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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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1183934 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
2 e% ^! k( U/ M. CNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 : F+ d7 ^, L# d; d7 |" P
+ Author Affiliations1 x* I; o5 O) _9 _0 O2 T

& a3 q) i6 y) s( g& L( o0 O1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan . k( o9 @# U; T0 g! m$ `0 y( N: Q
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
" J% G2 o: f  F, j0 S3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan : T+ M% {# t" {6 v9 n" s0 T1 F9 x# D
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan ! A* t) v% F& R: A8 k# y0 l
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ! t- B, w$ V* ~% Z* d1 o- v; N
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan " \2 s& ~- Y) N6 O
7Kinki University School of Medicine, Osaka 589-8511, Japan
% Y% D1 X  e, G+ ~- g4 Z. r, \8Izumi Municipal Hospital, Osaka 594-0071, Japan
! V* L- q: n" F7 B9 a+ U+ |6 V' H9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan . \6 D& R7 b2 E) @1 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 . A$ E" ?2 O9 H7 @0 A$ E1 B
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. 7 k$ e) D7 i4 y- H2 |8 |( ^

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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
7 X4 C: D3 Z+ P# r
9 d0 E+ z7 v5 u  L2 l5 pAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
9 ^; l3 M* q' P1 x( F/ Y: Z- v
  f: z* I* w4 f- TAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  $ a4 e+ d- K, o) ]
* E# _% l0 H6 S
Published online on: Thursday, December 1, 2011 - j" R8 o) `1 v8 y1 G

, a) }( L  v& B# K1 j; T& DDoi: 10.3892/ol.2011.507
3 U9 T; i) h: l2 v* ]( w* o* ~) E; `. a
Pages: 405-410
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# b7 s% x, R6 X7 t' k5 b& F3 bAbstract:
! A' n' `) R, x% xS-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.0 w. @! s2 o- L3 Y

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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
5 W7 W* o7 M% N$ H* `" Q" ]  fF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ) X! U! }# l  [: m0 l% D1 f
+ Author Affiliations3 U% ^+ J( o& U) o! Y
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
5 M; n5 i. W% c$ x2 T: P2Department of Thoracic Surgery, Kyoto University, Kyoto - j5 I' d0 f0 _5 r  S
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 9 z  K( b9 i+ r
&#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 E5 v) M' sReceived September 3, 2010. 9 ?/ |4 q) q$ e8 ^
Revision received November 11, 2010.
7 ]8 x) W4 i7 h7 iAccepted November 17, 2010.
( E- r& w  i- v% AAbstract
# f5 q, b  I- w7 E$ fBackground: 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.
% w9 S" q4 z2 r+ R; gPatients 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. ; S8 ?1 z6 S4 Z- I
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.
/ T% G+ p* O! c3 A8 `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。
- x; z( \' w/ R! F( R+ o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?) W8 m9 o4 u6 x& Y9 R1 s! I
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; E6 _  H" X8 j9 \6 j" C
http://clinicaltrials.gov/ct2/show/NCT015235873 f% v) U6 ]; W& ~9 I, A
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
' x1 Z& c5 x3 ?6 f' }# 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 * }; y5 W8 |3 F3 G+ Z: t- y
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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。3 J# ?1 K( d9 A" B% ~3 t' w
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 ; i8 }# E0 P* h1 `# y6 j$ a0 A
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。) N3 P7 H. M. x8 y: T1 y& t& |
至今为止,未出 ...

% |& |) z* q) g! ]/ j& {没有副作用是第一追求,效果显著是第二追求。+ v! n( V5 G5 X
不错。

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