显著是第二追求。
0 O2 J# @# p: H* T不错。

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