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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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1203225 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
' I' c  e; W# W# y: Z4 yNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
$ J9 R; i9 {) h$ j+ J3 c* ]/ L+ Author Affiliations) d0 I. W7 k# P
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
) n& o- h4 V( x( K; v, G2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 1 n2 i! A1 y5 C4 r6 ?& L" U
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan * i! g, Z5 Q" T* h7 c- {
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
' |3 j: A5 ^8 L3 B) `7 t4 }( J5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
& b, |2 E) V" q  |! ~2 K" O6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan ( F% T  \( d1 `4 K
7Kinki University School of Medicine, Osaka 589-8511, Japan
7 ^4 v# X7 b. t9 j1 }8Izumi Municipal Hospital, Osaka 594-0071, Japan 6 b5 w: v& n6 d" u, c/ u. H6 i7 H8 l* o
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 8 {/ {  B" k8 \9 Q8 k5 `1 f
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
5 z' P. N! [4 A7 z. 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. + A) @8 _) B7 t

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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 ; [+ U4 D6 T/ s4 i5 G& N* X

' h5 q2 `+ o- [Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
4 C& K# n. P8 c2 w' ^  b! }, s8 i% M
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  1 N$ e1 ?6 H& ^7 u/ D

$ k; z5 I+ ^. A" Y0 m& l( i. HPublished online on: Thursday, December 1, 2011
6 b: r" f& ~. v/ W5 v! l$ ^% v7 b" }# @& l: \4 e
Doi: 10.3892/ol.2011.507
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Pages: 405-410 * Q9 y$ @$ W: q( G

) z0 ^- {+ y2 I! H2 j" ?4 lAbstract:0 g3 i  D: y( y6 f5 O( J
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.. @% a4 p3 P7 }0 B, ^) s

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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) }! {& L+ M5 }  x
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
' }  j0 u  M/ }' w  `1 M/ W" T+ Author Affiliations+ ]- Y  d; I( S
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 0 x0 C* d9 y5 I% ~# h: @$ p! C. @
2Department of Thoracic Surgery, Kyoto University, Kyoto 9 Y* y) ]/ `# b+ N6 [
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
$ |" C( ]$ Q% h  K; J&#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 5 I& c' y  l0 ]6 C& z" _
Received September 3, 2010.
4 _/ O! ~$ {" }" xRevision received November 11, 2010. * {  S. T8 D4 A* |- [( M% T  l
Accepted November 17, 2010. + J& t" `" R+ P
Abstract7 ^+ \9 W/ k* i) [5 K; R3 z
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.
6 W; b! Q! g7 T+ f& {$ P2 WPatients 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.
* P2 D$ P& G$ l: xResults: 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.
" k9 x/ c( N& O, f5 VConclusion: 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。: |' J  f# o6 n4 Y& l
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?; s) g1 G& |) G
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
0 C( g9 k6 v7 I* E  N7 _& k: O* dhttp://clinicaltrials.gov/ct2/show/NCT01523587& M! H* [4 b: A0 C5 k
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
" d' H4 A8 y$ L( r3 x: Thttp://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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- |# V' B9 F( K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。& r0 ^! `9 s4 \4 Y1 f
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
( A. x4 ?' p! D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。
9 x! Z3 P5 u7 j: D) x* w  w* u至今为止,未出 ...

! A5 K9 D" ^0 ^3 |3 x7 a没有副作用是第一追求,效果显著是第二追求。
) ~" o+ B% V* a! }; d# P不错。

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