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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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1365311 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" ]9 g+ O4 C# z3 E& G
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
- g: x% E% `- }$ I+ Author Affiliations" n/ O" m( G6 P5 T; }; o! Z

/ {) f3 \  p. O+ ^* y0 J1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 6 w; w; g/ k2 c# H* v4 M, R0 `  Z: E
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 9 ^* I% m, b& Z  ~4 h( \
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
: O" M/ `6 K2 ?$ ~4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
  g( @8 F4 S3 ?5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ! w4 ?+ n- y; C2 y* g5 r  m
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
2 j/ v, Y" m! a& g9 n( m7Kinki University School of Medicine, Osaka 589-8511, Japan
# Q9 v& ^  Y0 `- F: J8Izumi Municipal Hospital, Osaka 594-0071, Japan # A+ C5 I! B- l( k
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 5 I8 d3 j" E, T: d. W3 ?0 E4 `
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   ]# w+ {+ M9 x- W8 a9 v" T
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. & E6 k; f; L# c0 w4 E
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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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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato   |- r* C; u7 Z! W' {$ J

) F. R3 V% Y* J; @" HAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  9 D7 M# y8 ?7 j8 N

7 {5 z. J8 H& m, N/ {3 DPublished online on: Thursday, December 1, 2011
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: @7 d: _3 X& C; m$ q4 JDoi: 10.3892/ol.2011.507
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) ]" q( d6 j; `" dPages: 405-410
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Abstract:8 W0 l2 N9 @2 \8 p  M( c
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 population0 P8 [1 H4 N5 f, h# D
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3   c2 T+ e* Y) \1 Q) k. q
+ Author Affiliations* q+ d' l6 |5 W4 A7 J7 [9 v2 @( ~
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ! S/ _# m" ~8 t' a0 \2 g
2Department of Thoracic Surgery, Kyoto University, Kyoto
) o# m) P. V* w3 ^; P" o3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan / `: k/ j/ L4 b& L9 g
&#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
6 R/ x5 |6 D3 KReceived September 3, 2010. ) ^0 F: a( y0 Z/ f' W1 G) v
Revision received November 11, 2010.
, i. }* r4 l7 X4 qAccepted November 17, 2010.   k7 \2 R3 L$ A7 C  k8 H  x. ?
Abstract
0 |+ `* q; g9 j, t) bBackground: 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 j9 z7 S- G2 i3 PPatients 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. + q2 U7 E5 |5 _- o
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.
( L1 s! D0 r/ G, m: }4 m0 S- Z- YConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 1 [6 Y; U% Z  {0 n8 V$ ^$ \% 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。
2 l  x  J' D0 Q6 w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 ?4 E& V! ~  Y5 Z2 {' [
http://clinicaltrials.gov/ct2/show/NCT01523587
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8 e5 v( Y$ Q* X* fBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
3 k7 ^" w# `# ?" j. shttp://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。
9 h$ |! h7 R# e) h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 8 h6 `# e4 [6 q) v* 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。
# @9 K# Z5 N6 b  R7 C至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。9 `) x! m8 S' s5 W
不错。

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