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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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1207716 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
6 G+ ~+ A% ^! [4 B( INOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
- l( _1 t0 \# Y( y- V( `) J( ~8 n9 B+ Author Affiliations0 _7 D9 [0 X; W9 g+ c: I
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
6 L: B. m5 h) ^9 {7 D" U2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan / u# e6 B4 b, d; H7 V
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
& W. M3 E0 e9 a8 `4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
& V* S4 Y- ^# z% a$ c5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan   ?. H! a3 [1 ~
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan ' t) `' T/ t; X* v5 T3 w7 Y+ b
7Kinki University School of Medicine, Osaka 589-8511, Japan ' S3 `( w: B: k3 p- q7 Y
8Izumi Municipal Hospital, Osaka 594-0071, Japan
) N$ a/ M% c- m+ s$ A9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
0 }4 h7 a- }0 _) s9 g8 LCorrespondence 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
* x0 M/ n: J9 qAbstractBackground: 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 5 U: W8 [( Y5 _8 K3 U9 P
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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 0 v* o" Q# M% T( O7 u; D

8 g3 R. u6 z* {) ]5 lAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
  `. N' {; W+ a) b! ]  }  J; L- N+ d) G+ u  y$ `3 R2 W' q
Published online on: Thursday, December 1, 2011
6 U7 |6 X- ^! G9 ~5 u9 V( j/ H- F
Doi: 10.3892/ol.2011.507
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' u- d; G1 o1 x1 ~4 U- \Pages: 405-410 2 Q* f0 k# E6 I
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Abstract:1 O; v: W4 r6 Q
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
$ G( Z, r9 [3 c  g9 nF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
' g% {, D! ^8 k7 U; i: z$ k9 Y) q8 S+ Author Affiliations
, M; t& e8 x; C# S1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
! e- e  k, W2 ^8 z1 Y/ G: ?7 d2Department of Thoracic Surgery, Kyoto University, Kyoto * ?* ~% f4 |% |; V7 G7 B) e
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
, @: r9 p$ ~4 H/ d4 ?4 p) N, u2 U&#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
) c% l( X1 h' O7 T) yReceived September 3, 2010. 4 L: `; n- f1 m
Revision received November 11, 2010. - c3 h0 M" Y- V- h/ O2 H5 `+ S" h
Accepted November 17, 2010.
$ n; j) m, ]5 [  |  hAbstract" Y0 |+ k, I  f8 P5 `! K
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. ; [* z. @. I9 d' Q
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.
$ T& w! @0 {% M7 q$ V1 f# K; W6 \  xResults: 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 E. s3 r6 U  o9 @# aConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. , Z( W/ m) k; U$ `- M# l  a1 s
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。
2 i! d0 K% G' S. R0 f+ G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 Chemotherapy4 ^: L. x$ v( Y: U. z  a, h. ^
http://clinicaltrials.gov/ct2/show/NCT01523587$ a1 A& f: M$ Z: H2 t1 n5 f

8 Q/ h2 o: f9 y7 p  zBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
# _: Q5 b- X/ f# 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 # z9 [8 R( W1 M: @& N
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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。
$ I! k; `4 N4 T' w. G" f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
, h% d6 h1 X" I7 h6 L. W5 L# I) m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。: L- j: e1 D( O: f' g9 R
至今为止,未出 ...

: z4 R5 n7 y1 y* c1 P3 {+ j1 T1 b没有副作用是第一追求,效果显著是第二追求。
% \9 T* R9 s$ r: E) o; f/ j不错。

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