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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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1397140 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
+ ]" j8 m' K4 ?' eNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
0 d2 U" ~1 d8 ~  U, x+ Author Affiliations
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3 s( O, a  N; U4 x2 V' P1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan - G) O# y) L6 c  ^  o6 w+ Q
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
: ^' h1 U- w0 H6 d3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
7 t; B1 G/ E' z, @( {4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan ( ?0 f$ y- Y4 I1 ^; ?
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
; [- {1 g/ |8 D$ _0 G+ H* F6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
% {5 {" j4 P+ i/ y: V( T6 u7Kinki University School of Medicine, Osaka 589-8511, Japan , c3 {' U+ y% s' L) }
8Izumi Municipal Hospital, Osaka 594-0071, Japan 3 k2 ]" F7 c4 Y( d: e% _" F
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 2 i$ h: n, ?* [+ v: \
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 8 o5 c. R: @8 a
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. 9 V+ q0 C# ^! S9 Y
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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 ' y* Z- E( W' u3 l
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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
7 ^( R6 F$ l5 s7 d! x: Q3 U+ F2 p( B8 X0 \* p
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 z- {$ w6 A+ j9 p" Q+ K: hPublished online on: Thursday, December 1, 2011 " e$ Y/ M7 A2 ^( O! j  v
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Doi: 10.3892/ol.2011.507 + h5 K% w1 c, A! Q7 N8 J& {5 z

( G/ L3 h1 S8 e. NPages: 405-410
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7 A, j: F2 i; L  ]Abstract:4 c" W3 T2 g1 o+ S, O
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/ ^0 C2 O2 w+ ~: |0 b' F9 q
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
/ P( V, G; I" e# \/ x+ Author Affiliations8 t& t- |5 F) J7 z5 f+ Z0 L
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
% [3 {, t8 c2 ]2Department of Thoracic Surgery, Kyoto University, Kyoto
8 x5 e. s/ Q9 h5 {" `1 A& I( U9 D- T3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
: Q4 o2 h+ h' O. V&#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 + E& x, L: W6 a% k( y' f) i
Received September 3, 2010. / ?; c; o1 ?1 G
Revision received November 11, 2010.
2 p! A* `& p7 ?  k6 ?( o8 nAccepted November 17, 2010. 2 J3 s% l. ]8 g; B! t( h: ?8 k) q- I4 t
Abstract, L1 _  A+ i0 |* n+ [: F8 T
Background: 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. ' N5 u% p6 Q& R/ B1 b8 q4 Z
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. 6 ], R4 R. I# O" f3 F
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. 8 S% a0 ]. Y, p0 C7 e: J. S% U
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。
& v! S0 V2 l1 F4 q5 f3 c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?- i! ^& V& W' F3 x6 e; U: k: k
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 Chemotherapy3 |* v& H% q# Y( d, x/ w
http://clinicaltrials.gov/ct2/show/NCT01523587) ~: Q) e1 Q* ~, r
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC  P/ b2 V4 U# d3 j7 |/ c
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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- h/ T- Q3 `# s& b+ L1 m/ l; K5 U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。" X# y  \* }: m8 R9 A8 c( z( `
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
, {9 O. Q4 J/ y+ S8 U0 b& N2 D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。# Y4 s& R2 ^; x; b
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。
7 s7 c, [! ?7 f2 ^0 m不错。

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