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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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1465331 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
5 e6 }7 n+ u; rNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
0 n5 t' l8 p8 _. f# e+ Author Affiliations
8 ~4 j+ Z) }. W" }& A: M' h3 C2 w
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
( E9 y7 l: J/ G/ ^, J1 i2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
! K9 o0 E, t- u  }( N3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan , i# q6 r$ ?( X/ ^& u
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
3 U7 K, j1 ?% H6 Z& s5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ! o/ @1 b" p+ _  ~/ h6 x/ {
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
% x  U& w9 D8 M; }) Y& j7Kinki University School of Medicine, Osaka 589-8511, Japan . m; ]5 s2 {$ r2 D
8Izumi Municipal Hospital, Osaka 594-0071, Japan 9 B2 |: W3 x* Y/ @- _# t: x, I$ ]
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 7 _% h. }* K( h$ G# O. T# S) B7 ]
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 1 Q! D) S% x' Z5 K) W
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. ; |# M" G. H& e! Z: h* Z

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 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 - Y: R6 v" k* o$ ]2 T

0 z6 G( ~( m/ J. _" ~3 y) dAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 0 @9 J4 z# b2 Z& H

- Y! g- H$ C3 f6 oAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  ! e! T6 o7 ^5 o8 ^& u5 g

- S/ N$ b5 e. `% {Published online on: Thursday, December 1, 2011
, N3 P& F* N* O3 u" @( H' `& v  A3 j. J% |& y
Doi: 10.3892/ol.2011.507
, q- Z* f! e+ k0 I  Y+ o2 D5 S' W# h7 F' ?! q9 k7 x) ]; j/ L
Pages: 405-410 & ?8 n- `9 {% n" ]$ _3 v

6 K: ^6 l# ]* R7 fAbstract:
7 ?$ [$ |0 Q2 B. q2 mS-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
+ k8 h7 `& y- Q: [+ p# D/ JF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 8 T, y% i0 _+ h4 o4 a; F
+ Author Affiliations
2 u5 J, P& y( v: w3 g# r1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
, E8 p/ ~( z+ ?" B2 \& ~2 S  l' {2Department of Thoracic Surgery, Kyoto University, Kyoto   w. E# {8 e. J) S% A' q6 J5 d
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan * n/ i* _& N# ?  d5 H" R
&#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
3 b) \. @  Z9 T) _) q8 VReceived September 3, 2010.
( D2 U! q- j) w- h4 H0 D+ T3 GRevision received November 11, 2010.   L1 R( V& C9 n
Accepted November 17, 2010.
& m& l$ s$ X- X0 o$ P3 p0 UAbstract
$ b( a6 @! y/ u# MBackground: 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. 7 s" m# U- Z/ g: A
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. 6 h3 M* n5 L4 z
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. " A5 u8 ~0 B- m0 D+ N1 H9 B/ Q
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。" ~. ?! @# l3 o, A! V5 F
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?! m" F$ l' b7 \+ p/ s2 s, v
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 g2 \0 C& J& n2 S" ^% K3 u
http://clinicaltrials.gov/ct2/show/NCT01523587! w: g: q9 E; Z5 }/ ]# M
3 Q- P$ A) x3 t  w
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
8 ?+ U% H8 g3 g9 b" @: {  t2 s( Fhttp://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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$ T- i- t  A( k+ ]3 _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。8 v* P( N$ u0 U4 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 , O% c, H1 S: w% U1 S  ~
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 F; [8 t; o( j8 t' |6 e, S3 W至今为止,未出 ...

! g' C0 c% V' Z# F没有副作用是第一追求,效果显著是第二追求。3 z- c* ^$ w! N( Q) w2 ]
不错。

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