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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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1259194 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 Type6 g. b# \' f7 n$ o. B: v
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
6 P& K6 t  ?! W( F" R8 W3 I+ Author Affiliations8 Q1 g( y' P! \3 f4 n4 v
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 9 |/ Q; M9 J- c9 M
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
- _/ Z  h4 ^4 z) Q4 U# R4 ]3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan % P6 g  f8 T( U, a  ]6 C3 V
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
: \! v( Q$ w9 q7 p9 [7 F5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ! {- ~1 v8 \# U4 R
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan , m5 E! M7 w- r8 D6 j3 m
7Kinki University School of Medicine, Osaka 589-8511, Japan 7 \3 C+ ~! m* _9 p. D2 C
8Izumi Municipal Hospital, Osaka 594-0071, Japan 8 |  S0 j& P  i' F6 ~6 K5 {
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan ! |0 p6 Z6 X2 p, G) A
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 * L4 K) m3 `9 M1 B
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. / L; n+ k, ]- U7 O4 N

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 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 + E1 ^, F* I& B) N7 B9 ?; I( A

( A  `. e- I* e" k5 k% f3 f8 C+ dAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato " v: i. e  S2 b1 d. |! s! ?6 [
, a- ~; C# o/ C  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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5 o. E) o) ~: U5 KPublished online on: Thursday, December 1, 2011
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Doi: 10.3892/ol.2011.507
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1 U" |( y& [5 [Pages: 405-410
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Abstract:2 X! j5 O# p' H% g8 }, _; E) F
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
7 |2 N* {1 T" E& h) o  lF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
) \, o1 T$ L% L( |  R3 O( E+ Author Affiliations
% D, C4 u9 u6 c1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
( F/ A: m& e6 P: h2Department of Thoracic Surgery, Kyoto University, Kyoto 5 P! t1 `  {+ b: |
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
  t+ v# y/ _; T$ j&#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 9 M7 r% ^/ f% R. g' P. h6 ]2 \
Received September 3, 2010. : S3 W; s- v$ s  @/ u% L
Revision received November 11, 2010.
- {2 O4 w) {, q, O2 f7 y. y5 kAccepted November 17, 2010.
, n8 Z9 M3 S6 u( q8 `Abstract8 m0 Y- L. j. j- @, V4 a
Background: 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. 9 O% I. L7 O* `" W5 x/ 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.
. {2 Q9 c; o+ i) m: L. U0 f5 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.
' |8 R5 @3 z/ @% H  g: G) ?! GConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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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。
0 f- Y$ j) S4 f! J7 _: 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?7 `; K* }5 V; T0 m) m6 c
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
. ?! `* h1 _# O; \2 ~; e8 Jhttp://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC  ^1 e  p- ~6 |
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( K# e7 F$ s- N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
" E/ y  G9 A- d8 U0 W. L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。
" W6 ?6 ]. @5 t* g* l- |至今为止,未出 ...

# ^/ N; K, R* |# }& X( F7 F没有副作用是第一追求,效果显著是第二追求。
- q8 I2 U6 D% a' z& e9 U! H不错。

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