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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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1144768 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. f9 G$ ~4 {  h+ ~
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
& H# H9 H( N- T+ Author Affiliations: F8 A* C/ N8 r' \% [6 u
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan & g0 P* W  Y* }* o1 _  o
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan , n' t+ H& W% L  M+ ~5 y" ^# i6 B
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ) N; t; m7 T( ~) C! m6 ]1 c2 _
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
, g# u7 j4 F( l" R5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
( P7 ?% \* J! M: }, e/ H+ a6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
! z4 w" i: r0 E8 K7Kinki University School of Medicine, Osaka 589-8511, Japan
5 L7 o5 }+ T# p% Z9 \+ a7 J8Izumi Municipal Hospital, Osaka 594-0071, Japan
- r2 X  E) a$ r7 z+ M2 J9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
: i! T5 M, }. R( n4 J( S& r( X4 ACorrespondence 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+ Y0 y: n, ^; H! vAbstractBackground: 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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( W; s0 F- F6 N, y4 ^0 xAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 3 Z; b* ^. G6 R& Y) E5 W) ~  _- a

' z+ o- q+ d8 m3 S# B- H7 s# F* VAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  * G" r$ O. |% Y8 p' Y/ n
: f! |' N1 S, R  k5 X2 G
Published online on: Thursday, December 1, 2011 + R4 o8 _( T; ^' ]0 m% e; E( E$ n

" R1 x% P1 ]. S& k5 D# ^  r2 {Doi: 10.3892/ol.2011.507
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$ U6 t7 q. Y4 h# a' P7 mPages: 405-410 9 C* c; O, k7 A, w3 F
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Abstract:6 q) b- B* i* A
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.6 o: k, ]5 _  B& @
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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( p+ j  g2 O3 q' {7 F: D6 X
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ( g! W1 G# O% q: ?4 D
+ Author Affiliations% H$ t( [+ r( S
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 6 T# D; D& L. _/ i
2Department of Thoracic Surgery, Kyoto University, Kyoto ( u/ ]. N' }9 J8 ^' u* V, ^
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
* f% ^3 ?. s8 S6 m, H( y$ n&#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 ?4 `* F- d0 Z4 @/ U! h" BReceived September 3, 2010. ; E  C* ^' k1 J1 U! ?; v! G4 B
Revision received November 11, 2010.
/ w! X/ e: F! m5 s1 h& h7 k0 AAccepted November 17, 2010.
: n  G- K# `5 G1 e. U; C( nAbstract0 @! c0 J' q0 s% [5 T& f5 J' ^1 \
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. , f$ @" j; j- R3 _" ?
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.
+ s4 `. |5 r' A0 t/ yResults: 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. ' r/ H* N6 b9 ^$ K
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。" V! Z2 m. V# M4 I
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?% Z% {" S0 w, r$ z0 o7 r- N# c
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
  Z+ ?! M3 Y1 o3 M$ Chttp://clinicaltrials.gov/ct2/show/NCT01523587- V3 W# e6 M1 A$ p/ H

- R2 K0 U) a# @* Q6 f, I9 t+ ~$ {BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
( U- ?/ M5 |; D! [, z' r3 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 ) t9 s2 t& z4 y+ V) F# v) M
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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。
; C* ]. D/ ?' s+ B) B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
/ r: o( H. U- o8 m) h$ a5 ?* _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。! }5 M( n$ Y% j' g2 J& b& H
至今为止,未出 ...

7 C2 p7 P1 u: K+ b" \没有副作用是第一追求,效果显著是第二追求。% s, n& i$ }& @% z0 \0 [
不错。

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