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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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1157768 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
. }3 ^. q9 E0 ]. j+ PNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 , h, S! P; }" D" v( C- s" X$ A
+ Author Affiliations& k7 T  ?, O2 p; T% s0 ^
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
& Z1 ]1 O* [& V2 T! a: O+ v5 T* ~( C2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
7 u3 B0 B# D' @+ a3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ; J- b. W7 a% Z+ u, O! A
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
4 y* U- U, {# h) K9 @/ B4 M) E! }5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan . Q! m( ]1 \0 \% D/ L+ O3 ^! o
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
9 k4 ?. e9 o8 P: T7Kinki University School of Medicine, Osaka 589-8511, Japan
6 B8 t$ m5 E) T0 M' v+ ?/ s8Izumi Municipal Hospital, Osaka 594-0071, Japan
9 O& U6 p, I+ W  M5 r9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 3 I: _6 S, U) W3 I& I
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 4 P6 N4 n5 K3 w. e4 z9 w
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 ) n; h' S  _0 R3 j( {/ W( i: |8 d

2 H9 T4 [$ p) Q: I+ tAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ' d4 N7 o$ F2 r" L
% ^& J4 s4 u$ B6 {% H
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
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# M: H% r( \/ p0 B, P1 Z0 |Doi: 10.3892/ol.2011.507
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Pages: 405-410 , k! z( Y! e& S' B/ y, d# X

' y& @; g$ n- W' K* v- j9 VAbstract:
' D" b1 I" ]# |! @  h6 |3 QS-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% H, v5 Z0 r2 v. R2 Y( U
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 9 j# D' {; m7 e: U) |1 Y, _6 E
+ Author Affiliations3 A2 M4 o# U1 k# l# ~# J8 d0 w. M
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu   ^' S7 s2 b6 ~; H/ L, i
2Department of Thoracic Surgery, Kyoto University, Kyoto ( y' s4 y7 y6 r' }0 D. H- ~- Y
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan ; [4 U4 v8 i8 e' o: s" o+ h: |
&#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
" t+ h! L( O4 F: qReceived September 3, 2010. 8 I6 G( f2 t/ x, A. N2 ?6 ]$ W
Revision received November 11, 2010.
% q% @; ~8 x' E6 D7 T" \/ P/ x4 ~Accepted November 17, 2010. 7 U: Q) Q7 i6 ~
Abstract
, r" o6 I+ A+ K- t7 m+ O; N8 [( 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.
$ q* S" x) w6 I9 DPatients 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.
4 D: e* M6 J+ Z! L6 f) x( uResults: 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.
6 S3 [( f# t  Z0 vConclusion: 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。
8 f  h3 q5 P4 V" h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: _' T* s$ U6 M$ B; k0 k
http://clinicaltrials.gov/ct2/show/NCT01523587
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; z8 i1 [. v! _& u  }% YBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
$ c# U2 F" x$ l( B$ M1 D2 U" thttp://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 3 k, f! d9 N0 b* j
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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。  O. B, c0 U! c3 r& \
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
3 G# K, A- {- i, ^* N; ?0 [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。
% v/ E' C4 @. l! ?4 \5 O至今为止,未出 ...

' B% k; n( g1 s$ m: m6 i没有副作用是第一追求,效果显著是第二追求。
/ L% P2 n; \; r! w, k. q不错。

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