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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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1250037 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" L+ `9 r4 L% ]; _6 D: G" i5 e
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
' F+ T: D7 |5 B+ Author Affiliations
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' [; r4 w& i  P1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
0 y- H% d4 v+ R! j2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 5 }! @. c. V7 q- K) I
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan + \! A6 B6 }" b7 ~) V
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan + z6 {, i3 \5 B7 ~) |. G9 u
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
& W$ H6 E+ f9 K  Q6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
* P7 ^% q/ [3 \8 C9 S% E/ \7Kinki University School of Medicine, Osaka 589-8511, Japan / [( O* U8 M7 S* g" |% e, e
8Izumi Municipal Hospital, Osaka 594-0071, Japan
0 S! V+ {0 b0 P+ y2 E9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 9 r" Y# c, e6 c3 n. W  d5 @
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 & |7 j" B7 I0 p0 N
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. 8 E9 n0 x# S( Y# q
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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 * e( f( P- P3 {' ~, @/ [

7 U0 \3 O, t' UAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 7 j* F, p! L( O
: f" u7 N6 P& G" I8 C8 d4 @. K- o( R
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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: G+ U- u# i) ^0 Z5 C6 ePublished online on: Thursday, December 1, 2011
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/ T0 x4 T2 ?) ^" mDoi: 10.3892/ol.2011.507
4 Y2 E7 b$ B6 Y  L3 ]; _2 ]6 N, I! [$ C
Pages: 405-410
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Abstract:, _( _" b. M2 j" W$ f4 i
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.+ x5 g9 r0 h, \3 r8 @3 `' O, N

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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 population6 Y$ }; ?8 u# B; l1 @7 x. H& ^8 d
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
) a) ^* S2 Q" c* x1 o+ Author Affiliations; G" i, O& M7 d3 C' S  o6 G, l; Q
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
- y3 u2 \4 L1 U/ [2 E/ y# q2Department of Thoracic Surgery, Kyoto University, Kyoto
: T- f! q& B$ i  x% |2 a  T* b' j3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
$ @- `# c0 w: m) P  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 ' M9 @8 D. Z8 l2 _* N
Received September 3, 2010.
9 f5 t( t  M3 [9 b: JRevision received November 11, 2010.
- N" ^$ N/ }7 ~2 eAccepted November 17, 2010.
# B6 P8 ]! a+ y( gAbstract
( {" f" S, ~4 ?& j' M( oBackground: 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. ; C! d' ^1 D( A/ P' M6 d  u
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.
9 d- I4 ]' }3 N$ W2 k6 qResults: 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. $ D5 t8 N: s2 Q6 D! n4 j
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. : W  g& k. {2 M, Z9 d
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。+ A7 ]8 G; n4 X2 a4 J0 y
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
+ M+ a# P( y) b9 ^7 r2 J' n0 yhttp://clinicaltrials.gov/ct2/show/NCT01523587
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9 a- D) ?" P  E- G; DBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
& e6 f! K' E7 D" Ehttp://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。# Y* \( G! T+ o* v7 @+ S
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
& N! Z- i4 c4 j( j( r$ g. n3 _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。
" H$ b0 R6 Z# z; ^- ]至今为止,未出 ...

& H$ x8 N4 Z$ e" I, O( h没有副作用是第一追求,效果显著是第二追求。- H/ `. Z5 l# v5 A
不错。

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