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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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1154530 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 Type4 @9 w( ~" }. X8 T4 w
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
. E# u% A+ K& @. d+ Author Affiliations
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* e3 ]" q2 j' Q/ R& |1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
' N) {( V# A3 C# I- T2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
9 O! h6 e$ ^" j  g, n* }1 E3 ?# f5 h3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 7 z1 w2 ]$ w! ]
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 6 |( M/ \# p1 b
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan : D; D! [9 l( v, t" _6 p$ _: _! V' A
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan , w% y* C+ v4 W! h( z4 K  D( L
7Kinki University School of Medicine, Osaka 589-8511, Japan
& u% u7 Y+ o# ]6 z( {8Izumi Municipal Hospital, Osaka 594-0071, Japan # _0 F, j& G, ?# G0 j" R
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 3 k# n) d" U* d0 y- E$ v
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 . f) U/ c# a- d; r9 t: J
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 + }, x, _) s6 n+ n: i; q

7 P$ Z" A* j1 J! S$ tAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 1 J8 N+ R3 d% s* W; ]" w
* J0 e5 s$ R& R, i0 n2 V
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  + A# g/ o; Z* C$ Q
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Published online on: Thursday, December 1, 2011
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3 J) Y) U! P  R& w) N% LDoi: 10.3892/ol.2011.507 5 D0 h- X! q) A% D  b/ P' k
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Pages: 405-410
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" H4 A$ D4 V) e5 ~: _# r, }1 _6 lAbstract:2 I" Y% `0 a& X  z
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.
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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# K& [$ m9 |4 `' U0 H0 G
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 9 C' u  b4 ?# x5 K6 b' s
+ Author Affiliations; Y) `4 S( S; p( Q4 L
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
  _$ G# q2 M! h1 |  ?! g% X2Department of Thoracic Surgery, Kyoto University, Kyoto 2 X. L5 g% J' l1 n9 r
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 8 b8 b' l" }# a! x! D9 A
&#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 7 z1 M- c# i1 y4 T4 V+ ]4 a& B
Received September 3, 2010.
/ L" b% s& s5 i% RRevision received November 11, 2010.
0 b$ C* o& N& z' r  XAccepted November 17, 2010.
" o% ^8 q! D. V5 [9 L+ gAbstract) d! r# ]  ^& U; ^! Q
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.
3 ]/ E( q6 {( G; }# g2 Y* OPatients 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.
. q& i, X' H+ P2 M6 j/ PResults: 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.
6 Q1 O2 t* h9 Z2 c4 R& t* tConclusion: 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。
- o. x& _( x6 h7 w3 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?
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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; l! W0 B' q2 E
http://clinicaltrials.gov/ct2/show/NCT01523587! x" f+ I4 [+ y3 f

7 {) o5 F9 ^0 y) o8 t6 c. W# Y, R* `BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC, w6 T1 r( g! F" V
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 $ B2 M4 q6 z* |. O) R1 B" I

  L5 `, ]) \; e6 V7 e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。
% Q! V5 l% b! ?  O/ E  I* v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 + R! s5 p9 A" u+ [7 j
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。. _. D0 _. r6 y) {! V/ M6 Z
至今为止,未出 ...

9 L& I" u' C: Q3 N7 P没有副作用是第一追求,效果显著是第二追求。9 `( F% b) |/ s; E  ^8 S! E
不错。

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