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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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1204616 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' _( q8 p* K: d
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9   c( }  k2 C! f3 ~( K8 \. i
+ Author Affiliations' b; ]8 k) }$ S: l: j
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 2 K5 `1 v7 X# F/ {9 _' d9 @
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
& k( `: A3 l3 @# w- u/ X4 S3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
1 W: k, @% P7 v: l8 W4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan # q, O+ t, ?$ J. ]
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
" I& q2 Q% q/ V1 a6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan - P- m; ?3 y; _% s
7Kinki University School of Medicine, Osaka 589-8511, Japan / J$ J; _/ s+ y4 s/ d/ Q
8Izumi Municipal Hospital, Osaka 594-0071, Japan 0 ^2 H& y1 m0 \& P
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
7 P3 N' h0 v# _+ D6 D3 T" ]# PCorrespondence 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 9 f) ?0 K* E  ]
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. % n* [4 f8 D3 `, k

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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 ) z3 Q" B  L3 }3 N
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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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2 @- x. y- u" v6 Y' mAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  ( z, p! _( B2 `: K# [3 c
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Published online on: Thursday, December 1, 2011
6 }" f) `9 U6 \* u& u+ d/ e+ ]9 |" V! u, u& X% P
Doi: 10.3892/ol.2011.507 ( C9 ?3 U: [* V$ M
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Pages: 405-410 ; _6 S7 [7 ~& \! k" X
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Abstract:) c# A: G  `- \% `) ~8 E6 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 population( Y+ ^3 v2 }3 Y5 ~' Q7 I& T' ]- x
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 3 ?2 c) _$ s) V7 p, n6 h
+ Author Affiliations
8 ?( Z* U' A8 Q& v& U- a5 i1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
$ A8 M* P5 d: i0 M, _2Department of Thoracic Surgery, Kyoto University, Kyoto 4 i) _7 g& J% y2 G6 S( h. n
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan + o# O) l; K' d
&#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
+ G! g! w. F( Q' W$ w/ q& P+ W1 tReceived September 3, 2010. 0 y+ M* e- W" o& b* @& W
Revision received November 11, 2010.
* r5 B3 _  e1 ?1 _+ aAccepted November 17, 2010. 8 d; O0 c+ @( K6 ]: R0 H2 m0 h
Abstract
2 ]; K% h5 a: K6 Q! RBackground: 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. * \# R, i9 L4 n
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 I) p4 O& c& `9 t5 U
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.
5 f8 l% m' q- Z* A) d8 r  GConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. + V# \* t& _+ p* v) m
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。
* J3 A6 T) p* B, }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% y" d, c: Y7 h6 K
http://clinicaltrials.gov/ct2/show/NCT015235875 L: j; [% E% B- a/ n" ~) P2 L

$ O2 d/ v/ G2 v. O  n2 b# _BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC: ]4 I0 L% R1 p; k
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 3 L: ~3 a$ I3 q3 C$ B! }5 {

  J+ f. I3 G  H! E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。5 N$ g: U7 }: k( Y5 m, G- h5 Q
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

  S" ~5 ]6 T% D3 I5 A5 H4 ?没有副作用是第一追求,效果显著是第二追求。
2 _) X. z! x# w7 \' W6 R" H不错。

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