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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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1224583 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) x9 p! Y; U& n, k0 e4 i7 ]
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 * w% S8 Q6 a3 z1 {
+ Author Affiliations; ~! M/ R; F. y0 i

1 p5 W/ X6 W0 H# C$ D4 k# I1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 1 d* L5 {" F1 ^- U, l
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
9 |9 u6 R; a9 D/ S; S5 m3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
  ~6 Y! _- l1 B' M! E5 @4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
" z: ?# T% m3 F$ V- h2 S5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan + [3 O* M1 L3 t  |# a) C" d. J3 J
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 4 E$ L* N0 r$ \# O
7Kinki University School of Medicine, Osaka 589-8511, Japan
! u! _, F* ~# d/ `& P8Izumi Municipal Hospital, Osaka 594-0071, Japan
. E% y: ~1 L% a8 ?# {' X) b- s; e9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
! M+ X7 H. q4 y: c! L  f, b9 c, y1 PCorrespondence 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+ j6 u1 E- o7 ~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. / @$ S% e# N; [  U8 p& Z( G
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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 3 X4 Y5 u! g& c
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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
( [* U: F$ j7 H4 i# x* _% v0 j  F# V9 X" e/ m" A1 X& s" t+ `
Affiliations: 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
& X5 S: P9 `; D! f" o' `3 u& c; N6 ^# T( \# y& y
Doi: 10.3892/ol.2011.507 , A1 f; T+ a6 u9 r" E9 T( ^. G
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Pages: 405-410
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% @  Z1 q$ k, \* @+ n# E2 KAbstract:' Y  A0 E: n" X% a. \' i, ?
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 population/ ~7 A% U/ M/ W& g
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 9 R6 G1 R+ n( }, P
+ Author Affiliations2 \# f0 v* d1 L! M3 X) ^
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
4 f1 A  I3 [: h! T! M" @% C; x2Department of Thoracic Surgery, Kyoto University, Kyoto
' \( E0 X) d" E1 k# H3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan % g* r$ {$ {% X1 B
&#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 t- w: K. e& ?, t' h
Received September 3, 2010.
8 }- r2 }$ c  I% QRevision received November 11, 2010. / r( }" R8 Z3 P: D7 X( p/ X
Accepted November 17, 2010.
. h% _# J) G6 H2 }, F" N1 O$ KAbstract8 f0 u) \% G2 |2 @& w7 w3 `' p% O
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. 2 P' y$ q+ ?) o5 W% X/ D& O3 Q
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 U3 E: G/ F: D/ n  v1 J% WResults: 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. ) `8 D8 D( Q# V8 |4 j" J8 p
Conclusion: 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。0 m% M4 {/ {" _4 x/ V
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# Q  g3 }- J4 H
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 D/ {3 t! H( |3 N% D. W# \http://clinicaltrials.gov/ct2/show/NCT01523587; S$ O( |- R- w" z

8 B$ {: C% f; f% y0 K' Q( u! p2 t2 cBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
, y& M4 Q5 {+ k6 dhttp://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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& u3 ^% ^+ U/ j# Z1 H4 B) ~0 q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。
) b6 i# l' A& ~( i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 1 _  g& {6 Q- d' ^8 T! c: k
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。
) V0 m  B1 j2 u至今为止,未出 ...
$ \( p( B" Y1 ^9 J" p% ?& U
没有副作用是第一追求,效果显著是第二追求。
+ w/ P* A. M6 ]6 j4 e& `不错。

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