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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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1232569 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
+ I! \" l2 ~9 ]: p7 GNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
; `, |( \1 t4 H% H+ L6 X- e" }/ V+ Author Affiliations; [- l  w% u- n  k$ M

$ l- A$ {6 _3 j3 q& E1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan & e( |: Y" I( N
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan : q# ]* s, Y3 S* W. {# _8 L
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
+ S% @5 `- z, g4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 6 I0 b; B6 E/ t9 v; M1 E
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
. {* Y$ P: f9 [9 I6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan % S" s6 Q$ a3 P5 e5 A6 p
7Kinki University School of Medicine, Osaka 589-8511, Japan + O4 y1 ]& B2 u: C
8Izumi Municipal Hospital, Osaka 594-0071, Japan
: z9 m0 ~, O* d1 J) x3 |8 f, f9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
  l' H; X; O9 S# o" r9 c4 sCorrespondence 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 & V# Q3 y4 K) X& O. b; F. Q$ I0 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. ) u9 `0 c$ P2 ~, y9 ]# I

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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 # {& k2 R1 k! t# l# r7 h
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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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1 J+ H% z; q/ f& }8 G, X* VAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  9 _% h2 ]' e& o. x9 ^& @
% p" e8 t' h2 y& r: _: \9 o% D
Published online on: Thursday, December 1, 2011
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Doi: 10.3892/ol.2011.507 0 Q- r# y1 _# f) N3 X5 U( K7 U
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Pages: 405-410
6 i" ^1 `  r* h8 c( M/ }" i/ P5 C* d! K5 M6 U4 A- Z, Z0 |
Abstract:
/ y; a, J8 t1 fS-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.$ j5 \# `- q  Q( {/ g1 v4 U6 {

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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' K! g2 o8 a/ f4 d
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 . W' \5 w* n5 s1 P% I$ V, P
+ Author Affiliations
& k( q5 c# K! K8 Y  o1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu : y! a% p. T' d$ F9 n) E
2Department of Thoracic Surgery, Kyoto University, Kyoto
: j! d  {$ Z; r4 l8 D3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 5 w" o1 T! _+ m, p1 F5 k% o3 {) a
&#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 0 |) P$ _& P9 i+ I. c. F/ R
Received September 3, 2010. 5 E- i. l' ^$ c$ D& q) a2 ^
Revision received November 11, 2010. ! L- ]) F  ^$ q; G7 W$ h
Accepted November 17, 2010.
* z3 F! k/ A0 U; w" U; oAbstract
1 Y  u& w9 s% @) _. nBackground: 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. 0 I1 G& @5 F" L  Z9 o+ ^" G
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.
- n/ C# u" h* n7 [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.
: c4 T- R$ t0 c8 l% `$ _Conclusion: 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。7 B- I; M; x0 c4 U& D3 I' Y
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
: A8 G. o- k( L' V# d  W* Ahttp://clinicaltrials.gov/ct2/show/NCT01523587
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) y9 Z) x: U1 `BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
* e, M/ Q5 I* \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 , `7 H8 M$ h7 I

% X# Z4 D4 H5 f8 R+ V$ l/ n3 q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。
+ y# _* }$ m/ |! G6 G9 x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
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没有副作用是第一追求,效果显著是第二追求。
) u0 P3 q+ i1 i* `0 b% x" e4 R不错。

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