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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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1204323 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
) x9 Z6 o) E1 d& g& |8 MNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 3 V7 q/ p, l/ v3 G/ a
+ Author Affiliations
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- p! W9 X% k# k8 {+ F1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ) b# B) x: @8 W* o+ I
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan / ?, x) t' E# `! [6 U$ m
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
7 [& V3 J/ L) R- u4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 9 C+ I+ a# @4 T, ]- A1 e( r
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan , @1 z# E2 _$ b7 a1 \' w  |
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan $ [& F! m% R% x/ s* T. U
7Kinki University School of Medicine, Osaka 589-8511, Japan ' n  \8 w. c3 M6 F
8Izumi Municipal Hospital, Osaka 594-0071, Japan
+ i( o1 g1 a9 k& Q  n9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan " O! G- j" v: K1 z/ x* k
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
- c8 b* A' [* R5 k# Q. ]+ Q. q+ uAbstractBackground: 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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) F& `! M* V* pAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato + Y* x( f' K. B# W' ^) A& M: U
2 m$ x. ]2 H) Y- p$ I
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
3 V9 k5 G" _. ^2 \
, h9 V  K1 x# }. PPublished online on: Thursday, December 1, 2011
% U* P7 r% {$ ~3 ]. T, G& I( [' Y. U, l( W: }
Doi: 10.3892/ol.2011.507   f; d0 ?" b7 k+ j' a8 Y& {5 S1 f
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Pages: 405-410
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Abstract:
4 t0 O# B' ~+ A+ O+ E. }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.+ Y% s  a+ k1 Q2 x: f/ v

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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
2 n5 R1 J0 e- K5 FF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
# _, [- B9 s0 U* }& D+ Author Affiliations& H- H# J: i7 Q5 ^
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
9 Y4 I! j; t  Y% J3 a9 q& p3 o* y, v2 k" S2Department of Thoracic Surgery, Kyoto University, Kyoto
" V$ b' @8 d/ ~! R3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan # X9 u' J5 ~! K9 O. m7 b
&#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 J8 A" Y% A0 _- f  a
Received September 3, 2010. 7 X4 L- G* |' T: w0 l/ r9 {, A
Revision received November 11, 2010. 4 L# \0 {" H, u7 e4 {
Accepted November 17, 2010.
. @' o6 y9 @; Q$ b; F# |Abstract
+ g1 q/ n0 {( l$ e4 G; yBackground: 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.
8 z7 _, Z! I; z  d1 M9 L% \; ?' 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. - G+ w; y2 w7 E  S+ V, l
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. " Q" S7 l3 G- @; ^& Y2 V
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 2 x' ]/ h* K$ l, W; h
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。
, |) H9 A/ V0 e  V0 a/ 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?, i& S/ D# b/ T; N/ i8 C# j/ l
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 Chemotherapy9 u0 Q! b: O+ U5 ^) {7 X
http://clinicaltrials.gov/ct2/show/NCT01523587
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& d' X3 j& Y/ G7 xBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC/ `5 j2 C5 I9 h4 R
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
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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。) S  t- i4 s4 ~
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

1 s" y+ s. h" h2 C4 f没有副作用是第一追求,效果显著是第二追求。+ N5 D! N/ L" u. [. k" A8 N* T/ s
不错。

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