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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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1464951 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" ]9 V: |9 ~* ?4 \* i
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 , |0 g7 F$ F% f. k6 X
+ Author Affiliations
, B9 @' e1 P2 C. A# w) g' t) D$ Y+ S5 M0 T9 T3 V7 M9 T% A% |: |" d; }8 |
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 3 _/ A; r# a7 j6 Z; P
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
7 \% P" z5 _, c  R3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 1 f( f/ T+ a; P) [9 M  X! [
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
; P6 V+ e9 ^2 ?( r6 c  f# |. y5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan / v" b3 m2 y& {/ Q, Y7 t) u
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan # h* ^6 ^5 v; K) [
7Kinki University School of Medicine, Osaka 589-8511, Japan   ^$ C, \, j/ {; ~# B; u
8Izumi Municipal Hospital, Osaka 594-0071, Japan + w. }+ I: h) ~: W* {8 N
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
. n, v0 R* ]; t4 }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
! t% |! a' g& |5 v* d" T: y  Y0 ~5 i+ KAbstractBackground: 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 # h1 U5 k/ `4 o) o1 t0 `
2 y0 I1 X0 }* {& ~7 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  8 I3 [3 @# V* K' G. s, r# j
/ i: c: ^( K6 t$ o
Published online on: Thursday, December 1, 2011
/ l+ ^' R# \# g8 C* E- P0 L/ V  {* z% i
Doi: 10.3892/ol.2011.507 5 J) Y, d; i# G# i
5 ~5 m+ F; e  f4 {: l! c
Pages: 405-410   g3 s2 h! i4 A* V! d! |: n2 V

/ ~0 @' q/ L, tAbstract:
) r4 n# u  k7 V" c/ AS-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% m1 c/ }5 j4 o$ L$ p
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 2 ^2 S' ]1 J  {7 Q. D3 W
+ Author Affiliations
+ ?. f3 m. r# m% G1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ! L2 @: N& _' Q( \
2Department of Thoracic Surgery, Kyoto University, Kyoto $ F# a# e. Z) |
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
. W3 W+ a' Q: ]2 T&#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
: K0 m! `% a( m  ?+ ?2 iReceived September 3, 2010. 0 ~* [3 _" I; d9 G8 j1 h* Y" _6 K3 S; L8 L
Revision received November 11, 2010. 1 v; B7 K4 j; _4 C4 P4 A8 p$ C
Accepted November 17, 2010.
2 I% D+ v6 H9 [, Y% ?Abstract
8 s) w  W/ b& D$ QBackground: 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. * e8 ?4 N! M) a. z
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.
7 Q) W6 ~! F$ H9 i6 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. " t! A- S( P; z/ P1 y0 m
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 7 V* t7 n: c0 _: D& f
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。  A  y6 H2 u9 r! T: 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?# _; t4 I' U+ U* a) V/ G3 q
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
" N+ G. x, P' M, ahttp://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
$ L$ x* z, r$ x0 {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 $ b( I; w. K' E$ w/ @5 E# }" b
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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。. D- L+ P1 v: P, H: 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

$ `( \# T  E) c1 Q( E' s$ l7 I9 w' P没有副作用是第一追求,效果显著是第二追求。2 D9 P8 i. {* e$ R: ~0 h
不错。

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