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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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1141351 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! F" O# l& m$ l# p% w$ Y* l: |
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 4 p6 g7 w1 a/ y! M$ V3 ?8 \- X
+ Author Affiliations
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6 x3 ~. `' I& \: E% v1 J: h1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
: O. `( e. q! Q8 x6 V2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
0 x5 A; A. e7 R4 A; k3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
. k1 E/ x* I4 b  F, J/ {8 c4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan + Q8 j6 m6 M1 p3 j' T# A4 r
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan . g9 i! Z& l: J3 _3 M3 B
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 0 B! }/ \# W2 A# O9 s- l0 B) ]3 q
7Kinki University School of Medicine, Osaka 589-8511, Japan : X% j% \1 G. Z& g- n) S% l6 O
8Izumi Municipal Hospital, Osaka 594-0071, Japan
% L" Q! v3 G9 }6 ^4 y, D9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 7 y7 Q' y, t8 @5 m4 O- I
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 3 _) d  d( I( e; g9 U) [
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 8 }0 T3 c8 C* y/ d6 O

" H% k; E$ V. y& [0 {' }% QAffiliations: 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 , t. b1 h3 ?4 M
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Doi: 10.3892/ol.2011.507 ) o3 t8 w  X2 Q7 Z$ B7 D

- G  {& x2 z# _/ f; \3 ^7 nPages: 405-410
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% u# _0 L6 Q! V2 }; W# P8 A& eAbstract:6 \4 d5 `% t1 m; F; B4 r  @9 d
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
# J7 y' X% z: O' T- X: u' h1 l5 a( ]F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ; ~; K( ~3 _) ^/ J& L9 ~- I
+ Author Affiliations) N' y# {) J( i7 g1 G- X6 U, z4 J
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu + a1 n$ H' S) _- e2 K
2Department of Thoracic Surgery, Kyoto University, Kyoto
6 F; b2 N) y3 [3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
5 N, y: G2 _3 m. K&#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 D9 G8 P1 ?9 h; E3 n$ GReceived September 3, 2010.
# D8 h4 O9 b5 u3 f5 B0 h* [Revision received November 11, 2010. 1 z2 Q  C* M& q- G! j. }3 t  e1 R' m6 ~
Accepted November 17, 2010. 9 P( ]5 F; T& G
Abstract: \& V1 J0 F+ _+ S( Y1 U9 m) S
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.
  H0 M( J2 y7 q4 A1 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.
5 X- ?6 a# M$ m1 _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.
$ s% P- y; f* d  |' ?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。
4 Q! m9 K- W  z9 y( t' {( X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 Chemotherapy4 e" C' f/ S3 u! P5 n' b
http://clinicaltrials.gov/ct2/show/NCT01523587# D9 K4 S9 F+ J' {& `% c% y

* h! q& b7 x6 u  D* `1 ~4 F  PBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
5 w4 ]6 [0 x+ J, i( U0 v- J+ bhttp://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 # {. ^1 n$ ], ~
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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。
  b/ v$ G6 v9 @3 E( J' f. m) A& Q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 # P: C5 s- |+ S* L) m% Q* S6 x
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。
" G1 E3 N0 b( Q7 h4 Y9 T* d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。% ?. H1 L8 k5 W
不错。

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