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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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1119480 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
* R5 X! g9 X% a4 Y  x% B( f% D; mNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
' e4 }9 v% E: L8 ]4 Q. O+ Author Affiliations
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3 `5 u$ A! Z. Z1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
# n, G3 i2 J1 c% e5 z1 M, U4 {2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
! [% e8 i' N9 G! O3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
5 |& @8 U8 j/ T4 O' |4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan , x/ ^5 Q  ?+ u9 ?! U5 y6 C
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ) I- s) f! M0 r' f4 R& w
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 2 S* d! f, Z6 A! c
7Kinki University School of Medicine, Osaka 589-8511, Japan - {- p( L* a* A4 I* w1 q$ g
8Izumi Municipal Hospital, Osaka 594-0071, Japan - j$ J6 A. [; I5 \, s# q
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
$ g, t; J' t9 x4 O8 g1 d6 }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 ( c+ _1 F' g$ e: S4 |
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.
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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 ! ~! g  v, \  Q: P: }7 |! |
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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
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. C* f* b  h% a  z7 u( T6 |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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0 U. Y3 ?) J0 ]' g6 k# d7 T: X$ lPublished online on: Thursday, December 1, 2011 1 w0 Y( Y6 m8 [1 B" U4 r
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Doi: 10.3892/ol.2011.507
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Pages: 405-410
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Abstract:
  C% }% |7 ~; O4 o: uS-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.% a. g) c& Y0 G  d4 g6 C

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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 population4 K2 n8 S0 h$ b$ U, S
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
7 Z+ S! ?' L" q' u* X6 o8 x+ Author Affiliations% X+ K. E/ V- X( x
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
' C" I0 K( f$ n7 A. X( S& L) c; M$ C2Department of Thoracic Surgery, Kyoto University, Kyoto
. [2 r8 L9 w0 Y, f2 w/ W* ?3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
# H7 h4 h  O+ l( ?/ ?4 E2 n2 G8 O' X&#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 M3 Q5 Y- @6 Y, AReceived September 3, 2010. % t2 o$ F/ ]' U* H8 {/ c
Revision received November 11, 2010. # K" ]1 P8 {& j$ P2 e4 f
Accepted November 17, 2010.
0 m5 v0 g3 G3 J! _  g# @Abstract
: B, ]; `0 }" i9 G5 qBackground: 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. % Q8 L) \$ ^7 S/ S% _) F0 C. m6 K( P
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. ( e6 I, @/ g: s$ f( k5 c
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.
- J7 Q; {: b0 u9 U; R4 NConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. - ?0 ~8 D& V4 M7 ~: V
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。
% [' A& U$ Q3 B' z6 ^" U4 I+ g: |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?. {' T3 F$ J9 z* f
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 Chemotherapy0 g  f' ]; f" |( j# |
http://clinicaltrials.gov/ct2/show/NCT01523587- c: K+ [( z$ y2 L8 \

1 P1 A, j+ m* u8 o- a0 A1 PBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC3 P& T/ s6 G* ]7 V3 v" ~
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。
, u+ }8 W* H6 o' s; e' P9 u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 4 ]7 P0 `4 M& l2 ~. _) U8 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。
* P# @  C! o* ^& c% D0 s2 q) ]- P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。
+ z' a2 p9 I$ f6 n& G/ f不错。

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