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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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1243377 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. a/ e+ M3 ~" A
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
- z" p7 |" Y3 a' \! I, m3 @8 s4 u+ Author Affiliations
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9 J+ u* I. _! }1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
$ d1 D$ u8 o0 X  r9 m2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ! U1 X0 _, F( M& S* s1 {
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 5 h3 b7 E4 ]0 J4 `
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
, z/ f3 a7 ?/ h1 K) K2 X8 t3 P5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
+ E; K6 N( `! w0 q9 S: E: h8 I+ }) h6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
0 H1 W. b& v& ^' m* `$ l0 b7Kinki University School of Medicine, Osaka 589-8511, Japan
. g6 S0 ^5 h/ n4 \8Izumi Municipal Hospital, Osaka 594-0071, Japan ( [$ F1 Q& ]" r
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan   f, R2 s5 i& W. n! }8 S
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   O  h' K4 K7 ^4 s; H
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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3 `5 v$ ?1 R' x( x  e( r+ X! YAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
0 X1 h7 n; X& Y( H
- k* [/ B4 I6 z, ]7 iAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
$ F/ M: Q9 J% O: M
& M1 r1 ~0 Q4 M3 S% {; z% DPublished online on: Thursday, December 1, 2011
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; |$ q9 u# V; E( W4 O% kDoi: 10.3892/ol.2011.507
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Pages: 405-410 ; ]$ F4 `# D' I) F! b% L

# @' |* I5 ^1 ~( I9 lAbstract:
. o1 B. I1 {% N6 ^# q- Y) s+ CS-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
5 R7 F$ k5 ?2 _, LF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 7 A2 T" {6 E- A% ^' `/ j6 A
+ Author Affiliations
" b) Z6 T+ O( I, ^+ U% S8 h6 \1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
: q. G+ |5 i6 P5 n  u5 ~, }2Department of Thoracic Surgery, Kyoto University, Kyoto
  [1 p6 \4 V% l/ |8 K0 Y3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 9 {- r1 e' v7 F7 ~1 a5 W
&#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
( g' `$ X2 L+ K$ mReceived September 3, 2010. / v( C, ], q. z. ?! g
Revision received November 11, 2010. 9 }' Z$ ~; `" Z! v
Accepted November 17, 2010. " d2 ^2 Y$ a3 R  d
Abstract
! f9 i* S. v- O& ABackground: 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.
9 n  Q8 \1 H2 q% G* Z! QPatients 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. / N" m$ Q) U, y- ?$ ^4 G/ c
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. + e1 T( p8 ^& w. Z& k( Z* U
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. , B" c# i8 R- X9 H' E+ O1 g- ?$ |
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。
0 [0 C: h- q& M1 M2 t1 m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
, T1 @; z$ D* h) v  H8 w! |http://clinicaltrials.gov/ct2/show/NCT01523587
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9 i  I% g5 S" J+ S2 x' h4 ]/ ZBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
3 d& n) Q; b- G) h( H8 Qhttp://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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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。
7 x/ c7 M% o8 m/ a7 U" 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 ! C  [7 h7 y# G" y6 o9 U8 r
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。
3 h" T9 Q3 R! \2 {% K" T! `& R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。1 T0 O" k9 X& W1 z4 H. [/ S( K
不错。

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