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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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1156428 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
3 P3 U7 ^- s' w9 Z2 F% S# eNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 8 `+ e3 F' o7 j! E/ `6 B
+ Author Affiliations9 e2 [& @0 ^  i* L( O" W

& _1 U! L, G0 y, s4 \; P+ S$ J1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
9 \2 c1 |) j# ~) s  z3 e! s. j2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ( l/ O; f: W8 b+ C2 t0 r4 p7 u
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
0 |+ N+ ?, Q+ {$ U6 F$ m. Y- \, I4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
; D: d4 M$ O+ k! V5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
( P0 z6 P5 Q+ }: Z& Y0 l" }6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
- r" q2 S7 M2 u* S7Kinki University School of Medicine, Osaka 589-8511, Japan   J6 H6 f/ E% [; \+ u8 P8 N! F
8Izumi Municipal Hospital, Osaka 594-0071, Japan
% h7 {2 u( p" {6 @9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
8 j" L6 _& \" A% E) |4 P! `. bCorrespondence 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
( W4 A- k/ g% {0 V! i  ZAbstractBackground: 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 $ P5 N: r0 p& ^: l

, f2 T2 y8 g2 R- V2 RAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 7 \0 f6 I3 J& G
" k7 Y* L2 O4 ~: _2 V; H# m+ P
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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) n& Y4 H$ O6 I: F5 r' oPublished online on: Thursday, December 1, 2011
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Doi: 10.3892/ol.2011.507 # u/ R  m$ M- V# m3 N9 c# P9 F9 g" Q) b
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Pages: 405-410 . s/ Y9 L" }6 t: Z$ O
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Abstract:
+ F1 `- W( Z4 A; @6 i0 ?% |# DS-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.2 q& G6 g; O5 g
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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: S& [: ]% _+ h& [
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 0 _+ h! v; V  Z+ Q2 I
+ Author Affiliations2 E' L1 D4 V6 C: i' L. w1 B% Y( \; `
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu / d! P7 t# {5 W' E
2Department of Thoracic Surgery, Kyoto University, Kyoto
: A7 k4 R4 l. T( w; Q3 e" c9 q3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan + y: ^8 L; j) j: {5 {
&#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 O5 ]# ^+ w. u/ EReceived September 3, 2010. $ ?: j$ f# ]1 Q+ k5 p
Revision received November 11, 2010.
8 b; t. F3 b# O4 @Accepted November 17, 2010.
- d) n; Y- ]+ W8 R, V0 G8 U! aAbstract
0 Q/ @- z5 r7 R: I; Q7 B) F& L0 E. Q: lBackground: 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. . Z6 b( q7 x( a: g( @- o( f
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. . l- b, y' U1 z1 X  M3 ^
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.
/ a" ]+ p& `+ [4 I4 EConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ! L) }, z! z& L# r
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。
. N2 U7 h  K' e! u$ |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 Chemotherapy8 i* ?- V; m6 ?2 R
http://clinicaltrials.gov/ct2/show/NCT015235877 B  R8 _& w0 t8 l
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC  Y; n0 G# x0 v! A2 ?; L
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。
4 T( ~! d/ x, w( e- J4 y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 : h* ]* t1 T" e- Y" p  @) T, g
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。# ~- R6 i1 f; V3 q
至今为止,未出 ...

" l+ ?- T! C7 ^8 c. s* q# W6 q1 |没有副作用是第一追求,效果显著是第二追求。, p2 V9 t% J( ]. z3 l. H
不错。

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