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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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1214052 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
  H# B1 R0 Y; n8 w. f! q7 KNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
% p! E1 k2 r. }' B3 P. n2 [+ Author Affiliations
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: x( f6 j6 _0 v' X, E$ T( b1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 3 o# ]* X3 ?4 Y3 j/ m1 }, V" R9 p
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 5 f8 t9 j' [/ w7 _$ ~! [0 N
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 7 }: A# D! R& h  f2 N$ m" O- o
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
4 a$ k, j' z( m3 Z' L9 Z+ ?! `# Z/ Y- D5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan   Z. y  n+ d5 f9 w2 K
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
3 \* @0 b/ S& X& t9 }7Kinki University School of Medicine, Osaka 589-8511, Japan & P5 p: ?$ X0 h
8Izumi Municipal Hospital, Osaka 594-0071, Japan
& d7 T. c/ D) x5 i4 j5 i5 T" y0 ^9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
  Z  x+ @( G  g3 j4 J; VCorrespondence 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
5 O  N: {" q6 y2 q5 v. jAbstractBackground: 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. , P4 [( |# v* D$ B: |3 c* v  ]
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 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 , |/ l+ c: b- ^" z& w

5 g8 P/ l5 h, ]% a& V( G" uAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
) |3 Y% t$ C1 T, D5 }( w& z8 A" }) w% v, u( r4 }8 u% [/ 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  
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Published online on: Thursday, December 1, 2011 6 [& X$ x6 \9 W
  `: j, o. H3 X
Doi: 10.3892/ol.2011.507 , z% {6 e$ G" V4 e! F5 ^, x

  ?( Z$ t) {8 s4 Z- ^Pages: 405-410 ; c6 W7 j* c1 }& p

" f: I4 F. _1 n8 @Abstract:0 {9 Z! k0 I- h
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
4 g  E8 h% f4 V. J* O/ H. r3 jF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 1 K4 g1 n8 x* T6 o) a9 e
+ Author Affiliations2 ?. s! Y- v6 F9 R2 A( K
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
. `2 k( x  _3 h8 l9 v2Department of Thoracic Surgery, Kyoto University, Kyoto
5 S3 o- S, s0 U0 q% J" ]3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 4 _0 s7 R# m* n# }
&#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
  k4 [3 \& O; h; o0 `! CReceived September 3, 2010.
& Q+ I+ J3 O( E$ X8 FRevision received November 11, 2010. ' x% s' q( e1 N1 R5 j" b9 [9 C
Accepted November 17, 2010. + a$ a/ b6 n8 D) Z- g) _9 \( t$ h
Abstract
. z, S: w% X( R' J4 p7 rBackground: 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.
* \% u; {$ \/ U- A3 i" J* aPatients 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 W2 R! |# l4 I9 mResults: 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. ) M* m" ^8 I, P2 ?2 K* @
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. * y7 g; h9 a8 a" q( p8 ]$ {. L
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。
1 f- l, j# A1 S0 Q2 K! H7 B0 t& E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
  |1 S. t0 p! ^5 v7 Dhttp://clinicaltrials.gov/ct2/show/NCT01523587- G' i2 @, v& V* Z
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC( N; ]* b5 R% l) P0 @6 w* @
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 9 T, ~: n* e) k/ [  Q
7 {, L& ]: ^/ ?; {
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。* K, g1 `6 B" O* H+ P# c6 ]1 K
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 0 H7 g1 S2 J( h" e0 J" Q
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。( w/ D+ H) i6 z8 C
至今为止,未出 ...

) x4 e) n/ w$ ]- |; w0 T没有副作用是第一追求,效果显著是第二追求。
# g( |4 Q/ L; o: J不错。

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