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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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1305794 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 Type4 b  @+ l6 X! @4 @# j) H; r3 I2 m: W
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 3 M6 `  L/ Z! V' t& T1 Q
+ Author Affiliations, Q$ y# ]# b# z9 `! H( |

; T, F6 f6 g% b, C" a1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
$ n3 f  H2 [0 h% ~3 a% `) S2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 0 o+ ]8 H  d! `  B$ ^+ P
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
; H7 \; @$ W% Z+ W9 o! ^4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan . o* K& p1 B. O; `
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 3 m% o# m" a4 j; a
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
9 R  P: m1 n$ Z% o7Kinki University School of Medicine, Osaka 589-8511, Japan
1 O$ A! T0 }* l. |" U. q6 g% d8Izumi Municipal Hospital, Osaka 594-0071, Japan
3 M3 d. h- ]- R/ A) u2 o. e9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan * Y& I; M* T, F2 T
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 & h% T' g, P& s: f2 x
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
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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
+ ^! R/ A6 r* B8 u  Y5 f- P7 ?8 K/ ~' r5 R/ q) w
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 " |: _4 A  z1 G' W" I
, e8 Q# c6 M/ L9 z
Doi: 10.3892/ol.2011.507 4 q; ^. U, K. a+ U) \

& e5 o* q$ K9 e$ [( WPages: 405-410 , O3 V  Q; o* ~  `5 X$ e
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Abstract:5 e' X! \; L2 W
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.$ k* ]) r: D7 S2 \, p5 J# K

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 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  \! C# ~% H! z& V
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 8 w" U6 O$ e# M4 N8 Y+ [) N# w/ ^* ]7 H
+ Author Affiliations
8 h2 \4 `, R; A  D! \0 p9 t1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu   a1 {$ F, j& j, s/ z3 a
2Department of Thoracic Surgery, Kyoto University, Kyoto & |. ~; V  Y- ^) p* @
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
# G  @- D( R8 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
9 e# Z% ^$ E9 C3 i9 ZReceived September 3, 2010. ) w' w1 ]- l' ^) \% ]/ ?
Revision received November 11, 2010.
' ?- A' @& a8 EAccepted November 17, 2010. 5 G7 g* u( V6 q4 ^
Abstract
# n3 r$ R/ n3 |0 A0 ]. ?% VBackground: 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.
. N9 |" ]4 Z" ^! 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.
+ _" A3 S7 {! y# X2 v* wResults: 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. 7 I7 q! Q' N8 d/ G/ i0 a
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。+ A7 f- T* @+ i4 I5 t/ i
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?$ U5 k, _$ d0 P/ F) o* M2 X0 K3 A
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 Chemotherapy6 F7 K1 L2 W! N8 y% f1 R! P. j
http://clinicaltrials.gov/ct2/show/NCT01523587
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% i0 h5 P' Y9 R+ Y; j& M- U6 eBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
: _3 r5 d% c% `% bhttp://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 $ w  G+ V, I6 o9 u5 a/ N4 V
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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。
( G5 \! L: V" Q: z8 K& j/ K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

5 y3 l5 M' V, }3 l9 ~) Z没有副作用是第一追求,效果显著是第二追求。
6 Q% P, D7 c" h! R- u: r/ Q1 @2 L不错。

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