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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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1401468 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 Type1 \! }! q+ g! B, S8 g) T
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 3 t$ S, K' N( G* K1 M
+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
% n; M8 O% y- w9 [3 ^2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan & L* a2 S+ L- f' d6 B3 P& T
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 4 t7 _0 k. E  K  `% i. N
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 7 t6 g5 a& A7 m* \' t2 r+ o
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
0 o% p; D' M7 G- n: v1 i) p6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan + J7 p) t! h; T: T
7Kinki University School of Medicine, Osaka 589-8511, Japan 3 S' r, b7 o( y& d9 g1 l0 o6 q5 S+ I
8Izumi Municipal Hospital, Osaka 594-0071, Japan
6 B" }" j; z2 c* t& I7 x( y9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 7 U( ?( V$ c' L; ?
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 ; P3 _* |, y( Y; D7 |* q  u5 P
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. 2 q- u! g" p( b: ?
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 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 ) S* p5 Z$ h0 T9 s

/ F& k. l0 S! y0 e' [! EAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
; i3 T9 R7 q/ \" q$ a& M3 I& G
! m- ?4 ]7 ?7 A+ p7 n: d7 \Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan    n, ?3 f" I$ Y, L2 T) ]5 E- O: K0 R

6 H* [9 |3 o7 D9 }8 IPublished online on: Thursday, December 1, 2011
0 x1 |9 d& M- G( C0 p
* T4 E% v- r) \8 _6 Q6 NDoi: 10.3892/ol.2011.507 / u- m: G" @: N% U1 i2 C6 X

0 `3 ^! C( ^$ U9 j  l) u' hPages: 405-410
* J5 U3 {: l& j. C" o
) D5 l% ~8 u/ e4 p! ^$ g; XAbstract:$ [, a* u  D1 h) j: }3 R
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.4 Q( K! Y1 ^* x1 L, 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 population3 y, {7 ]$ N4 C1 w" W
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
* M; p4 A1 C6 F+ ]- ~7 G* V+ Author Affiliations
, Y* d+ k2 ]: q# j1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
/ }9 W3 c8 [' @" u2Department of Thoracic Surgery, Kyoto University, Kyoto
! b7 Y: I* u2 I9 V3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ) r- @1 C0 @- g; b. k) M0 L! u+ D
&#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 V* d  Z% K' `: h' b( p; T/ V2 YReceived September 3, 2010. % l; e* i1 A  t. x
Revision received November 11, 2010. $ f* l* U1 q! K" ]0 c
Accepted November 17, 2010.
" e" h# u% w4 q8 k5 j0 MAbstract
' S. [( {; B, X. O! o( zBackground: 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. 8 U' Y5 N7 L  X# U
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.
* s3 l! V' M: f9 @7 c0 cResults: 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. * Q7 T3 o3 }# s; J4 h
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 2 r4 N7 y  |4 w( f! B
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。; s1 G  L1 d, i" }: }& `1 K3 S
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 Chemotherapy! |' k% q/ K# K: D8 r' z
http://clinicaltrials.gov/ct2/show/NCT01523587
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0 v9 L& H* e  j1 a: d& KBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC* Y; F6 Z- A; ?/ z: ?
http://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 6 d% v' G3 a. t- _8 M0 y! a! E
6 {& h2 C9 o% _* Q' Q" g4 t- j' `
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。
1 `6 ~% X1 L( j! X) X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
# Q( r, N2 V& t) c' ^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。1 b  x: S6 w; n/ Z, O6 b" F8 p6 s
至今为止,未出 ...

9 j, j; |3 O  ?, e# {5 d  q8 m没有副作用是第一追求,效果显著是第二追求。- E1 K! ~6 L: I8 ?  T5 T1 b$ ^) N) t& T
不错。

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